CA2738496A1 - Compositions for proliferation of cells and related methods - Google Patents

Abstract

We have discovered that p63 inhibition results in increased cellular proliferation. We have also performed a screen for agents capable of increasing cellular proliferation, (e.g., of stem cells such as skin-derived precursors (SKPs)). The invention therefore invention provides compositions, methods, and kits for increasing proliferation of cells, using compounds that decrease p63 expression or activity or using the compounds described herein. The invention also features methods of using these compounds for increasing hair growth, improving skin health, or promoting skin repair in a subject.

Description

COMPOSITIONS FOR PROLIFERATION OF CELLS AND RELATED
METHODS

Background of the Invention The invention relates to compositions and methods useful in the proliferation of cells, particularly stem cells such as skin-derived precursors (SKPs). Also provided are methods for treating a subject having a disease or condition where an increase in SKP proliferation is desired.

Expensive growth factors are often required for cell proliferation, and even then, expansion is often not optimal. Thus, molecules which replace or enhance the actions of growth factors and allow increased expansion of cells in culture are desirable.

In addition, there are inadequate methods for regenerating skin or inducing hair growth in a subject (e.g., for treatment of a disease or condition where regenerating skin or inducing hair growth is beneficial).

Thus, there is a need for molecules that promote the proliferation and self-renewal of cells such as SKPs. These molecules may be highly advantageous for cosmetic and medical purposes.
Summary of the Invention We have discovered that p63 inhibits proliferation of skin-derived precursors (SKPs) and, further have screened for and identified compounds that increase proliferation of SKPs and neuroblastoma cells. On the basis of these discoveries, the invention features methods and compositions useful for increasing cell proliferation, as well as methods for increasing SKP
proliferation in subject (e.g., for treating diseases and conditions where increased SKP proliferation is desired).

Accordingly, in a first aspect, the invention features a method of increasing proliferation of a cell (e.g., cultured in vitro). The method includes contacting the cell with a sufficient amount of a compound that decreases (e.g., selectively decreases) p63 expression or activity, or a compound selected from the group consisting of acyclovir, alprostadil, aristolochic acid, carbadox, chlorpyrifos, cyclocreatine, 7,4'-dimethoxyisoflavone, dorzolamide, S(-)eticlopride, evoxine, guaifenesin, hydroxyprogesterone, kaempferol, linamarin, mexicanolide, MG 624, pramoxine, tannic acid, targinine, and yohimbic acid, or an analog thereof, under conditions that support cell proliferation. The cell may be from a tumor cell line, may be a stem cell (e.g., a SKP), or any cell described herein capable of proliferation. The cell may be a human or non-human cell (e.g., from a mammal such as a mouse or rat). In certain embodiments, the compound is a p63 antibody, or an antigen-binding fragment thereof; an RNAi molecule that decreases p63 expression, or a nucleic acid encoding the RNAi molecule; or a polypeptide substantially identical to a dominant negative form of p63, a fragment thereof, or a nucleic acid encoding such a polypeptide, where the polypeptide or the fragment has dominant negative p63 activity. In embodiments where the cell is cultured in vitro, the culture may include at least one additional growth factor (e.g., FGF2, EGF, NGF, or a combination thereof). The method may involve no substantial change in the differentiation rate of the cells.

In another aspect, the invention features a composition including (a) an isolated cell (e.g., a stem cell such as a SKP, or any cell described herein) and (b) a compound selected from the group consisting of acyclovir, alprostadil, aristolochic acid, carbadox, chlorpyrifos, cyclocreatine, 7,4'-dimethoxyisoflavone, dorzolamide, S(-)eticlopride, evoxine, guaifenesin, hydroxyprogesterone, kaempferol, linamarin, mexicanolide, MG 624, pramoxine, tannic acid, targinine, and yohimbic acid, or an analog thereof, where the compound is present in an amount sufficient to promote proliferation of the stem cell.

2 In another aspect, the invention features a composition including (a) an isolated cell (e.g., a stem cell such as a SKP, or any cell described herein) and (b) a compound that decreases p63 expression or activity, where the compound is present in an amount sufficient to promote proliferation of the cell.

In either of the above two aspects, the composition may further include a growth factor (e.g., FGF2, EGF, NGF, or a combination thereof). The composition may be capable of supporting cell proliferation.

In another aspect, the invention features a kit including (a) a compound that decreases p63 expression or activity (e.g., any described herein) or a compound selected from the group consisting of acyclovir, alprostadil, aristolochic acid, carbadox, chlorpyrifos, cyclocreatine, 7,4'-dimethoxyisoflavone, dorzolamide, S(-)eticlopride, evoxine, guaifenesin, hydroxyprogesterone, kaempferol, linamarin, mexicanolide, MG 624, pramoxine, tannic acid, targinine, and yohimbic acid, or an analog thereof;
and (b) instructions for use of (a) to promote cell proliferation, hair growth, skin repair, or skin health.

In another aspect, the invention features a composition including (a) a compound that decreases p63 expression or activity (e.g., any described herein) or a compound selected from the group consisting of acyclovir, alprostadil, aristolochic acid, carbadox, chlorpyrifos, cyclocreatine, 7,4'-dimethoxyisoflavone, dorzolamide, S(-)eticlopride, evoxine, guaifenesin, hydroxyprogesterone, kaempferol, linamarin, mexicanolide, MG 624, pramoxine, tannic acid, targinine, and yohimbic acid, or an analog thereof, and (b) a topically suitable excipient. The composition may be in the form of a cream or a lotion (e.g., a moisturizing lotion).

In another aspect, the invention features a method of increasing SKP
proliferation in a subject. The method includes administering to the subject a sufficient amount of (a) a compound that inhibits p63 expression or activity;
or (b) a compound selected from the group consisting of acyclovir, alprostadil, aristolochic acid, carbadox, chlorpyrifos, cyclocreatine,

3 7,4'-dimethoxyisoflavone, dorzolamide, S(-)eticlopride, evoxine, guaifenesin, hydroxyprogesterone, kaempferol, linamarin, mexicanolide, MG 624, pramoxine, tannic acid, targinine, and yohimbic acid, or an analog thereof.
The compound can be administered topically, systemically, or by any route described herein. In certain embodiments, the compound that inhibits p63 expression or activity is a p63 antibody or an antigen-binding fragment thereof;
an RNAi molecule that inhibits p63 expression or a nucleic acid encoding the RNAi molecule; or a polypeptide substantially identical to a dominant negative form of p63, a fragment thereof, or a nucleic acid encoding such a polypeptide, where the polypeptide or the fragment has dominant negative p63 activity.
In another aspect, the invention features a method of promoting hair growth in a subject. The method includes administering to the subject a sufficient amount of (a) a compound that inhibits p63 expression or activity or (b) a compound selected from the group consisting of acyclovir, alprostadil, aristolochic acid, carbadox, chlorpyrifos, cyclocreatine, 7,4'-dimethoxyisoflavone, dorzolamide, S(-)eticlopride, evoxine, guaifenesin, hydroxyprogesterone, kaempferol, linamarin, mexicanolide, MG 624, pramoxine, tannic acid, targinine, and yohimbic acid, or an analog thereof.
The compound may be administered topically, systemically, or by any route described herein. In certain embodiments, the compound that inhibits p63 expression or activity may be a p63 antibody or an antigen-binding fragment thereof; an RNAi molecule that inhibits p63 expression or a nucleic acid encoding the RNAi molecule; or a polypeptide substantially identical to a dominant negative form of p63, a fragment thereof, or a nucleic acid encoding the polypeptide, where the polypeptide or the fragment has dominant negative p63 activity.

In another embodiment, the invention features a method of repairing skin in a subject, the method including administering a sufficient amount of (a) a compound that inhibits p63 expression or activity or (b) a compound selected from the group consisting of acyclovir, alprostadil, aristolochic acid, carbadox,

4 chlorpyrifos, cyclocreatine, 7,4'-dimethoxyisoflavone, dorzolamide, S(-)eticlopridc, evoxine, guaifenesin, hydroxyprogesterone, kaempferol, linamarin, mexicanolide, MG 624, pramoxine, tannic acid, targinine, and yohimbic acid, or an analog thereof. In certain embodiments, the subject has a wound, and the compound is administered in an amount sufficient to improve healing of the wound. The compound may be administered topically, systemically, or by any route described herein. In certain embodiments, the compound that inhibits p63 expression or activity is a p63 antibody or an antigen-binding fragment thereof;
an RNAi molecule that inhibits p63 expression or a nucleic acid encoding the RNAi molecule; or a polypeptide substantially identical to a dominant negative form of p63, a fragment thereof, or a nucleic acid encoding such a polypeptide, where the polypeptide or the fragment has dominant negative p63 activity.

In another aspect, the invention features a method of improving skin health in a subject for example, by reducing skin aging (or the appearance of aging) or reducing wrinkles. The method includes administering to the subject a sufficient amount of (a) a compound that inhibits p63 expression or activity or (b) a compound selected from the group consisting of acyclovir, alprostadil, aristolochic acid, carbadox, chlorpyrifos, cyclocreatine, 7,4'-dimethoxyisoflavone, dorzolamide, S(-)eticlopride, evoxine, guaifenesin, hydroxyprogesterone, kaempferol, linamarin, mexicanolide, MG 624, pramoxine, tannic acid, targinine, and yohimbic acid, or an analog thereof.
The compound may be administered topically, systemically, or by any route described herein. In certain embodiments, the compound that inhibits p63 expression or activity is a p63 antibody or an antigen-binding fragment thereof;

an RNAi molecule that inhibits p63 expression or a nucleic acid encoding the RNAi molecule; or a polypeptide substantially identical to a dominant negative form of p63, a fragment thereof, or a nucleic acid encoding the polypeptide, where the polypeptide or the fragment has dominant negative p63 activity.

In any of the above methods, the subject may be a human.

5 In another aspect, the invention features a method of identifying a compound capable of altering cell proliferation, the method including (a) contacting (e.g., in vitro) a SKP (e.g., human or non-human SKP, such as a mouse or rat SKP) with a candidate compound, and (b) determining the proliferation rate of the SKP, where an alteration in the proliferation rate of the SKP in the presence of the compound as compared to in the absence of the compound, indicates that the compound alters the rate of cell proliferation.
In certain embodiments, the compound is selected from a chemical library.

In embodiments of the above aspects of the invention where the subject is administered acyclovir or analog thereof, the subject may not suffer from, or be diagnosed with, herpes (e.g., genital herpes) or chicken pox. In embodiments where the subject is administered alprostadil or an analog thereof, the subject may not suffer from, or be diagnosed with erectile dysfunction or be in need of weight loss (e.g., be overweight or obese). In embodiments where the subject is administered aristolochic acid or an analog thereof, the subject may not be in need of weight loss (e.g., be overweight or obese). In embodiments where the subject is administered dorzolamide or an analog thereof, the subject may not have, or may not be diagnosed with, increased intraocular pressure (e.g., ocular hypertension or open-angle glaucoma). In embodiments where the subject is administered guaifenesin or an analog thereof, the subject may not be in need of an expectorant (e.g., suffering from a cold, an allergy, or airway infection). In embodiments where the subject is administered hydroxyprogesterone, the subject may not be suffering from, or may not be diagnosed with, congenital adrenal hyperplasia, 2 1 -hydroxylase deficiency, or breast neoplasms, or is not at risk of having a preterm birth.
In embodiments where the subject is administered pramoxine, the subject may not be in need of a topical anesthetic (e.g., due to itching, burning, or other pain).
In embodiments where the subject is administered yohimbic acid, the subject may not be suffering from erectile dysfunction, panic disorder, alcoholism, or depression.

6 In any of the above aspects, the SKP may express any one, two, three, four, five, or more of the markers for SKPs described herein, or may not express any one, two three, four, five, or more of the markers not expressed by SKPs. In any of the above aspects, the analogs of the compounds may be any analog described herein.

By "decreasing expression" of a gene or protein is meant reducing (e.g., by 5%,10%,25%, 50%, 75%, 90%, 95%, 99%, or 99.9%) in the amount the gene or protein produced. Decreased expression may occur, for example, by a reduction in transcription, translation, or mRNA processing.
By "decreased activity" is meant a reduction (e.g., by 5%, 10%, 25%, 50%, 75%, 90%, 95%, 99%, or 99.9%) by in the total activity of a protein in a cell. Reduction of activity may result, for example, from direct inhibition of the protein (e.g., by a compound that specifically binds the protein), increased degradation or processing, or decreased expression of the protein.

By a compound or composition that "selectively inhibits" a target protein (e.g., p63) is meant a compound or composition that decreases expression or activity of the target protein and (a) binds specifically to the target protein (e.g., a small molecule or an antibody) and decreases its activity, (b) binds specifically to an mRNA encoding the target protein, thereby decreasing expression of the protein, or (c) prevents the target protein from performing its normal function (e.g., by binding to a binding partner of the target protein).

A compound which "specifically binds" a target molecule is a compound which recognizes and binds the target, but which does not substantially recognize and bind other molecules.

By "subject" is meant a human or non-human animal (e.g., a mammal).
By a cell which does "not express" a protein or gene is meant that expression of the protein or gene cannot be detected by standard methods. In the case of cell surface markers, expression can be measured by flow cytometry, using a cut-off value as obtained from negative controls (i.e., cells known to lack the antigen of interest) or by isotype controls (i.e., measuring

7 non-specific binding of the antibody to the cell). Thus, a cell that "does not express" a marker appears similar to the negative control for that marker. For gene expression, a gene "does not express" if the presence of its mRNA cannot be visually detected on a standard agarose gel following standard PCR
protocols.
A nucleic acid molecule or polypeptide is said to be "substantially identical" to a reference molecule if it exhibits, over its entire length, at least 50% or 55% identity, preferably at least 60%, 65%, or 70% identity, more preferably at least 75% or 85% identity, and most preferably at least 90%, 95%, or 99% identity to the sequence of the reference molecule. For polypeptides, the length of comparison sequences is at least 16 amino acids, preferably at least 20 amino acids, more preferably at least 25 amino acids, and most preferably at least 35 amino acids. For nucleic acid molecules, the length of comparison sequences is at least 50 nucleotides, preferably at least 60 nucleotides, more preferably at least 75 nucleotides, and most preferably at least 110 nucleotides.

The term "antibody" is used in the broadest sense and specifically covers, for example, single monoclonal antibodies against p63, antibody compositions with polyepitopic specificity, single chain antibodies, nanobodies, and fragments of antibodies. "Antibody" includes intact immunoglobulin or antibody molecules, polyclonal antibodies, multispecific antibodies (e.g., bispecific antibodies formed from at least two intact antibodies), and immunoglobulin fragments (such as Fab, F(ab')2, or Fv), so long as they exhibit any of the desired properties (e.g., antigen binding) described herein.

"Antibody fragments" comprise a portion of an intact antibody, generally the antigen binding or variable region of the intact antibody.
Examples of antibody fragments include Fab, Fab', F(ab')2, and Fv fragments, diabodies, single chain antibody molecules, and multispecific antibodies formed from antibody fragments.

8

9 PCT/US2009/058723 "Humanized" forms of non-human (e.g., murine) antibodies are specific chimeric immunoglobulins, immunoglobulin chains, or fragments thereof (such as Fv, Fab, Fab', F(ab')2 or other antigen-binding subsequences of antibodies) which contain minimal sequence derived from non-human immunoglobulin.
A "human antibody" is one which possesses an amino acid sequence which corresponds to that of an antibody produced by a human and/or has been made using any of the techniques for making human antibodies known in the art. A "human antibody" includes antibodies comprising at least one human heavy chain polypeptide or at least one human light chain polypeptide.
By "small molecule" is meant a molecule having a molecular weight of less than about 1000 Da (e.g., less than 900, 800, 700, 600, 500, or 400 Da).
In the generic descriptions of compounds of this invention, the number of atoms of a particular type in a substituent group is generally given as a range, e.g., an alkyl group containing from 1 to 4 carbon atoms or C1a alkyl.

Reference to such a range is intended to include specific references to groups having each of the integer number of atoms within the specified range. For example, an alkyl group from 1 to 4 carbon atoms includes each of C1, C2, C3, and C4. A C1_12 heteroalkyl, for example, includes from 1 to 12 carbon atoms in addition to one or more heteroatoms. Other numbers of atoms and other types of atoms may be indicated in a similar manner.

As used herein, the terms "alkyl" and the prefix "alk-" are inclusive of both straight chain and branched chain groups and of cyclic groups, i.e., cycloalkyl. Cyclic groups can be monocyclic or polycyclic and preferably have from 3 to 12 ring carbon atoms, inclusive. Exemplary cyclic groups include cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl groups.

By "C1-4 alkyl" is meant a branched or unbranched hydrocarbon group having from 1 to 4 carbon atoms. A C1-4 alkyl group may be substituted or unsubstituted. Exemplary substituents include alkoxy, aryloxy, sulfhydryl, alkylthio, arylthio, halide, hydroxyl, fluoroalkyl, perfluoralkyl, amino, aminoalkyl, disubstituted amino, quaternary amino, hydroxyalkyl, carboxyalkyl, and carboxyl groups. C1-4 alkyls include, without limitation, methyl, ethyl, n-propyl, isopropyl, cyclopropyl, cyclopropylmethyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, and cyclobutyl.
By "C2_4 alkenyl" is meant a branched or unbranched hydrocarbon group containing one or more double bonds and having from 2 to 4 carbon atoms. A
C2_4 alkenyl may optionally include monocyclic or polycyclic rings, in which each ring desirably has from three to six members. The C2-4 alkenyl group may be substituted or unsubstituted. Exemplary substituents include alkoxy, aryloxy, sulfhydryl, alkylthio, arylthio, halide, hydroxyl, fluoroalkyl, perfluoralkyl, amino, aminoalkyl, disubstituted amino, quaternary amino, hydroxyalkyl, carboxyalkyl, and carboxyl groups. C2-4 alkenyls include, without limitation, vinyl, allyl, 2-cyclopropyl- l -ethenyl, 1-propenyl, 1-butenyl, 2-butenyl, 3 -butenyl, 2-methyl- l -propenyl, and 2-methyl-2-propenyl.
By "C2_1 alkynyl" is meant a branched or unbranched hydrocarbon group containing one or more triple bonds and having from 2 to 4 carbon atoms. A
C2_+ alkynyl may optionally include monocyclic, bicyclic, or tricyclic rings, in which each ring desirably has five or six members. The C2-4 alkynyl group may be substituted or unsubstituted. Exemplary substituents include alkoxy, aryloxy, sulfhydryl, alkylthio, arylthio, halide, hydroxy, fluoroalkyl, perfluoralkyl, amino, aminoalkyl, disubstituted amino, quaternary amino, hydroxyalkyl, carboxyalkyl, and carboxyl groups. C2-4 alkynyls include, without limitation, ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, and 3-butynyl.

By "C2_6 heterocyclyl" is meant a stable 5- to 7-membered monocyclic or 7- to 14-membered bicyclic heterocyclic ring which is saturated, partially unsaturated, or unsaturated (aromatic), and which consists of 2 to 6 carbon atoms and 1, 2, 3, or 4 heteroatoms independently selected from N, 0, and S
and including any bicyclic group in which any of the above-defined heterocyclic rings is fused to a benzene ring. The heterocyclyl group may be substituted or unsubstituted. Exemplary substituents include alkoxy, aryloxy, sulfhydryl, alkylthio, arylthio, halide, hydroxy, fluoroalkyl, perfluoralkyl, amino, aminoalkyl, disubstituted amino, quaternary amino, hydroxyalkyl, carboxyalkyl, and carboxyl groups. The nitrogen and sulfur heteroatoms may optionally be oxidized. The heterocyclic ring may be covalently attached via any heteroatom or carbon atom which results in a stable structure, e.g., an imidazolinyl ring may be linked at either of the ring-carbon atom positions or at the nitrogen atom. A nitrogen atom in the heterocycle may optionally be quaternized. Preferably when the total number of S and 0 atoms in the heterocycle exceeds 1, then these heteroatoms are not adjacent to one another.

Heterocycles include, without limitation, 1H-indazole, 2-pyrrolidonyl, 2H,6H-1,5,2-dithiazinyl, 2H-pyrrolyl, 3H-indolyl, 4-piperidonyl, 4aH-carbazole, 4H-quinolizinyl, 6H- 1,2,5-thiadiazinyl, acridinyl, azocinyl, benzimidazolyl, benzofuranyl, benzothiofuranyl, benzothiophenyl, benzoxazolyl, benzthiazolyl, benztriazolyl, benztetrazolyl, benzisoxazolyl, benzisothiazolyl, benzimidazalonyl, carbazolyl, 4aH-carbazolyl, b-carbolinyl, chromanyl, chromenyl, cinnolinyl, decahydroquinolinyl, 2H,6H-1,5,2-dithiazinyl, dihydrofuro[2,3-b]tetrahydrofuran, furanyl, furazanyl, imidazolidinyl, imidazolinyl, imidazolyl, 1 H-indazolyl, indolenyl, indolinyl, indolizinyl, indolyl, isobenzofuranyl, isochromanyl, isoindazolyl, isoindolinyl, isoindolyl, isoquinolinyl, isothiazolyl, isoxazolyl, morpholinyl, naphthyridinyl, octahydroisoquinolinyl, oxadiazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, oxazolidinyl, oxazolyl, oxazolidinylperimidinyl, phenanthridinyl, phenanthrolinyl, phenarsazinyl, phenazinyl, phenothiazinyl, phenoxathiinyl, phenoxazinyl, phthalazinyl, piperazinyl, piperidinyl, pteridinyl, piperidonyl, 4-piperidonyl, pteridinyl, purinyl, pyranyl, pyrazinyl, pyrazolidinyl, pyrazolinyl, pyrazolyl, pyridazinyl, pyridooxazole, pyridoimidazole, pyridothiazole, pyridinyl, pyridyl, pyrimidinyl, pyrrolidinyl, pyrrolinyl, pyrrolyl, quinazolinyl, quinolinyl, 4H-quinolizinyl, quinoxalinyl, quinuclidinyl, carbolinyl, tetrahydrofuranyl, tetrahydroisoquinolinyl, tetrahydroquinolinyl, 6H-1,2,5-thiadiazinyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, thianthrenyl, thiazolyl, thienyl, thienothiazolyl, thienooxazolyl, thienoimidazolyl, thiophenyl, triazinyl, 1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,5-triazolyl, 1,3,4-triazolyl, and xanthenyl. Preferred 5 to 10 membered heterocycles include, but are not limited to, pyridinyl, pyrimidinyl, triazinyl, furanyl, thienyl, thiazolyl, pyrrolyl, pyrazolyl, imidazolyl, oxazolyl, isoxazolyl, tetrazolyl, benzofuranyl, benzothiofuranyl, indolyl, benzimidazolyl, 1H-indazolyl, oxazolidinyl, isoxazolidinyl, benzotriazolyl, benzisoxazolyl, oxindolyl, benzoxazolinyl, quinolinyl, and isoquinolinyl. Preferred 5 to 6 membered heterocycles include, without limitation, pyridinyl, pyrimidinyl, triazinyl, furanyl, thienyl, thiazolyl, pyrrolyl, piperazinyl, piperidinyl, pyrazolyl, imidazolyl, oxazolyl, isoxazolyl, and tetrazolyl.

By "C6-12 aryl" is meant an aromatic group having a ring system comprised of carbon atoms with conjugated 7t electrons (e.g., phenyl). The aryl group has from 6 to 12 carbon atoms. Aryl groups may optionally include monocyclic, bicyclic, or tricyclic rings, in which each ring desirably has five or six members. The aryl group may be substituted or unsubstituted. Exemplary substituents include alkyl, hydroxy, alkoxy, aryloxy, sulfhydryl, alkylthio, arylthio, halide, fluoroalkyl, carboxyl, hydroxyalkyl, carboxyalkyl, amino, aminoalkyl, monosubstituted amino, disubstituted amino, and quaternary amino groups.

By "C7-14 alkaryl" is meant an alkyl substituted by an aryl group (e.g., benzyl, phenethyl, or 3,4-dichlorophenethyl) having from 7 to 14 carbon atoms.
By "C3-10 alkheterocyclyl" is meant an alkyl substituted heterocyclic group having from 3 to 10 carbon atoms in addition to one or more heteroatoms (e.g., 3-furanylmethyl, 2-furanylmethyl, 3-tetrahydrofuranylmethyl, or 2-t etrahydro furanylmethyl) .

By "C1_7 heteroalkyl" is meant a branched or unbranched alkyl, alkenyl, or alkynyl group having from 1 to 7 carbon atoms in addition to 1, 2, 3, or 4 heteroatoms independently selected from the group consisting of N, 0, S, and P. Heteroalkyls include, without limitation, tertiary amines, secondary amines, ethers, thioethers, amides, thioamides, carbamates, thiocarbamates, hydrazones, imines, phosphodiesters, phosphoramidates, sulfonamides, and disulfides. A
heteroalkyl may optionally include monocyclic, bicyclic, or tricyclic rings, in which each ring desirably has three to six members. The heteroalkyl group may be substituted or unsubstituted. Exemplary substituents include alkoxy, aryloxy, sulfhydryl, alkylthio, arylthio, halide, hydroxyl, fluoroalkyl, perfluoralkyl, amino, aminoalkyl, disubstituted amino, quaternary amino, hydroxyalkyl, hydroxyalkyl, carboxyalkyl, and carboxyl groups. Examples of C1_7 heteroalkyls include, without limitation, methoxymethyl and ethoxyethyl.
By "halide" or "halogen" is meant bromine, chlorine, iodine, or fluorine.
By "fluoroalkyl" is meant an alkyl group that is substituted with a fluorine atom.

By "perfluoroalkyl" is meant an alkyl group consisting of only carbon and fluorine atoms.

By "carboxyalkyl" is meant a chemical moiety with the formula -(R)-COOH, wherein R is selected from C1_7 alkyl, C2_7 alkenyl, C2_7 alkynyl, C2_6 heterocyclyl, C6_12 aryl, C7_14 alkaryl, C3_10 alkheterocyclyl, or C1-7 heteroalkyl.

By "hydroxyalkyl" is meant a chemical moiety with the formula -(R)-OH, wherein R is selected from C1_7 alkyl, C2_7 alkenyl, C2_7 alkynyl, C2_6 heterocyclyl, C6_12 aryl, C7_14 alkaryl, C3_10 alkheterocyclyl, or C1_7 heteroalkyl.

By "alkoxy" is meant a chemical substituent of the formula -OR, wherein R is selected from C1_7 alkyl, C2_7 alkenyl, C2_7 alkynyl, C2_6 heterocyclyl, C6_12 aryl, C7_14 alkaryl, C3_10 alkheterocyclyl, or C1_7 heteroalkyl.

By "aryloxy" is meant a chemical substituent of the formula -OR, wherein R is a C6_12 aryl group.

By "alkylthio" is meant a chemical substituent of the formula -SR, wherein R is selected from C1_7 alkyl, C2_7 alkenyl, C2_7 alkynyl, C2_6 heterocyclyl, C6-12 aryl, C7_14 alkaryl, C3_10 alkheterocyclyl, or C1_7 heteroalkyl.

By "arylthio" is meant a chemical substituent of the formula -SR, wherein R is a C6-12 aryl group.

By "quaternary amino" is meant a chemical substituent of the formula -(R)-N(R')(R")(R"')+, wherein R, R', R", and R"' are each independently an alkyl, alkenyl, alkynyl, or aryl group. R may be an alkyl group linking the quaternary amino nitrogen atom, as a substituent, to another moiety. The nitrogen atom, N, is covalently attached to four carbon atoms of alkyl, heteroalkyl, heteroaryl, and/or aryl groups, resulting in a positive charge at the nitrogen atom.

Other features and advantages of the invention will be apparent from the following Detailed Description, the drawings, and the claims.

Brief Description of the Drawings Figure IA is a photograph of a gel showing that wild-type SKPs express TAp63 mRNA, whereas SKPs from p63 null mice do not.

Figure lB is photograph of a gel showing that SKPs from both wild-type and p63 null mice express p53, but do not express p73. GAPDH is shown as a control.

Figure 1 C is a set of photomicrographs showing that p63 is expressed in wild-type SKPs, but not in SKPs from p63 null mice (top panels). Hoescht stained cells are shown in the corresponding lower panels.

Figure 1 D is a set of photomicrographs showing that both SK-Ps from both wild-type and p63 null mice express the SKP markers fibronectin, nestin, vimentin, and SMA.

Figure 1 E is a set of photomicrographs showing that the proliferation marker K1167 is expressed at higher levels in SKPs from p63 null mice than in wild-type SKPs. Results using whisker and back cells from neonatal mice, as well as using whisker cells from one-month-old mice, are shown.

Figure IF is graph showing increasing Ki167 expression in p63 null mice as compared to wild-type mice in SKPs taken from E18, P1, and P30 mice.

Figure 1G is a graph showing that newborn TAp63-/- and E18 p63-/-SKPs self-renewed approximately 4 times more robustly than did wild-type SKPs and SKPs from one-month-old mice proliferated and self-renewed about 1.5 fold more than wild-type SKPs.

Figure 1 H is a photograph of a gel showing that the p57 mRNA
expression is reduced in SKPs from p63 null mice as compare to those from wild-type mice.

Figure I I is a set of photomicrographs showing p57 expression in wild-type, p63-/-, and TAp63-/- cells.

Figure 1J is a photograph of a gel showing that, using RT-PCR, p63 is was bound to a previously defined binding site in the p57 promoter.

Figure 1K is a graph showing the percentage of p57 positive cells in wild-type and in Tap63-/- cells.

Figure 1 L is a set of photomicrographs showing immunostaining for p57Kip2 and Ki67 in TAp63-/- SKPs, plated on an adherent 4-well chamber slides, two days after transfection with or without a pCMV-p57Kip2 expression vector. Cells were counterstained with Hoechst 33258. Transfected p57-positive cells were never double-labelled for Ki67. The images are taken at 200x magnification with n=3 independent experiments.

Figure 2A is a set of photomicrographs showing that wild-type and p63-/- SKPs are capable of differentiating to neural and mesoderm subtypes. Left, neurofilament medium (NFM) expression; center, smooth muscle actin (SMA) expression; right, glial fibrillary acidic protein (GFAP) and S 100J3 expression.

Figure 2B is a set of photomicrographs showing that both wild-type and p63-/- SKPs, when transplanted into the neural crest migratory stream of HH
stage 18 chicks in ovo, migrated into neural crest targets.
Figure 3 is a schematic diagram of an exemplary screening procedure described herein.

Figures 4A shows a schematic diagram of the sphere formation assay employed to confirm the hits identified in the screen.

Figure 4B is a graph showing the effects of increasing concentrations of rapamycin on sphere formation in various cell lines.

Figure 4C is a graph showing inhibition of tumor formation by rapamycin and vinblastine.

Figure 5 is a graph showing the effects of MG 624 on SKPs (left) and neuroblastoma (right) proliferation at various concentrations. At 200 nM, SKP
proliferation was increased.

Figures 6A-6E are graphs showing dose-response curves for proliferation of human SKPs in response to MG624 (Figure 6A), GSK3(3 (Figure 6B), pramoxine (Figure 6C), kaempferol (Figure 6D), and alprostadil (Figure 6E) in presence of EGF and FGF2.

Detailed Description We have discovered that the p63 pathway is involved in inhibition of proliferation of skin-derived precursors (SKPs). The invention thus features methods of increasing proliferation of a cell (e.g., a stem cell such as a SKP) by inhibiting p63 expression or activity.

In addition, we have performed a screen to identify agents useful for enhancing cellular proliferation. This screen resulted in identification compounds including acyclovir, alprostadil, aristolochic acid, carbadox, chlorpyrifos, cyclocreatine, 7,4'-dimethoxyisoflavone, dorzolamide, S(-)eticlopride, evoxine, guaifenesin, hydroxyprogesterone, kaempferol, linamarin, mexicanolide, MG 624, pramoxine, tannic acid, targinine, and yohimbic acid.

On this basis, these compounds, or analogs of these compounds, can be used to increase proliferation of cells, including SKPs or neuroblastoma cells. As SKPs are known to be involved in skin regeneration and hair growth, stimulation of SKPs using these compounds can enhance skin repair (e.g., wounded skin), improve dermal maintenance or skin health, or promote hair growth in a subject.

Cells The compounds identified herein may be used to increase proliferation of any cell that is capable of proliferation, such as tumor cell lines (e.g., neuroblastoma) or stem cells. In certain embodiments, the cell is a stem cell such as a SKP cell. Other stem cells include embryonic stem cells and adult stem cells such as mesenchymal cells and hematopoietic stem cells.

SKPs are described in U.S. Patent Application Publication Nos.
2004/0033597 and 2007/0248574. SKPs can express at least one, two, three, or more of the following molecular markers: nestin, WNT- 1, vimentin, versican, fibronectin, S1000, slug, snail, twist, Pax3, Sox9, Dermo-1, and SHOX2. SKPs may also express increased levels of slug, snail, twist, and Pax3 relative to central nervous system neural stem cells. Desirably, the multipotent stem cells of the invention do not express measurable levels of at least one, two, three, or more of the following molecular markers: tyrosinase, c-kit, tryp- 1, and DCT, which are markers of melanoblasts and melanocytes. The multipotent stem cells also may not express of one or more of the following markers of Schwann cells: MBP, P0, p75NTR, and SOX10.

SKPs are capable of differentiating into various non-neural cells (e.g., hair follicle cell, bone cell, smooth muscle cell, or adipocyte) and neural cells (e.g., a neuron, astrocyte, Schwann cell, or oligodendrocyte).

SKPs can be isolated as described in the art. In one example, dorsal or facial skin from mouse embryos (E15-19), mouse or rat neonates (P2-P6), or adults (3 weeks and older) was dissected from the animal and cut into 2-3 mm2 pieces. Tissue was digested with 0.1% trypsin for 10-45 min at 37 C, mechanically dissociated and filtered through a 40 m cell strainer (Falcon).
Cell culture The cells (e.g., SKPs) may be cultured under standard cell culture conditions, such as those described herein or known in the art. In one example, SKPs are cultured as described in Toma et al. (Nat. Cell Biol. 3:778-784, 2001).
Dissociated cells (e.g., as described above) were pelleted and plated in DMEM-F 12, 3:1 (Invitrogen), containing 20 ng/ml EGF and 40 ng/ml FGF2 (both from Collaborative Research), hereafter referred to as proliferation medium. Cells were cultured in 25 cm2 tissue culture flasks (Falcon) in a 37 C, 5% CO2 tissue culture incubator. SKPs were passaged by mechanically dissociating spheres and splitting 1:3 with 75% new medium and 25%
conditioned medium from the initial flask. For neuronal differentiation, SKP

spheres or primary dissociated skin cells were mechanically dissociated and plated on chamber slides (Nunc) coated with poly-D-lysine/laminin in DMEM-F12 3:1 supplemented with 40 ng/ml FGF2 and 10% FBS (BioWhittaker) for 5-7 days. Cells were then cultured an additional 5-7 days in the same medium without FGF2 but with the addition of 10 ng/ml NGF (Cedar Lane), 10 ng/ml BDNF (Peprotech), and 10 ng/ml NT3 (Peprotech). For Schwann cell differentiation, dissociated spheres were cultured in DMEM-F12 3:1 supplemented with 10% FBS for 7 days, then switched to the same medium supplemented with 4 M forskolin (Sigma).

Compounds that decrease p63 expression or activity The compositions, methods, and kits of the invention may employ a compound that decreases p63 expression or activity. These compounds can be used either in place of or in addition to other growth factors (e.g., FGF2 or EGF). In certain embodiments, the addition of a compound that decreases p63 expression or activity allows for the use of a reduced concentration of another growth factor or factors (e.g., FGF2 or EGF). Exemplary compounds include RNAi molecules that target p63 mRNA, antibodies that specifically bind p63, and dominant negative forms of p63.

p63 RNAi molecules RNAi molecules such as siRNA molecules that target p63 are known in the art or can be designed and tested for RNA interference activity. p63 RNAi molecules are commercially available (e.g., from Santa Cruz Biotechnology, Inc., Santa Cruz, CA, Catalog No. sc-36161). Additional RNAi molecules (e.g., siRNA molecules) can be designed based on the human p63 mRNA
sequence (NCBI accession Nos. NM_003722, NM_001114978, NM_001114979, NM_001114980, NM_001114981, and NM_001114982) or the corresponding mouse (NCBI accession Nos. NM_011641, NM_001127259, NM_001127260, NM_001127261, NM_001127262, NM_001127263, NM_001127264, NM_001127265) or rat (NCBI accession Nos.
NM_001127339, NM_001127341, NM_OO1127342, NM_001127343, NM_001127344, and NM_019221) sequences.

p63 antibodies Anti-p63 antibodies may be employed in the compositions, methods, and kits of the invention. Any antibody or antibody variant (e.g., monoclonal, polyclonal, human, humanized, single chain), a fragment thereof, or a nanobody can be employed.

Such antibodies are commercially available (e.g., from Abcam, Inc., Cambridge, MA, Catalog No. ab735, or from Santa Cruz Biotechnology, Inc., Catalog No. sc-843 1). Additional antibodies (polyclonal or monoclonal) against p63 or regions of p63 can also be generated using methods known in the art.

Humanized antibodies can be generated following the method of Winter and co-workers (Jones et al., Nature, 321:522-525, 1986; Riechmann et al., Nature, 332:323-327 (1988); Verhoeyen et al., Science, 239:1534-1536 (1988)), by substituting rodent CDRs or CDR sequences for the corresponding sequences of a human antibody.

Accordingly, such "humanized" antibodies are chimeric antibodies wherein substantially less than an intact human variable domain has been substituted by the corresponding sequence from a non-human species. In practice, humanized antibodies are typically human antibodies in which some CDR residues and possibly some FR residues are substituted by residues from analogous sites in rodent antibodies.
Human monoclonal antibodies can be made by the hybridoma method, as is known in the art (see, e.g., Kozbor, J. Immunol. 133, 3001, 1984, and Brodeur et al., Monoclonal Antibody Production Techniques and Applications, pp. 51-63 (Marcel Dekker, Inc., New York, 1987)).
Nanobodies can be generated by immunization of an animal (e.g., a camel or llama) which produces nanobodies, which can then be purified using standard techniques.

Single chain Fv fragments may be produced such as described in Iliades et al., FEBS Letters, 409:437-441 (1997). Coupling of such single chain fragments using various linkers is described in Kortt et al., Protein Engineering,

10:423-433 (1997).

The compositions, methods, and kits of the invention can also include a p63 antibody fragment (e.g., a fragment of a murine, human or humanized antibody, and antibody variants). Such fragments can be derived by proteolytic digestion of intact antibodies (see, e.g., Morimoto et al., J. Biochem.
Biophys.
Methods 24:107-117 (1992) and Brennan et al., Science 229:81, 1985) or can be produced directly by recombinant host cells. For example, Fab'-SH
fragments can be directly recovered from E. coli and chemically coupled to form F(ab')2 fragments (Carter et al., Bio/Technology 10:163-167, 1992).
Single chain Fv fragments may be produced such as described in Iliades et al., FEBS Letters, 409:437-441 (1997). Coupling of such single chain fragments using various linkers is described in Kortt et al., Protein Engineering, 10:423-433, 1997.

Triabodies can also be used in the compositions, methods, and kits of the invention. Such antibodies are described for instance in Iliades et al., supra and Kortt et al., supra.
The antibodies of the present invention may be modified by conjugating the antibody to an agent (e.g., any of the compounds described herein).
Further antibody modifications are also contemplated. For example, the antibody may be linked to one of a variety of nonproteinaceous polymers, e.g., polyethylene glycol, polypropylene glycol, polyoxyalkylenes, or copolymers of polyethylene glycol and polypropylene glycol. The antibody also may be entrapped in microcapsules prepared, for example, by coacervation techniques or by interfacial polymerization (for example, hydroxymethylcellulose or gelatin-microcapsules and poly-(methylmethacylate) microcapsules, respectively), in colloidal drug delivery systems (for example, liposomes, albumin microspheres, microemulsions, nano-particles and nanocapsules), or in macroemulsions. Such techniques are disclosed in Remington: The Science and Practice of Pharmacy, 20th edition, 2000, ed. A.R. Gennaro, Lippincott Williams & Wilkins, Philadelphia. To increase the serum half-life of the antibody, one may incorporate a salvage receptor binding epitope into the antibody (especially an antibody fragment), as described in U.S. Pat. No. 5,739,277, for example. A
"salvage receptor binding epitope" is an epitope of the Fe region of an IgG
molecule (e.g., IgGl, IgG2, IgG3, or IgG4) that is responsible for increasing the in vivo serum half-life of the IgG molecule.
Dominant negative p63 Dominant negative forms of p63, polypeptides substantially identical to such dominant negative forms and having dominant negative activity, or fragments thereof having dominant negative activity can be used in the compositions, methods, and kits of the invention. Forms of p63 with the N-terminal transactivation domain are termed TAp63, whereas those lacking this domain (AN-p63 isoforms) have dominant negative activity. See, e.g., Ghioni et al., Mol Cell Biol 22:8659-8668, 2002. Exemplary sequences encoding dominant negative proteins are known in the art and include DN p63 alpha (NCBI accession Nos. AAG45610 and AAC62636 (human); AAP87985 and AAC62644 (mouse)); DN p63 beta (NCBI accession Nos. AAG45611 and AAC62638 (human); AAP87986 and AAC62643 (mouse)); and DN p63 gamma (NCBI accession Nos. AAG45612 and AAC62634 (human);
AAP87987 and AAC62642 (mouse)). Other dominant negative p63 polypeptides can sequences substantially identical to those sequences, or may contain chemical modifications, as is known in the art.

Gene therapy Decreases in p63 expression or activity may also be achieved through introduction of a gene vector into a subject. To increase cellular proliferation, enhance skin repair or skin health, or promote hair growth, p63 expression or activity may be decreased, for example, by administering to a subject a vector containing a polynucleotide sequence encoding a dominant negative form of p63 or an RNAi molecule that targets p63 mRNA, operably linked to a promoter capable of driving expression in targeted cells. Any standard gene therapy vector and methodology may be employed for such administration.
Compounds Based on the results of the screen described herein, we have identified compounds capable of increasing proliferation. Accordingly, these compounds, or analogs of these compounds, may be used in methods for increasing proliferation (e.g., without affecting differentiation) in vivo or in vitro of any type of cell capable of proliferation (e.g., stem cells, such as SKPs). The compounds may be used in conjunction with any cell culture techniques known in the art. Use of these compounds may allow for reduced concentrations of other growth factors. In addition, the compounds can also be used to treat a disease or condition where increases in SKP proliferation are desirable (e.g., those described herein).

Acyclovir The compositions, methods, and kits of the invention may include acyclovir or an analog thereof. Acyclovir has the structure:
O
HN N
HZN N N
~/OH

Analogs of acyclovir are described in U.S. Patent No. 4,199,574 and have the structure:
R, N N
N R

where X is sulfur or oxygen, R1 is H, halogen, OH, C1_4 alkoxy, azide, thio, C1_6 alkylthio, amino, C1_6 alkylamino or dialkylamino; R2 is H, halogen, C1.4 alkylthio, acylamino, amino or azide; R3 is H, straight or branch chain or cyclic C1_6 alkyl, C1_6 hydroxyalkyl, benzyloxyalkyl, or phenyl; R4 is H, OH, or alky;
R5 is H, OH, NH2, C1_4 alkyl, C1_4 hydroxyalkyl, benzyloxy, benzoyloxy, benzoyloxymethyl, sulfamoyloxy, phosphate carboxypropiamyloxy, straight chain or cyclic acyloxy having from 1 to 8 carbon atoms e.g., acetoxy or substituted carbamoyl group of formula NH.CO-Z wherein Z is alkyl, aryl or aralkyl optionally substituted by one or more of sulfonyl, amino, carbamoyl or halogen; R6 is H or alkyl (e.g., when X is 0 and R2, R3, R4, and R6 are H, Rl is not amino or methylamino when R5 is hydrogen or hydroxy), or a salt thereof.

Other analogs of acyclovir include 1-O-hexadecylpropanediol-3-p-acyclovir, 1-O-hexadecylpropanediol-3-phosphoacyclovir, 1-O-octadecyl-sn-glycero-3-phospho-acyclovir, 2'-O-glycyl acyclovir, 2,6-diamino-9-(2-hydroxyethoxymethyl)purine, 3,9-dihydro-3-((2-hydroxyethoxy)methyl)-6-ethyl-9-oxo-5H-imidazo(1,2-a)purine, 3-methyl-cyclosal-PCVMP, 6-deoxypenciclovir, 8-fluoropenciclovir, 9-((1,3-dihydroxy-2-propylthio)methyl)guanine, 9-((2-aminoethoxy)methyl)guanine, 9-(2'-(9"-octadecenoyloxy)ethoxymethyl)guanine, 9-(3,4-dihydroxybutyl)guanine, 9-(4-hydroxy-2-(hydroxymethyl)butyl)-guanine triphosphate, 9-(4-hydroxybutyl)guanine, acyclovir (3-glucoside, acyclovir diphosphate dimyristoylglycerol, acyclovir fluorophosphate, acyclovir monophosphate, acyclovir monophosphate-lactosaminated serum albumin conjugate, acyclovir phosphite, acyclovir triphosphate, acyclovir-5'-(phenyl methoxy alaninyl)phosphate, BIOLF 143, bis(2-(guanin-9-ylmethoxy)ethoxy)-4-(methylsulfonyl)phenyl phosphate, BRL 42359, bucyclovir triphosphate, desciclovir, diamminechloro(9-(2-hydroxyethoxymethyl)guan-7-yl)platinum(II), famciclovir, y-glutamylacyclovir, ganciclovir, guanin-9-yl methyloxy-2-ethyl bis(S-acetyl-2-thioethyl) phosphate, guanin-9-yl methyloxy-2-ethyl bis(S-pivaloyl-2-thioethyl) phosphate, penciclovir, penciclovir triphosphate, tyrosylacyclovir, val-valacyclovir, and valacyclovir.

Additional analogs are described in U.S. Patent Nos. 4,806,642, 4,957,924, 5,580,571, 6,214,811, and 6,031,096.

Prostaglandins The compositions, methods, and kits of the invention may include a prostaglandin such as alprostadil (prostaglandin El), or an analog thereof.
Alprostadil has the formula:

O O
OH

HO OH
Analogs of alprostadil are described in U.S. Patent No. 3,735,005 and have the formula:

~\\ OR, (CH2),,CH3 where R1 is hydrogen or a C1_8 alkyl group, R2 is a member selected from the group consisting of H, C1_8 alkyl, and the acyl group of a hydrocarbon carboxylic acid of 2 to 18 carbon atoms; R3 is OH, n is 3, 4, or 5, and OR2 and R3 may have an a or (3 configuration. Exemplary of lower alkyl containing from 1 to 8 carbon atoms suitable for include branched or straight chain hydrocarbon groups such as methyl, ethyl, propyl, isopropyl, butyl, tert-butyl, pentyl, and hexyl. Exemplary acyl groups include acetyl, propionyl, butyryl, hexanoyl, octanoyl, lauroyl, palmitoyl, stearoyl, and oleoyl. Other alprostadil analogs are described in U.S. Patent No. 5,219,885. Other prostaglandins that can be used in the invention are described below.

Other prostaglandins include 2-chloro-4-hydroxy-5-(6-methoxycarbonyl-2-hexyenylidene)-4-n-octyl-2-cyclopentanone, 4-fluoroenisoprost, 7-hydroxy-5,11 -dioxotetranorprostane- 1, 1 6-dioic acid, AY 22093, bromovulone III, carijenone, claviridenone E, claviridenone F, claviridenone G, clavubicyclone, MR 256, NEPP11 compound, NEPP6 compound, NEPP6-biotin, prostaglandin endoperoxides, prostaglandins A, prostaglandins B, prostaglandins D, prostaglandins E, prostaglandins F, prostaglandins I (e.g., epoprostenol), RS
61756-007, S 1033, tricycloclavulone.

Prostaglandins A include 13,14-dihydro- l 5-deoxy-A-prostaglandin-A 1-methyl ester, 13,14-dihydro-A7-prostaglandin Al methyl ester, 15-keto-13,14-dihydroprostaglandin A2, 16,16-dimethylprostaglandin A2 methyl ester, 5-(4-N,N-dimethylaminophenylmethylene)-4-hydroxy-2-(1-methylimidazol-2-ylthio)-4-(4-phenylbutyl)-2-cyclopentenone, 8-isoprostaglandin A2, chlorovulone I, clavulone II, clavulones, prostaglandin Al, prostaglandin A2, prostaglandin A2 isopropyl ester, and TEI 3313.

Prostaglandins B include 15-ketoprostaglandin B 1, 16,16-dimethyl-15-dehydroprostaglandin B 1 trimer, 19-hydroxyprostaglandin B2, di-Calciphor, OC 5181, OC 5186, prostaglandin B 1, prostaglandin B2, and prostaglandin Bx.
Prostaglandins D include 9-chloro- l 5-cyclohexyl- 11, 15-dihydroxypentanor-5,13-prostadienoic acid, 9-fluoro- l 5-cyclohexyl- 11, 15-dihydroxypentanor-5,13-prostadienoic acid, 9-fluoro-15-hydroxy-16-phenoxy-17,18,19,20-tetranor-5,13-prostadienoic acid, 9-hydroxy-11,15-dioxo-2,3,18,19-tetranorprost-5-ene-1,20-dioic acid, prostaglandin D2, and prostaglandin D3.

Prostaglandin D2 analogs include 11, 15 -dioxo-9-hydroxy-2,3,4,5-tetranorprostan- 1,20-dioic acid, 11-methoxime prostaglandin D2, 11-methyleneprostaglandin D2, 13,14-dihydro- l 5-ketoprostaglandin D2, 15-deoxy-A(12,14)-prostaglandin J2, 15-deoxyprostaglandin J2, 15-methylprostaglandin D2, 9-deoxy-9,10-didehydro-12,13-didehydro-13,14-dihydroprostaglandin D2, 9-deoxy-A-9-prostaglandin D2, anhydrolevulgandin D2, A(12)-prostaglandin J(2), prostaglandin D2 4-azidophenacyl ester, prostaglandin D2 methyl ester, and TS-002.

Prostaglandins E include 17-isolevuglandin E4, 6(9)-oxy- 11, 15-dihydroxy-prosta-7,13-dienoic acid, anhydrolevuglandin E2, levuglandin E2, lymphocytic thyroid stimulator (non-immunoglobulin), alprostadil, dinoprostone, prostaglandin-inositol cyclic phosphate, Ro 22-1327, and suppressor active peptide (thermal injury.) Prostaglandin El analogs include 11,15-bisdeoxyprostaglandin El, 11-deoxy-l0-hydroxyprostaglandin E1 methyl ester, 11-deoxy-13,14-dihydro-8-azaprostaglandin E(1), 11-deoxy-16,16-trimethyleneprostaglandin E 1, 11 -deoxy- 1 6-phenoxy- 17,18,19,20-tetranorprostaglandin E 1, 11 -deoxy-4,4-dimethyl-4-silaprostaglandin E 1, 11-deoxy-8-azaprostaglandin E(l), 11-deoxyprostaglandin E 1, 11 -deoxyprostaglandin E 1 4-hydroxyphenyl ester, 13,14-dihydro-15-ketoprostaglandin El, 13,14-dihydroprostaglandin El, 15(S)-15-methylprostaglandin El, 15-cyclohexyl-omega-pentanor-7-thiaprostaglandin El, 15-fluoro-11,15-dideoxyprostaglandin El, 15-keto-13,14-dihydro-6-ketoprostaglandin El, 15-keto-prostaglandin E0, 15-ketoprostaglandin E, 16,16-dimethyl-A2-prostaglandin El, 16,18-ethano 20-ethyl-6-oxoprostaglandin El, 16,18-ethano-20- ethyl- 6-oxoprostaglandin El leucinamide, 17,18-dehydroprostaglandin El, 18-hydroxyprostaglandin El, 19-hydroxyprostaglandin El, 20-dimethyl-7-thiaprostaglandin El methyl ester, 20-hydroxyprostaglandin El, 3,7-dithia(11 a,13 E,15 S)-11,15-Dihydroxy-9-oxoprost-13-en- l -oic acid, 3-oxa-4,5,6-nor-(3,7-inter)-3-phenyleneprostaglandin El methyl ester, 3-oxa-4,5,6-nor-3,7-inter-3-phenyleneprostaglandin El, 3-oxa-4,5,6-trinor-3,7-inter-3-phenyleneprostaglandin El amide, 4-thiaprostaglandin El, 5(6)-epoxyprostaglandin E 1 a, 5,6-dihydroxyprostaglandin E 1, 6-ketoprostaglandin El, 7-keto-9,9-ethylenedioxiprostanoid, 7-oxo-15-methylprostaglandin El methyl ester, 8-azaprostaglandin E1, alibra, AY 23626, butaprost, 5-17-tetranorprostaglandin El, enisoprost, gemeprost, isoprostaglandin El, limaprost, limaprost-alfadex, lubiprostone, MDL 646, MR 356, NP 01A, NP 07 A, NP 13 A, ONO 1082, ONO 1206, ONO-DI-004, ornoprostil, prostaglandin E0, prostaglandin E1 ethyl ester, prostaglandin El methyl ester, prostaglandin Ela-cyclodextrin, prostaglandin El-hexyl-sepharose, prostaglandin E3, SC
29169, SC 31391, SC-46275, SPM 206, tetranorprostaglandin El, TFC 612, and TR4161.

Dinoprostone (prostaglandin E2) analogs include 11-deoxy,16,16-dimethyl prostaglandin E2, 11-deoxy-11,12-methanoprostaglandin E2, 11-deoxy-11 a-(2-hydroxyethylthio)-prostaglandin E2 methyl ester, 11-deoxy-15-keto-13,14-dihydro-11 beta, l 6-cycloprostaglandin E2, 11-deoxyprostaglandin E2-1-alcohol, 12-isoprostaglandin F(2a), 13,14-didehydroprostaglandin E2, 13,14-dihydro-16-phenyl-Q-tetranorprostaglandin E2, 13,14-dihydroprostaglandin E2, 15-deoxy-16-hydroxy- l 6-vinylprostaglandin E2, 15-fluoro- l 5-deoxyprostaglandin E2, 15-hydroperoxyprostaglandin E2, 15-keto-13,14-dihydroprostaglandin E2, 15-keto-13,14-dihydroprostaglandin E2-thyroglobulin conjugate, 15-ketoprostaglandin E2, 16-methyl prostaglandin E2, 16-methyl-13,14-didehydroprostaglandin E2, 16-methyl-16-methoxyprostaglandin E2, 16-methyl-20-methoxy-prostglandin E2, 17,17-dimethylprostaglandin E2, 17-(4-azidophenyl)- 1 8,19,20-trinorprostaglandin E2, 17-phenyltrinorprostaglandin E2, 18,18,20-trimethylprostaglandin E2, 18-hydroxyprostaglandin E2, 19,20-dehydroprostaglandin E2, 19-hydroxyprostaglandin E2, 1 a, l b-dihomoprostaglandin E2, 20-hydroxyprostaglandin E2, 20-isopropylidene prostaglandin E2, 20-methyl-13,14-didehydroprostaglandin E2, 8,12-epi-prostaglandin E2, 8-isoprostaglandin E2, 9-deoxy-9-chloro- I 5-deoxy- 16-hydroxy- 17,17-trimethylene- 19,20-didehydroprostaglandin E2, 9-enol-prostaglandin E2 methyl ester trimethylsilyl ether, FCE 20700, HOE 260, N-acetylprostaglandin E2 carboxamide, ONO AE 248, prostaglandin D2 ethanolamide, prostaglandin E2 azidophenacyl ester, prostaglandin E2 ethanolamide, prostaglandin E2 glyceryl ester, prostaglandin E2 methyl ester, prostaglandin E2 methyl oxime, prostaglandin F2a ethanolamide, prostamide H2, sulprostone, trimoprostil, and viprostol.

Prostaglandins F analogs include (5Z)-7-((1R,2R, 3R,5S)-2-((1E)-3,3-difluoro-4-phenoxy -1-butenyl)-3,5-dihydroxycyclopentyl)-5-heptenoic acid, 15-cis-(4-n-propylcyclohexyl)-16,17,17,19,20-pentanor-9-deoxy-6,9-a-nitriloprostaglandin Fl, 2,3-dinor-6-oxoprostaglandin Fl 1, 5(6)-epoxyprostaglandin Fla, 5,6-dihydroxyprostaglandin Fl, 5,7-dihydroxy-1 l-ketotetranorprostanoic acid, alfaprostol, butyryl prostaglandin F 1 butyl ester, C22-prostaglandin F4a, 6-Ketoprostaglandin F 1 a, lymphocytic thyroid stimulator (non-immunoglobulin), Dinoprost, prostaglandin F-main urinary metabolite, prostaglandin F 1, prostaglandin F 1(3, prostaglandin F2(3, prostaglandin F3a, and tafluprost.

6-Ketoprostaglandin Fla analogs include 2,3-dinor-6-ketoprostaglandin F 1 a, 5-hydroxy-6-ketoprostaglandin F 1 a, 6,15-diketo-13,14-dihydroprostaglandin F 1 a, 6,15-diketoprostaglandin F 1 a, 6-ketoprostaglandin F l a-thyroglobulin conjugate, 6-ketoprostaglandin F l a-tyramide, A(17)-6-ketoprostaglandin F 1 a, and endothelin- 1,2-6-ketoprostaglandin F 1 a.
Dinaprost (prostaglandin F2a) analogs include 1-ethyl (5Z)-7-((1R,2R, 3R,5S)-2-((1E)-3,3-difluoro-4-phenoxy -1-butenyl)-3,5-dihydroxycyclopentyl)-5-heptenoate, 1-methyl (5Z)-7-((1R,2R, 3R,5S)-2-((1E)-3,3-difluoro-4-phenoxy -1-butenyl)-3,5-dihydroxycyclopentyl)-5-heptenoate, 11-fluoro-11-dehydroxyprostaglandin F2a, 11-fluoro-1 l-deoxyprostaglandin F2a, 11-ketotetranorprostaglandin F2a, 13,14-dihydroprostaglandin F2a, 13,14-dihydroxy-l5-ketoprostaglandin F2a, 15-fluoro-l5-deoxyprostaglandin F2a, 15-keto-13,14-dihydroprostaglandin F2a, 15-keto- l 7-phenyl- 18,19,20-trinorprostaglandin F2a- 1 -isopropyl ester, 15-ketoprostaglandin F2a, 15-propionat-prostaglandin F2a-isopropyl ester, 16,16-dimethylprostaglandin F2a, 16-(3-chlorophenoxy)-17,18,19,20-tetranorprostaglandin F2a, 16-aminoprostaglandin F2a methyl ester, 16-fluoromethyleneprostaglandin F2a, 17-azaprostaglandin F2a, 17-phenyl- 1 8,19,20-trinor-prostaglandin F2a-1-isopropyl ester, 17-phenyl-18,19,20-trinorprostaglandin F2a, 17-phenylprostaglandin F2a, 18,19,20-trinor- l 7-cyclohexyl- 13,14-dehydroprostaglandin F2a methyl ester, 19-hydroxyprostaglandin F, 1 a, lb-dihomoprostaglandin F2, 2,3-dinor-5,6-dihydro-15-F-isoprostane, 2,3-dinor-5,6-dihydro-8-iso-prostaglandin F2a, 2,3-dinor-5,6-dihydroisoprostane F2a-III, 2-decarboxy-2-(P-methylphosphinico)-16-phenoxytetranorprostaglandin F2a, 20-methyl-13,14-(didehydroprostaglandin) F2a, 3-(3,5-dihydroxy-2-(oxodecyl)cyclopentyl)propionic acid, 6-keto-prostaglandin F2a, 7-(3,5-dihydroxy-2-(3-oxodecyl)cyclopentyl)hept-5-enoic acid, 8,12-iso-isoprostane F2a-III, 8,12-iso-isoprostane F2a-VI, 8-epi-prostaglandin F2a, 9-chloro-15-cyclohexyl-11,15-dihydroxy-3-oxa-16,17,18,19,20-pentanor-5-prostenoic acid, AFP-157, AL 6598, AL 8810, AL 8810 ethylamide, AL-3138, AY 24366, delprostenate, dinoprost tromethamine, etiproston, etiproston tromethamine, fluprostinol, ICI 79939, isopropyl unoprostone, N-dimethylaminoprostaglandin F2a, PhXa 85, prostaglandin F2 ethyl ester, prostaglandin F2 isopropyl ester, prostaglandin F2 methyl ester, prostaglandin F2a 11-methyl ether, prostaglandin F2a 15-methyl ether, prostaglandin F2a 9-methyl ether, prostaglandin F2a N-dimethylamide, ZK 110841, ZK 118182, and ZK 71677.

Epoprostenol analogs include 10,10-difluoro-13-dehydroprostacyclin,

11-desoxyprostacyclin, 13,14-dehydroprostaglandin 12, 13,14-dehydroprostaglandin 12 methyl ester, 13,14-didehydro-20-methylcarboprostacyclin, 13,14-dinor-inter-p-phenylene carbacyclin, 15-cyclopentyl-7-oxo-prostaglandin 12-ephedrine, 15-deoxy-(16-m-tolyl)-17,18,19,20-tetranorisocarbacyclin methylester, 15-deoxy- l 6-m-tolyl-17,18,19,20-tetranorisocarbacyclin, 15-fluoro-13,14-dehydrocarbacyclin, 15-ketoprostaglandin 12, 16-tolyl-17,18,19,20-tetranorisocarbacyclin, 17,20-dimethylisocarbacyclin, 19-(3-azidophenyl)-20-norisocarbacyclin, 2,2,10,10-tetrafluoro-13-dehydroprostacyclin, 20-methyl-13,14-didehydro-2,4-inter-3-phenylene prostaglandin 12, 3-oxa-9(O)-methano-delta(6,9)prostaglandin 1(1), 3-oxacarbacyclin, 3-oxahomoisocarbacyclin, 4,5-didehydroisocarbacyclin, 5,6-dihydroprostacyclin, 5-hydroxyprostaglandin I, 5-methyleneisocarbacyclin, 5-nitroprostaglandin 11, 5-nitroprostaglandin 12, 6,9-thiaprostacyclin, 6a-carbaprostaglandin 13, 7-fluoroprostacyclin, 7-oxo-cyclopentyl-prostaglandin

12, 7-oxo-prostaglandin 12-ephedrine, 7-oxoprostaglandin 12, 7a-homo-2-norprostacyclin, 9-0-methanoprostaglandin I, AFP 03, AFP 06, AFP 07, APS

306, benzodioxane prostacyclin, beraprost, bicyclo(4.3.0)non-2-ene homoisocarbacyclin, carbaprostacyclin, carboprostacyclin, CG 4303, Chinoin 7284, Chinoin 7384, cicaprost, ciprostene, CL 115999, dehydro-15-cyclohexylcarbaprostacyclin, dihomo-prostaglandin 1(2), FCE 21258, HOE
892, homoisocarbacyclin, KP 10614, MM 706, naxaprostene, nileprost, nitriloprostaglandin 12, ONO 41483, OP 2507, OP 41483-a-cyclodextrin, piriprost, prostaglandin 12 11-methyl ether, prostaglandin 12 15-methyl ether, prostaglandin 12 methyl ester, prostaglandin 13, R 59274, SC 39902, SM 10902, SM 10906, taprostene, TEl 1324, TEI 3356, TEI 4343, TEI 9090, TFC 132, tilsuprost, treprostinil, TRY 200, TTC 909, TY 10957, TY 11223, U 56467, U
68215, and U 72382.

Synthetic prostaglandin analogs include (+)(-)-8,12-trans-9-oxo-prosta-5,14-dienoic acid, 11-methoxime prostaglandin D2, 9a, I I a,15a-trihydroxy-16-phenoxy-17,18,19,20-tetranorprosta-4,5,13-trienoic acid, 9-chloro-15-cyclohexyl- 11, 1 5-dihydroxypentanor-5,13-prostadienoic acid, 9-fluoro- 15-cyclohexyl- 11, 1 5-dihydroxypentanor-5,13 -prostadienoic acid, AL- 12182, EMD
33290, EP 045, EP 092, GIF 0010, GIF 0037, Iloprost, synthetic prostaglandin endoperoxides, synthetic prostaglandins A, synthetic prostaglandins E, synthetic prostaglandins F, and U 62840. Iloprost analogs include 2,6-dichloro-4-aminophenol iloprost, eptaloprost, and iloprost phenacyl ester. Synthetic prostaglandin endoperoxides include 9,11 -azo- 1 3-oxa- l 5-hydroxyprostanoic acid, 9,11-iminoepoxyprosta-5,13-dienoic acid, prostaglandin H2 9-cyclic ether, prostaglandin H2 methyl ester, and U 44069. Synthetic prostaglandins A
include 16,16-dimethylprostaglandin Al, 9-oxo-15-hydroxy-A7,10,13-prostatrienoic acid methyl ester, GSH-prostaglandin Al, HR 546, punaglandin III, and TE19826. Synthetic prostaglandins E include 16,16-dimethylprostaglandin E, 1 6-hydroxy-16-methyl-9-oxo-prosta-10,13-dien- l -oic acid methyl ester, CL 115574, CL 116069, CP 48630, 16,16-dimethylprostaglandin E2 or an analog thereof (e.g., 11-methyl-16,16-dimethylprostaglandin E2, 16,16-dimethylprostaglandin E2 (4-acetamidobenzamido)phenyl ester, 16,16-dimethyprostaglandin E2 4-benzaldehyde semicarbazone ester, 19-hydroxy-16,16-dimethylprostaglandin E2, 9- deoxy- 1 6,16-dimethyl-tetranor-9-methyleneprostaglandin E2, and meteneprost), enprostil, GR 63799X, arbaprostil or a analog thereof (e.g., 15-deoxy- l 6-methyl-16-hydroxy-3,4-didehydroprostaglandin E2 methyl ester and 15-methylprostaglandin E2 methyl ester), misoprostol or an analog thereof (e.g., 2-demethoxycarbonyl-2-ethoxycarbonyl- l l -deoxymisoprostol, Arthrotec, diclofenac-misoprostol, misoprostol acid, and SC 53450), ONO-747, rioprostil, Ro 22-6923, RS 20216, RS 61565, and Wy 17186.

Aristolochic acid The compositions, methods, and kits of the invention may include the use of aristolochic acid, or an analog thereof. Aristolochic is a phospholipase A
inhibitor. The structure of aristolochic acid is:

OH

O-/ O"
Analogs of aristolochic acid include 7-(deoxyadenosin-N(6)-yl)aristolactam II, 7-(deoxyadenosin-N(6)-yl)aristolactam I, 7-(deoxyguanosin-N(2)-yl)aristolactam II, 7-(deoxyguanosin-N(2)-yl)aristolactam I, 7-methoxyaristolochic acid A, 7-methoxyaristololactam IV, 9-ethoxyaristolactone, 9-ethoxyaristololactam, 9-hydroxy aristolochic acid I, aristolactam I, aristolic acid, aristolochic acid C, aristolochic acid E, aristolochic acid II, aristololactam BII, aristololactam IVa, aristololactam-glucoside, aristoloside, methyl aristolate, and N-((6'-p-coumaroyl)glucopyranosyl)aristolactam.

Carbadox The compositions, methods, and kits of the invention may include the use of carbadox, or an analog thereof. The structure of carbadox is:

I

~NH
O- N

N+

Analogs of carbadox are described in U.S. Patent No. 3,371,090 and have the formula:

R, N\ R3 W RZ

where each of R1 and R2 is individually selected from the group consisting of H
and C1_8 alkyl; R3 is selected from the group consisting of NHCONH2, NHC(S)NH2, NHCNHNH2, NHR4, NHCOOR5, NHCOR6, OR7, where R4 is selected from the group consisting of C1_8 alkyl, phenyl, benzyl, and hydroxyalkyl containing from 2 to 4 carbon atoms; R5 is selected from the group consisting of lower alkyl, hydroxyalkyl containing from 2 to 4 carbon atoms, and haloalkyl containing from 2 to 4 carbon atoms; R6 is selected from the group consisting of C1_8 alkyl and phenyl; and R7 is selected from the group consisting of hydrogen and C1_8 alkyl.

Chlorpyrifos The compositions, methods, and kits of the invention may include the use of chlorpyrifos, or an analog thereof. The structure of chlorpyrifos is:

CI

II/
CI / O-P\
-CI
Analogs of chlorpyrifos are described in U.S. Patent No. 3,244,586 and have the structure:
Z R, II
R-O- /
P
R' where R is pyridyl optionally substituted with one or more (e.g., 2, 3, 4) halogen groups, Z is 0 or S, and each R' independently represents C1_8 alkoxy, amino, or C1_8 alkylamino.

Cyclocreatine Creatines, such as cyclocreatine, may be used in the compositions, methods, and kits of the invention. Cyclocreatine has the structure:

HO

~N
--c O
Creatine analogs are described in U.S. Patent No. 5,998,457 and have the structure:

X-A-Y
ZZ
wherein Y is -COOHNHOH, -NO2, -SO3H, -C(=O)NHSO2J, or -P(=O)(OH)(OJ), where J is H, C1_6 alkyl, C2_6 alkenyl, or aryl;

A is C, CH, C1_5 alkyl, C2_5 alkenyl, C2.5 alkynyl, or C1_5 alkoyl, each having 0-2 substituents selected independently from K, where K is C1_6 alkyl, C2.6 alkenyl, C1_6 straight alkoyl, and C4_6 branched alkoyl, having 0-2 substituents independently selected from Br, Cl, epoxy, and acetoxy; a 1-2 ring aryl group optionally heterocyclic having 0-2 substituents independently selected from -CH2L and -COCH2L, where L is Br, Cl, epoxy, or acetoxy; and 3) -NH-M, where M is H, C1-4 alkyl, C2_4 alkenyl, C1-4 alkoyl, and C4 branched alkoyl;
X is NR1, CHRI, CR1, 0, or S, where R1 is H; K, where K is C1_6 alkyl, C2.6 alkenyl, C1_6 straight alkoyl, and C4_6 branched alkoyl, having 0-2 substituents independently selected from Br, Cl, epoxy, and acetoxy; a 1-2 ring aryl group optionally heterocyclic having 0-2 substitutions of -CH2L and -COCH2L where L is Br, Cl, epoxy, or acetoxy; a C5_9 a-amino-w-methyl-w-adenosylcarboxylic acid attached by the co-methyl carbon; a C5_9 a-amino-w-aza-w-methyl-w-adenosylcarboxylic acid attached by the w-methyl carbon; and a C5_9 a-amino-w-thia-w-methyl-w-adenosylcarboxylic acid attached by the w-methyl carbon;

Z1 and Z2 are chosen independently from the group consisting of: =0, -NHR2, -CH2R2, -NRZOH; where Z1 and Z2 are not both =0 and where R2 is H;
K, where K is C1-6 alkyl; C2-6 alkenyl, C1_6 straight alkoyl, and C4_6 branched alkoyl and contains 0-2 substituents independently selected from Br, Cl, epoxy, and acetoxy; a 1-2 ring aryl group optionally heterocyclic containing 0-2 substituents independently selected from -CH2L and -COCH2L where L is Br, Cl, epoxy, or acetoxy; a C4-8 a-amino-carboxylic acid attached via the w-carbon; B, where B represents -CO2H-NHOH, -SO3H, -NO2, OP(=O)(OH)(OJ), or -P(=O)(OH)(OJ), where J is H, C1_6 alkyl, C2_6 alkenyl, or aryl, and B is optionally connected to the nitrogen by C1_2 alkyl, C2 alkenyl, or C1-2 alkoyl; -D-E, where D is C1_3 alkyl, C2_3 alkenyl, C1_3 straight alkoyl, aryl, or aroyl; and E is -(P03),NMP, where n is 0-2 and NMP is ribonucleotide monophosphate connected by the 5'-phosphate, 3'-phosphate, or the aromatic ring of the base; -[P(=O)(OCH3)(O)]m Q, where in is 0-3 and Q is a ribonucleoside connected via the ribose or the aromatic ring of the base; -[P(=O)(OH)(CH2)]m Q, where in is 0-3 and Q is a ribonucleoside connected via the ribose or the aromatic ring of the base; and an aryl group containing 0-3 substituents chosen independently from Cl, Br, epoxy, acetoxy, -OG, -C(=O)G, and -CO2G, where G represents C1_6 alkyl, C2_6 alkenyl, C1_6 straight alkoyl, C4_6 branched alkoyl, and where E may be attached to any point to D, and if D is alkyl or alkenyl, D may be connected at either or both ends by an amide linkage; and -E, where E represents -(PO3),INMP, where n is 0-2 and NMP is a ribonucleotide monophosphate connected by the 5'-phosphate, 3'-phosphate, or the aromatic ring of the base; -[P(=O)(OCH3)(O)]m Q, where in is 0-3 and Q is a ribonucleoside connected via the ribose or the aromatic ring of the base; -[P(=O)(OH)(CH2)],n Q, where in is 0-3 and Q is a ribonucleoside connected via the ribose or the aromatic ring of the base; and an aryl group containing 0-3 substituents chose independently from the group consisting of Cl, Br, epoxy, acetoxy, -OG, -C(=O)G, and -CO2G, where G represents C1_6 alkyl, C2_6 alkenyl, C1_6 straight alkoyl, C4_6 branched alkoyl; and if E is aryl, E
may be connected by an amide linkage;

if Rl and at least one R2 group are present, R1 may be connected by a single or double bond to an R2 group to form a 5-7 member ring;

if two R2 groups are present, they may be connected by a single or a double bond to form a 4-7 member ring; and if Rl is present and Z1 or Z2 is -NHR2, -CH2R2, or -NR2OH, then R1 may be connected by a single or double bond to the carbon or nitrogen of either Z1 or Z2 to form a 4-7 member ring.

7,4'-dimethoxyisoflavone Isoflavones such as 7,4'-dimethoxyisoflavone can be used in the compositions, methods, and kits of the invention. 7,4'-dimethoxyisoflavone has the structure:

0 o Isoflavone analogs include (3R)-4'-methoxy-2',3,7-trihydroxyisoflavanone, (3R)-6,2' -dihydroxy-7-methoxy-4' , 5' -methylenedioxyisoflavan, (R)-3',5-dihydroxy-4',7-dimethoxyspiro(2H-1-benzopyran- 3(4H),7'-bicyclo(4.2.0)-octa(1,3,5)-trien)-4-one, 10,11-dihydroxydracaenone C, 2",6"-O-diacetyloninin, 2"-O-glycosylisovitexin, 2',4',7-trihydroxyisoflavone, 2'-hydroxy-5'-methoxybiochanin A, 2'-hydroxy-5,6,7-trimethoxyisoflavonoid, 2' -hydroxy-6,4',6",4"'-tetramethoxy(7-0-7")-bisisoflavone, 2'-methoxybonducellin, 2'-methoxydihydrobonducellin, 2,7,4'-trihydroxyisoflavanone, 2-methoxy-3,8,9-trihydroxy coumestan, 3',4',7-trihydroxyisoflavone, 3',7-dihydroxy-2',4',5',8-tetramethoxyisoflavan, 3',7-dihydroxyisoflavan, 3'-chloro-5,7-dihydroxyisoflavone, 3'-hydroxy-6,4'-dimethoxy-7-O-glucopyranozylisoflavone, 3' -methoxypuerarin, 3' -prenyl-4' -methoxyisoflavone-7-0-beta-(2"-O-4-coumaroyl)glucopyranoside, 3(2H)-isoflavene, 3-(3-bromophenyl)-5,7-dihydroxy-4-oxo-4H-chromene-2-carboxylic acid ethyl ester, 3-(4'-methoxybenzyl)-7,8-methylenedioxychroman-4-one, 3-(4-hydroxybenzyl)-5-hydroxy-6,7,8-trimethoxychroman-4-one, 4',5,6,7-tetrahydroxy-8-methoxyisoflavone-7-0-beta-D-galactopyranosyl-(1-3)-O-beta-D-xylopyranosyl-(1-4)-O-alpha-L-rhamnopyranoside, 4',5,7-trihydroxy-6,8-dimethylisoflavone, 4',5-dihydroxy-2',3'-dimethoxy-7-(5-hydroxyoxychromen-7y1)-isoflavanone, 4',5-dihydroxy-7-0-methylisoflavone-3'-0-(3"-cinnamoyl)glucoside, 4',7,8-trihydroxyisoflavone, 4',7-dimethoxy-2-isoflavonol, 4',8-dihydroxyl-7-methoxylisoflavone, 4'-methoxypuerarin, 4'-0-coumaroyl-isovitexine, 4'-O-methyl equol, 4'-O-methylalpinumisoflavone, 5,4'-dimethoxy-3'-prenylbiochanin A, 5,6,6'-trimethoxy-3',4'-methylenedioxyisoflavone 7-0-(2"-0-4-coumaroylglucopyranoside), 5,6,7-trihydroxy-3-(3,4, 5-trimethoxyphenyl)-1H-benzopyran-4-one, 5,7,4'-trihydroxy-2'-methoxyisoflavone, 5,7,4'-trihydroxy-3'-(3-hydroxy-3-methylbutyl)isoflavone, 5,7,8,4'-tetrahydroxyisoflavone, 5,7-dihydroxy-2',3',5',6'-tetramethoxy isoflavone, 5,7-dihydroxy-2',4',5'-trimethoxyisoflavanone, 5,7-dihydroxy-2'-methoxy-3',4'-methylenedioxyisoflavanone, 5,7-dihydroxy-3-(3-hydroxy-4-methoxybenzyl)-6-methoxychroman-4-one, 5-hydroxy-2',4',5'-trimethoxy-2",2"-dimethylpyrano(5",6": 6,7)isoflavanone, 5-methoxyxanthocercin A, 6"-O-malonyldaidzin, 6"-O-xylosyltectoridin, 6,7,4'-trihydroxyisoflavan, 6,7,4'-trihydroxyisoflavanone, 6,7,4'-trihydroxyisoflavone, 6,7,8,3',4',5'-hexamethoxyisoflavone, 6,7-dihydroxy-4'-methoxyisoflavanone, 6-aldehydo-7-methoxyiso-ophiopogonanone B, 6-chloro-3(2H)-isoflavene, 6-hydroxy-7,2',4',5'-tetramethoxyisoflavone, 6-hydroxybiochanin A, 6-hydroxydaidzein, 6-0-glucuronopyranosyl-2',5,6-trihydroxyisoflavone, 2'-O-sulfate, 6-oxazolinylisoflavan, 7,2'-dihydroxy-3',4'-dimethoxyisoflavane-7-0-glucoside, 7,3',4'-trihydroxy-5-0-alpha-L-rhamnopyranosylisoflavone, 7,3',4'-trihydroxy-5-0-beta-D-(2"-acetyl)-xylopyranosylisoflavone, 7,3'-dihydroxy-4'-methoxy-5' -(gamma,gamma-dimethylallyl)isoflavone, 7,3'-dihydroxy-4'-methoxyisoflavone, 7,3'-dihydroxy-6",6"-dimethyl-4",5"-dehydropyrano(2",3":4',5')isoflavone, 7,3'-dihydroxyl-5'-methoxyisoflavone, 7,4' -dimethoxy-5-hydroxyisoflavone, 7,4' -dioxyethoxydaidzein, 7,4' -disuccinic acid monoester-O-ethoxydaidzein, 7,6'-dihydroxy-3'-methoxyisoflavone, 7,8,3',4',5'-pentamethoxyisoflavone, 7,8,4'-trihydroxyisoflavone, 7,8,4'-trimethoxyisoflavone, 7,8-dihydroxy-2',4',5'-trimethoxyisoflavan, 7-hydroxy-2',3',4',5',8-pentamethoxyisoflavan, 7-hydroxy-4'-methoxy-3'-prenylisoflavone, 7-hydroxy-6,4'-dimethoxy-isoflavonequinone, 7-methoxy-4'-hydroxy-3' -diethylaminomethylisoflavone, 7-0-(carboxypropyl)-4' -hydroxyisoflavone, 7-0-beta-glucopyranosyl-4'-hydroxy-5-methoxyisoflavone, 7-0-methyleucomol 5-0-glucopyranoside, 7-0-methyleucomol 5-0-neohesperidoside, 7-0-methyleucomol 5-0-rutinoside, 7-0-methylisolupalbigenin, 8-chloro-3',4',5,7-tetrahydroxyisoflavone, 8-hydroxydaidzein, 8-hydroxyglycitein, 8-isopentenylnaringenin, 8-methoxy-5,6,4'-trihydroxyisoflavone-7-0-glucopyranoside, 8-methoxyvestitol, 8-prenyldaidzein, 8-prenylmucronulatol, acetylpuerarin, afromosin, alpinumisoflavone, astraisoflavanin, auriculasin, bavadin, bidwillon B, biochanin A 7-0-(apiofuranosyl-(1-5)-apiofuranosyl-(1-6)-glucopyranoside), bolusanthol A, bolusanthol B, bolusanthol C, cabreuvin, cajanol, calycosin-7-0-beta-D-glucoside, calycosin-7-0-glucopyranoside, chungkookjang, CJY
compound, CK 122, claussequinone, colutehydroquinone, colutequinone, coromandelin, coumestrol, daidzein, daidzein 7-0-beta-D-glucuronide-4'-O-sulfate, daidzein-4',7-yl diglucopyranosiduronic acid, daidzein-4'-O-sulfate, daidzein-4,7-diglucoside, daidzein-7,4'-di-O-sulfate, daidzein-7-yl glucopyranosiduronic acid, daidzin, dalbergion 4'-O-glucopyranoside, dalcongestin, dalnigrein7-0-beta-D-apiofuranosyl-(1-6)-beta-D-glucopyranoside, dalpatein 7-0-beta-D-apiofuranosyl-(1-6)-beta-D-glucopyranoside, dehydroequol, derrubone, desmodianone A, desmodianone B, desmodianone C, dichotomitin, dihydrobonducellin, dihydrodaidzein, dihydrodaidzin, dihydrogenistin, dihydroisoderrondiol, dihydrolicoisoflavone, duartin, echinoisoflavanone, EMD 16795, equol, eriotriochin, erycristagallin, euchrenone b 10, eurycarpin A, eurycarpin B, formononetin, fremontin, fremontone, fujiflavone P40, furowanin B, gancaonin A, genistein, genistein 4',7'-bis(6-deoxytalopyranoside), genistein 7-(6-deoxytalopyranoside), genistein 7-0-alpha-L-rhamnopyranoside-4' -O-(6"'-O-alpha-L-rhamnopyranosyl)-beta-sophoroside, genistein 7-0-beta-D-glucopyranoside-4'-0-(6"'-O-alpha-L-rhamnopyranosyl)-beta-sophoroside, genistin, glabrene, glabrizoflavone, glaziovianin A, glicoisoflavanone, glisoflavanone, glycitein, glycitin, haginin A, hydroxyethylpuerarin, indicanine C, intricatinol, ipriflavone, irigenin, irilin A, irilin B, irilin D, irilone, irisone A, irisone B, isocytisoside, isocytisoside-7-0-glucopyranoside, isoflavanone, isovitexin 2"-O-glucoside, isovitexin-4'-O-glucoside, judaicin (isoflavone), kakkalide, kievitone, kraussianone 1, kraussianone-1, kraussianone-2, kwakhurin, lanceolarin, licoisoflavone A, licoisoflavone B, lupinalbisone A, lupinalbisone B, mahuangchiside, malonylgenistin, manuifolin D, manuifolin E, manuifolin F, manuifolin Q, menoflavon, methylaminium 4',7-dihydroxyisoflavone-3'-sulfonate, methylophiopogonanone B, millewanin G, millewanin H, munetone, muscomin, N99-596 A, N99-596 B, nigrolineaisoflavone A, 0-desmethylangolensin, O-methylclaussequinone, ormosidin, osajaxanthone, osajin, pallidifloric acid methyl ester, pallidiflorin, pentandrin, pentandrin glucoside, phaseollin (isoflavan), phenoxodiol, phytosoya, promensil, prunetin, prunetin-4'-O-beta-D-gentiobioside, psi-baptigenin, psi-tectorigenin, Pterocarpans, puerarin, robustic acid, rotenone, sativan, scandenone, senegalensin, sigmoidin I, sigmoidin J, sigmoidin K, smiranicin, sophoraisoflavanone D, sophoraisoflavone A, sophorol, soy isoflavone aglycone, tectoridin, tectorigenin, tectorigenin 7-0-(apiofuranosyl-(1-6)-glucopyranoside), tetrahydrodaidzein, tlatancuayin, torvanol A, triquetrumone A, triquetrumone B, triquetrumone C, triquetrumone D, ulexin C, ulexin D, vavain, vavain 3' -0-glucoside, vogelin A, vogelin B, vogelin C, vogelin H, vogelin I, vulgarin (isoflavones), warangalone, warangalone-4'-methyl ether, and yufengningxin. Analogs are also described in U.S Patent Nos. 2,764,596, 2,892,845, 2,892,846, 3,755,372, 3,907,830, 3,864,362, 4,841,077, and 4,264,509.

Dorzolamide The compositions, methods, and kits of the invention may use dorzolamide or an analog thereof. Dorzolamide has the structure:

NH

S=O
\S S O

1// S \O

Analogs of dorzolamide are described in U.S. Patent No. 4,677,115 and have the structure:

O
A S/

wherein A together with the two carbon atoms denoted as a and is the group:
R2 R= X a ::1 (CH2)n R3 'X or R2 R, wherein Xis S, SO, SO2 or CH2i Y is S, 0, or NR3 where R3 is H; C1_3 alkyl, or benzyl;
n is 1 or 2;

R1, R2, R3, R4 are independently:
H;

OR5 where R5 is H, C1_5 alkyl optionally substituted with OH or NR6R7 where R6 and R7 are independently H or C1_5 alkyl or are joined together form a heterocycle with the nitrogen to which they are attached (e.g., piperidino, morpholino, or piperazino), C1.5 alkanoyl optionally substituted with OH, NR6R7, NHCOR8, or COR8 where Rg is OH, NR6R7, or C1_5 alkoxy; or COR9, where R9 is NR6R7 or a 5- or 6-membered aromatic heterocycle such as pyridyl, imidazolyl, pyrazinyl, thiazolyl, thienyl, or oxazolyl;
NR6R7;

NHR10 wherein Rlu is SO2NR6R7, S02R11 where R11 is C1_5 alkyl, or CONR6R7, C1_5 alkyl, optionally substituted with OR5, CN, NR6R7, or COR8, S02R11;
S02NR6R7, or halo, such as Cl, Br, or F;

R1 and R3, or R2 and R4 taken together represent a double bond; R1 and R2, or R3 and R4 taken together represent =0, or =NOR12 where R12 is H or C1.3 alkyl;
and one of the CH2 groups of -(CH2)ri is optionally substituted with -COR8, -CH2R8, or -CH2COR8.

S(-)eticlopride S(-)eticlopride, or an analog thereof can be used in the compositions, methods, and kits of the invention. S(-)eticlopride has the structure:
CI

H
NN
OH O

Analogs of eticlopride are described in U.S. Patent No. 4,789,683 and have the formula:

OA, H
N
Rl where R1 and R2 are independently H, a halogen, CN, C1_6 alkyl, or acyl; R3 is C1_6 alkyl, a C2_6 alkenyl, or C6_12 aryl optionally substituted with F, Cl, Br, CF3, C1_6 alkyl, or C1_6 alkoxy, Al and A2 are independently H, C1_6 alkyl group, acyl, C1_6 alkoxycarbonyl, or a dialkylcarbamyl group, (e.g., provided that when Al and A2 are the same lower alkyl group and R3 is ethyl, R1, R2, or both are selected among CN, C1_6 alkyl, and acyl); or a physiologically acceptable salt or optical isomers thereof.

Evoxine Evoxine, or an analog thereof, may be used in the compositions, methods, and kits of the invention. Evoxine has the structure:

O
HO O \ N O
OH O

Evoxine acts as a sedative and is an antagonist of strychnine and pentylenetrazole.

Guaifenesin Guaifenesin, or an analog thereof, may be used in the compositions, methods, and kits of the invention. Guaifenesin has the structure:

HO'--~O
OH
Gauifenesin is used as an expectorant.

Hydroxyprogesterones 17u-Hydroxyprogesterone (CAS No. 68-96-2), or an analog thereof, may be used in the compositions, methods, and kits of the invention. 17a-Hydroxyprogesterone has the structure:

O

H H
O /
Other hydroxyprogesterone compounds include 11 a-broinoacetoxyprogesterone, 11,14-dihydroxypregn-4-ene-3,20-dione, 11-hydroxyprogesterone, 11-hydroxyprogesterone 11-glucuronide, 12a-hydroxyprogesterone, 14-hydroxypregna-1,4-diene-3,20-dione, 14-hydroxyprogesterone, 15,17-dihydroxyprogesterone, 15-hydroxyprogesterone, 16a,17a-isopropylidenedioxyprogesterone, 16 a-bromoacetoxyprogesterone, 16,17-epoxy-3-hydroxypregn-5-en-20-one, 16-hydroxyprogesterone, 16-methylene-17 a-acetoxyprogesterone, 16-methylene-17 a-hydroxyprogesterone, 17 a,20 (3-dihydroxypregn-4-en-3-one, 17 a-acetoxy-2',2',6 13-trifluoro-6 (3,7 (3- dihydro-16-methylenecyclopropa(6,7)progesterone, 17,20- dihydroxy-4-pregnen-3 -one, 17-(bromoacetoxy)progesterone, 17-acetoxy-11-oxaprogesterone, 17-acetoxy-7-oxaprogesterone, 17-a-hydroxy-progesterone caproate, 17-hydroxypregn-4-ene-3-one, 17-hydroxyprogesterone 17-(9-oxo-10-chlorodecanoate), 17-hydroxyprogesterone heptanoate, 17a-hydroxy-6-methylene-progesterone, 18-hydroxyprogesterone, 19-hydroxyprogesterone, 2-bromoacetoxyprogesterone, 21-amino- l 7-hydroxyprogesterone, 21-bromoacetoxyprogesterone, 3-0-glucopyranosyl-3,15-dihydroxypregn-5-en-20-one, 4-pregnen-20,21-diol-3-one, 6 0-acetoxyprogesterone, 6,17,20-trihydroxypregn-4-ene-3-one, 6-bromoacetoxyprogesterone, 6-hydroxy-6-methyl-17-acetoxyprogesterone, 6-hydroxyprogesterone, 6-trifluoromethyl- l 6-methylene- 17 a-hydroxy-4,6-pregnadiene-3,20-dione 17-acetate, 7 a-carboxymethyl-17-hydroxyprogesterone, 7 (3-carboxymethyl-17-hydroxyprogesterone, 7,14-dihydroxypregn-4-ene-3,20-dione, 7-hydroxyprogesterone, caprovestrol, deluteval, flumedroxone, 17a-acetoxy-3 (3-butanoyloxy-6-methyl-pregna-4,6-dien-20-one, 17a- acetoxy- 3 13-isopropyloxy-6-methylpregna-4,6-dien-20-one, 17a-acetoxy-3 (3-phenylpropionyloxy-6-methylpregna-4,6-dien-20-one, 17-a-hydroxyprogesterone, Injectable No. 1, methylene-dehydroacetoxy-progesterone, pregna-l,4-diene-l1-ol-3,20-dione, primosiston, progesterone 11-glucuronide-alkaline phosphatase conjugate, progesterone 11-hemisuccinate, progesterone 11-hemisuccinate-(2-iodohistamine), thymine-hydroxyprogesterone, and trophobolen.

Kaempferol Kaempferol, or an analog thereof, may be used in the compositions, methods, and kits of the invention. The structure of kaempferol is:
OH
HO O

OH
OH O
Analogs of kaempferol include (6"'-O-(delphinidin 3-0-(6"-O-p-coumaroylglucoside) 7-0-glucosyl)) (6""-O-(kaempferol 3-0-glucoside, 7-0-xyloside, 4'-O-glucosyl))succinate, (6"'-O-(delphinidin 3-0-(6"-O-p-coumaroylglucoside) 7-0-glucosyl)) (6""-O-(kaempferol 3,7-di-O-glucoside, 4'-O-glucosyl))succinate, 3,4'-dimethylkaempferol, 3,7-O-dimethylkaempferol, 3-hydroxy-2,3-dihydroapigenyl-(I-4',0,11-3')-dihydrokaempferol, 3-methylkaempferol, 3-0-((xylopyranosyl(1-3)-rhamnopyranosyl(1-6))(apiofuranosyl(1-2)))-galactopyranosyl kaempferol, 3-0-(3-((3-(6"'-acetyl)-D-glucopyranosyl(1-2))-D-glucopyranosyl kaempferol, 3-0-glucosyl-1-6-glucosylkaempferol, 3-0-rhamnopyranosylkaempferol-7-O-glucopyranoside, 4"'-acetylvitexin-2"-O-rhamnoside, 6,8-di-C-methylkaempferol 3-methyl ether, 6,8-dihydroxyafzelin, 6-hydroxykaempferol-3-0-glucoside, 6-methoxykaempferol 3-0-rhamnoside, 7-0-acetyl-3-O-glucosylkaempferol, 7-0-a-L-rhamnopyranosyl-kaempferol-3-0-a-L-rhamnopyranoside, 7-0-a-L-rhamnopyranosyl-kaempferol-3-O-3-D-glucopyranoside, 8-lavandulylkaempferol, 8-methoxykaempferol-3-0-glucoside, afzelin 3"-O-gallate, amoenin A3, astragalin, camelliaside A, camelliaside C, clitorin, des-methylicariine, kaempefrol-3-0-arabinofuranoside-7-0-rhamnopyranoside, kaempferide, kaempferide 3-0-glucopyranosyl-1-2-0-(rhamnopyranosyl-l-6)glucopyranoside, kaempferide 3-0-neohesperidoside, kaempferol 3-(2(Gal)-(4-acetylrhanmosyl)robinobioside), kaempferol 3-(2(Gal)-rhamnosylrobinobioside), kaempferol 3-(2,4-di-(4-coumaroyl)rhamnoside), kaempferol 3-arabinoside, kaempferol 3-gentiobioside, kaempferol 3-glucosyl(1-3)rhamnosyl(1-6)galactoside, kaempferol 3-0-((6""-feruloyl)-(3-D-glucopyranosyl-(1-3 ))-(a-L-rhamnopyranosyl-(1-6))- f 3-D-glucopyranoside, kaempferol 3-0-(2"-O-galloylrutinoside), kaempferol 3-0-(2(G)-(E)-coumaroyl-3 (G)-O-(3-D-glucosyl-3 (R)-O-(3-D-glucosylrutinoside), kaempferol 3-0-(apiofuranosyl-(1 "'-2")-rhamnopyranosyl-(1""-6"))-galactopyranoside, kaempferol 3-O-a-L-3"-acetyl-arabinofuranoside, kaempferol 3-0-a-rhamnopyranosyl(1-2)-(3-galactopyranoside-7-0-f3-glucopyranoside, kaempferol 3-O-a-rhamnopyranosyl-(1-2)-p-galactopyranoside, kaempferol 3-0-apiofuranoside 7-0-a-rhamnosyl-(1 "'-6"')-O-galactopyranoside, kaempferol 3-0-apiofuranoside 7-O-rhamnosyl-(1""-6"')-O- (2'"-O-E-caffeoylgalactopyranoside), kaempferol 3-0-apiofuranosyl-1-6-glucopyranoside, kaempferol 3-0-glucopyranoside-6"-(3-hydroxy-3-methyl glutarate), kaempferol 3-0-glucopyranosyl-1-4-rhamnopyranosyl-1-6-galactopyranoside, kaempferol 3-0-neohesperidoside, kaempferol 3-0-rhamnopyranosyl(1-2)-galactopyranoside-7-O-arabinofuranoside, kaempferol 3 -0-rhamnopyranosyl(1-6)-galactopyranoside-7-0-arabinofuranoside, kaempferol 3 -0-rhamnopyranosyl-1-6-glucopyranosyl- l -6-galactopyranoside, kaempferol 3-0-rhamnopyranosyl-1-6-0-(glucopyranosyl-1-3-0-rhamnopyranosyl-1-2)-O-galactopyranoside, kaempferol 3-0-rhamnoside, kaempferol 3-0-sophoroside, kaempferol 3-0-sophoroside-7-0-glucoside, kaempferol 3 -rhamnosyldiglucoside, kaempferol 7-neohesperidoside, kaempferol 7-0-(2,3-di-E-p-coumaroyl-a-L-rhamnoside), kaempferol 7-0-(2-E-p-coumaroyl-a-L-rhamnoside), kaempferol 7-0-glucoside, kaempferol rhanmorobinoside, kaempferol-2,4-dicoumaroyl-3-0-glucoside, kaempferol-3-(4-coumaroyl triglucoside), kaempferol-3-(3-D-(6-0-trans-p-coumaroyl)glucopyranoside, kaempferol-3-0-((xylopyranosyl(1-3)-rhamnopyranosyl(1-6))(rhamnopyranosyl(1-2)))galactopyranoside, kaempferol-3-0-(2,3,4-tri-O-acetyl-a-l-rhamnopyranoside), kaempferol-3-0-(2,3-di-0-acetyl-a-1-rhamnopyranoside), kaempferol-3-0-(6",4"-di-p-coumaroyl)mannopyranoside, kaempferol-3-O-(6"-p-coumaroyl)mannopyranoside, kaempferol-3-O-(6-trans-caffeoyl)-f -D-glucopyranosyl-(1- 2)-(3-D-glucopyranoside-7-O-f -D-glucopyranoside, kaempferol-3-O-(apiofuranosyl-(1 "'-2"))-galactopyranoside, kaempferol-3-O-(rhamnopyranosyl-rhamnopyranosyl-(1-6)-galactoside), kaempferol-3-O-a-L-(6"-ethyl)-rhamnopyranoside, kaempferol-3-O-a-L-(6"-methyl)-rhamnopyranoside, kaempferol-3-O-a-L-5"-acetyl-arabinofuranoside, kaempferol-3-O-a-L-arabifuranoside, kaempferol-3-O-(3-D-(6"-O-p-coumaroyl)galactopyranoside, kaempferol-3-O-(3-D-galactoside, kaempferol-3-O-13-D-glucopyranoside-7-O-a-L-arabinofuranoside, kaempferol-3-O-galactoside, kaempferol-3-O-glucopyranoside-6"-(3-hydroxy-3-methyl glutarate)-7-O-glucopyranoside, kaempferol-3-0-glucopyranosyl-1-4-rhamnopyranoside, kaempferol-3-0-glucoside, kaempferol-3-O-glucosyl(1-2)rhamnoside, kaempferol-3-O-rutinoside, kaempferol-4',7-dimethyl-3-0-glucoside, kaempferol-7-O-a-L-rhamnopyranoside, lespenefril, mauritianin, morindaoside, nigeglanoside, siparunoside, and trifolin acetate.
Linamarin Linamarin, or an analog thereof, may be used in the compositions, methods, and kits of the invention. The structure of linamarin is:

HON
O Y-1j;
Hot',---- 0 HO bH
Linamarin is a cyanogenic glucoside found in the leaves and roots of plants such as cassava, lima beans, and flax.

Mexicanolide Mexicanolide, or an analog thereof, may be used in the compositions, methods, and kits of the invention. The structure of mexicanolide is:

O O

t-d'X O O Mexicanolide is found in the Spanish cedar (Cedrela odorata L).

MG 624, or an analog thereof, may be used in the compositions, methods, and kits of the invention. The structure of MG 624 is:

N
O

Analogs of MG 624 are described in Mantegazza et al., Arch. Int.
Pharmacodyn., 4:371, 1955 and Gotti et al., Br. J. Pharmacol. 124:1197, 1998.

Pramoxine Prainoxine, or an analog thereof, may be used in the compositions, methods, and kits of the invention. The structure of pramoxine is:

o 0 o ~/-\
N

Pramoxine is used as a topical anesthetic, often in treatment of insect bites.
Tannic acid Tannic acid or tannic complexes may be used in the compositions, methods, and kits of the invention. Tannic acid is a polymer made up of a glucose molecule attached by ester linkages and to one or more gallic acid units, which, in turn, may be further attached to additional gallic acid units.
Tannic acid can have the structure:
OH
OH
OH
HO OH O OH OH
HO O
O O OH
HO / I O O OH

OH HO O O O OH

O O / /
OH O OH
HO OOH
HO
OH
Tannic acid is used topically to treat injuries such as burns, and has been shown to have some antineoplastic effects.

Targinine Targinine, or an analog thereof, may be used in the compositions, methods, and kits of the invention. The structure of targinine is:
O

HN
H2N~N

Analogs of targinine are described in U.S. Patent No. 4,698,442 and have the structure:

O
H2N Y", OH

(CH2)n \
NH
/ \ i R2 R~ N
where n is 1-5; R1 is C1-12 alkyl, C1_4 halogen substituted alkyl, or NHR3 where R3 is C1.12 alkyl, C3_12 cycloalkyl, phenyl, benzyl, C1_4 halogen substituted alkyl, morpholino, or (CH2),,N(R4)2 where n is 1-5 and R4 is C1_4 alkyl; R2 is H or R3;

or R1 and R2 comprise a ring represented by the following structural formulas:
HN N ' \
HN ~N
A-~K (CH2)m N N HN 'J"' NH
`\ /
, x X, , and B B

where m is 0-6; A and B are independently H, C1_6 alkyl, or C3_12 cycloalkyl;
and X is halo or A (e.g., provided that wherein n is 3 and R1 is -NHR3, wherein R3 is methyl and R2 is H or methyl are excluded).

Yohimbic acid Yohimbic acid, or an analog thereof, may be used in the compositions, methods, and kits of the invention. The structure of yohimbic acid is:

\ / 'Z6 H H
O~, OH

OH
Analogs of yohimbic acid are described in U.S. Patent Nos. 2,796,420, 2,841,586, 2,977,367, 2,998,556, 3,120,532, 3,126,390, 3,139,434, 3,337,559, and 3,940,387. Analogs of yohimbic acid include yohimbine, 1-methylyohimbine, 10-hydroxyyohimbine, 11-hydroxy-yohimbine, 11-hydroxyyohimbine, 14-(4-nitrobenzoyloxy)yohimbine, 14-benzoyloxyyohimbine, 17-hydroxy-20-yohimban-16-(N-(4-azido-3-iodo)phenyl)carboxamide, 5-carboxytetrahydroalstonine, 9-methoxy-3-epi-alpha-yohimbine, raubasine, apoyohimbine, iodinated rauwolscine, NMI 187, rauwolscine 4-aminophenylcarboxamide, rauwolscine, Reserpine or an analog thereof (e.g., 16,18-reserpinediol, adelphan-esidrex, adelphane, aldatense, Bendigon, bietaserpine, Briserin, bromoreserpine, butiserpazide, caprinol, CD
3400, Crystepin CH, deserpidine, dibromoreserpine, enderpins, FH 109 C, Hyparez, meprocalm, methyl reserpate, Nortensin, Regroton, rescinamine, rescinnamine, reserpic acid, reserpine methonitrate, sinepres, and syrosingopine), and trimethoxybenzoylyohimbine.

Treatment of a subject The invention also provides methods for increasing cellular proliferation, enhancing skin repair or skin health, and promoting hair growth by administration of a compound that decreases expression or activity of p63 (e.g., dominant negative forms of p63, a p63 antibody, or a compound selected from the group consisting of acyclovir, alprostadil, aristolochic acid, carbadox, chlorpyrifos, cyclocreatine, 7,4'-dimethoxyisoflavone, dorzolamide, S(-)eticlopride, evoxine, guaifenesin, hydroxyprogesterone, kaempferol, linamarin, mexicanolide, MG 624, pramoxine, tannic acid, targinine, and yohimbic acid, or an analog thereof, to a subject in need thereof. The compounds can be further modified using standard chemical, physical, or biochemical methods.

Formulation of pharmaceutical compositions The administration of any compound or composition described herein may be by any suitable means that results in a concentration of the compound that increases cellular proliferation, enhances skin repair or skin health, or promotes hair growth. The compound may be contained in any appropriate amount in any suitable carrier substance, and is generally present in an amount of 1-95% by weight of the total weight of the composition. The composition may be provided in a dosage form that is suitable for the oral, skin (e.g., topical or by patch), cutaneous, parenteral (e.g., intravenous or intramuscular), rectal, nasal, vaginal, inhalant, ocular, or intracranial administration route. Thus, the composition may be in the form of, e.g., tablets, capsules, pills, powders, granulates, suspensions, emulsions, solutions, gels including hydrogels, pastes, ointments, creams, plasters, drenches, osmotic delivery devices, suppositories, enemas, injectables, implants, sprays, or aerosols. The pharmaceutical compositions may be formulated according to conventional pharmaceutical practice (see, e.g., Remington: The Science and Practice of Pharmacy, 20th edition, 2000, ed. A.R. Gennaro, Lippincott Williams & Wilkins, Philadelphia, and Encyclopedia of Pharmaceutical Technology, eds. J. Swarbrick and J. C.
Boylan, 1988-1999, Marcel Dekker, New York).

Pharmaceutical compositions may be formulated to release the active compound immediately upon administration or at any predetermined time or time period after administration. The latter types of compositions are generally known as controlled release formulations, which include (i) formulations that create substantially constant concentrations of the agent(s) of the invention within the body over an extended period of time; (ii) formulations that after a predetermined lag time create substantially constant concentrations of the agents of the invention within the body over an extended period of time; (iii) formulations that sustain the agent(s) action during a predetermined time period by maintaining a relatively constant, effective level of the agent(s) in the body with concomitant minimization of undesirable side effects associated with fluctuations in the plasma level of the agent(s) (sawtooth kinetic pattern);
(iv) formulations that localize action of agent(s), e.g., spatial placement of a controlled release composition adjacent to or in the diseased tissue or organ;
(v) formulations that achieve convenience of dosing, e.g., administering the composition once per week or once every two weeks; and (vi) formulations that target the action of the agent(s) by using carriers or chemical derivatives to deliver the compound to a particular target cell type. Administration of the compound in the form of a controlled release formulation is especially preferred for compounds having a narrow absorption window in the gastro-intestinal tract or a relatively short biological half-life.

Any of a number of strategies can be pursued in order to obtain controlled release in which the rate of release outweighs the rate of metabolism of the compound in question. In one example, controlled release is obtained by appropriate selection of various formulation parameters and ingredients, including, e.g., various types of controlled release compositions and coatings.
Thus, the compound is formulated with appropriate excipients into a pharmaceutical composition that, upon administration, releases the compound in a controlled manner. Examples include single or multiple unit tablet or capsule compositions, oil solutions, suspensions, emulsions, microcapsules, molecular complexes, microspheres, nanoparticles, patches, and liposomes.
Topical formulations Pharmaceutical compositions according to the present invention can be formulated for topical administration. Subjects can be administered effective amounts of a compound described herein by means of a solution (e.g., drops), ointment, gel, or aerosol (e.g., nebulizer). The composition is typically administered to the affected area by topically applying, for example, one to four drops of a solution or suspension, or a comparable amount of an ointment, gel, or other solid or semisolid composition, once, twice, three times, or more than three times per day. These formulations can be made according to known and conventional methods for preparing such formulations.

For compounds of the invention that are not highly soluble in water at physiological conditions, a solubilizing excipient may be used to increase solubility. Solubilization is taken to mean an improvement in the solubility by virtue of surface-active compounds that can convert substances that are insoluble or virtually insoluble in water into clear, or opalescent, aqueous solutions without changing the chemical structure of these substances in the process. Excipients used for this purpose are restricted to those that are safe for administration to humans. Typically such co-solvents are employed at a level of about 0.01% to 2% by weight.

A variety of solubilizing excipients may be used for the formulation of a compound of the invention, including compounds belonging to the following classes: polyethoxylated fatty acids, PEG-fatty acid diesters, PEG-fatty acid mono-ester and di-ester mixtures, polyethylene glycol glycerol fatty acid esters, alcohol-oil transesterification products, polyglycerized fatty acids, propylene glycol fatty acid esters, mixtures of propylene glycol esters and glycerol esters, mono- and diglycerides, sterol and sterol derivatives, polyethylene glycol sorbitan fatty acid esters, polyethylene glycol alkyl ethers, sugar esters, polyethylene glycol alkyl phenols, polyoxyethylene-polyoxypropylene block copolymers, sorbitan fatty acid esters, lower alcohol fatty acid esters, or ionic surfactants.

The compounds described herein can also be formulated as part a lotion such as a moisturizing lotion. Exemplary lotion formulations are described in U.S. Patent Nos. 4,595,586; 4,459,285; 3,867,528; 3,265,571; 4,512,978;
4,564,462; 4,165,385; 3,062,721; 3,949,071; 4,482,537; 4,295,985; 2,507,236;
and 3,987,775.

Solid dosage forms for oral use Formulations for oral use include tablets containing the active ingredient(s) in a mixture with non-toxic pharmaceutically acceptable excipients, and such formulations are known to the skilled artisan (e.g., U.S.P.N.: 5,817,307, 5,824,300, 5,830,456, 5,846,526, 5,882,640, 5,910,304, 6,036,949, 6,036,949, 6,372,218, hereby incorporated by reference). These excipients may be, for example, inert diluents or fillers (e.g., sucrose, sorbitol, sugar, mannitol, microcrystalline cellulose, starches including potato starch, calcium carbonate, sodium chloride, lactose, calcium phosphate, calcium sulfate, or sodium phosphate); granulating and disintegrating agents (e.g., cellulose derivatives including microcrystalline cellulose, starches including potato starch, croscarmellose sodium, alginates, or alginic acid); binding agents (e.g., sucrose, glucose, sorbitol, acacia, alginic acid, sodium alginate, gelatin, starch, pregelatinized starch, microcrystalline cellulose, magnesium aluminum silicate, carboxymethylcellulose sodium, methylcellulose, hydroxypropyl methylcellulose, ethylcellulose, polyvinylpyrrolidone, or polyethylene glycol);
and lubricating agents, glidants, and anti-adhesives (e.g., magnesium stearate, zinc stearate, stearic acid, silicas, hydrogenated vegetable oils, or talc).
Other pharmaceutically acceptable excipients can be colorants, flavoring agents, plasticizers, hurnectants, buffering agents, and the like.

The tablets may be uncoated or may be coated by known techniques, optionally to delay disintegration and absorption in the gastrointestinal tract and thereby providing a sustained action over a longer period. The coating may be adapted to release the compound in a predetermined pattern (e.g., in order to achieve a controlled release formulation) or it may be adapted not to release the agent(s) until after passage of the stomach (enteric coating). The coating may be a sugar coating, a film coating (e.g., based on hydroxypropyl methylcellulose, methylcellulose, methyl hydroxyethylcellulose, hydroxypropylcellulose, carboxymethylcellulose, acrylate copolymers, polyethylene glycols, and/or polyvinylpyrrolidone), or an enteric coating (e.g., based on methacrylic acid copolymer, cellulose acetate phthalate, hydroxypropyl methylcellulose phthalate, hydroxypropyl methylcellulose acetate succinate, polyvinyl acetate phthalate, shellac, and/or ethylcellulose).
Furthermore, a time delay material such as, e.g., glyceryl monostearate or glyceryl distearate, may be employed.

The solid tablet compositions may include a coating adapted to protect the composition from unwanted chemical changes, (e.g., chemical degradation prior to the release of the active substances). The coating may be applied on the solid dosage form in a similar manner as that described in Encyclopedia of Pharmaceutical Technology, supra.

The compositions of the invention may be mixed together in the tablet, or may be partitioned. In one example, a first agent is contained on the inside of the tablet, and a second agent is on the outside, such that a substantial portion of the second agent is released prior to the release of the first agent.
Formulations for oral use may also be presented as chewable tablets, or as hard gelatin capsules wherein the active ingredient is mixed with an inert solid diluent (e.g., potato starch, lactose, microcrystalline cellulose, calcium carbonate, calcium phosphate, or kaolin), or as soft gelatin capsules wherein the active ingredient is mixed with water or an oil medium, for example, peanut oil, liquid paraffin, or olive oil. Powders and granulates may be prepared using the ingredients mentioned above under tablets and capsules in a conventional manner using, e.g., a mixer, a fluid bed apparatus, or spray drying equipment.

Parenteral compositions A composition containing a compound described herein or identified using the methods of the invention may be administered parenterally by injection, infusion, or implantation (subcutaneous, intravenous, intramuscular, intraperitoneal, or the like) in dosage forms, formulations, or via suitable delivery devices or implants containing conventional, non-toxic pharmaceutically acceptable carriers and adjuvants. The formulation and preparation of such compositions are well known to those skilled in the art of pharmaceutical formulation.
Compositions for parenteral use may be provided in unit dosage forms (e.g., in single-dose ampoules), or in vials containing several doses and in which a suitable preservative may be added (see below). The composition may be in form of a solution, a suspension, an emulsion, an infusion device, or a delivery device for implantation, or it may be presented as a dry powder to be reconstituted with water or another suitable vehicle before use. Apart from the active agent(s), the composition may include suitable parenterally acceptable carriers and/or excipients. The active agent(s) may be incorporated into microspheres, microcapsules, nanoparticles, liposomes, or the like for controlled release. Furthermore, the composition may include suspending, solubilizing, stabilizing, pH-adjusting agents, tonicity adjusting agents, and/or dispersing agents.

As indicated above, the pharmaceutical compositions according to the invention may be in a form suitable for sterile injection. To prepare such a composition, the suitable active agent(s) are dissolved or suspended in a parenterally acceptable liquid vehicle. Among acceptable vehicles and solvents that may be employed are water, water adjusted to a suitable pH by addition of an appropriate amount of hydrochloric acid, sodium hydroxide or a suitable buffer, 1,3-butanediol, Ringer's solution, dextrose solution, and isotonic sodium chloride solution. The aqueous formulation may also contain one or more preservatives (e.g., methyl, ethyl, or n-propyl p-hydroxybenzoate). In cases where one of the compounds is only sparingly or slightly soluble in water, a dissolution enhancing or solubilizing agent can be added, or the solvent may include 10-60% w/w of propylene glycol or the like.

Dosages The dosage of any compound described herein depends on several factors, including: the administration method, the amount of increase in cellular proliferation, skin repair, hair growth, or skin health enhancement desired, and the age, weight, and health of the subject to be treated.

With respect to the treatment methods of the invention, it is not intended that the administration of a compound to a subject be limited to a particular mode of administration, dosage, or frequency of dosing; the present invention contemplates all modes of administration, including oral, cutaneous, subcutaneous, intramuscular, intravenous, intraperitoneal, intravesicular, intraarticular, intralesional, or any other route sufficient to provide a dose adequate to increase cellular proliferation, enhance skin repair or skin health, or promote hair growth treat. The compound may be administered to the subject in a single dose or in multiple doses. For example, a compound described herein may be administered once a week for, e.g., 2, 3, 4, 5, 6, 7, 8, 10, 15, 20, or more weeks. It is to be understood that, for any particular subject, specific dosage regimes should be adjusted over time according to the individual need and the professional judgment of the person administering or supervising the administration of the compound. For example, the dosage of a compound can be increased if the lower dose does not provide sufficient activity in the treatment of a metabolic disorder (e.g., diabetes or obesity). Conversely, the dosage of the compound can be decreased if the metabolic disorder is reduced or eliminated.

While the attending physician ultimately will decide the appropriate amount and dosage regimen, a therapeutically effective amount of a compound described herein may be, for example, in the range of 0.0035 gg to 20 g/kg body weight/day or 0.0 10 gg to 140 g/kg body weight/week. Desirably a therapeutically effective amount is in the range of 0.025 gg to 10 g/kg, for example, at least 0.025, 0.035, 0.05, 0.075, 0.1, 0.25, 0.5, 1.0, 1.5, 2.0, 2.5, 3.0, 3.5, 4.0, 5.0, 6.0, 7.0, 8.0, or 9.0 gg/kg body weight administered daily, every other day, or twice a week. In addition, a therapeutically effective amount may be in the range of 0.05 g to 20 g/kg, for example, at least 0.05, 0.7, 0.15, 0.2, 1.0, 2.0, 3.0, 4.0, 5.0, 6.0, 7.0, 8.0, 10.0, 12.0, 14.0, 16.0, or 18.0 g/kg body weight administered weekly, every other week, or once a month. Furthermore, a therapeutically effective amount of a compound may be, for example, in the range of 100 g/m2 to 100,000 g/m2 administered every other day, once weekly, or every other week. In a desirable embodiment, the therapeutically effective amount is in the range of 1000 g/m2 to 20,000 g/m2, for example, at least 1000, 1500, 4000, or 14,000 g/m2 of the compound administered daily, every other day, twice weekly, weekly, or every other week.

Example 1 p63 inhibits cellular proliferation To determine whether there is a cell-autonomous requirement for tumor antigen p63 (TAp63) in the maintenance of dermal stem cells, we isolated and analyzed SKPs from wild-type and p63 null mice. We used RT-PCR to characterize the p53 family members expressed in cultured wild-type SKPs.
Consistent with the expression of p63 in dermal sheath cells in vivo, SKPs expressed TAp63 mRNA, whereas p63 expression was not observed in cells taken from p63-/- mice (Figure lA). These cells did not express dominant negative p63 (dNp63) or p73, and p53 levels were similar in p63-/- and p63+/+
SKPs (Figure 1B). Immunostaining with anti-p63 confirmed that wild-type, but not p63-/-, SKPs expressed detectable levels of p63 protein (Figure 1 Q. Thus, of the p53 family members, SKPs express only TAp63 and p53.
To determine whether TAp63 is necessary for maintenance of SKPs, the cells were isolated from the skin of TAp63-/- and TAp63+/+ mice at various times postnatally. Immunocytochemical analysis of SKP spheres for fibronectin, nestin, vimentin, and versican demonstrated that there were no overt differences in expression of these markers for SKPs with the loss of TAp63 (Figure 1D). By contrast, immunostaining for the proliferation marker Ki67 demonstrated that TAp63-/- neonatal SKPs proliferated approximately 2-3-fold more than their wild-type counterparts. Similar results were obtained when SKPs were isolated from the rudimentary dermis that is present in E18 p63-/- mice (Figures 1E and IF). To determine whether this increased proliferation reflected increased self-renewal, SKPs were dissociated to single cells, plated at low density in medium containing methylcellulose, and the percentage of cells that initiated a new sphere was determined. As seen in the proliferation assay, newborn TAp63-/- and El 8 p63-/- SKPs self-renewed approximately 4 times more robustly than did wild type SKPs (Figure 1 G).
When TAp63-1- SKPs were isolated from 1 month old mice, they still proliferated and self-renewed more than did wild-type SKPs, although the magnitude of the increase was reduced to approximately 1.5-fold (Figure 1 G).
In spite of this hyperproliferation, TAp63-/- and TAp63+/+ SKPs were both able to differentiate into both neural and mesodermal cell types under previously defined conditions (Figure 2A), and, when transplanted into the neural crest migratory stream of cHH stage 18 chicks in ovo, both populations of SKPs migrated into neural crest targets (Figure 2B). Thus, TAp63 regulates SKP proliferation and self-renewal, but does not overtly affect their phenotype or differentiation capacity.

Thus, TAp63 may normally function to dampen the self-renewal rate of SKPs, potentially as a mechanism to ensure that the SKPs last for the lifetime of the animal. One p63 target that decreases cellular proliferation is p57. RT-PCR analysis demonstrated that p57 mRNA levels were reduced in TAp63-/-and p63-/- SKPs (Figure 1H). Immunocytochemistry for p57 confirmed this result, and demonstrated that p57 protein levels were decreased in SKPs in the absence of TAp63 (Figure 11). To confirm that p57 is a direct target of p63 in SKPs, as it is in human keratinocyte HaCat cell line (Beretta et al., Cell Cycle.
4:1625-1631, 2005), we performed chromatin immunoprecipitations using an antibody for p63. RT-PCR of the associated DNA demonstrated that p63 was bound to a previously defined binding site in the p57 promoter (Figure 1J).
Thus, TAp63 regulation of SKPs' self-renewal likely involves regulation of p57.

To quantify the number of p57 positive cells in TAp63-/- cells and in wild-type cells, both types of cells were stained as shown in Figure 11, and the percentage of p57 positive cells was calculated. From these results, approximately 50% of the wild-type cells were identified as being p57 positive, whereas only 18% of the TAp63-/- cells were p57 positive (Figure 1K).

We also determined whether the hyperproliferation phenotype in TAp63-/- SKPs could be rescued by p57Kip2 (p57). To do this, TAp63-/- SKPs were plated on an adherent substrate, transfected with either the empty vector or a p57Kip2 expression vector, and immunostained two days later for p57Kip2 and Ki67. Under these conditions, approximately 45% of TAp63-/- cells transfected with the empty vector were dividing, as monitored by Ki67 expression, and none of them expressed p57Kip2 (Figure 1L). By contrast, approximately 20% of the cells transfected with p57Kip2 expressed detectable levels of this protein, and none of these transfected cells coexpressed Ki67 (Figure 1 L). Thus, p57Kip2 completely rescued the hyperproliferation, indicating that TAp63 regulates SKPs self-renewal at least in part by regulating p57Kip2.

Example 2 Screen for compounds that enhance cellular proliferation To identify molecules (e.g., small molecules) that promote proliferation of SKPs, a simple, reproducible and robust assay that measures cell proliferation using Alamar Blue dye, which yields a fluorescent signal in a response to metabolic activity, was developed. Compounds (5 M) were added in singlet to 96-well uncoated plates, 3000 early passage dissociated sphere cells were robotically seeded, and plates were incubated in basal growth medium. After 30 hours, Alamar Blue was added and its reduction assessed after another 24 hours. Typically, there is an 8-10 fold difference in Alamar Blue reduction between positive and negative controls. A compound was identified as a hit if Alamar Blue reduction is increased by three standard deviations from the mean of all the compounds in a particular screen. In our assay, the variability of signals are low, with CV values ranging from 3.5-4.5%
and the dimensionless statistical parameters Z' and Z factors >0.5, indicative of an excellent assay. The chemical libraries we used include the LOPAC, Prestwick, Biomol, and Spectrum collections, which comprise 3,500 unique low-molecular weight compounds, including both natural products and synthetic chemicals, known drugs and drug-like compounds, and phosphatase and kinase inhibitors. These screens were done at the same time as high-throughput screens using human neuroblastoma tumor cells with the goal of identifying drugs that are cytotoxic for cancer but not for normal cells (SKPs) (Figure 3).

Using this screen, we identified several compounds that enhance the proliferation of human SKPs, shown in the Table below:

Acyclovir Dorzolamide hydrochloride Mexicanolide Alprostadil S(-)Eticlopride hydrochloride MG 624 Aristolochic acid Evoxine Pramoxine hydrochloride Carbadox Guaifenesin Tannic acid Chlorpyrifos Hydroxyprogesterone Targinine hydrochloride Cyclocreatine Kaempferol Yohimbic acid 7,4'-Dimethoxyisoflavone Linamarin To confirm these hits dose-response curves (IC50s) were determined using human neuroblastoma tumor cells in our standard Alamar Blue proliferation assay. In addition, we monitored proliferation over one week by quantifying cell numbers with trypan blue, and further, examined sphere formation over one week (as described in Figure 4) with at least 3 independent human SKP cell isolates. The high-throughput screens with human neuroblastoma tumor cells identified several small molecules that are effective in inhibiting proliferation of multiple neuroblastoma patient samples in vitro and xenograft neuroblastoma tumors in vivo (Figure 4).
Example 3 Characterization of MG 624 The proliferative effects of MG 624 on SKPs and neuroblastoma tumor initiating cells have also been studied in detail. Dose response curves for proliferation of human SKPs and neuroblastoma tumor initiating cells in response to MG 624 were generated in the presence of EGF and FGF2. At 200 nM MG 624, SKP cell proliferation is enhanced (Figure 5).

Example 4 Dose-response for proliferation of human SKPs To characterize enhancement of proliferation brought about by the agents identified above, dose-response curves for MG624, GSK3 fi, pramoxine, kaempferol, and alprostadil in presence of EGF and FGF2 were generated (Figures 6A-6E). In all cases, enhanced proliferation at 100 nM concentration of each agent was observed as compared to cells grown in the absence of the agent.

Other embodiments All patents, patent applications, and publications mentioned in this specification are herein incorporated by reference, including U.S. Provisional Application No. 61/101,443, filed September 30, 2008, to the same extent as if each independent patent, patent application, or publication was specifically and individually indicated to be incorporated by reference.
What is claimed is:

Claims (46)

1. A method of increasing proliferation of a cell, said method comprising contacting said cell with a sufficient amount of:
(a) a compound that decreases p63 expression or activity, or (b) a compound selected from the group consisting of acyclovir, alprostadil, aristolochic acid, carbadox, chlorpyrifos, cyclocreatine, 7,4'-dimethoxyisoflavone, dorzolamide, S(-)eticlopride, evoxine, guaifenesin, hydroxyprogesterone, kaempferol, linamarin, mexicanolide, MG 624, pramoxine, tannic acid, targinine, and yohimbic acid, or an analog thereof, under conditions that support cell proliferation.

2. The method of claim 1, wherein said cell is from a tumor cell line or is a stem cell.

3. The method of claim 2, wherein said stem cell is a skin-derived precursor (SKP).

4. The method of any of claims 1-3, wherein said compound selectively decreases p63 expression or activity.

5. The method of any of claims 1-4, wherein said compound is a p63 antibody, or an antigen-binding fragment thereof.

6. The method of any of claims 1-4, wherein said compound is an RNAi molecule that decreases p63 expression, or a nucleic acid encoding said RNAi molecule.

7. The method of any of claims 1-4, wherein said compound is a polypeptide substantially identical to a dominant negative form of p63, a fragment thereof, or a nucleic acid encoding said polypeptide, wherein said polypeptide or said fragment has dominant negative p63 activity.

8. The method of any of claims 1-7, wherein said cell is being cultured in vitro.

9. The method of claim 8, wherein said cell culture further comprises an additional growth factor.

10. The method of claim 9, wherein said growth factor is FGF2 or EGF.

11. The method of any of claims 1-10, wherein said contacting does not substantially alter the differentiation rate of said cell.

12. A composition comprising:
(a) an isolated stem cell; and (b) a compound selected from the group consisting of acyclovir, alprostadil, aristolochic acid, carbadox, chlorpyrifos, cyclocreatine, 7,4'-dimethoxyisoflavone, dorzolamide, S(-)eticlopride, evoxine, guaifenesin, hydroxyprogesterone, kaempferol, linamarin, mexicanolide, MG 624, pramoxine, tannic acid, targinine, and yohimbic acid, or an analog thereof, wherein said compound is present in an amount sufficient to promote proliferation of said stem cell.

13. A composition comprising:
(a) an isolated stem cell; and (b) a compound that decreases p63 expression or activity, wherein said compound is present in an amount sufficient to promote proliferation of said stem cell.

14. The composition of claim 12 or 13, wherein said stem cell is a SKP.

15. The composition of claim 12 or 13 further comprising a growth factor.

16. The composition of claim 15, wherein said growth factor is FGF2 or EGF.

17. The composition of any of claims 12-16, wherein said composition can support proliferation of said cells.

18. A composition comprising:

(a) a compound that decreases p63 expression or activity or a compound selected from the group consisting of acyclovir, alprostadil, aristolochic acid, carbadox, chlorpyrifos, cyclocreatine, 7,4'-dimethoxyisoflavone, dorzolamide, S(-)eticlopride, evoxine, guaifenesin, hydroxyprogesterone, kaempferol, linamarin, mexicanolide, MG 624, pramoxine, tannic acid, targinine, and yohimbic acid, or an analog thereof; and (b) a carrier suitable for topical administration.

19. The composition of claim 18, wherein said carrier is a lotion.

20. A kit comprising:

(a) a compound that decreases p63 expression or activity or a compound selected from the group consisting of acyclovir, alprostadil, aristolochic acid, carbadox, chlorpyrifos, cyclocreatine, 7,4'-dimethoxyisoflavone, dorzolamide, S(-)eticlopride, evoxine, guaifenesin, hydroxyprogesterone, kaempferol, linamarin, mexicanolide, MG 624, pramoxine, tannic acid, targinine, and yohimbic acid, or an analog thereof; and (b) instructions for use of (a) to promote cell proliferation, hair growth, skin repair, or skin health.

21. A method of increasing SKP proliferation in a subject, said method comprising administering to said subject a sufficient amount of:

(a) a compound that inhibits p63 expression or activity; or (b) a compound selected from the group consisting of acyclovir, alprostadil, aristolochic acid, carbadox, chlorpyrifos, cyclocreatine, 7,4'-dimethoxyisoflavone, dorzolamide, S(-)eticlopride, evoxine, guaifenesin, hydroxyprogesterone, kaempferol, linamarin, mexicanolide, MG 624, pramoxine, tannic acid, targinine, and yohimbic acid, or an analog thereof.

22. The method of claim 21, wherein said compound is administered topically or systemically.

23. The method of claim 21 or 22, wherein said compound that inhibits p63 expression or activity is a p63 antibody or an antigen-binding fragment thereof.

24. The method of claim 21 or 22, wherein said compound that inhibits p63 expression or activity is an RNAi molecule that inhibits p63 expression or a nucleic acid encoding said RNAi molecule.

25. The method of claim 21 or 22, wherein said compound that inhibits p63 expression or activity is a polypeptide substantially identical to a dominant negative form of p63, a fragment thereof, or a nucleic acid encoding said polypeptide, wherein said polypeptide or said fragment has dominant negative p63 activity.

26. A method of promoting hair growth in a subject, said method comprising administering to said subject a sufficient amount of:
(a) a compound that inhibits p63 expression or activity; or (b) a compound selected from the group consisting of acyclovir, alprostadil, aristolochic acid, carbadox, chlorpyrifos, cyclocreatine, 7,4'-dimethoxyisoflavone, dorzolamide, S(-)eticlopride, evoxine, guaifenesin, hydroxyprogesterone, kaempferol, linamarin, mexicanolide, MG 624, pramoxine, tannic acid, targinine, and yohimbic acid, or an analog thereof.

27. The method of claim 26, wherein said compound is administered topically or systemically.

28. The method of claim 26 or 27, wherein said compound that inhibits p63 expression or activity is a p63 antibody or an antigen binding fragment thereof.

29. The method of claim 26 or 27, wherein said compound that inhibits p63 expression or activity is an RNAi molecule that inhibits p63 expression or a nucleic acid encoding said RNAi molecule.

30. The method of claim 26 or 27, wherein said compound that inhibits p63 expression or activity is a polypeptide substantially identical to a dominant negative form of p63, a fragment thereof, or a nucleic acid encoding said polypeptide, wherein said polypeptide or said fragment has dominant negative p63 activity.

31. A method of repairing skin in a subject, said method comprising administering a sufficient amount of:
(a) a compound that inhibits p63 expression or activity; or (b) a compound selected from the group consisting of acyclovir, alprostadil, aristolochic acid, carbadox, chlorpyrifos, cyclocreatine, 7,4'-dimethoxyisoflavone, dorzolamide, S(-)eticlopride, evoxine, guaifenesin, hydroxyprogesterone, kaempferol, linamarin, mexicanolide, MG 624, pramoxine, tannic acid, targinine, and yohimbic acid, or an analog thereof.

32. The method of claim 31, wherein said subject has a wound, and said compound is administered in an amount sufficient to improve healing of said wound.

33. The method of claim 31 or 32, wherein said compound is administered topically or systemically.

34. The method of any of claims 31-33, wherein said compound that inhibits p63 expression or activity is a p63 antibody or an antigen-binding fragment thereof.

35. The method of any of claims 31-33, wherein said compound that inhibits p63 expression or activity is an RNAi molecule that inhibits p63 expression or a nucleic acid encoding said RNAi molecule.

36. The method of any of claims 31-33, wherein said compound that inhibits p63 expression or activity is a polypeptide substantially identical to a dominant negative form of p63, a fragment thereof, or a nucleic acid encoding said polypeptide, wherein said polypeptide or said fragment has dominant negative p63 activity.

37. A method of improving skin health in a subject, said method comprising administering to said subject a sufficient amount of:

(a) a compound that inhibits p63 expression or activity; or (b) a compound selected from the group consisting of acyclovir, alprostadil, aristolochic acid, carbadox, chlorpyrifos, cyclocreatine, 7,4'-dimethoxyisoflavone, dorzolamide, S(-)eticlopride, evoxine, guaifenesin, hydroxyprogesterone, kaempferol, linamarin, mexicanolide, MG 624, pramoxine, tannic acid, targinine, and yohimbic acid, or an analog thereof.

38. The method of claim 37, wherein said administration of said compound reduces wrinkles in the skin of said subject.

39. The method of claim 37, wherein said compound is administered topically or systemically.

40. The method of claim 37 or 39, wherein said compound that inhibits p63 expression or activity is a p63 antibody or an antigen-binding fragment thereof.

41. The method of claim 37 or 39, wherein said compound that inhibits p63 expression or activity is an RNAi molecule that inhibits p63 expression or a nucleic acid encoding said RNAi molecule.

42. The method of claim 37 or 39, wherein said compound that inhibits p63 expression or activity is a polypeptide substantially identical to a dominant negative form of p63, a fragment thereof, or a nucleic acid encoding said polypeptide, wherein said polypeptide or said fragment has dominant negative p63 activity.

43. The method of any of claims 21-42, wherein said subject is a human.

44. A method of identifying a compound capable of altering cell proliferation, said method comprising:
(a) contacting a SKP with a candidate compound; and (b) determining the proliferation rate of said SKP, wherein an alteration in the proliferation rate of said SKP in the presence of said compound as compared to in the absence of said compound, indicates that said compound alters the rate of cell proliferation.

45. The method of claim 44, wherein said SKP cell is a human, mouse, or rat cell.

46. The method of claim 44 or 45, wherein said compound is selected from a chemical library.