AU2001292631B2 - MUC1 extracellular domain and cancer treatment compositions and methods derived therefrom - Google Patents

Description

MUCl EXTRACELLULAR DOMAIN AND CANCER TREATMENT COMPOSITIONS AND METHODS DERIVED THEREFROM

This application claims priority to Provisional Application Serial No. 60/231,841, filed September 11, 2000. The United States government may own rights in the present invention pursuant to grant number R21-CA87421from the National Cancer Institute, National Institutes of Health, Department of Health and Human Services.

FIELD OF THE INVENTION

The present invention relates generally to the field of cancer therapy and more specifically to the use of modulators or agents that interact with MUCl as a point on intervention in cancer therapy.

BACKGROUND OF THE INVENTION

The human MUCl mucin glycoprotein is expressed on the apical borders of secretory epithelial cells on the luminal surface of most glandular epithelia (Kufe et al, 1984). In carcinomas, MUCl is highly overexpressed throughout the entire cell membrane and cytoplasm (Kufe et al, 1984; Perey et al, 1992). As such, the aberrant pattern of MUCl expression in carcinoma cells may confer a function for MUCl normally found at the apical membrane to the entire cell membrane. The hallmark of MUCl mucin is an ectodomain comprising a glycosylated 20 amino acid extracellular sequence that is tandemly repeated 25-100 times in each molecule (Strouss & Decker, 1992). The mucin glycosylation level appears to be lower in cancer cells than normal cells of ductal epithelial tissue (Kufe, U.S. Pat. No. 5,506,343). This hypoglycosylation results in the exposure of tumor-specific epitopes that are hidden in the fully glycosylated mucin.

Over ninety percent of breast cancers show an increased expression of MUCl

(also known as Mucin, Epithelial Membrane Antigen, Polymorphic Epithelial Mucin, Human Milk Fat Globule Membrane antigen, Episialin, DF-3, etc., see Barry & Sharkey, 1985). Several clinical studies have suggested that mucinous tumor antigens expressed on the cell surface of tumor cells associate with poor prognosis of a variety of cancer types (Itzkowitz et al, 1990).

MUCl is expressed as both a transmembrane form and a secreted form (Finn et al, 1995). The repeating sialyl epitopes of MUCl (the 'ectodomain') are shed into the serum (Reddish et al, 1996). The N-terminal ectodomain (the extracellular domain that is cleaved) of MUCl consists of a variable number of the 20-amino acid tandem repeats that are subject to O-glycosylation. This mucin extends far above the cell surface and past the glycocalyx making it easily available for interactions with other cells. The C-terminal region of MUCl includes a 37 amino acid transmembrane domain and a 72 amino acid cytoplasmic tail that contains sites for tyrosine phosphorylation. A approximately 45- amino acid extracellular domain remains following cleavage of the ectodomain. It is not known what enzyme is responsible for the cleavage of the ectodomain at this time. The extracellular domain or "MUCl/ECD," remaining, after cleavage of the ectodomain, typically includes the amino acid sequence:

TDNNHDVETQFNQYKTEAASRYNLTISDNSNSDVPFPFSAQSGAG. The cytoplasmic domain of MUCl ("MUC1/CD") encompasses multiple sub- domains that are important in intracellular signaling in cancer cells. β-Catenin binds directly to MUC1/CD at a SAGΝGGSSL motif (Yamamoto et al, 1997). β-Catenin, a component of the adherens junctions of mammalian epithelium, binds to cadherins at the intracellular surface of the plasma membrane and performs a signaling role in the cytoplasm as the penultimate downstream mediator of the wnt signaling pathway (Takeichi, 1990; Novak & Dedhar, 1999). The ultimate mediator of the wnt pathway is a nuclear complex of β-catenin and lymphoid enhancer factor/T cell factor (Lef/Tcf) which stimulates the transcription of a variety of target genes (see e.g., Molenaar et al, 1996; Brunner et al, 1997). Defects in the β-catenin-Lef/Tcf pathway are involved in the development of several types of cancers (Novak & Dedhar, 1999).

Glycogen synthase kinase 3β (GSK3β) also binds directly to MUCl/CD and phosphorylates serine in a DRSPY site adjacent to the β-catenin binding motif, thereby decreasing the association between MUCl and β-catenin (Li et al, 1998). In addition, the c-Src tyrosine kinase also binds to and phosphorylates a MUCl/CD SPYEKV motif, resulting in an increased interaction between MUCl/CD and β-catenin and a decreased interaction between MUCl/CD and GSK3β (Li et al, 2001). MUCl associates also constitutively with the epidermal growth factor receptor

(EGF-R, HER1) at the cell membrane and activated EGF-R induces phosphorylation of the MUCl/CD SPYKEN motif (Li et al, 2001(a)). EGF-R mediated phosphorylation of MUCl/CD appears to increase the interaction of MUCl with c-Src and β-catenin and downregulate the interaction between MUCl and GSK3β. These results support a model wherein MUCl integrates the signaling among c-Src, β-catenin and GSK3β pathways and dysregulation of this integrated signaling by aberrant overexpression of MUCl in cancer cells could promote the transformed phenotype (Li et al, 2001(a)).

The Armadillo protein pl20^ctn also binds directly to MUCl/CD resulting in the nuclear localization of pi 20 (Li & Kufe, 2001). PI 20 has been implicated in cell transformation and altered patterns of pl20 expression have been observed in carcinomas (see e.g., Jawhari et al, 1999; Shimazui et al, 1996). P120 is a v-Src tyrosine kinase substrate, binds to E-cadherin, and is implicated as a transcriptional coactivator (Reynolds et al, 1989; Reynolds et al, 1994; Daniels & Reynolds, 1999). The observations that pl20 localizes to both cell junctions and the nucleus have supported a role for pl20, like β-catenin, in the regulation of both cell adhesion and gene transcription. Decreased cell adhesion resulting from association of MUCl and pl20 may be involved in increased metastatic potential of MUCl -expressing tumor cells.

Thus the available evidence indicates that MUCl/CD functions to transfer signals from the extracellular domain to the nucleus, and utilizes signaling mechanisms that have been implicated in adhesion receptor and growth factor signaling and cellular transformation. It is desirable to identify compositions and methods related to modulation of the MUCl -mediated signaling and its putative role in cellular transformation. SUMMARY OF THE INVENTION

The present invention encompasses methods of use and pharmaceutical compositions relating to the discovery that the extracellular domain of MUCl provides binding domains for endogenous ligands and that such binding is related to an oncogenic function of MUCl and the proliferation of cancer cells.

Broadly the invention relates to cancer treatment compositions and methods employing agents or treatment methodologies that comprise or include antagonists of MUCl/ECD modulated cell proliferation. Preferred are methods and compositions that comprise agents that bind to MUCl/ECD or that bind to MUCl/ECD ligands that activate the oncogenic function of MUCl.

Thus, one aspect of the present invention provides for a method for inhibiting the proliferation of cancer cells, comprising administration of an effective amount of a MUCl/ECD antagonist. MUCl/ECD antagonists are agents that downregulate or reduce the quantity of MUCl/ECD presented on cell surfaces, or downregulate the level of wild- type MUCl/ECD ligands available for binding to MUCl/ECD, and/or MUCl/ECD binding inhibitors. A "MUCl/ECD binding inhibitor" means a compound that inhibits the binding of MUCl wild-type ligands, which may suitably include neuregulin 2 isoform 5 (SEQ ID NO: 2), neuregulin 2 isoform 6 (SEQ ID NO: 3), and appropriate fragments thereof, to MUCl ECD or a compound that inhibits the binding of an antibody that binds to an epitope within SEQ ID NO. 4 to MUCl/ECD. Appropriate fragments of neuregulin 2 isoform 5 (SEQ ID NO: 2) and neuregulin 2 isoform 6 (SEQ ID NO: 3) are those that bind to MUCl/ECD. MUCl/ECD binding inhibitors include antibodies, polypeptides and small molecules that inhibit such binding. A "MUCl/ECD-Pl binding inhibitor" means a MUCl/ECD binding inhibitor identified by inhibition of the binding to MUCl/ECD of an antibody the binds to an epitope within SEQ ID NO. 4.

In one embodiment of the invention, the MUCl/ECD inhibitor is the polypeptide of SEQ ID NO: 1, or a fragment comprising at least four consecutive amino acids of SEQ ID. NO: 1 such as TD V, NVHD, VHDV, DVET, VETQ, ETQF, TQFN, QFNQ, FNQY, NQYK, QYKT, YKTE, KTEA, TEAA, EAAS, AASR, ASRY, SRYN, RYNL, YNLT, NLTI, LTIS, TISD, ISDN, SDVS, DNSV, NSNS, SNSD, NSDN, SDNP, DNPF, NPFP, PFPF, FPFS, PFSA, FSAQ, SAQS, AQSG, QSGA, and SGAG. In other embodiments, the MUCl/ECD inhibitor is a conservative variant of the foregoing peptides. In another embodiment, the MUCl/ECD binding inhibitor is the polypeptide of SEQ ID NO: 4, SEQ TD NO: 5, or conservative variants thereof.

In another embodiment of the present invention, the MUCl/ECD inhibitor is an antibody that binds to one or more epitopes in the MUCl/ECD sequence SEQ ID NO: 1. In other embodiments of the invention, the MUCl/ECD inhibitor is an antibody that binds to an epitope within SEQ ID NO: 2 or SEQ ID NO: 3. The antibody may be a polyclonal or a monoclonal antibody. Monoclonal antibodies may be humanized or human monoclonal antibodies. It may also be a bispecific antibody or a fragment which comprises an antigen binding region. In some embodiments, the antibody is conjugated to a chemotherapeutic agent, radioisotope, toxin, or an effector that induces a cytolytic or cytotoxic immune response. Such conjugates may comprise a cytokine, an antimetabolite, an anthracycline, a vinca alkaloid, an antibiotic, an alkylating agent, a naturally derived toxin, or an Fc region of a IgGl immunoglobulin.

In another embodiment, the method further comprises the administration of a chemotherapeutic agent or radiation in combination with a MUCl/ECD antagonist. Chemotherapeutic agents typically include alkylating agents, topoisomerase inhibitors, antimetabolites, tubulin interactive agents, anti-hormonal agents, ornithine decarboxylase inhibitors and tyrosine kinase inhibitors.

In various embodiments, the cancer cells are selected from the group consisting of skin cancer cells, prostate cancer cells, lung cancer cells, brain cancer cells, breast cancer cells, ovarian cancer cells, cervical cancer cells, liver cancer cells, pancreatic cancer cells; colon cancer cells, stomach cancer cells and leukemia cells.

Another aspect of the invention is a method for reducing tumor growth in a mammal comprising administration of a therapeutic amount of a chemotherapeutic agent or radiation and an effective amount of a MUCl/ECD antagonist. In a preferred embodiment, the mammal is human. In one embodiment the method is for treating refractory tumors comprising administration of a therapeutic amount of a chemotherapeutic agent or radiation and an effective amount of a MUCl/ECD antagonist subsequent to treatment with one or more chemotherapeutic agents. In various embodiments, the tumor is a tumor of the skin, prostate, lung, brain, breast, ovary, cervix, liver, pancreas, colon, stomach or heampoietic system. Other aspects of the invention relate to pharmaceutical compositions comprising

MUCl/ECD antagonists and a pharmaceutically acceptable carrier. Wherein the antagonist is a MUCl/ECD binding inhibitor that may be the polypeptide of SEQ ID NO:

1 or a fragment comprising at least four consecutive amino acids, or conservative variants thereof, and a pharmaceutically acceptable carrier. In some embodiments, the MUCl/ECD inhibitor may be the polypeptide of SEQ ID NO: 4, SEQ ED NO: 5, or conservative variants thereof. In other embodiments, the pharmaceutical composition comprises an antibody that is a MUCl/ECD binding inhibitor and binds to an epitope within sequences of the peptides selected from the group consisting of SEQ ID NO: 1, SEQ ID NO: 2 and SEQ ID NO: 3 and a pharmaceutically acceptable carrier. The present invention also encompasses methods for screening MUCl/ECD binding inhibitor activity. One embodiment comprises a method of identifying a compound that inhibits the binding of ligands to MUCl/ECD, the method comprising: (a) providing a polypeptide comprising SEQ ED. NO: 1 or SEQ ED NO: 5; (b) contacting said polypeptide with a test compound and a ligand to the extracellular domain of MUCl selected from the group consisting of antibodies to MUCl ECD that stimulate MUCl mediated cancer cell proliferation and wild type ligands that bind to MUCl/ECD and stimulate cancer cell proliferation; and (c) determining whether the binding of said antibody to MUCl/ECD or wild type ligand is decreased relative to an appropriate control. Appropriate controls include, but are not limited to, assays wherein test compounds are excluded. In one embodiment the MUCl/ECD antibody that stimulates MUCl mediated cancer cell proliferation is an antibody that binds to an epitope within SEQ ED NO. 4. In other embodiments, the wild type ligands may suitable include neuregulin 2 isoform 5 (SEQ ED NO: 2) and appropriate fragments thereof and neuregulin

2 isoform 6 (SEQ ED NO: 3) and appropriate fragments thereof, wherein appropriate fragments are those that bind to the SEQ ED NO: 1 and have suitable growth stimulatory activity.

Another embodiment is a method of identifying a compound that inhibits the proliferation of MUCl -expressing cancer cells, the method comprising: (a) providing a population of MUCl -expressing cancer cells; (b) contacting said population of MUC1- expressing cancer cells with a test compound and a ligand to the extracellular domain of MUCl selected from the group consisting of antibodies to MUCl/ECD that stimulate MUCl mediated cancer cell proliferation and wild type ligands that bind to MUCl ECD and stimulate cancer cell proliferation; and (c) determining whether the proliferation of the population of MUCl -expressing cancer cells is decreased by comparison to an appropriate control. Appropriate controls include, but are not limited to, proliferation assays wherein test compounds are excluded. En one embodiment the MUCl/ECD antibody that stimulates MUCl mediated cancer cell proliferation is an antibody that binds to an epitope within SEQ ED NO. 4. In other embodiments, the wild type ligands may suitable include neuregulin 2 isoform 5 (SEQ ED NO: 2) and appropriate fragments thereof and neuregulin 2 isoform 6 (SEQ ED NO: 3) and appropriate fragments thereof, wherein appropriate fragments are those that bind to the SEQ ED NO: 1 and have suitable growth stimulatory activity.

The present invention also provides methods for identifying compounds that downregulate MUCl/ECD expression. The method comprises: (a) providing a population of MUCl -expressing cancer cells; (b) contacting said population of MUC1- expressing cancer cells with a test compound; (c) utilizing an anti-MUCl/ECD antibody to identify polypeptides comprising MUCl/ECD in the MUCl -expressing cancer cells; and (d) determining whether the expression of polypeptides comprising MUCl/ECD is decreased in comparison to controls wherein the test compound was excluded.

The present invention also encompasses pharmaceutical compositions comprising compounds identified by the foregoing methods and a pharmaceutically acceptable carrier. BRIEF DESCRIPTION OF THE DRAWINGS

The following drawings form part of the present specification and are included to further demonstrate certain aspects of the present invention. The invention may be better understood by reference to one or more of these drawings in combination with the detailed description of specific embodiments presented herein.

FIG. 1: Effect of anti-MUCl-Pl antibody on proliferation of ZR-75-1 breast carcinoma cells.

FIG. 2: Effect of anti-MUCl-Pl antibody on proliferation of SW480 cells stably expressing an empty vector (SW480/V) or MUCl (SW480/MUC1). FIG. 3: Effect of ZR-75-1 conditioned medium on proliferation of SW480 cells stably expressing an empty vector (SW480/V) or MUCl (SW480/MUC1).

FIG. 4: Effect of MUCl on H₂O₂ and taxol-induced apoptosis in HeLa cells stably expressing an empty vector (HeLa/N) or MUCl (HeLa/Mucl). The results are expressed as the percentage apoptosis (mean±SE) of three separate experiments.

DETAILED DESCRIPTION OF THE INVENTION I. Polypeptides

The polypeptides of the present invention can be created by synthetic techniques or recombinant techniques which employ genomic or cDNA cloning methods. Polypeptides can be routinely synthesized using solid phase or solution phase peptide synthesis. Methods of preparing relatively short polypeptides peptides, such as P0 (SEQ

ED NO: 9), PI (SEQ ED NO: 4), P2 (SEQ ED NO: 6) and P3 (SEQ ED NO: 7), by chemical synthesis are well known in the art. Such polypeptides could, for example be produced by solid-phase peptide synthesis techniques using commercially available equipment and reagents such as those available from Milligen (Bedford, Mass.) or Applied Biosystems-

Perkin Elmer (Foster City, CA). Alternatively, segments of such polypeptides could be prepared by solid-phase synthesis and linked together using segment condensation methods such as those described by Dawson et al, (1994). During chemical synthesis of such polypeptides, substitution of any amino acid is achieved simply by replacement of the residue that is to be substituted with a different amino acid monomer. Wild-type MUCl/ECD ligand polypeptides can be identified as exemplified in Example 3 herein. Recombinant MUCl/ECD ligands can then be prepared by methods known in the art.

The polypeptides of the present invention include variant polypeptides. By "variant" polypeptide is intended a polypeptide sequence modified by deletion or addition of one or more amino acids at one or more sites in the sequence; or substitution of one or more amino acids at one or more sites within the sequence. Variant polypeptides encompassed by the present invention retain the desired biological activity of the polypeptide from which they are derived. Such variants will have at least 40%, 50%, 60%, 70%, generally at least 75%, 80%, 85%, preferably about 90% to 95% or more, and more preferably about 98% or more sequence identity to the amino acid sequence of the polypeptide from which they are derived. The percentage of sequence identity, also termed homology, between a polypeptide native and a variant sequence may be determined by comparing the two sequences using the Gap program (Wisconsin Sequence Analysis Package, Version 8 for Unix, Genetics Computer Group, University Research Park, Madison Wisconsin), which uses the algorithm of Smith and Waterman, (1981).

The polypeptides of the present invention also include variant polypeptides with one or more conservative substitutions. For the purposes of classifying amino acid substitutions as conservative, amino acids are grouped as follows: Group I (hydrophobic sidechains): norleucine, met, ala, val, leu, ile; Group EC (neutral hydrophilic side chains): cys, ser, thr; Group Ed (acidic side chains): asp, glu; Group EV (basic side chains): asn, gin, his, lys, arg; Group N (residues influencing chain orientation): gly, pro; and Group NI (aromatic side chains): tip, tyr, phe. Conservative substitutions involve substitutions between amino acids in the same class.

Also encompassed by the present invention are chemical derivatives of polypeptides. "Chemical derivative" refers to a subject polypeptide having one or more residues chemically derivatized by reaction of a functional side group. Such derivatized residues include, for example, those molecules in which free amino groups have been derivatized to form amine hydrochlorides, p-toluene sulfonyl groups, carbobenzoxy groups, t-butyloxycarbonyl groups, chloroacetyl groups or formyl groups. Free carboyl groups may be derivatized to form salts, methyl and ethyl esters or other types of esters or hyrazides. Free hydroxyl groups may be derivatized to form O-acyl or O-alkyl derivatives. The imadazole group of histidine may be derivatized to form N- imbenzylhistidine.

The term "polypeptide" as used herein indicates a molecular chain of amino acids and does not refer to a specific length of the product.

II. Antibodies The term "antibody" is used in the broadest sense and specifically covers monoclonal antibodies (including full length monoclonal antibodies), polyclonal antibodies, multispecific antibodies (e.g., bispecific antibodies), and antibody fragments, so long as they exhibit the desired biological activity.

Methods for generating polyclonal antibodies are well known in the art. Briefly, a polyclonal antibody is prepared by immunizing an animal with an antigenic composition and collecting antisera from that immunized animal. A wide range of animal species can be used for the production of antisera including rabbit, mouse, rat, hamster, guinea pig and goat.

As is well known in the art, a given composition may vary in its immunogenicity. It is often necessary therefore to boost the host immune system, as may be achieved by coupling a polypeptide immunogen to a carrier. Exemplary and preferred carriers are keyhole limpet hemocyanin (KLH) and bovine serum albumin (BSA). Other albumins such as ovalbumin, mouse serum albumin or rabbit serum albumin can also be used as carriers. Means for conjugating a polypeptide to a carrier protein are well known in the art and include glutaraldehyde, m-maleimidobenzoyl-N-hydroxysuccinimide ester, carbodiimide and bis-biazotized benzidine. As is also well known in the art, the immunogenicity of a particular immunogen composition can be enhanced by the use of non-specific stimulators of the immune response, known as adjuvants. Exemplary and preferred adjuvants include complete Freund's adjuvant (a non-specific stimulator of the immune response containing killed Mycobacterium tuberculosis), incomplete Freund's adjuvants and aluminum hydroxide adjuvant.

The serum for an immunized animal may be used as is for various applications or the desired antibody fraction may be purified by well-known methods, such as affinity chromatography using another antibody or a peptide bound to a solid matrix.

Monoclonal antibodies (MAbs) may be readily prepared through use of well- known techniques, such as those exemplified in U.S. Patent 4,196,265, incorporated herein by reference. Typically, this technique involves immunizing a suitable animal with a selected immunogen composition, e.g., a purified or partially purified expressed polypeptide. The immunizing composition is administered in a manner that effectively stimulates antibody producing cells.

The methods for generating monoclonal antibodies (MAbs) generally begin along the same lines as those for preparing polyclonal antibodies. The use of rats may provide certain advantages (Goding, 1986), but mice are preferred, with the BALB/c mouse being the most routinely used and generally gives a higher percentage of stable fusions.

Following immunization, somatic cells with the potential for producing antibodies, specifically B lymphocytes (B cells), are selected for use in the MAb generating protocol. These cells may be obtained from biopsied spleens, tonsils or lymph nodes, or from a peripheral blood sample. Spleen cells and peripheral blood cells are preferred. Often, a panel of animals will have been immunized and the spleen of animal with the highest antibody titer will be removed and obtaining lymphocytes from the spleen.

The antibody-producing B lymphocytes from the immunized animal are then fused with cells of an immortal myeloma cell, generally one of the same species as the animal that was immunized. Myeloma cell lines suited for use in hybridoma-producing fusion procedures preferably are non-antibody-producing, have high fusion efficiency, and have enzyme deficiencies that render them incapable of growing in certain selective media that support the growth of only the desired fused cells (hybridomas). Selected hybridomas are serially diluted and cloned into individual antibody-producing cell lines, which can then be propagated indefinitely to provide MAbs. En accordance with the present invention, fragments of the monoclonal antibody of the invention can be obtained from the monoclonal antibody produced as described above, by methods which include digestion with enzymes such as pepsin or papain and/or cleavage of disulfide bonds by chemical reduction. Alternatively, monoclonal antibody fragments encompassed by the present invention can be synthesized using an automated synthesizer, or by expression of full-length gene or of gene fragments in E. coli or other recombinant microorganisms and cell lines.

The present invention also encompasses various antibody conjugates. Conjugates with fluorescein markers are prepared be methods known in the art, such as conjugation in the presence of coupling agents or by reaction with an isothiocyanate. Conjugates with metal chelates are similarly produced. Other moieties to which antibodies may be conjugated include radionuclides such as ¹³¹ 1, ⁹⁰ Y, ¹⁰⁵ Rh, ⁴⁷ Sc, ⁶⁷ Cu, ²¹²Bi, ^2π At, ¹⁸⁸ Re, ¹⁰⁹ Pd, ⁴⁷ Sc, ²¹² Pb, and ¹⁵³ Sm and the like, as described in Gansow, 1991, which is herein incorporated by reference. Monoclonal antibodies of the invention can also be coupled to conventional chemotherapeutic agents such as an antimetabolite, an anthracycline, a vinca alkaloid, an antibiotic or an alkylating agent. Drugs that may be coupled to the antibodies for targeting include compounds such as doxorubicin, cyclophosphamide, cisplatin, adriamycin, estramustine, fluorouracil, ethinyl estradiol, mitoxantrone, methotrexate, finasteride, taxol, and megestrol. Methods of coupling may be direct via covalent bonds, or indirect via linking molecules, and will generally be known in the art for the particular drug selected and are made using a variety of bifunctional protein coupling agents. Examples of such reagents are SPDP, IE, bifunctional derivatives of imidoesters such a dimethyl adipimidate HCl, active esters such as disuccinimidyl suberate, aldehydes such as glutaraldehyde, bisazido compounds such as his (R-azidobenzoyl) hexanediamine, bisdiazonium derivatives such as bis-(R-diazoniumbenzoyl)ethylenediamine, diisocyanates such as tolylene 2,6-diisocyanate, and bis-active fluorine compounds such as l,5-difluoro-2,4-dinitrobenzene. (See, e.g., Thorpe et al, 1982, herein incorporated by reference). The antibodies of the present invention may also be conjugated with various toxin molecules or an effector such as IgGl immunoglobulin, which induces cytolytic or cytotoxic immune response. Thus, the two components may be chemically bonded together by any of a variety of well-known chemical procedures. For example, the linkage may be by way of heterobifunctional cross-linkers, e.g. SPDP, carbodiimide, glutaraldehyde, or the like. The toxin molecules may also be fused to the antibody or binding regions thereof by recombinant means, such as through the production of single chain antibodies. The genes encoding protein chains may be cloned in cDNA or in genomic form by any cloning procedure known to those skilled in the art (see e.g., Sambrook et al, 1989). The recombinant production of various immunotoxins is well- known within the art and can be found, for example in Thorpe et al, 1982(a), Waldmann, 1991, and Pastan et al., 1992, all herein incorporated by reference. A variety of toxin molecules are suitable for use as the cytotoxic domain in the antibody conjugates or fusion proteins described here. Any toxin known to be useful as the toxic component of an immunotoxin may be used, preferably a protein toxin that may be recombinantly expressed. Particularly useful as the cytotoxic domain are bacterial toxins such as Pseudomonas exotoxin A (PE), diphtheria toxin, shiga toxin and shiga-like toxin, and ^• ribosome inactivating toxins derived from plants and fungi, including ricin, -sarcin, restrictotocin, mitogellin, tricanthosin, saporin-G, saporin-1, momordin, gelonin, pokeweed antiviral protein, abrin, modeccin and others described in Genetically Engineered Toxins, ed. A. Frankel, Marcel Dekker, Inc., 1992, herein incorporated by reference, and any recombinant derivatives of those proteins (see Olsnes 1981; U.S. Pat. No. 4,675,382; and U.S. Pat. No. 4,894,443, herein incorporated by reference).

The antibody may also be a bispecific antibody which recognizes both the MUCl/ECD and an antigen which promotes the release of a cytokine such as EL-1, TNF alpha and CD16, CD2, CD3 L.C. CD28, which in turn, will activate the release of EFN gamma or TNF alpha, respectively.

The MAb's of the present invention encompass chimeric Mabs, including, "humanized" forms of non-human (e.g., murine) Mabs. Humanized MAbs are chimeric antibodies which contain minimal sequence derived from non-human immunoglobulin. For the most part, humanized antibodies are human immunoglobulins (recipient antibody) in which residues from a hypervariable region of the recipient are replaced by residues from a hypervariable region of a non-human species (donor antibody) such as mouse, rat, rabbit or nonhuman primate having the desired specificity, affinity, and capacity. In some instances, framework residues of the human immunoglobulin are replaced by corresponding non-human residues. Furthermore, humanized antibodies may comprise residues which are not found in the recipient antibody or in the donor antibody. These modifications are made to further refine antibody performance. En general, the humanized antibody will comprise substantially all of at least one, and typically two, variable domains, in which all or substantially all of the hypervariable regions correspond to those of a non-human immunoglobulin and all or substantially all of the framework regions are those of a human immunoglobulin sequence. The humanized antibody optionally also will comprise at least a portion of an immunoglobulin constant region (Fc), typically that of a human immunoglobulin. (see Jones et al, 1986; Riechmann et al, 1988; and Presta, 1992). Fully human MAbs are preferred in the therapeutic methods of the present invention.

"Single-chain FV or "sFv" antibody fragments of the present invention comprise the NH and NL domains of antibody, wherein these domains are present in a single polypeptide chain. Generally, the Fv polypeptide further comprises a polypeptide linker between the NH and NL domains which enables the sFv to form the desired structure for antigen binding (see Pluckthun, 1994).

HI. Screening and Diagnostic Assays

The present invention provides for methods for identifying compounds that inhibit the binding of various ligands to MUCl/ECD. The binding ligands include neuregulin 2 isoform 5 (SEQ ED NO: 2), neuregulin 2 isoform 6 (SEQ 3D NO: 3) and fragments of either isoform that bind to MUCl/ECD and, in a preferred embodiment, an antibody that binds to an epitope within SEQ ED NO: 4.

In one embodiment, the screening method utilizes an in vitro competitive binding assay, wherein the capacity of a test compound to inhibit the binding of the aforementioned ligands to a polypeptide comprising SEQ ED NOJ or SEQ ED NO: 5 is assessed. Ln such an assay, the polypeptide comprising MUCl/ECD derived sequences SEQ ED NOJ or SEQ ED NO: 5 may be conjugated to another protein or produced as a fusion protein, e.g., the GST-MUCl/ECD fusion protein exemplified herein in Example 3. Other suitable conjugates and fusion proteins may be made by one of skill in the art utilizing procedures know in the art. The polypeptides or MUCl/ECD ligands may be labeled with a radioisotope or fluorescent label (e.g., phycobiliproteins, such as phycoerythrin and allophycocyanins, fluorescein and Texas red). Alternatively an enzyme, such as peroxidase, may be used and conjugated either directly or indirectly via a biotin and avidin or streptavidin system. Decreased binding upon introduction of a test compound is indicative of competitive binding.

A compound that inhibits the binding of ligands to MUCl/ECD may be a modulator, that is an antagonist or agonist of the biological activity initiated by MUCl ECD binding by neregulin 2 isoforms 5 or 6. E.g., the antibody raised to polypeptide PI (SEQ ED. NO 4) is expected to inhibit binding of the wild-type ligands but acts as an agonist for the MUCl/ECD binding site, i.e., it stimulates proliferation of carcinoma cells. In contrast, appropriate compounds, such as the MUCl/ECD polypeptide SEQ ED NO. 1, will bind to the endogenous wild-type ligands thereby preventing binding to MUCl/ECD and consequently acting as an antagonist, i.e., preventing or decreasing the proliferation of carcinoma cells that would be otherwise observed upon binding of the MUCl/ECD ligands.

An alternative screening assay can discriminate between MUCl/ECD binding inhibitors that exhibit antagonist and agonist activity in regard to the proliferation of MUCl -expressing cancer cells. The method requires a population of MUCl-positive cancer cells, preferably human cancer cells. This could be a population of cells that constitutively expresses MUCl, but the population is preferably of a cell type engineered to express MUCl. The latter are more versatile in regard to providing cells for appropriate controls, e.g. cells engineered with an empty vector, and also for enabling the construction of cells expressing MUCl mutants. Examples of engineered MUCl cancer cells include, but are not limited to, SW480 and HCT116 colon cancer cells as exemplified in Examples 2 and 4 herein. Inhibition of MUCl/ECD ligand-induced cell proliferation will indicate a test compound with antagonist activity. Controls may comprise incubation of cancer cells engineered with an empty vector (i.e. MUC1- negative) or incubation of MUCl-positive cells in the absence of either the test compound or the MUCl/ECD ligand. One of the latter controls will identify agonists, i.e., stimulation of cancer cell proliferation observed in incubations in which the test compound is present and the MUCl/ECD ligand is absent. Specificity of the agonist activity is established by use of engineered MUCl-negative cells.

Yet another screening assay monitors MUCl ECD ligand induced phosphorylation of the intracellular domain of MUCl. Alternate screening methodologies employ monitoring of MUCl/ECD ligand induced association of MUCl with EGF-R, s-Src, β-catenin, GSK3β or pl20. Methods for monitoring such phosphorylation and protein associations are described in Li et al, (1998), Li et al, (2001), Li et al, (2001(a)) and Li & Kufe, (2001), all herein incorporated by reference. The present invention also provides for methods for identifying compounds that downregulate the expression of MUCl/ECD. In some embodiments of the invention, labeled antibodies to MUCl/ECD are utilized to visualize the expression of MUC/ECD in appropriate cell lines by flow cytometry or by immunohistochemistry, using methods know in the art. Alternatively, the expression of MUCl can be estimated by immunoblotting or by probing total cellular RNA with labeled DNA probes, e.g., as described in Example 7 herein.

Estimation of the expression of MUCl/ECD can also be used for diagnostic methodologies, wherein antibodies to MUCl ECD are utilized to investigated the expression of MUCl/ECD on or in cells derived from a subject. Such antibodies can also be utilized for imaging of cancer cells within a subject. Imaging is performed by labeling the anti-MUCl/ECD antibody, e.g., with a radiolabel, and injecting the antibody to a subject and monitoring the location of the antibody within the body of said subject. IV. Combination with Chemotherapeutic Agents

The present invention encompasses the use of the MUCl/ECD antagonists in combination with chemotherapeutic agents. While not being limited by any particular theory, MUCl inhibits the apoptotic response to genotoxic stress induced by certain chemotherapeutic agents, and thereby induces resistance to such agents. MUCl/ECD antagonists may be used to mitigate this MUCl mediated response to chemotherapeutic agents, thereby enhancing the effectiveness of such agents. In this regard, MUCl/ECD antagonists will be useful for the treatment cancer cells resistant to chemotherapeutic agents, including residual cancers remaining or reoccurring after cancer chemotherapy. The foregoing rational also pertains to the combination of MUCl/ECD antagonists and ionizing radiation.

The chemotherapeutic agents useful in the methods of the invention include the full spectrum of compositions and compounds which are known to be active in killing and/or inhibiting the growth of cancer cells. The chemotherapeutic agents, grouped by mechanism of action include DNA-interactive agents, antimetabolites, tubulin interactive agents, anti-hormonals, anti-virals, ODC inhibitors and other cytotoxics such as hydroxy- urea. Any of these agents are suitable for use in the methods of the present invention.

DNA-interactive agents include the alkylating agents, e.g., cisplatin, cyclophosphamide, altretamine; the DNA strand-breakage agents, such as bleomycin; the intercalating topoisomerase II inhibitors, e.g., dactinomycin and doxorubicin); the nonintercalating topoisomerase II inhibitors such as, etoposide and teniposide; and the DNA minor groove binder plicamycin.

The alkylating agents form covalent chemical adducts with cellular DNA, RNA and protein molecules and with smaller amino acids, glutathione and similar chemicals. Generally, these alkylating agents react with a nucleophilic atom in a cellular constituent, such as an amino, carboxyl, phosphate, sulfhydryl group in nucleic acids, proteins, amino acids, or glutathione. The mechanism and the role of these alkylating agents in cancer therapy is not well understood. Typical alkylating agents include: nitrogen mustards, such as chlorambucil, cyclophosphamide, ifosfamide, mechlorethamine, melphalan, uracil mustard; aziridine such as thiotepa; methanesulphonate esters such as busulfan; nitroso ureas, such as carmustine, lomustine, streptozocin; platinum complexes such as cisplatin, carboplatin; bioreductive alkylators, such as mitomycin and procarbazine, dacarbazine and altretemine; DNA strand-breaking agents including bleomycin.

Topoisomerases are ubiquitous cellular enzymes which initiate transient DNA strand breaks during replication to allow for free rotation of the strands. The functionality of these enzymes is critical to the replication process of DNA. Without them, the torsional strain in the DNA helix prohibits free rotation, the DNA strands are unable to separate properly, and the cell eventually dies without dividing. Topo I links to the 3'- terminus of a DNA single strand break, while Topo Et links to the 5 '-terminus of a double strand DNA break. DNA topoisomerase Et inhibitors include the following: intercalators such as amsacrine, dactinomycin, daunorubicin, doxorubicin, idarubicin and mitoxantrone; nonintercalators such as etoposide and teniposide; camtothecins including irinotecan (CPT-II) and topotecan. A representative DNA minor groove binder is plicamycin. The antimetabolites generally exert cytotoxic activity by interfering with the production of nucleic acids by one or the other of two major mechanisms. Some of the drugs inhibit production of the deoxyribonucleoside triphosphates that are the immediate precursours of DNA synthesis, thus inhibiting DNA replication. Some of the compounds are sufficiently like purines or pyrimidines to be able to substitute for them in the anabolic nucleotide pathways. These analogs can then be substituted into the DNA and RNA instead of their normal counterparts. The antimetabolites useful herein include: Mate antagonists such as methotrexate and trimetrexate; pyrimidine antagonists such as fluorouracil, fluorodeoxyuridine, azacitidine, cytarabine, and floxuridine; purine antagonists include mercaptopurine, 6-thioguanine, fludarabine, pentostatin; sugar modified analogs include cytarabine, fludarabine; ribonucleotide reductase inhibitors include hydroxyurea.

Tubulin interactive agents interfere with cell division by binding to specific sites on Tubulin, a protein that polymerizes to form cellular microtubules. Microtubules are critical cell structure units. When the interactive agents bind on the protein, the cell cannot properly form microtubules. Tubulin interactive agents include vincristine and vinblastine, both alkaloids and the taxanes (paclitaxel and docetaxel).

Although their mechanisms of action are different, both taxanes and vinca alkaloids exert their biological effects on the cell microtubles. Taxanes act to promote the polymerization of tubulin, a protein subunit of spindle microtubles. The end result is the inhibition of depolymerization of the microtubles, which causes the formation of stable and nonfunctional microtubles. This disrupts the dynamic equilibrium within the microtuble system, and arrests the cell cycle in the late G₂ and M phases, which inhibits cell replication. Like taxanes, vinca alkaloids also act to affect the microtuble system within the cells. In contrast to taxanes, vinca alkaloids bind to tubulin and inhibit or prevent the polymerization of tubulin subunits into microtubles. Vinca alkaloids also induce the depolymerization of microtubles, which inhibits microtuble assembly and mediates cellular metaphase arrest. Vinca alkaloids also exert effects on nucleic acid and protein synthesis; amino acid, cyclic AMP, and glutathione synthesis; cellular respiration; and exert immunosuppressive activity at higher concentrations.

Antihormonal agents exert cytotoxic activity by blocking hormone action at the end-receptor organ. Several different types of neoplasm require hormonal stimulation to propagate cell reproduction. The antihormonal agents, by blocking hormone action, deprive the neoplastic cells of a necessary stimulus to reproduce. As the cells reach the end of their life cycle, they die normally, without dividing and producing additional malignant cells. Antihormonal agents are typically derived from natural sources and include: estrogens, conjugated estrogens and ethinyl estradiol and diethylstibesterol, chlortrianisen and idenestrol; progestins such as hydroxyprogesterone caproate, medroxyprogesterone, and megestrol; androgens such as testosterone, testosterone propionate; fluoxymesterone, methyltestosterone.

Adrenal corticosteroids are derived from natural adrenal cortisol or hydrocortisone. They are used because of their anti-inflammatory benefits as well as the ability of some to inhibit mitotic divisions and to halt DNA synthesis, these compounds include prednisone, dexamethasone, methylprednisolone, and prednisolone. Leutinizing-releasing hormone agents or gonadotropin-releasing hormone antagonists are used primarily in the treatment of prostate cancer. These include leuprolide acetate and goserelin acetate. They prevent the biosynthesis of steroids in the testes.

Anti-hormonal agents include antiestrogenic agents such as tamoxifen, antiandrogen agents such as flutamide, and antiadrenal agents such as mitotane and aminoglutethimide.

ODC (or ornithine decarboxylase) inhibitors inhibit cancerous and pre-cancerous cell proliferation by depleting or otherwise interfering with the activity of ODC, the rate limiting enzyme of polyamine biosynthesis important to neoplastic cell growth. En particular, polyamine biosynthesis wherein ornithine is converted to the polyamine, putrescine, with putrescine being subsequently by converted to spermidine and spermine appears to be an essential biochemical event in the proliferation of neoplastic growth in a variety of cancers and cancer cell lines and the inhibition of ODC activity or depletion of ODC in such neoplastic cells has been shown to reduce polyamine levels in such cells leading to cell growth arrest; more differentiated cell morphology and even cellular senescence and death. In this regard, ODC or polyamine synthesis inhibitors are considered to be more cytotoxic agents functioning to prevent cancer reoccurrence or the conversion of pre-cancerous cells to cancerous cells than cytotoxic or cell killing agents. A suitable ODC inhibitor is eflornithine or α-difluoromethyl-ornithine, an orally available, irreversible ODC inhibitor, as well as a variety of polyamine analogs which are in various stages of pre-clinical and clinical research.

Other cytotoxics include agents which interfere or block various cellular processes essential for maintenance of cellular functions or cell mitosis as well as agents which promote apoptosis. In this regard, hydroxyurea appears to act via inhibitors of the enzyme ribonucleotide reductase whereas asparaginase enzymatically converts asparagine into non-functional aspartic acid thereby blocking protein synthesis in a tumor.

Compositions of the MUCl/ECD antagonists of present invention can also be used in combination with antibodies to HER-2, such as Trastuzumab (Herceptin (H)). n addition, the present invention also emcompasses the use of MUCl domain antoagonists in combination with epidermal growth factor recpetor-interactive agents such as tyrosine kinase inhibitors. Tyrosine kinase inhibitors suitably include imatinib (Norvartis), OSI- 774 (OSI Pharmaceuticals), ZD-1839 (AstraZeneca), SU-101 (Sugen) and CP-701 (Cephalon).

When used in the treatment methods of the present invention, it is contemplated that the chemotherapeutic agent of choice can be conveniently used in any formulation which is currently commercially available, and at dosages which fall below Or within the approved label usage for single agent use.

V. Ionizing Radiation En the present invention, the term "ionizing radiation" means radiation comprising particles or photons that have sufficient energy or can produce sufficient energy via nuclear interactions to produce ionization (gain or loss of electrons). An exemplary and preferred ionizing radiation is an x-radiation. Means for delivering x-radiation to a target tissue or cell are well known in the art. The amount of ionizing radiation needed in a given cell generally depends on the nature of that cell. Means for determining an effective amount of radiation are well known in the art. Used herein, the term "an effective dose" of ionizing radiation means a dose of ionizing radiation that produces cell damage or death when given in conjunction with the MUCl/ECD antagonists of the present invention, optionally further combined with a chemotherapeutic agent. Dosage ranges for x-rays range from daily doses of 50 to 200 roentgens for prolonged periods of time (3 to 4 weeks), to single doses of 2000 to 6000 roentgens. Dosage ranges for radioisotopes vary widely, and depend on the half -life of the isotope, the strength and type of radiation emitted, and the uptake by the neoplastic cells.

Any suitable means for delivering radiation to a tissue may be employed in the present invention, in addition to external means. For example, radiation may be delivered by first providing a radiolabeled antibody that immunoreacts with an antigen of the tumor, followed by delivering an effective amount of the radiolabeled antibody to the tumor. In addition, radioisotopes may be used to deliver ionizing radiation to a tissue or cell. VI. Downregulation of MUCl/ECD Expression

The present invention also encompass compounds that downregulate MUCl/ECD expression. One such compound is the isocoumarin NM-3 (2-(8-hydroxy-6-methoxy-l- oxo-1 H-2-benzopyran-3-yl) propionic acid). NM-3 and other isocoumarins suitable to downregulate the expression of MUCl/ECD are disclosed in U.S. patent No. 6,020,363, the entirety of which is herein incorporated by reference. Other suitable compounds include 2-substituted estradiol compounds such as 2-methoxyestradiol and 2- hydroxyrestradiol. These and other suitable estradiol derivatives are disclosed in U.S. Patent No. 6,239,123, the entirety of which is herein incorporated by reference. Other compounds suitable for downregulating MUCl/ECD expression include antisense oilgonucleotides that target nucleic acid molecules encoding MUCl, as described below.

VII. Antisense Oligonucleotides

The present invention also employs antisense compounds, particularly oilgonucleotides, for use in modulating the function of nucleic acid molecules encoding MUCl and MUCl/ECD wild-type ligands, such as neuregulin 2 isoforms 5 and 6. Inhibition of MUCl expression will decrease the levels of MUCl/ECD available for binding to MUCl/ECD ligands. Inhibition of the expression of the endogenous ligands of MUCl/ECD will prevent or decrease the proliferative effect on cancer cells associated with the binding of such ligands to MUCl/ECD. Antisense methodology takes advantage of the fact that nucleic acids tend to pair with "complementary sequences." By complementary, it is meant that polynucleotides are those capable of base-pairing according to the standard Watson-Crick complementary rules. The oligonucleotides of the present invention may be targeted wholly or in part to informational sequences, i.e., those coding for a protein, and other associated ribonucleotides such 5 '-untranslated regions, 3 '-untranslated regions, 5' cap regions and intron/exon junctions. Thus, the invention provides oilgonucleotides which specifically hybridize with nucleic acids, preferably mRNA, encoding MUCl and/or MUCl/ECD wild-type ligands such as neuregulin 2 isoforms 5 and 6. The overall effect of interference with mRNA is modulation of expression of neuregulin isoforms 5 and/or 6. Such modulation can be measured in ways that are routine in the art. In addition, effects on cancer cell proliferation or tumor growth can be assessed.

It is understood that an oligonucleotide need not be 100% complementary to its target nucleic acid sequence to be specifically hybridizable. An oligonucleotide is specifically hybridizable when binding of the oligonucleotide to the target interferes with the normal function of the target molecule to cause a loss of utility, and there is a sufficient degree of complementarity to avoid non-specific binding of the oligonucleotide to non-target sequences under conditions in which specific binding is desired, i.e., under physiological conditions in the case of in vivo assays or therapeutic treatment. The antisense compounds in accordance with this invention preferably comprise from about 4 to about 50 nucleobases. Particularly preferred are antisense oligonucleotides comprising from about 8 to about 30 linked nucleobases. The oligonucleotides used in accordance with this invention may be conveniently and routinely made through the well-known technique of solid phase synthesis. In the context of this invention, the term "oligonucleotide" refers to an oligomer or polymer of ribonucleic acid or deoxyribonucleic acid. This term includes oligonucleotides composed of naturally-occurring nucleobases, sugars and covalent intersugar (backbone) linkages as well as oligonucleotides having non-naturally-occurring portions which function similarly. Such modified or substituted oligonucleotides are often preferred over native forms because of desirable properties such as, for example, enhanced cellular uptake, enhanced binding to target and increased stability in the presence of nucleases. Examples of some preferred modified oligonucleotides include those containing phosphorothioates, phosphotriesters, methyl phosphonates, short chain alkyl or cycloalkyl intersugar linkages or short chain heteroatomic or heterocyclic intersugar linkages. Another additional or alternative modification of the oligonucleotides of the present invention involves chemically linking to the oligonucleotide one or more lipophilic moieties which enhance the cellular uptake of the oligonucleotide. Such lipophilic moieties may be linked to an oligonucleotide at several different positions on the oligonucleotide. Some preferred positions include the 3' position of the sugar of the 3' terminal nucleotide, the 5' position of the sugar of the 5' terminal nucleotide, and the 2' position of the sugar of any nucleotide. The antisense compounds of the present invention also include bioequivalent compounds, including pharmaceutically acceptable salts and prodrugs.

The terms "specifically hybridizable" and "complementary" are used to indicate a degree of complementarity sufficient to result in stable and specific binding between the antisense oligonucleotide and the target nucleic acid sequence. An oligonucleotide need not be 100% complementary to its target nucleic acid sequence to be specifically hybridizable. An oligonucleotide considered "specifically hybridizable" when binding of the oligonucleotide to the target interferes with the normal function of the target molecule to cause a loss of utility and decrease in expression of the product protein, and there is a sufficient degree of complementarity to avoid non-specific binding of the oligonucleotide to non-target sequences.

The neuregulin 2 protein family comprises a number of alternatively spliced isoforms (Ring et al, 1999). The coding sequences for neuregulin 2 isoforms 5 and 6 share the same nucleotide sequence from exons 1 through 6 of the neuregulin 2 gene that code for the first 416 amino acids of each protein but differ in the sequence coding for the carboxy terminal 10 amino acids of isoform 5 and for the carboxy terminal 6 amino acids of isoform 6. The coding DNA sequences of exons 1 through 6 are incorporated in SEQ ED NO: 10 through SED ED. NO: 15 respectively. The sequences coding for the first 416 amino acids of isoforms 5 and 6 are nucleotides 313 through 1012 of SEQ ED. NO 10, nucleotides 51-222 of SEQ ED. NO: 11, nucleotides 230-348 of SEQ ED NO: 12, nucleotides 100 through 220 of SEQ ED. NO: 13, nucleotides 111 through 187 of SEQ ED. NO: 14 and nucleotides 123 through 181 of SEQ ED. NO: 15. The sequences coding for the carboxy terminals of isoform 5 and isoform 6 are nucleotides 132 through 164 of SEQ ED NO: 16 and nucleotides 30 through 50 of SEQ ED NO: 17 respectively.

As SEQ ED NO: 16 and SEQ ED NO: 17 are apparently not shared by other neuregulin gene products, in a preferred embodiment, the antisense oligonucleotide comprises a sequence of at least 4 nucleotides that is complementary to a region between nucleotides 132 and 164 of SEQ ED. NO: 16 or nucleotides 30 through 50 of SEQ ED NO: 17. In a more preferred embodiment, the antisense oilgonucleotides comprises a sequence of at least 8 nucleotides that is complementary to a region between nucleotides 132 and 164 of SEQ ED. NO: 16 or nucleotides 30 through 50 of SEQ ED NO: 17.

In other embodiments, the antisense oligonucleotide comprises a sequence of at least 4 nucleotides that is complementary to a region between nucleotides 313 through 1012 of SEQ ED. NO 10, or a region between nucleotides 51-222 of SEQ ED. NO: 11, or a region between nucleotides 230-348 of SEQ ED NO: 12, or a region between nucleotides 100 through 220 of SEQ ED. NO: 13, or a region between nucleotides 111 through 187 of SEQ ED. NO: 14, or a region between nucleotides 123 through 181 of SEQ ED. NO: 15. Ln another embodiment the antisense oligonucleotide is at least 8 nucleotides that is complementary to a region of the one the foregoing nucleotides sequences.

In other embodiments, the antisense oligonucleotide comprises a sequence of at least 4 nucleotides, and preferably a sequence of at least 8 nucleotides, that is complementary to a non-coding region of SED ED NOS: 10 through 17.

En other embodiments of the invention, MUCl directed antisense oligonucleotides comprise a sequence of at least 4 nucleotides that is complementary to SEQ ED NO: 18. En preferred embodiments, the antisense oligonucleotides comprises a sequence of at least 8 nucleotides that is complementary to SEQ ED NO: 18

The present invention also encompasses expression vectors comprising an expression control system that directs production of a transcript of the foregoing antisense oilgonucleotides. In addition, the present invention provides for methods of hybridization comprising providing one of the forgoing antisense oilgonucleotides and contacting such oligonucleotide with a nucleic acid comprising the target sequence under conditions that permit hybridization of the oligonucleotide with the nucleic acid. Also included are methods of inhibiting translation of mRNA comprising providing one of the forgoing antisense oilgonucleotides and providing a cell comprising mRNA comprising the target sequence and introducing the oligonucleotide into the cell, wherein the oligonucleotide inhibits translation of the mRNA in the cell.

Another aspect of the present invention provides for pharmaceutical compositions comprising an antisense oligonucleotide of the invention and a pharmaceutically acceptable carrier. VIII. Vaccines

The present invention also encompasses the use of MUCl/ECD peptides, e.g,. SEQ ED NO: 1 or fragments thereof, wherein such fragments comprise four or more consecutive amino acids of SEQ ED NO. 1, in a vaccine wherein the host mammal generates antibodies to the polypeptide which also act against the host's own MUCl/ECD. Vaccine preparation techniques are generally known in the art as described by Duffy (1980), and references cited therein, all of which are incorporated herein by reference.

The MUCl/ECD peptides may be conjugated to a carrier molecule such as a protein or Ficoll. The carrier protein is preferably one with a molecular weight of at least about 40,000 dalton and more preferably at least about 60,000 dalton. The vaccine formulation may comprise a pharmaceutically acceptable carrier and may also include adjuvant systems for enhancing the immunogenicity of the formulation, such as oil-in water systems and other systems known in the art. Since the peptides or conjugates may be broken down in the stomach, the vaccine is preferably administered parenterally (for instance, subcutaneous, intramuscular, intravenous, or intradermal injection). The dosage will depend on the specific activity of the vaccine and can be readily determined by routine experimentation. The formulations may be presented in unit-dose or multi-dose containers, for example, sealed ampoules and vials and may be stored in a freeze-dried condition requiring only the addition of the sterile liquid carrier immediately prior to use.

IX. Formulations

The MUCl ECD antagonists including binding inhibitors or oligonucleotides employed in the compositions and methods of the present invention can be formulated in a variety of conventional pharmaceutical formulations and administered to cancer patients, in need of treatment, by any one of the drug administration routes conventionally employed including oral, intravenous, intraarterial, parental or intrapenitoneal.

For oral administration the compositions of the present invention may be formulated, for example, with an inert dilutent or with an assimiable edible carrier, or enclosed in hard or soft shell gelatin capsules, or compressed into tablets, or incorporated directly with the food of the diet. For oral therapeutic administration, the active compound may be incorporated with excipients and used in the form of ingestible tablets, buccal tablets, troches, capsules, elixirs, suspensions, syrups, wafers, and the like. Such compositions and preparations may, of course, be varied and may conveniently be between about 2 to about 60% of the weight of the unit. The amount of active compounds in such therapeutically useful compositions is such that a suitable dosage will be obtained.

The tablets, troches, pills, capsules and the like may also contain the following: a binder, a gum tragacanth, acacia, cornstarch, or gelatin; excipients, such as dicalcium phosphate; a disintegrating agent, such as corn starch, potato starch, alginic acid and the like; a lubricant, such as magnesium stearate; and a sweetening agent, such as sucrose, lactose or saccharin may be added or a flavoring agent, such as peppermint, oil of wintergreen, or cherry flavoring. When the dosage unit for is a capsule, it may contain, in addition to materials of the above type, a liquid carrier. Various other materials may be present as coatings or to otherwise modify the physical form of the dosage unit. For instance, tablets, pills, or capsules may be coated with shellac, sugar or both. A syrup or elixir may contain the active compounds sucrose as a sweetening agent methyl and propylparabens as preservatives, a dye and flavoring, such as cherry or orange flavor. Of course, any material used in preparing a dosage unit form should be pharmaceutically pure and substantially non-toxic in the amounts employed. In addition, other chemotherapeutic compounds may be incorporated into sustained-release preparation and formulations.

Ln regard to formulations comprising oligonucleotides, colloidal dispersion systems may be used as delivery vehicles to enhance the in vivo stability of the oligonucleotides and/or to target the oligonucleotides to a particular organ, tissue or cell type. Colloidal dispersion systems include, but are not limited to, macromolecule complexes, nanocapsules, microspheres, beads and lipid-based systems including oil-in- water emulsions, micelles, mixed micelles, liposomes and lipid: oligonucleotide complexes of uncharacterized structure. Pharmaceutical formulations of the compositions of the present invention which are suitable for injectable use include sterile aqueous solutions or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersions. In all cases the form must be sterile and must be fluid to the extent that each syringability exists. It must be stable under the conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms, such as bacteria and fungi. The carrier can be a solvent or dispersion medium containing, for example, by the use of a coating, such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants. The prevention of the action of microorganisms can be brought about by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, sorbic acid, thimerosal, and the like. In many cases, it will be preferable to include isotonic agents, for example, sugars or sodium chloride. Prolonged absorption of the injectable compositions can be brought about by the use in the compositions of agents delaying absorption, for example, aluminum monostearate and gelatin.

Sterile injectable solutions are prepared by incorporating the compositions of the present invention in the required amount in the appropriate solvent with various of the other ingredients enumerated above, as required, followed by filtered sterilization. Generally, dispersions are prepared by incorporating the various sterilized active ingredients into a sterile vehicle which contains the basic dispersion medium and the required other ingredients from those enumerated above. Ln the case of sterile powders for the preparation of sterile injectable solutions, the preferred methods of preparation are vacuum-drying and freeze-drying techniques which yield a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof.

As used herein, "pharmaceutically acceptable carrier" includes any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents and the like. The use of such media and agents for pharmaceutical active substances is well known in the art. Except insofar as any conventional media or agent is incompatible with the active ingredient, its use in the therapeutic compositions is contemplated. Supplementary active ingredients can also be incorporated into the composition.

X. Treatment Methods Tumors that can be suitably treated with the methods of the present invention include; but are not limited to, tumors of the brain (glioblastomas, medulloblastoma, astrocytoma, oligodendroglioma, ependymomas), lung, liver, spleen, kidney, lymph node, small intestine, pancreas, blood cells, colon, stomach, breast, endometrium, prostate, testicle, ovary, skin, head and neck, esophagus, bone marrow, blood and other tissue. The tumor may be distinguished as metastatic and non-metastatic. Pre-malignant lesions may also be suitably treated with the methods of the present invention.

The treatment with the MUCl/ECD antagonists of the present invention may precede or follow irradiation and/or chemotherapy by intervals ranging from seconds to weeks and/or be administered concurrently with such treatments. In embodiments where the MUCl/ECD antagonists and irradiation and/or chemotherapy are applied separately to the cell, steps should be taken to ensure that a significant period of time does not expire between the time of each delivery, such that the combination of the two or three treatments would still be able to exert an advantageously combined effect on the cell. In such instances, it is contemplated that one would contact the cell with the treatment agents or modalities within amount 0J to 25 h of each other and, more preferably, within about 1 to 4 h of each other, with a delay time of only about 1 h to about 2 h being most preferred. Ln some situations, it is desirable to extend the time period of treatment significantly, however, where several days (2, 3, 4, 5, 6 or 7) or several weeks (1, 2, 3, 4, 5, 6, 7 or 8) lapse between the respective administrations. In any case, the invention contemplates that the MUCl/ECD antagonists may be given before, after or even simultaneously with the ionizing radiation and/or chemotherapeutic agent.

Some chemotherapeutic agents transiently induce MUCl expression on cancer cells 0.5 to 12 hours after contact of the carcinoma cells with the chemotherapeutic agents. Thus, in some embodiments the administration of MUCl/ECD binding inhibitors, especially antibodies to the MUC/ECD sequence SEQ ED NO. 1, optionally conjugated to a toxin or radionucleotide, is coordinated with the increased expression of MUCl on the cancer cells. In other embodiments, agents other than chemotherapeutic agents may be used to increase MUCl expression prior to treatment with a MUCl binding inhibitor, especially antibodies to the MUC/ECD sequence SEQ ED NO. 1, optionally conjugated to a toxin or radionucleotide.

In the methods of the present invention, the actual dosage of MUCl/ECD antagonists employed will depend on a variety of factors including the type and severity of cancer being treated, and the additive or synergistic treatment effects of the MUCl/ECD antagonists and the other treatment modality or modalities selected.

EXAMPLES OF THE INVENTION Example 1: Peptides

The MUCl/ECD polypeptide sequence, as typically found in MUCl-expressing cells, is provided by SEQ ED NO: 1. A number of polypeptide sequences have been synthesized by standard techniques. These include peptides PI (SEQ ED NO: 2), P2 (SEQ ED NO: 5) and P3 (SEQ ED NO:6), which are polypeptide fragments of MUCl/ECD. PI (SEQ ED NO: 2) represents amino acids 5 through 20 of MUCl/ECD (SEQ ED NO: 1) with a cysteine added at the carboxy terminal. P2 (SEQ ED NO: 5) represents amino acids 13 through 28 of MUCl ECD (SEQ ED NO: 1) with a cysteine added at the carboxy terminal. P3 (SEQ ED NO: 6) represents amino acids 27 through 44 of MUCl/ECD (SEQ ED NO: 1) with a cysteine at the carboxy terminal. Ln addition, the synthesized polypeptide sequence SEQ ED NO: 7 incorporates amino acids 6 through 24 of MUCl/ECD (SEQ ED NO: 1) with a cysteine added at the carboxy terminal. The synthesized polypeptide P0 (SEQ ED NO: 8) incorporates a 19 amino acid sequence occurring in the MUCl protein occurring just prior to the amino terminus of MUCl/ECD and represents the a potential cleavage site. A cysteine was again added at the carboxy terminal of the sequence at it occurs in the MUC 1 sequence. Example 2: Anti-MUCl-Pl Antibody

A. Generation of Antibody

The polypeptide PI (SEQ. ED NO: 4), contains the QYK motif and other sequences homologous to ligand binding domains of cytokine receptors (Zrihan-Licht, et al, 1994). A polyclonal antibody was raised in rabbits against polypeptide PI (SEQ ED NO. 4) conjugated to KLH. Serum was prepared by standard methods.

Polyclonal antibodies were also raised against the polypeptide SEQ ED NO: 7, whereby the immunogen was formed by conjugating the polypeptide SEQ ED NO: 7 to

KLH. Antibodies have been obtained from 2 rabbits, designated 3402-1 and 3402-2. Both serum and affinity purified antibody preparations have been prepared by standard methodologies.

B. Stimulation of Human Carcinoma Cells by Anti-MUCl-Pl-Antibody Human ZR-75-1 carcinoma cells were grown to 80% confluence in RPMI 1640 medium containing 10% fetal bovine serum (FBS) and then passed onto a 6-well plate at lxlO⁴ cells per well. After overnight starvation in medium containing 0.1% FBS, anti- MUCl-Pl antibody was added to each well it the amounts indicated in FIG. 1 and incubated for 48 hours. Cell numbers were quantified after another 3 days of incubation in the presence of 0J % FBS. As shown in FIG. 1, anti-MUCi-Pl stimulates the growth of ZR-75-1 cells in a dose dependent fashion. To assess the specificity of anti-MUCl-Pl antibody stimulation, human MUC1- negative SW480 colon cancer cells were stably transfected to express empty vector (SW480/V) or MUCl (SW480/MUC1). SW80 colon cancer cells were transfected with either pCMN-EE-akl-dhfr vector or pCMN-EE-akl-dhfr-MUCl using lipofectamide (Ligtenburger et al, 1992). Cells were grown in the presence of 800 μg/ml G418 (neomycin) and serially diluted to single-cell populations. Single cell clones that express MUCl (SW480/MUC1) were selected. Both SW480 cells types were grown to 80 % confluence in DMEM containing 10% FBS and plated onto 6-well plates at 5xl0⁴ cells per well. After overnight starvation in medium containing 0.1% FBS, anti-MUCl-Pl antibody was added at the indicated concentrations and incubated for 48 hr. Cell numbers were quantified after a further day of incubation (3 days total). As shown in FIG. 2, anti- MUCl-Pl stimulates the growth of SW480/MUC1 cells but not SW48-0/N cells. These findings confirm that the anti-MUCl-Pl antibody stimulates the growth of human carcinoma cells by specifically interacting with MUCl.

Example 3: Endogenous MUCl ECD Ligands

The finding that anti-MUCl-Pl stimulates growth of human carcinoma cells is suggestive of the potential existence of natural MUCl ECD ligands. To investigate this potential, ZR-75-1 cells were screened as a possible source of MUCl ligand(s). Conditioned medium was prepared by culturing ZR-75-1 cells in RPMI 1640 medium containing 0.1% FBS for 72 hr and then preparing a supernatant. The conditioned medium was added to SW480/V and SW480/MUC1 cells that were growth arrested in DME containing 0.1% FBS as previously described. Conditioned medium was added at the concentration indicated in Fig. 3 and the cells were maintained for 3 days prior to quantification of cell numbers. As shown in FIG. 3, ZR-75-1 cells express a soluble ligand that stimulates carcinoma cell growth by binding to MUCl.

To identify the soluble MUCl ligand(s), a fusion protein comprising the MUCl/ECD (SEQ ED. No: 1) and glutathione S-transferase (GST) was prepared. GST was amplified by PCR using a set of primers as follows: 5'-ATTAGGCTAGCCTGGTTCCGCGTGGTTCTATGTCCCCTATACTAGGTTA-3', and 5'-CAAGGGGATCCCTACGGAACCAGATCCGATTTTGG-3', and inserted between the Nhel and BamHI sites of pET-lld (the "pET-lld-GST vector"). MUCl/ECD was amplified by PCR using a set of primers as follows: 5'-TCTGGCCATGGGAGAAGGTACCATCAAT-3', and 5'-AGCGCGCTAGCCCAGCCTGGCACCCCAGC-3', and inserted between the Ncol and Nhel sites of pETl ld-GST vector (the "pETl ld-GST-MUCl/ECD" vector).

The GST fusion protein was prepared by incubating logarithmically growing E. coli BL21(D3)pLysS cells transformed with pETl ld-GST-MUCl ECD or pETl ld-GST with 0.1 mM isopropyl-β-D-thiogalatopyranoside for 6 hr at 25 °C. Cells were pelleted and resuspended in PBS containing 20 % sucrose, 5 mM MgCl₂, 0.5 % NP-40, then sonicated. Debris was removed by centrifugation at 10,000 x g for 30 min. at 4 °C. The supernatant was applied to bulk glutathione sepharose 4B and incubated for 4 hr at 4 °C prior to washing and packing into a column. The fusion protein was eluted with 10 mM glutathione in 50 mM Tris-HCl, pH 9.5. The purified fusion protein was dialyzed with PBS. Cytosolic fractions of cultured cells were prepared by harvesting ZR75-1 cells in

PBS containing 40mM EDTA. After washing with PBS, cells were resuspended with ice-cold homogenized buffer (20 mM Hepes-KOH, pH 7.5, 10 mM KC1, 1.5 mM MgCl₂, 1 mM dithiothreitol, 1 mM EGTA, 1 mM EDTA and protease inhibitors cocktail (Roche) and put on ice for 15 min. The suspension was homogenized with a Dounce homogenizer. The homogenate was centrifuged at 1,00 x g for 5 min at 4 °C. The supernatant was collected as a cytosol fraction and stored at 0 °C.

The GST-MUC1/ECD fusion protein (1.8 mg) was immobilized on 400 μl of glutathione-sepharose 4B, which was packed into a column and equilibrated with buffer A (30 mM Tris-HCl, pH 7.5, 5 mM MgCl₂, 1 mM EDTA, and 1 mM dithiothreitol). The cytosolic fraction was first precleared by passing it through a glutathione-sepharose 4B column and was then loaded onto the GST-MUC1/ECD affinity column which was then washed twice with 2 x 10 ml of buffer A. The protein bound to the column was eluted by the addition of 2 ml of buffer B (buffer A containing 0J5 M NaCl), and fractions of 0.4 ml each were collected. The second and third fractions were mixed and loaded on sodium dodecyl sulfate-polyacyralmide gel electrophoresis (SDS-PAGE). As a control, the GST protein (1.5 mg) was immobilized on 400 μl of glutathione-sepharose 4B and the experiment performed as described above. The results demonstrated that MUCl/ECD binds to a 45 kDa protein. A similar experiment was performed with lysates of human MCF-7 breast carcinoma cells confirmed the binding of MUCl/ECD with a 45 kDa protein.

The 45 kDa from the GST-MUC1/ECD adsorbate was excised from the gel, dehydrated with acetonitrile, and then redhydrated with 100 mM ammonium bicarbonate. The gel pieces were then suspended in 12.5 ng/μl trypsin/50 mM ammonium bicarbonate. Digestion was carried out at 37 °C for 10-12 hr. The masses of the trypsin-digested peptides were analyzed by matrix assisted laser desorption/ionization-time of flight-mass spectroscopy (MALDI-TOF-MS) using a Voyager DE-PRO (Perceptive Biosystem Luc, Framingham, MA). Two related proteins, designated ML-1 and ML-2, were identified by mass fingerprinting. The sequences of ML-1 (SEQ ED NO: 3) and ML-2 (SEQ ED NO: 4) are as those previously disclosed for two neuregulin isoforms, NRG2 splice isoform 5 and NRG2 splice isoform 6 respectively.

Example 4: MUCl as an Oncogene

A. MUCl supports growth in soft agar The expression of MUCl was shown to be functionally significant regarding the exhibition of the malignant phenotype. Cell lines that stably express MUCl were generated. HCT116 colon cancer cells were transfected with pE ES-puro2 vector or pERES-puro2-MUCl by lipofectamine and selected for puromycin-resistance. Studies were performed with human MUCl -negative HCT116 colon cancer cells with single clones that stably express either the empty vector (VCT116/V) or MUCl (HCT116/MUC1). The HCT 116/V and HCT116/MUC1 cells were assayed for anchorage-independent growth in soft agar. Cells (1 x 10⁵ / 60 mm dish) were suspended in 0.33% agarose-containing DMEM medium supplemented with 10 % FBS and layered over an agarose plug (0.5 % agarose in DMEM supplemented with 10 % FBS). The cells were incubated to 4 weeks, during which time fresh medium was added to the plates every week. Colonies larger than 70 μm in diameter were counted after 4 weeks. Expression of wild-type MUCl was associated with a marked increase in the size and number of colonies compared to that obtained with HCT/116/V cells. These findings were confirmed by similar studies performed with SW480/V and SW480/MUC1 cells wherein MUCl expression was again shown to support anchorage-independent growth of SW480 cells.

B. MUCl supports human tumor formation in nude mice

To assess the effects of MUCl on human tumor growth in vivo. Five to six week old athymic, Balbc/nu/nu mice (Taconic, Germantown, NY) were injected subcutaneously in the right flank with 1 x 10⁶ HCT116/V or HCT 116/MUCl cells. Tumors (4 mice/group) were measured twice a week. Tumor volumes were calculated by the following formula: ^(length x width²). Experiments were terminated when tumor volume exceeded 2 cm³. Measurements of tumor volume over time demonstrated little HCT116/V cell growth. By comparison there was a marked increase in the growth of HCT116/MUC1 tumors.

Example 5: MUCl Expression is Induced by Oxidative and Genotoxic Stress

To determine whether MUCl is induced in response to oxidative stress, MCF-7 cells were treated with hydrogen peroxide. Cell lysates were analyzed by immunoblotting with anti-DF3/MUCl antibody. Lysates were prepared by suspending MCF-7 cells in lysis buffer (50 mM Tris, pH 7.6, 150 mM NaCl, 1 mM PMSF, 3 mM NaF, 1 mM sodium vandate, lmM DTT with protease inhibitors and either 1% NP-40 or 1% Brij-96) for 30 min. on ice. Lysates were cleared by centifugation and equal amounts of proteins were resolved by SDS-PAGE. Proteins were then transferred to nitrocellulose filters, blocked by incubation in 5 % non-fat dry milk in PBS with 0.05 % Tween-20 and probed with anti-MUCl antibody (Pandey et al, 1995). Anti-actin was used as a control. The results demonstrated that MUCl is rapidly and transiently induced in response to oxidative stress while there was no effect of hydrogen peroxide on levels of actin expression.

Similar studies were performed with genotoxic agents. The results demonstrate that treatment of MCF-7 cells with daunorubicin is associated with a rapid and transient induction of MUCl, and not actin, expression. The available evidence indicates that MUCl is induced by diverse cytotoxic agents, including taxol, cisplatin and ionizing radiation.

Example 6: MUCl Inhibits the Apoptotic Response to Oxidative and Genotoxic Stress

To determine whether MUCl inhibits the apoptotic response to oxidative stress,

HeLa cells stably expressing the empty vector or MUCl were treated with 1 mM hydrogen peroxide for 1 hr. DNA content was assessed by staining ethanol-fixed cells with propidium iodide and monitoring by FACScan (Beckton Dickerson). Numbers of cells with sub-Gl DNA content were determined with a MODFIT LT program, (Verity Software House, Topsham, ME) (Yuan et al, 1997). The cells were analyzed for induction of sub-Gl DNA by flow cytometry as a marker of apoptosis. As shown in FIG. 4, the results demonstrate that MUCl inhibits the apoptotic response to oxidative stress. The induction of apoptosis in cells treated with 0.01 mM taxol for 20 hr was assessed by measuring sub-Gl DNA content of HeLa cells expressing empty vector or MUCl. As shown in FIG. 4, as with oxidative stress, taxol-induced apoptosis was inhibited by MUCl expression.

Example 7: Effect of NM-3 on MUCl Expression

MCF-7 cells were treated with NM-3 (2-(8-hydroxy-6-methoxy-l-oxo-l H- - benzopyran-3-yl) propionic acid) at 100-400 μg/ml for 48 hr. DF3 antigen levels were visualized by immunoblot analysis with DF3 MAb (Kufe, U.S. Patent 5,506,343, herein incorporated by reference). A decrease in the intracellular levels of DF3 antigen of NM-3 treated cells relative to non-treated cells was observed. Similar results were found in ZR-75-1 and BT-20 cell lines. The NM-3 mediated decrease of intracellular DF3 antigen was shown to be both dose- and time dependent. To determine whether NM-3 impaired the extracellular localization of the MUCl DF3 antigen, the antigen levels in cell culture medium supematants and on MCF-7 cells after NM-3 treatment were investigated. The levels of DF3 antigen were reduced in both localizations. These findings suggest that NM-3 inhibits MUCl protein expression.

Hybridization studies were performed to determine whether the effect of NM-3 on MUCl -expression was detectable at the transcriptional level. A ³²P-labaelled DF3 DNA probe hybridized to two transcripts of 4.5 and 7.0 kb in total cellular RNA after NM-3 treatment on MCF-7 cells for 48 hr. The levels of both mRNA were decreased relative to controls wherein MCF-7 cells were incubated in the absence of NM-3. The same results were observed using ZR-75-1 and BT-20 cell lines. These findings suggest that DF3 expression is regulated at the transcriptional level after NM-3 treatment on those cell lines. To determine whether NM-3 inhibits the expression of cellular surface proteins as well, the level of epidermal growth factor receptor (EGF-R) expression after NM-3 treatment was tested on MCF-7, ZR-75-1 and BT-20 cell lines. Compared to controls wherein cells were incubated in the absence of NM-3, there were no detectable changes in EGF-R expression after NM-3 treatment. These results indicate a selective effect of NM-3 on MUCl expression without inhibition of surface molecular expression.

The present invention has been shown by both description and examples. The

Examples are only examples and cannot be construed to limit the scope of the invention.

One of ordinary skill in the art will envision equivalents to the inventive process described by the following claims that are within the scope and spirit of the claimed invention.

REFERENCES

The following references, to the extent that they provide exemplary procedural or other details supplementary to those set forth herein, are specifically incorporated herein by reference.

Barry & Sharkey, Hum. Pathol., 16:225-7, 1985.

Brunner et al., Nature, 385:829-833, 1997.

Daniels & Reynolds, Mol. Cell. BioL, 19:3614-23, 1999.

Dawson et al, Science 266:776, 1994.

Duffy, in Vaccine Preparation Techniques, Noyes Data Corporation of Park Ridge, N.J., 1980.

Finn et al, Immunol. Rev. 145:61-89, 1995.

Gansow, Int. J. Rad Appl. Lustrum. [B], Nucl. Med. Biol. 18:369-381, 1991.

Goding, In: Monoclonal Antibodies: Principles and Practice, 2d ed., Orlando,

Fla.,Academic Press, pp. 60-61, 1986. Itzkowitz et al., Cancer, 66: 1960-6, 1990.

Jawhari et al, J. Pathol, 189:180-85, 1999.

Jones et al., Nature 321 :522-525, 1986.

Kufe et al., Hybridoma, 3:223-232, 1984.

Li et al, Mol Cell BioL, 18:7216-24, 1998. Li et al., J. Biol. Chem., 276:6061-64, 2001.

Li et al, J. Biol Chem, e-publication manuscript C100359200, August 1, 2001(a).

Li & Kufe, Biochem Biophys. Res. Commun., 281, 440-43, 2001.

Ligtenburger et al., Cancer Res., 15:2318-2324, 1992.

Molenaar et al, Cell, 86:391-399, 1996. Novak & Dedhar, Cell Mol. Life Sci., 523-37, 1999.

Olsnes & Pihl, Pharmac. Ther. 25:355-381, 1981.

Pandey et al, Cancer Res., 55:4000-4003, 1995.

Pastan et al, Ann. Rev. Biochem. 61:331-354, 1992.

Perey et al, Cancer Res., 52:2563-68, 1992. Pluckthun in The Pharmacology of Monoclonal Antibodies, vol. 113:269-315,

Rosenburg and Moore eds. Springer- Verlag, New York, 1994.

Presta, Curr. Op. Struct Biol. 2:593-596, 1992.

Reddish et al, Cancer Immunol. Lmmunother., 42:303-9, 1996. Reynolds et al, Mol. Cell. Biol. 9:629-38, 1989.

Reynolds et al, Mol. Cell. Biol, 14:8333-41, 1994.

Riechmann et al, Nature 332:323-329, 1988.

Ring et al, Human Genet., 104:326-32, 1999.

Sambrook et al, Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. 1989.

Shimazui et al, Cancer Res., 56:4154-58, 1996.

Smith & Waterman, Adv. Appl. Math., 2:482-489, 1981.

Strouss & Decker, Crit. Rev. Biochem. Mol. Biol, 27:57-92, 1992.

Takeichi, Annu. Rev. Biochem., 59:237-52, 1990. Thorpe et al, Immunological Rev. 62: 119-158, 1982.

Thorpe et al, Monoclonal Antibodies in Clinical Medicine, pp. 168-190 Academic Press,

NY 1982(a).

Waldmann, Science, 252:1657, 1991.

Yamamoto et al, J. Biol. Chem. 272:12492-94, 1997. Yuan et al, PNAS, 94: 1437-1440, 1997.

Zrihan-Licht, et al, FEBS Let., 356:130-36, 1994.

U.S. Pat. No. 4,675,382

U.S. Pat. No. 4,894,443,

U.S. Pat. No. 5,506,343

Claims (49)

WHAT IS CLAIMED IS:

1. The use of a MUCl extracellular domain antagonist for the manufacture of a medicant to inhibit the proliferation of MUCl -expressing cancer cells.

2. The use of a MUCl extracellular domain antagonist of claim 1, wherein said MUCl extracellular domain antagonist downregulates the expression of the MUCl extracellular domain.

3. The use of a MUCl extracellular domain antagonist of claim 1, wherein said MUCl extracellular domain antagonist is a MUCl extracellular domain binding inhibitor.

4. The use of a MUCl extracellular domain antagonist of claim 3, wherein said MUCl extracellular domain binding inhibitor is the polypeptide of SEQ ED NO: 1, or a fragment comprising at least four consecutive amino acids of SEQ ED. NO: 1, or conservative variants thereof.

5. The use of a MUCl extracellular domain antagonist of claim 3, wherein said MUCl extracellular domain binding inhibitor is the polypeptide of SEQ ED NO: 4 or SEQ ED NO: 5 or conservative variants thereof.

6. The use of a MUCl extracellular domain antagonist of claim 3, wherein said MUCl extracellular domain binding inhibitor is an antibody or fragment thereof that binds to an epitope within sequences of the peptides selected from the group consisting of SEQ ED NO: 1, SEQ ED NO: 2 and SEQ ED NO: 3.

7. The use of a MUCl extracellular domain antagonist of claim 3, wherein said MUCl extracellular domain binding inhibitor is an antibody or fragment thereof that binds to an epitope within sequence of SEQ ED NO: 1.

8. The use of a MUCl extracellular domain antagonist of claim 6, wherein said antibody is a monoclonal antibody.

9. The use of a MUCl extracellular domain antagonist of claim 8, wherein said monoclonal antibody is humanized.

10. The use of a MUCl extracellular domain antagonist of claim 8, wherein said monoclonal antibody is a human antibody.

11. The use of a MUCl extracellular domain antagonist of claim 6, wherein said antibody is a bispecific antibody.

12. The use of a MUCl extracellular domain antagonist of claim 6, wherein said fragment comprises an antigen binding region.

13. The use of a MUCl extracellular domain antagonist of claim 6, wherein said antibody or fragment thereof is conjugated to a chemotherapeutic agent, radioisotope, toxin, or an effector that induces a cytolytic or cytotoxic immune response.

14. The use of a MUCl extracellular domain antagonist of claim 13, wherein said antibody or fragment thereof is conjugated to a cytokine, an antimetabolite, an anthracycline, a vinca alkaloid, an antibiotic, an alkylating agent, a naturally derived toxin, or an Fc region of a IgGl immunoglobulin.

15. The use of a MUCl extracellular domain antagonist of claim 1, wherein said effective amount of a MUCl extracellular antagonist is administered as a composition comprising said MUCl extracellular domain antagonist and a pharmaceutically acceptable carrier.

16. The use of a MUCl extracellular domain antagonist of claim 1, further comprising administration of a chemotherapeutic agent or radiation.

17. A use of a MUCl extracellular domain antagonist for the manufacture of a medicant for use in combination with a chemotherapeutic agent or radiation for the treatment of cancer.

18. The use of a MUCl extracellular domain antagonist of claim 17, wherein said MUCl extracellular domain antagonist downregulates the expression of the MUCl extracellular domain.

19. The use of a MUCl extracellular domain antagonist of claim 17, wherein said MUCl extracellular domain antagonist is a MUCl extracellular domain binding inhibitor.

20. The use of a MUCl extracellular domain antagonist of claim 19, wherein said MUCl extracellular domain binding inhibitor is the polypeptide of SEQ ED NO: 1, or a fragment comprising at least four consecutive amino acids of SEQ ED. NO: 1, or conservative variants thereof.

21. The use of a MUCl extracellular domain antagonist of claim 19, wherein said MUCl extracellular domain binding antagonist is the polypeptide of SEQ ED NO: 4 or SEQ ED NO: 5 or conservative variants thereof.

22. The use of a MUCl extracellular domain antagonist of claim 19, wherein said MUCl extracellular domain binding inhibitor is an antibody or fragment thereof that binds to an epitope within sequences of the peptides selected from the group consisting of SEQ ED NO: 1, SEQ ED NO: 2 and SEQ ED NO: 3.

23. The use of a MUCl extracellular domain binding antagonist of claim 19, wherein said MUCl extracellular domain binding antagonist is an antibody or fragment thereof that binds to an epitope within sequence of SEQ ED NO: 1.

24. The use of a MUCl extracellular domain antagonist of claim 22, wherein said antibody is a monoclonal antibody.

25. The use of a MUCl extracellular domain antagonist of claim 24, wherein said monoclonal antibody is humanized.

26. The use of a MUCl extracellular domain antagonist of claim 24, wherein said monoclonal antibody is a human antibody.

27. The use of a MUCl extracellular domain antagonist of claim 22, wherein said antibody is a bispecific antibody.

28. The use of a MUCl extracellular domain antagonist of claim 22, wherein said fragment comprises an antigen binding region.

29. The use of a MUCl extracellular domain antagonist of claim 22, wherein said antibody or fragment thereof is conjugated to a chemotherapeutic agent, radioisotope, toxin, or an effector that induces a cytolytic or cytotoxic immune response.

30. The use of a MUCl extracellular domain antagonist of claim 29, wherein said antibody or fragment thereof is conjugated to a cytokine, an antimetabolite, an anthracycline, a vinca alkaloid, an antibiotic, an alkylating agent, a naturally derived toxin, or an Fc region of a IgGl immunoglobulin.

31. The use of a MUCl extracellular domain antagonist of claim 17, wherein said chemotherapeutic agent is selected from the group consisting of alkylating agents, topoisomerase inhibitors, antimetabolites, tubulin interactive agents, anti-hormonal agents, ornithine decarboxylase inhibitors and tyrosine kinase inhibitors.

32. A pharmaceutical composition comprising the polypeptide of SEQ ED NO: 1, or a fragment comprising at least four consecutive amino acids of SEQ ED. NO: 1, or conservative variants thereof, and a pharmaceutically acceptable carrier.

33. The composition of claim 32, wherein said polypeptide is the polypeptide of SEQ ED NO: 5, or conservative variants thereof.

34. A pharmaceutical composition comprising the polypeptide of SEQ ED NO: 4 or conservative variants thereof, and a pharmaceutically acceptable carrier.

35. A pharmaceutical composition comprising an antibody or fragment thereof that binds to an epitope within sequences of the peptides selected from the group consisting of SEQ ED NO: 1, SEQ ED NO: 2 and SEQ ED NO: 3 and a pharmaceutically acceptable carrier.

36. The composition of claim 35, wherein said antibody or fragment thereof binds to an epitope within sequence of SEQ ED NO: 1.

37. The composition of claim 36, wherein said antibody is a monoclonal antibody.

38. The composition of claim 37, wherein said monoclonal antibody is humanized.

39. The composition of claim 37, wherein said monoclonal antibody is a human antibody.

40. The composition of claim 35, wherein said antibody is a bispecific antibody.

41. The composition of claim 35, wherein said fragment comprises an antigen binding region.

42. The composition of claim 35, wherein said antibody or fragment thereof is conjugated to a chemotherapeutic agent, radioisotope, toxin, or an effector that induces a cytolytic or cytotoxic immune response.

43. The composition of claim 42, wherein said antibody or fragment thereof is conjugated to a cytokine, an antimetabolite, an anthracycline, a vinca alkaloid, an antibiotic, an alkylating agent, a naturally derived toxin, or an Fc region of a IgGl immunoglobulin.

44. A method of identifying a compound the inhibits the binding of ligands to the extracellular domain of MUCl, the method comprising:

(a) providing a polypeptide comprising the polypeptide of SEQ ED. NO: 1 or the polypeptide of SEQ ED NO: 5;

(b) contacting said polypeptide test compound and an antibody that binds to an epitope within SEQ ED NO: 4;

(c) determining whether the binding of said antibody that binds to an antibody to an epitope within SEQ ED NO: 4 to the polypeptide SEQ ED. NO: 1 or the polypeptide of SEQ ED NO: 5 is decreased relative to an appropriate control.

45. A pharmaceutical composition comprising a compound identified by the method of claim 44 and a pharmaceutically acceptable carrier.

46. A method of identifying a compound that inhibits the proliferation of MUC1- expressing cancer cells, the method comprising:

(a) providing a population of MUCl -expressing cancer cells;

(b) contacting said population of MUCl-positive cancer cells with a test compound and an antibody that binds to an epitope within SEQ ED NO: 5; (c) determining whether the proliferation of said population of MUCl -expressing cancer cells is decreased by comparison to an appropriate control.

47. A pharmaceutical composition comprising a compound identified by the method of claim 46 and a pharmaceutically acceptable carrier.

48. A method of identifying a compound that downregulates the expression the extracellular domain of MUCl, the method comprising:

(a) providing a population of MUCl -expressing cancer cells;

(b) contacting said population of MUCl-expressing cancer cells with a test compound;

(c) utilizing an anti-MUCl/ECD antibody to identify polypeptides comprising MUCl/ECD in the MUCl/ECD-expressing cancer cells; and

(d) determining whether the expression of polypeptides comprising MUCl/ECD is decreased in comparison to controls wherein the test compound was excluded.

49. The use of a NM-3 for the manufacture of a medicant to downregulate the expression of the extracellular domain of MUCl/ECD in a cancer.