EP1242050A2 - Survivin promotion of angiogenesis - Google Patents
Survivin promotion of angiogenesisInfo
- Publication number
- EP1242050A2 EP1242050A2 EP00990262A EP00990262A EP1242050A2 EP 1242050 A2 EP1242050 A2 EP 1242050A2 EP 00990262 A EP00990262 A EP 00990262A EP 00990262 A EP00990262 A EP 00990262A EP 1242050 A2 EP1242050 A2 EP 1242050A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- survivin
- agent
- expression
- angiogenesis
- cell
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
- C07K14/4701—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals not used
- C07K14/4747—Apoptosis related proteins
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/475—Growth factors; Growth regulators
- C07K14/515—Angiogenesic factors; Angiogenin
Definitions
- the invention relates generally to the modulation of survivin to induce or inhibit angiogenesis.
- apoptosis preserves tissue and organ homeostasis by eliminating senescent or damaged cells (Vaux et al, 1999). This process involves different gene families of inhibitors and stimulators of cell death, and culminates with activation of intracellular cysteine proteases known as caspases (Salvesen et al, 1997). Aberrations of the apoptosis moieties are known to contribute to human diseases, including cancer (Thompson, 1995) and vascular disorders (Rudin et al, 1997).
- the endothelium is one of the most critical sites for the control of apoptosis in vascular injury and vascular remodeling (Karsan et al, 1996).
- a heterogeneous group of "protective"genes activated by nuclear factor KB, opposes cell death and proinflammatory changes in endothelial cells (EC) induced by cytokines, i.e. tumor necrosis factor (TNF ⁇ ) (Bach et al, 1997).
- TNF ⁇ tumor necrosis factor
- Inhibition of apoptosis may also be obligatorily required during vascular remodeling and new blood vessel formation (Risau, 1997).
- EC specific mitogens including vascular endothelial cell growth factor (VEGF) or basic fibroblast growth factor (bFGF), transduce survival signals critically maintaining EC viability, in vivo (Benjamin et al, 1997; Alon et al, 1995; Yuan et al, 1996).
- VEGF vascular endothelial cell growth factor
- bFGF basic fibroblast growth factor
- angiopoietin-1 is an endothelium-specific ligand essential for embryonic vascular stabilization, branching morphogenesis, and post-natal angiogenesis.
- Ang-1 angiopoietin-1
- EC receive cues from growth factors to initiate mitosis, migration and organization of endothelial cells into primitive angiotubes and patent vascular networks (Risau 1997; Hanahan 1997). These processes critically depend on preservation of endothelial. cell viability.
- Ang-1 does not stimulate endothelial cell growth, but rather promotes stabilization of vascular networks and branching morphogenesis, in vivo and in vitro (Davis et al, 1996; Koblizek et al, 1998; Papapetropoulos et al, 1999; Witzenbichler et al, 1998). Little is known about the signaling requirements of these responses, and it is unclear if the role of Ang-1 in angiogenesis includes protection of EC from apoptosis (Papapetropoulos et al, 1999; Kontos et al, 1998).
- LAP apoptosis
- BIR Cys/His baculovirus IAP repeats
- IAP proteins Block apoptosis induced by various stimuli in vitro (Duckett et al, 1996; Liston et al., 1996), and promotes abnormally prolonged cell survival in the developmentally- regulated model of the Drosophila eye, in vivo (Hay et al, 1995).
- Survivin has recently been identified as a novel member of the IAP family.
- Survivin is a 16.5 kDa cytoplasmic protein containing a single partially conserved BIR domain, and a highly charged carboxyl-terminus coiled-coil region instead of a RING finger, which inhibits apoptosis induced by growth factor (IL-3) withdrawal when transferred in B cell precursors (Ambrosini et al, 1997).
- IL-3 growth factor 3
- survivin is undetectable in adult tissues, but becomes prominently expressed in all the most common human cancers of lung, colon, breast, pancreas, and prostate, and in ⁇ 50% of high-grade non-Hodgkin's lymphomas, in vivo. Moreover, survivin does not bind caspases in a cell-free system (Roy et al, 1997). Although survivin has been characterized as a cell cycle regulated apoptosis inhibitor, the role of survivin on EC viability and angiogenesis has not been previously discovered.
- Angiogenesis i.e. the formation of new blood vessels from existing ones (Risau, W., 1997) is an indispensable process for organ and tissue development, and genetic dysregulation of these mechanisms has been associated with embryonic lethality (Hanahan, D. 1997).
- angiogenesis provides for beneficial compensatory mechanisms that increase blood supply in response to hypoxia or during tissue repair and/or remodeling (Carmeliet, P., 2000).
- the same process may have disastrous consequences in cancer, where increased vascularization due to de novo vessel formation contributes to tumor progression and metastatic dissemination (Hanahan et al, 1996).
- Targeted inhibition of angiogenesis by either disrupting cell-cell (Stromblad et al, 1996) and cell-matrix interactions (Brooks et al, 1998) or by interfering with receptor-initiated intracellular signals (Lin et al, 1998; Claeson- elsh et al, 1998), results in rapid involution of newly formed blood vessels in vitro and in vivo, and the appearance of classical morphologic features of apoptosis in the targeted endothelium (Alon et al, 1995; Yuan et al, 1996; Lin et al, 1998).
- the continuous suppression of EC apoptosis may constitute one of the critical requirements of angiogenesis, consistent with the up regulation of protective genes of the bcl-2 (Gerber et al, 1998a; Nor et al, 1999) or IAP (O'Connor et al, 2000a; Tran et al, 1999; Papapetropoulos et al, 2000) gene families in endothelium stimulated by VEGF or Ang-1.
- the present invention is based on the discovery that angiogenesis stimulation strongly induces survivin expression in endothelium during vascular remodeling and angiogenesis, in vitro and in vivo.
- Survivin expression and function affect endothelial cell viability during the proliferative and the stabilizing phase of angiogenesis.
- Therapeutic manipulation of survivin expression/function in endothelium may influence compensatory or pathologic (tumor) angiogenesis.
- the present invention is also based on the discovery that Ang-1 prevents endothelial cell apoptosis by activating a critical survival messenger, Akt, and by up- regulating survivin.
- Akt critical survival messenger
- survivin a critical survival messenger
- the activation of anti-apoptotic pathways mediated by Akt and survivin in endothelial cells may contribute to Ang-1 stabilization of vascular structures during angiogenesis, in vivo.
- targeted manipulation of Ang-1 /Akt/Survivin may be exploited to improve endothelial cell viability and favor therapeutic angiogenesis, in vivo.
- the present invention provides methods of promoting or inhibiting angiogenesis and methods of treating conditions by inducing compensatory angiogenesis.
- the disclosed methods are useful for treating ischemic diseases caused by myocardial infarction, peripheral vascular occlusion, brain ischemia, or stroke.
- the disclosed methods of inhibiting angiogenesis are useful for treating vasculoproliferative disease such as cancer, restenosis, vascular bypass graft occlusion, or transplant coronary vasculopathy.
- the disclosed methods comprise providing to a cell or tissue an apoptosis modulating agent, wherein the.
- agent is selected from the group consisting of a survivin polypeptide, a survivin transgene, a survivin antisense molecule, a survivin peptidomimetic, or an agent that modulates the expression or activity of survivin in a cell or tissue, such as Ang-1 or Akt.
- the agent is provided in an implant.
- the implant maybe a stent and the implant maybe coated or impregnated with a survivin transgene that is operatively linked to an expression control element in a vector.
- the survivin transgene or antisense molecule is contained within a transfection facilitating composition, such as a transfection facilitating lipid or a transfection facilitating particle.
- the present invention includes a method of inhibiting angiogenesis comprising administering an agent that inhibits survivin.
- agents that inhibit survivin include, but are not limited to, survivin antibodies, survivin antisense molecules, inhibitors of Akt phosphorylation, and other inhibitors of survivin function or expression.
- the method inhibits the angiogenesis of tumors or inhibits the metastasis of cancerous cells and the agent is a survivin antisense molecule.
- the method inhibits VEGF induced functions such as ceramide or TNF ⁇ induced apoptosis and capillary formation and maintenance. Most preferably, the method inhibits VEGF induced capillary formation and maintenance.
- survivin is involved not only in the proliferative phase of angiogenesis but also the remodeling and stabilizing phase of angiogenesis.
- Survivin antisense molecule is sufficient to induce endothelial cell apoptosis and regression of the capillary-like structures.
- the present invention contemplates the use of inhibitors of survivin expression and function as agents that inhibits angiogenesis, such as an antagonist. In another aspect, the present invention contemplates the use of survivin and inducers of survivin expression and function as agents that promotes angiogenesis, such as an agonist.
- Figures lA-C Modulation of survivin expression in EC.
- Quiescent EC were incubated with medium or serum (10% FCS), VEGF (100 ng/ml), bFGF (5 ng/ml), TNF ⁇ (10 ng/ml) or IL-1 (2 ng/ml) for 16 h at 37°C.
- Cells were harvested, SDS-extracted and analyzed for expression of survivin or ⁇ -actin, by immunoblotting.
- B. Control or EC were stimulated with the indicated increasing concentrations of VEGF for 16 h at 37°C and analyzed for expression of survivin or ⁇ - actin by immunoblotting.
- Total RNA was extracted from EC stimulated with 100 ng/ml VEGF at the indicated time intervals, separated on agarose-formaldehyde denaturing gels and hybridized with probes to survivin or control ⁇ -actin.
- Figures 2A-D Expression of survivin in three-dimensional EC culture.
- EC were grown in three-dimensional fibronectin-collagen gels, paraffin- embedded and analyzed for survivin expression by immunohistochemistry.
- A. Survivin expression in control, two-dimensional EC culture.
- B. Survivin expression in three- dimensional EC culture.
- C. Control staining of three-dimensional EC culture with preimmune antibody.
- D. Two (2-D)- or three (3-D)-dimensional EC cultures were harvested, homogenized in a tissue grinder, and analyzed for survivin expression by immunoblotting.
- FIGS 3A-F Expression of survivin in proliferating and non-proliferating skin capillaries.
- Figures 4A-B Anti-apoptotic function of survivin in EC.
- Sub-confluent bovine aortic EC were fransfected with GFP-vector or GFP- survivin by lipofectin, cultivated for 35 h at 37°C and treated with 5 ng/ml TNF ⁇ /5 ⁇ g/ml cycloheximide for additional 8-h at 37°C.
- GFP-expressing cells were analyzed for DNA content by propidium iodide staining and flow cytometry. The percentage of cells with hypodiploid DNA content (sub-Gl -fraction) is indicated in parenthesis for each condition tested.
- Untreated or EC fransfected with GFP-vector or GFP-survivin were incubated with the indicated concentrations of TNF ⁇ /10 ⁇ g/ml cycloheximide, harvested, and analyzed for caspase-3 activity by hydrolysis of the fluorogenic substrate DEVD-AMC in the presence or in the absence of the caspase-3 inhibitor DEVD-CHO. Data are the mean ⁇ SD of replicates of a representative experiment.
- FIGS. 5A-D Ang-1 stimulates Akt phosphorylation and kinase activity.
- MVEC were incubated with Ang-1 (250 ng/ml) for 15 min and analyzed for Akt phosphorylation (serine 473, upper panel) or total Akt expression (lower panel) by Western blotting.
- Cells were treated as described, and cell lysates prepared for Akt kinase assays (see B). 20 ⁇ g of protein was separated on SDS-polyacrylamide gel electrophoresis gel (SDS-PAGE) and transferred onto a polyvinylidene difluoride membrane (Millipore).
- Akt was immunoprecipitated from MVEC and analyzed for kinase activity using histone 2B as a substrate.
- Cells were washed twice with PBS and lysed with cell lysis buffer (1% Nonidet P-40, 10% glycerol, 137 mM NaCl, 20 mM Tris-HCl, pH 7.4, 20 mM NaF, 2 ⁇ g/ml leupeptin, 1 mM phenylmethylsulfonyl fluoride). Lysates were precleared with protein G-agarose for 30 min at 4°C, and immunoprecipitated for 2 h with anti- Akt antibodies in the presence of 2 mg/ml bovine serum albumin with or without 16 ⁇ g/ml competitor peptides (Santa Cruz).
- cell lysis buffer 1% Nonidet P-40, 10% glycerol, 137 mM NaCl, 20 mM Tris-HCl, pH 7.4, 20 mM NaF, 2 ⁇ g/ml leupeptin, 1 mM phenylmethylsulfonyl fluoride. Lysates were precle
- Immunoprecipitates were washed twice with cell lysis buffer, once with water, and once with kinase buffer (20 mM HEPES, pH 7.2, 10 mM MgCl 2 , 10 mM MnCl 2 ). Immunoprecipitated proteins were incubated in 50 ⁇ l of kinase buffer containing 2 ⁇ g of histone H2B (Roche Molecular Biochemicals) and [ 32 P-]ATP (5 ⁇ M, 10 ⁇ Ci) for 30 min at room temperature. Kinase reactions were stopped by the addition of SDS sample buffer and samples subjected to Cerekenov counting and SDS-PAGE followed by autoradiography. Parallel samples were processed to confirm equal amounts of immunoprecipitated Akt. C.
- MVEC Time-dependent activation of Akt by Ang-1.
- MVEC were incubated with Ang-1 for increasing amount of time and Akt activation detennined as above.
- D Ang-1 induced Akt phosphorylation is blocked by soluble Tie-2 and Ang-2, but not by soluble Tie 1.
- MVEC were incubated with vehicle (TBS plus CHAPS), or the various indicated combinations of Ang-1 (250 ng/ml), Ang-2 (alone (2.5 ⁇ g/ml), soluble Tie 1 or Tie 2 receptors (2.5 ⁇ g/ml) for 15 min before determination of Akt phosphorylation or total Akt expression by Western blotting.
- Ang-1 -induced Akt phosphorylation is blocked by soluble Tie-2, but not by Tie 1 or Ang-2.
- data are representative of at least 3 experiments.
- FIGS. 6A-C Ang-1 inhibits endothelial cell apoptosis via a PI-3 kinase/Akt pathway.
- MVEC were plated onto bacteriological dishes in serum-free media for 18h in the absence or presence of Ang-1 (250 ng/ml) or wortmannin (WM, 200 nM), before determination of apoptosis by propidium iodide staining and flow cytometry .
- MVEC were plated on bacteriological dishes in serum free medium in the presence or either vehicle (TBS containing CHAPS) or Ang-1 (250ng/ml). Cells were incubated for 18hr and both floating and adherent cells were collected.
- MVEC were fixed for 1 hour in 70% ethanol and stained with a solution containing 500 ⁇ g/ml RNAase H and 50 ⁇ g/ml propidium iodide and analyzed by using a fluorescence activated Cell sorter (FACS). At least 5000 events were analyzed, and the percentage of cells in the sub-Gl population calculated.)
- FACS fluorescence activated Cell sorter
- MVEC with hypodiploid (apoptotic) DNA content is indicated.
- FIGS 7A-D Ang-1 induces survivin expression via a PI-3 kinase/Akt pathway.
- MVEC were co-transfected with plasmids encoding a promoterless luciferase cassette (pLUC-42), or a 1.2 kb survivin promoter fragment (pLUC-cycl.2) with ⁇ - galactosidase and relative luciferase activity was determined.
- D. VEGF and Ang-1 increase survivin protein expression.
- HUVEC were treated with VEGF (50 ng/ml) or Ang-1 (250 ng/ml) under the various conditions tested, were harvested after 18 h and analyzed for survivin, actin and bcl-2 protein expression by Western blotting. Numbers below the survivin panel indicate relative levels based on densitometry. For all panels, data are representative of 2-4 experiments.
- FIGS 8A-B Survivin mediates the anti-apoptotic effect of Ang-1.
- the experimental conditions are the same as in B, except that EC extracts treated with control or the survivin antisense oligonucleotide were analyzed with an antibody to bcl-2 by Western blotting.
- molecular weight markers in kDa are indicated on the left.
- WB Western blot.
- FIGS 10A-D Inhibition of VEGF cytoprotection by survivin targeting.
- DAPI 4,6- diamidino-2-phenylindole
- Photographs of phase contrast or DAPI staining of each field are from a representative experiment out of at least three independent determinations.
- FIGS 11A-C Modulation of Caspase Activity by Survivin Targeting.
- Starved EC were transfected with the indicated oligonucleotides and incubated in the absence (-Ceramide) or presence (+Ceramide) of ceramide.
- Cell extracts were analyzed for caspase-3 activity by hydrolysis of the fluorogenic substrate DEVD-AMC, in the presence or in the absence of DEVD-CHO (A), or by DNA content by propidium iodide staining and flow cytometry (B). Data are expressed as the mean ⁇ SD of three independent experiments. In B, the percentage of apoptotic cells with hypodiploid, sub- Gl, DNA content is indicated. .
- the experimental conditions are as in Figure 10, except that quiescent EC were transfected with the indicated antisense oligonucleotides, stimulated with VEGF and exposed to C-6 ceramide. Cells were analyzed for nuclear morphology by DAPI staining after a 12 h culture at 37°C. Data are the mean ⁇ SEM of three independent transfection experiments.
- Figure 14 Effect of survivin targeting on VEGF-induced EC migration/chemotaxis.
- EC were transfected with control or the survivin antisense oligonucleotide, stimulated with VEGF and exposed to the indicated increasing concentrations of VEGF or control SPP-1 in a Boy den chamber. After a 5 h incubation at 37°C, migrated cells were counted microscopically by Giemsa. Data are the mea+SEM of triplicates of a representative experiment out of three independent determinations.
- Figure 15 Effect of survivin targeting on capillary formation.
- EC transfected with the control or the survivin antisense oligonucleotide were cultured in collagen gels in the presence of PMA, and stabilized in the absence (None) or presence of VEGF.
- Three-dimensional capillary networks were analyzed by phase contrast microscopy during a 3-d culture at 37°C. Pictures are representative of one experiment out of at least three independent determinations. Magnification xlOO.
- the present invention is based in part on the discovery that survivin is a growth factor-inducible protective gene expressed by endothelial cells during angiogenesis. Stimulation of quiescent endothelial cells with mitogens, including vascular endothelial growth factor or basic fibroblast growth factor, induced up to ⁇ 16-fold up-regulation of survivin. Mitogen stimulation rapidly increased survivin RNA expression in endothelial cells, which peaked after 6-10 h culture and decreased by 24-h. Inflammatory cytokines, tumor necrosis factor or interleukin-1 did not induce survivin expression in endothelial cells.
- the present invention is also based on the discovery that Ang-1 acting via the Tie-2 receptor induces phosphorylation of the survival serine/threonine kinase Akt (or protein kinase B). This is associated with up-regulation of survivin in endothelial cells and protection of endothelium from death-inducing stimuli. Moreover, a dominant negative survivin mutant negates the ability of Ang-1 to protect cells from undergoing apoptosis. The activation of anti-apoptotic pathways mediated by Akt and survivin in endothelial cells may contribute to Ang-1 stabilization of vascular structures during angiogenesis, in vivo.
- the present invention is based on the finding that an antisense oligonucleotide to the apoptosis inhibitor survivin suppressed survivin expression in endothelial cells induced by vascular endothelial cell growth factor (VEGF).
- VEGF vascular endothelial cell growth factor
- the survivin antisense oligonucleotide did not affect anti-apoptotic bcl-2 levels in endothelium.
- antisense targeting of survivin abolished the anti-apoptotic function of VEGF against TNF ⁇ - or ceramide-induced cell death, enhanced caspase-3 activity, promoted the generation of a ⁇ 17 kDa active caspase- 3 subunit, and increased cleavage of the caspase substrate, poly-ADP ribose polymerase.
- the survivin antisense oligonucleotide had no effect on endothelial cell viability in the absence of VEGF.
- Antisense oligonucleotides to platelet-endothelial cell adhesion molecule-1 (PECAM-1, CD31), lymphocyte function : associated molecule-3 (LFA-3, CD58) or intercellular adhesion molecule-1 (ICAM-1, CD54) did not reduce the anti apoptotic function of VEGF in endothelium.
- antisense survivin targeting induced rapid regression of three- dimensional capillary networks but did not affect endothelial cell migration chemotaxis.
- the present invention provides methods of modulating this pathway to increase endothelial cell viability in compensatory angiogenesis or to facilitate endothelial cell apoptosis and promote vascular regression during tumor angiogenesis.
- the present invention employs survivin protein, as well as allelic variants of the survivin protein, and conservative amino acid substitutions of the survivin protein.
- survivin protein or "survivin” refers in part to a protein that has the amino acid sequence of human survivin.
- the term also includes naturally occurring allelic variants of survivin, which include naturally occurring proteins that have a slightly different amino acid sequence than that specifically recited above. Allelic variants, though possessing a slightly different amino acid sequence than those recited above, will still have the requisite ability to inhibit cellular apoptosis.
- the survivin family of proteins also refers to survivin proteins that have been isolated from organisms in addition to humans.
- the survivin proteins of the present invention further include conservative variants of the survivin proteins herein described.
- a conservative variant refers to alterations in the amino acid sequence that do not adversely affect the ability of the survivin protein to bind to a survivin binding or signaling partner and/or to inhibit cellular apoptosis.
- a substitution, insertion or deletion is said to adversely affect the survivin protein when the altered sequence prevents the survivin protein from associating with a survivin binding or signaling partner and/or prevents the survivin protein from inhibiting cellular apoptosis.
- the overall charge, structure or hydrophobic/hydrophilic properties of survivin can be altered without adversely affecting the activity of survivin.
- the amino acid sequence of survivin can be altered, for example to render the peptide more hydrophobic or hydrophilic, without adversely affecting the activity of survivin.
- allelic variants will have the ability to inhibit cellular apoptosis.
- Such proteins will ordinarily have an amino acid sequence having at least about 75% amino acid sequence identity with the human survivin sequence, more preferably at least about 80%, even more preferably at least about 90%, and most preferably at least about 95%.
- Identity or homology with respect to such sequences is defined herein as the percentage of amino acid residues in the candidate sequence that are identical with the known peptides, after aligning the sequences and introducing gaps, if necessary, to achieve the maximum percent homology, and including any conservative substitutions as being homologous.
- the survivin proteins of the present invention include molecules having full length amino acid sequence of naturally occurring proteins; fragments thereof or peptides having a consecutive sequence of at least about 3, 5, 10, 15, or more amino acid residues of the survivin protein; amino acid sequence variants of such sequence wherein an amino acid residue has been inserted N- or C-terminal to, or within, the sequence of a naturally occurring survivin protein; amino acid sequence variants of the disclosed survivin sequence, or their fragments as defined above, that have been substituted by another residue.
- Contemplated variants further include those containing predetermined mutations by, e.g., homologous recombination, site-directed or PCR mutagenesis, and the corresponding survivin proteins of other animal species, including but not limited to rabbit, rat, murine, porcine, bovine, ovine, equine and non-human primate species, and the alleles or other naturally occurring variants of the survivin family of proteins; and derivatives wherein the survivin protein has been covalently modified by substitution, chemical, enzymatic, or other appropriate means with a moiety other than a naturally occurring amino acid (for example a detectable moiety such as an enzyme or radioisotope.
- a detectable moiety such as an enzyme or radioisotope.
- the present invention also includes or employs survivin peptidomimetics.
- Survivin peptidomimetics are compounds that mimic the activity of survivin peptides. They are structurally similar to survivin peptides but have a chemically modified peptide backbone. Peptidomimetics may have significant advantages over polypeptide embodiments, including, for example: more economical production; greater chemical stability; enhanced pharmacological properties (half-life, absorption, potency, efficacy, etc); altered specificity (e.g., a broad-spectrum of biological activities); reduced antigenicity; and others.
- nucleic acid is defined as RNA or DNA that encodes a peptide as defined above, or is complementary to a nucleic acid sequence encoding such peptides, or hybridizes to such a nucleic acid and remains stably bound to it under stringent conditions, or encodes a polypeptide sharing at least 75% sequence identity, preferably at least 80%, and more preferably at least 85%, with the peptide sequences.
- genomic DNA, cDNA, mRNA and antisense molecules as well as nucleic acids based on an alternative backbone or including alternative bases whether derived from natural sources or synthesized.
- stringent conditions are conditions in which hybridization yields a clear and detectable sequence. Stringent conditions are those that (1) employ low ionic strength and high temperature for washing, for example, 0.015M NaCl/0.0015M sodium titrate/0.1% SDS at 50°C, or (2) employ during hybridization a denaturing agent such as formamide, for example, 50% (vol/vol) formamide with 0.1% bovine serum albumin/0.1% Ficoll/0.1% polyvinylpyrrolidone/50 mM sodium phosphate buffer at pH 6.5 with 750 mM NaCl, 75 mM sodium citrate at 42°C.
- formamide for example, 50% (vol/vol) formamide with 0.1% bovine serum albumin/0.1% Ficoll/0.1% polyvinylpyrrolidone/50 mM sodium phosphate buffer at pH 6.5 with 750 mM NaCl, 75 mM sodium citrate at 42°C.
- Another example is use of 50% formamide, 5 x SSC (0.75M NaCl, 0.075 M sodium citrate), 50 mM sodium phosphate (pH 6.8), 0.1% sodium pyrophosphate, 5 x Denhardfs solution, sonicated salmon sperm DNA (50 (g/ml), 0.1% SDS, and 10% dextran sulfate at 42°C, with washes at 42°C. in 0.2 x SSC and 0.1% SDS.
- a skilled artisan can readily determine and vary the stringency conditions appropriately to obtain a clear and detectable hybridization signal.
- the present invention further employs fragments of the survivin encoding nucleic acid molecule.
- a fragment of a survivin encoding nucleic acid molecule refers to a small portion of the entire protein encoding sequence. The size of the fragment will be determined by the intended use. For example, if the fragment is chosen so as to encode an active portion of the survivin protein, such as the C-terminal coils or the IAP motif, the fragment will need to be large enough to encode the functional region(s) of the Survivin protein.
- An antisense survivin molecule is complementary to and capable of hybridizing or annealing with the RNA encoded by a survivin gene (the "sense gene").
- An antisense survivin molecule is used to inhibit the expression of the survivin gene thereby inhibiting angiogenesis and preventing and, treating diseases associated with angiogenesis.
- Antisense nucleic acids are preferably constructed by inverting the coding region of the sense gene relative to its normal presentation for transcription to allow for transcription of its complement, hence the complementariness of the respective RNAs encoded by these DNA's.
- the antisense DNA should preferably be expressed at approximately the same time as the sense gene if the antisense nucleic acid is to be expressed in the cell. The timing must be approximate in the sense that the antisense RNA must be present within the cell to block the function of the RNA encoded by the sense gene. To accomplish this result, the coding region of the antisense DNA is often placed under the control of the same promoter as found in the sense gene thereby causing both to be transcribed at the same time.
- nucleic acid molecules complementary to a portion of the survivin mRNA transcript including the translation initiation codon are particularly preferred.
- nucleic acid molecules complementary to a portion of the survivin mRNA transcript lying within about 40 nucleotides upstream (the 5' direction) or about 40 nucleotides downstream (the 3' direction) from the translation initiation codon are particularly preferred.
- antisense oligonucleotides which hybridize or anneal to at least a portion of the survivin mRNA in a cell may be used in the methods of the invention.
- Such oligonucleotides are typically short in length and fairly easily diffusible into a cell.
- Such antisense oligonucleotides include, but are not limited to, polydeoxynucleotides containing 2'-deoxy-D-ribose, polyribonucleotides containing D-ribose, any other type of polynucleotide which is an N-glycoside of a purine or pyrimidine base, or other polymers containing nonnucleotide backbones (e.g., protein nucleic acids and synthetic sequence specific nucleic acid polymers commercially available) or nonstandard linkages, providing that the polymers contain nucleotides in a configuration which allows for base pairing and base stacking such as is found in DNA and RNA.
- nonnucleotide backbones e.g., protein nucleic acids and synthetic sequence specific nucleic acid polymers commercially available
- RNA and DNA:RNA hybrids may include double- and single-stranded DNA, as well as double- and single-stranded RNA and DNA:RNA hybrids, and also include, as well as unmodified forms of the polynucleotide or oligonucleotide, known types of modifications, for example, labels which are known to those skilled in the art, "caps", methylation, substitution of one or more of the naturally occurring nucleotides with analogue, internucleotide modifications such as, for example, those with uncharged linkages (e.g., methyl phosphonates, phosphorotriesters, phosphoramidates, carbamates, etc) and with charged linkages or sulfur-containing linkages (e.g., phosphorothioates, phosphorodithioates, etc.), those containing pendant moieties, such as, for example, proteins (including nucleases, nuclease inliibitors, toxins, antibodies, signal peptides, poly-L-lys
- nucleoside as used concerning survivin antisense nucleic acid molecules, include those moieties which contain not only the known purine and pyrimidine bases, but also other heterocyclic bases which have been modified. Such modifications include methylated purines and pyrimidines, acylated purines and pyrimidines, or other heterocycles. Modified nucleosides or nucleotides will also include modifications on the sugar moiety, e.g., wherein one or more of the hydroxyl groups are replaced with halogen, aliphatic groups, or are functionalized as ethers, amines, or the like.
- Angiogenesis is the process by which new blood vessels are formed (Folkman et al. 1992). Thus, angiogenesis is essential in reproduction, development, and wound repair. However, inappropriate angiogenesis can have severe consequences. For example, it is only after many solid tumors are vascularized as a result of angiogenesis that the tumors begin to grow rapidly and metastasize. Because angiogenesis is so critical to these functions, it must be carefully regulated in order to maintain health.
- the angiogenesis process is believed to begin with the degradation of the basement membrane by proteases secreted from EC activated by mitogens such as vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (bFGF). The cells migrate and proliferate, leading to the formation of solid endothelial cell sprouts into the stromal space, then, vascular loops are formed and capillary tubes develop with formation of tight junctions and deposition of new basement membrane.
- VEGF vascular endothelial growth factor
- bFGF basic fibroblast
- the rate of angiogenesis involves a change in the local equilibrium between positive and negative regulators of the growth of micro vessels.
- Abnormal angiogenesis occurs when the body loses its control of angiogenesis, resulting in either excessive or insufficient blood vessel growth.
- conditions such as myocardial infarction, peripheral vascular occlusion, brain ischemia, or stroke may result from the absence of angiogenesis normally required for natural healing.
- excessive blood vessel proliferation may favor tumor growth and spreading, blindness, psoriasis and rheumatoid arthritis.
- EC endothelial cell
- Alternative methods for regulating angiogenesis are still desirable for a number of reasons. For example, it is believed that native endothelial cell (EC) number and/or viability decreases over time. Thus, in certain patient populations, e.g., the elderly, the resident population of ECs that is competent to respond to administered angiogenic cytokines may be limited. Moreover, while agents promoting or inhibiting angiogenesis may be useful at one location, they may be undesirable at another location. Thus, means to more precisely regulate angiogenesis at a given location are desirable.
- EC endothelial cell
- the present invention provides a method of regulating angiogenesis by providing survivin or a modulator of survivin expression to a cell or tissue.
- a modulator of survivin expression is a molecule that alters the expression of survivin in a cell.
- the present invention provides methods of inducing angiogenesis.
- the present invention is based on the findings that survivin, an apoptosis inhibitor, is expressed by EC during angiogenesis and vascular remodeling, that Ang-1 prevents EC apoptosis by phosphorylation of Akt, and by up-regulating survivin, and that phosphorylation of Akt is required for survivin expression. Since inhibition of apoptosis may be required during vascular remodeling and angiogenesis, survivin and agents that increase the expression of survivin or the activity of survivin are useful for inducing angiogenesis.
- survivin activity refers to the activities associated with survivin, for example, inhibition of apoptosis by survivin.
- survivin, Ang-1, Akt, or any other agent that increases the expression of survivin or promotes the functional activity of survivin can be used to induce angiogenesis.
- Administering the molecules in an amount that is effective to inhibit apoptosis may be sufficient to induce angiogenesis.
- an apoptosis inhibiting amount of survivin, Ang-1, Akt, and or other agent that increases the expression of survivin would be effective in treating diseases and conditions that require inducing compensatory angiogenesis. Examples of diseases and conditions that can be treated by these molecules include myocardial infarction, peripheral vascular occlusion, brain ischemia, and stroke.
- the present invention provides methods of inhibiting angiogenesis using agents that inhibit the expression of survivin.
- An example of an inhibitor of survivin expression is an antisense molecule.
- a modulator that inliibits the expression of survivin or a survivin dominant negative mutant can be used such as the C84A mutant (see Li et al, (1999), which is herein incorporated by reference in its entirety).
- An antisense survivin molecule or an agent that inliibits the expression of survivin is useful to prevent diseases or conditions such as restenosis, vascular bypass graft occlusion, transplant coronary vasculopathy, rheumatoid arthritis, psoriasis, ocular neovascularization, diabetic retinopathy, neovascular glaucoma, angiogenesis dependent tumors, and tumor metastasis.
- Agents that inhibit the functions of survivin are also useful in inhibiting angiogenesis, especially in cancerous cells to prevent metastases.
- agents include, but are not limited to, survivin antibodies, inhibitors of Akt phosphorylation, and inhibitors of survivin function.
- Gene therapy is a method for delivering functionally active therapeutic or other forms of genes into targeted cells.
- Initial efforts of gene transfer into somatic tissues have relied on indirect means called ex vivo gene therapy, wherein target cells are removed from the body, transfected or infected with vectors carrying recombinant genes, and re-implanted into the body.
- Techniques currently used to transfer DNA in vitro into cells include calcium phosphate-DNA precipitation, DEAE-Dextran transfection, electroporation, liposome mediated DNA transfer or transduction with recombinant viral vectors. These transfection protocols have been used to transfer DNA into different cell types including epithelial cells (U.S. Pat. No.
- Viral vectors are often the most efficient gene therapy system, and recombinant replication-defective viral vectors have been used to transduce (i.e., infect) cells both ex vivo and in vivo.
- Such vectors include retroviral, adenovirus and adeno-associated and herpes viral vectors.
- the survivin transgene or survivin antisense molecule can be subcloned into an appropriate vector and transferred into a cell or tissue by gene transfer techniques discussed above.
- the survivin transgene or the survivin antisense molecule can be provided to the cell or tissue using a transfection facilitating composition, such as cationic liposomes containing desired polynucleotide.
- a transfection facilitating composition such as cationic liposomes containing desired polynucleotide.
- the desired polynucleotide is the survivin transgene or the survivin antisense molecule.
- the present invention provides a method of delivering endothelial cells engineered to express an apoptosis inhibiting amount of survivin to a patient.
- Genetically engineered endothelial cells preferably autologous, may be implanted directly into the patient, where they produce and deliver survivin.
- autologous endothelial cells are engineered to express an apoptosis inhibiting amount of survivin.
- autologous cells derived from the patient are stably transfected with the nucleic acid encoding the desired protein. They are harvested from tissue culture dishes, placed in an implantation device, and implanted at a variety of sites including subcutaneous, intraperitoneal, intrasplenic, intraomental, inguinal, intrathecal, intraventricular, and intramuscular sites, as well as within lymph nodes or within adipose tissue.
- vascular endothelial growth factor As described above, the localized induction of angiogenesis using a Hydrogel-coated angioplasty balloon as the gene delivery system has been successfully demonstrated (Takeshita et al, 1996; Isner et al, 1996). These trials demonstrated the sustained expression of the VEGF gene in the vessel wall which subsequently augmented neovascularization in the ischemic limb.
- delivery systems may be used to provide a survivin encoding nucleic acid molecule or transgene to a patient in need thereof.
- Such a system may also be used to locally deliver an agent which modulates survivin expression in contacted cells.
- both a survivin encoding nucleic acid molecule and the VEGF gene may be delivered in combination or sequentially to induce localized angiogenesis.
- survivin or an agent that modulates survivin expression can be provided to the tissue as an implant.
- the preparation of implants requires such supports suitable for being placed in contact with cells and various factors promoting the adhesion of tliese cells to the support if necessary, under conditions such that the different constituents present conserve their principal natural structural and functional properties.
- suitable implant materials are fibrous collagen and type II collagen.
- the implant material is coated or impregnated with the agent that is to be provided to the cell or tissue.
- Other implantation device consists of a solid, unitary piece of collagen gel (a "collagen matrix") in which the cells are embedded (U.S. Pat. No. 4,485,096).
- PTFE polytetrafluoro-ethylene
- the implant can be provided to the cell or tissue as a stent.
- Implantable stents are small tubes of a few millimeters in diameter and a few centimers in length used to deliver therapeutic agents directly to the target site. Stents are suitable for local delivery of viral vectors encoding a survivin nucleic acid molecule or survivin inducing molecule to target sites and are often designed to be capable of degradation into products that are nontoxic to the cells of the vessel wall where they are implanted (Raiasubramanian et al, 1994).
- biodegradable polymeric material for making stents are mixtures of poly-L-lactic acid (PLLA) and Poly-E- caprolactone (PLC) (Raiasubramanian et al, 1994) and poly-beta-hydroxybutanoic acid (US Patent No. 5,935,506).
- the stents can be impregnated with a survivin nucleic acid molecule, a survivin antisense molecule, or an agent that induces survivin expression to be delivered and surgically implanted at the target site.
- the agents that promotes or inhibits angiogenesis can be administered via parenteral, subcutaneous, intravenous, intramuscular, intraperitoneal, transdermal, or buccal routes. Alternatively, or concurrently, administration may be by the oral route.
- the dosage administered will be dependent upon the age, health, and weight of the recipient, kind of concurrent treatment, if any, frequency of treatment, and the nature of the effect desired.
- a survivin irihibiting agent such as a survivin antibody, an inhibitor of survivin expression or function, or an inhibitor of Akt phosphorylation, is administered systemically or locally to the individual being treated.
- an agent such as survivin itself, Ang-1, Akt, or any other agent that increases the expression of survivin or induces the function of survivin is administered systemically or locally to the individual. As described below, there are many methods that can readily be adapted to administer such agents.
- the present invention contemplates compositions containing one or more agents that promotes or inhibits angiogenesis. While individual needs vary, a determination of optimal ranges of effective amounts of each component in the composition is within the skill of the art.
- Typical dosages comprise 0.1 to 100 mg/kg body wt.
- the preferred dosages comprise 0.1 to 10 mg/kg body wt.
- the most preferred dosages comprise 0.1 to 1 mg/kg body wt.
- compositions of the present invention may contain suitable pharmaceutically acceptable carriers comprising excipients and auxiliaries which facilitate processing of the active compounds into preparations which can be used pharmaceutically for delivery to the site of action.
- Suitable formulations for parenteral administration include aqueous solutions of the active compounds in water-soluble form, for example, water-soluble salts.
- suspensions of the active compounds as appropriate oily injection suspensions may be administered.
- Suitable lipophilic solvents or vehicles include fatty oils, for example, sesame oil, or synthetic fatty acid esters, for example, ethyl oleate or triglycerides.
- Aqueous injection suspensions may contain substances which increase the viscosity of the suspension include, for example, sodium carboxymethyl cellulose, sorbitol, and/or dextran.
- the suspension may also contain stabilizers. Liposomes can also be used to encapsulate the agent for delivery into the cell.
- the pharmaceutical formulations for systemic administration according to the invention may be formulated for enteral, parenteral or topical administration. Indeed, all three types of formulations may be used simultaneously to achieve systemic administration of the active ingredient.
- Suitable formulations for oral administration include hard or soft gelatin capsules, pills, tablets, including coated tablets, elixirs, suspensions, syrups or inhalations and controlled release forms thereof.
- the agents that induce or inhibit angiogenesis may be used alone or in combination, or in combination with other therapeutic or diagnostic agents.
- the agents may be coadministered along with other compounds typically prescribed for these conditions according to generally accepted medical practice, such as chemotherapeutic agents.
- the present invention contemplates the use of agents that modulate survivin expression or function in combination with an immunomodulatory agent in an immunosuppressive therapy, such as those used to treat patients who have received a transplant or graft.
- an immunosuppressive therapy such as those used to treat patients who have received a transplant or graft.
- Transplants of healthy organs or cells into a patient suffering from a disease are often rejected by the body due to an immune response initiated in response to the foreign tissue or cells.
- the only method to inhibit this immune response is to administer chronic nonspecific immunosuppression agents.
- Agents that modulate survivin expression or function can inhibit or induce angiogenesis depending on the condition, and immunomodulatory agents can suppress undesirable immune response. The combination would facilitate the recovery of patients who have undergone transplantation.
- Human umbilical vein EC were maintained in Ml 99 medium supplemented with 20% fetal calf serum (FCS), 50 ⁇ g/ml Endothelial Cell Growth Supplement (ECGS), 100 ⁇ g/ml heparin, 100 ⁇ g/ml penicillin, 100 ⁇ g/ml streptomycin (all from Life Technologies, Grand Island, NY), in 5% CO 2 at 37°C.
- Bovine aortic EC were isolated and maintained in culture as described by De Luca et al (1994). Subconfluent EC were rendered quiescent by a 24 h-culture in M199 plus 0.1% FCS. Cells were detached with 0.05% trypsin/0.02% EDTA, seeded in C6-well plates (Costar Corp., New Bedford, MA), grown to 70% confluency and used between passage 2 and 3.
- Protein normalized aliquots of cell extracts were electrophoresed on a 13.5% SDS polyacrylamide gel, transferred to nylon membranes (Millipore, Corp.) for 1 h at 1 A, and immunoblotted with 1 ⁇ g/ml of a rabbit antibody to survivin followed by chemiluminescence (Amersham, Arlington Heights, IL). 18 Samples were analyzed for equal protein loading by immunoblotting with a mouse antibody to ⁇ -actin. For Northern hybridization, serum-deprived EC were stimulated with 100 ng/ml VEGF and harvested at increasing time intervals between 1.5- 24 h culture at 37°C.
- EC were suspended at a density of 3x10 6 /ml in a liquefied matrix of rat-tail type I collagen (1.5 mg/ml) and human plasma-derived fibronectin (0.15 mg/ml) in Ml 99, pH 7.5.
- a liquefied matrix of rat-tail type I collagen 1.5 mg/ml
- human plasma-derived fibronectin 0.15 mg/ml
- Binding of the primary antibody was revealed by addition of 3,3'-diaminobenzidine,.or, alternatively, 3-amino-9-ethylcarbazol (AEC, Vector), as a substrate. Control experiments were carried out in the absence of primary antibody, or in the presence of preimmune rabbit IgG.
- the cDNA of wild type survivin (Ambrosini et al, 1997) was inserted in frame in the EcoRI site of Green Fluorescence Protein (GFP)-encoding plasmid, p ⁇ GFPcl (Clontech, San Francisco). The correct orientation and reading frame of p ⁇ GFPcl fusion plasmid were confirmed by DNA sequencing.
- Bovine aortic EC were seeded in C6-well plates at 40-50% confluency and transfected with GFP-vector or GFP-survivin by lipofectin for 6 h at 37°C.
- the EC monolayer was placed in complete growth medium for 35 h at 37°C, and incubated with 5 ng/ml TNF ⁇ plus 5 ⁇ g/ml cycloheximide for additional 8h at 37°C.
- Cells floaters plus attached cells
- bovine EC transfected with GFP-vector or GFP-survivin were treated with control medium or 5-10 ng/ml TNF ⁇ plus 10 g/ml cycloheximide for 8-h at 37°C.
- Cells were harvested, and analyzed for caspase-3 activity by hydrolysis of the fluorogenic substrate Ac-DEVD- AMC (N-Acetyl- Asp-Glu- Val- Asp-aldehyde, Pharmingen, San Diego, CA), in the presence or in the absence of the caspase-3 inhibitor Ac-DEVD-CHO. Fluorescence emissions were quantitated on a spectrofluorometer with excitation wavelength of 360 nm and emission of 460 nm.
- Bovine lung microvascular endothelial cells (MVEC, Vectek, Albany, NY) were cultured in Dulbecco's Modified Eagle's Medium containing 10% fetal bovine serum (FBS), L-glutamine and antibiotics (penicillin and streptomycin). Cells (up to passage 12) were used for the experiments; cultures had typical cobblestone morphology and stained uniformly for von WiUebrand factor, as assessed by indirect immunofluorescence.
- Ang-1 A recombinant form of Ang-1 was used in all of the experiments.
- This form of Ang-1 differs from the native Tie2 ligand in that it possesses a modified NH2-terminal sequence and a mutation in Cys245 that make it easier to produce and purify.
- Microvascular endothelial cells were treated with Ang-1. Changes in the anti-apoptotic serine/threonine kinase, Akt (or protein kinase B) were analyzed. Stimulation of MVEC with Ang-1 increased Akt phosphorylation on serine 473 (Fig. 5A), threonine 308 (not shown) and up-regulated Akt kinase activity (Fig. 5B), in a reaction suppressed by the PI3 kinase inhibitor, wortmannin (WM; Fig. 5B). Ang-1 stimulated Akt phosphorylation in a time-dependent manner with maximal activation occurring within 15-30 min, and sustained phosphorylation lasting for up to 2 h (Fig.
- Ang-1 stimulated phosphorylation of Akt on Ser 473 was antagonized by preincubation of Ang-1 with soluble Tie 2 receptor, but not by incubation with soluble Tiel receptor bodies (5D).
- Ang-1 induced Akt phosphorylation was partially blocked by the physiological antagonist of Ang-1, angiopoeitin-2 (Ang-2; Maisonpierre et al, 1997).
- Ang-2 alone weakly activated Akt in MVEC. Therefore, Ang-1 via the Tie 2 receptor stimulates Akt activation through a PI-3 kinase dependent mechanism.
- MVEC in serum free media and plated onto petri dishes for 18 h underwent extensive apoptosis as determined by appearance of a hypodiploid cell population (-25% versus 2% of control, adherent cultures) by propidium iodide staining and flow cytometry (Fig. 6A).
- Ang-1 inhibited apoptosis by 75%, in a reaction reversed by WM (Fig. 6A).
- MVEC were infected with adenoviral ⁇ -galactosidase or activation deficient Akt (AA-Akt; Fujio et al, 1999) and determined the degree of apoptosis. Transduction of MVEC with AA-Akt abrogated the cytoprotective effect of Ang-1 against anoikis, whereas a control adenovirus encoding ⁇ -galactosidase was ineffective. MVEC were infected with 100 MOI of adenovirus containing the ⁇ - galactosidase, HA-tagged activation deficient phosphorylation mutant Akt (AA-Akt, Fujio et al, 1999).
- Ang-1 Treatment of MVEC with Ang-1 rapidly induced a time-dependent increase in survivin RNA levels (Li et al, 1998), which peaked 12 h after stimulation and remained sustained for up to 24 h (Fig 7A). In contrast, Ang-1 did not up-regulate bcl-2 RNA expression in MVEC (Fig. 5A). Consistent with a receptor-mediated response, preincubation of Ang-1 with soluble Tie-2 receptor abolished Ang-1 induction of survivin RNA in MVEC (Fig. 7B).
- MVEC survivin- luciferase promoter construct
- Ang-1 stimulated a 3-7-fold up- regulation of survivin transcriptional activity, which persisted for up to 24 h after stimulation
- VEGF or Ang-1 strongly induced expression of survivin protein in HUVEC, an effect abrogated by WM, or by transduction with AA-Akt (Fig. 7D).
- Human umbilical vein endothelial cells (HUVEC ) were used in these experiments due to greater sensitivity of the survivin antibody with human survivin.
- HUVEC were isolated from umbilical veins and cultured on gelatin coated tissue culture flasks in Ml 99 containing 20%) fetal bovine serum (FBS), 50 ⁇ g/ml EC growth supplement (ECGS, a commercial preparation that contains mainly acidic fibroblast growth factor), 100 ⁇ g/ml porcine heparin, lOU/ml penicillin and 100 ⁇ g/ml streptomycin.
- FBS fetal bovine serum
- ECGS a commercial preparation that contains mainly acidic fibroblast growth factor
- 100 ⁇ g/ml porcine heparin 100 ⁇ g/ml porcine heparin
- lOU/ml penicillin 100 ⁇ g/ml streptomycin.
- Two to three individual donors were pooled at passage one and used up to passage, three. Cultures had typical cobblestone morphology and stained uniformly for von WiUebrand factor, as assessed by indirect immunofluoresence. Identical results were obtained using MVEC.
- MVEC was transfected with cDNAs containing green fluorescent protein (GFP) fused to wild-type-survivin (GFP-survivin), or to a dominant negative Cys 84 ⁇ >Ala survivin mutant (GFP-C84A survivin). Cytoprotection in response to apoptosis-inducing stimuli (Li et al, 1999b) was determined. Fusion of survivin with GFP does interfere with its biological activity (Li et al, 1999b).
- the survivin-GFP (Cys84-Ala) construct is a mutation in the BIR1 domain. It is targeted to the mitotic spindle similar to endogenous survivin but is devoid of its anti-apoptotic function.
- DNA encoding survivin is assembled into a mammalian expression vector containing the cytomegalovirus promoter (Takeshita et al, 1996).
- the biologic activity of survivin obtained from cells transfected with this construct, phSurvivin, is confirmed before performing arterial gene transfer.
- the plasmid pGSVLacZ containing a nuclear- targeted -galactosidase sequence coupled to the simian virus 40 early promoter is used for control transfection experiments (Takeshita et al, 1996).
- the femoral artery is completely excised from its proximal origin as a branch of the external iliac artery, to the point distally at which it bifurcates into the saphenous and popliteal arteries.
- tl rombotic occlusion of the external iliac artery extends retrograde to its origin from the common iliac artery. Consequently, blood supply to the distal limb is dependent on the collateral arteries, which may originate from the internal iliac artery.
- An interval of 10 days between the time of surgery and gene transfer is allowed for postoperative recovery of the rabbits and development of endogenous collateral vessels.
- a baseline angiogram is performed.
- the internal iliac artery of the ischemic limb of a number of animals is transfected with phSurvivin percutaneously using a 2mm hydrogel-coated balloon catheter (SliderTM, Boston Scientific, Watertown massachusetts).
- the angioplasty balloon is prepared (ex vivo) by advancing the deflated balloon through a 5 Fr.
- Teflon sheath (Boston Scientific); applying the solution of plasmid DNA from a conventional pipette to the 20 ⁇ m layer of hydrogel coating the external surface of the inflated balloon; and finally, deflating the balloon, retracting same into the protective sheath, and re-inflating the balloon to prevent backflow of blood into the sheath (and onto the coated balloon) after introduction into the circulation.
- the sheath and angioplasty catheter are then introduced via the right carotic artery and advanced to the lower abdominal aorta using a 0.014-inch guide- wire (Hi- Torque Floppy IITM; Advanced Cardiovascular System, Temecula, California) under fluoroscopic guidance.
- the balloon catheter is then advanced into the internal iliac artery of the ischemic limb, inflated for 1 minute at 4 to 6 atmospheres, deflated and withdrawn.
- An identical protocol is used to transfect the internal iliac arter of control animals with the plasmid pGSVLacZ. Heparin is not administered at the time of transfection or angiography.
- Gene expression is evaluated at the mRNA level by RT-PCR in rabbits in wliich the iliac artery was transfected using the hydrogel balloon catheter, as described above. Transfected arterial segments are obtained at 7, 14, 21, and 30 days posttransfection. Remote tissues such as brain, heart, liver, lung, spleen, testes, are also retrieved ⁇ 7 days posttransfection for analysis of survivin mRNA. Total cellular RNA is isolated using TRI reagent (Molecular Research Center, Cincinnati, Ohio) according to the manufacturer's instructions. Extracted DNA is treated with DNase I (0.5 ⁇ l, 10 U/ ⁇ l, Rnase-free, Message Clean kit; GenHunter, Boston, Massachusetts) at 37°C for 30 minutes to eliminate DNA contamination.
- DNase I 0.5 ⁇ l, 10 U/ ⁇ l, Rnase-free, Message Clean kit; GenHunter, Boston, Massachusetts
- RNA sample is subjected to 1% nondenaturing mini-agarose gel electrophoresis.
- Each RNA sample is used to make cDNA in a reaction containing deoxynucleotides, RNasin (Promega, Madison, Wisconsin), random hexanucleotide primers (Promega), and Moloney murine leukemia virus reverse transcriptase (GIB CO BRL, Gaithersburg, Maryland). Reactions are incubated at 42°C for 1 hour, then at 95°C for 5 minutes to terminate the reaction.
- PCR amplification is performed for 30 cycles at 94°C for 20 seconds, ending with 5 minutes at 72°C.
- Oligonucleotide primers selected from a specific region of the nucleic acid encoding survivin is used to amplify that region or fragment of survivin.
- RT-PCR products are analyzed by 2% agaose gel electrophoresis.
- LacZ-Tf arteries are harvested on Day 5, and ⁇ -galactosidase activity is determined by incubation with 5-bomo-4-chloro-3-indolyl- ⁇ -D-galactoside chromogen (X-Gal; Sigma Chemical Company, St. Louis Missouri) as previously described (Takeshita etal, 1996). After staining with X-Gal solution, tissues are paraffin-embedded, sectioned, and counterstained with hematoxylin-eosin.
- Nuclear localized ⁇ -galactosidase expression of the plasmid pGSVLacZ could not result from endogenous ⁇ -galactosidase activity; , accordingly, histochemical identification of ⁇ -galactosidase within the cell nucleus is interpreted as evidence for successful gene transfer and gene expression. Cytoplasmic or other staining is considered nonspecific for the purpose of the present study.
- Calf blood pressure is measured in both hindlimbs using a Doppler flowmeter (model 1059, Parks Medical Electonics, Aloha, Oregon) immediately before transfection (Day 0) as well as on Day 30.
- the hindlimbs are shaved and cleaned, the pulse of the posterior tibial artery is identified using a Doppler probe, and the systolic blood pressure in both limbs is determined using standard techniques (Takeshita et al, 1996).
- the calf blood pressure ratio is defined for each rabbit as the ratio of systolic pressure of the ischemic limb to systolic pressure of the normal limb.
- a 3 Fr. Infusion catheter (Tracker- 18, Target Therapeutic, San Jose, California) is introduced into a common carotid artery through a small cutdown and advanced to the internal iliac artery of the ischemic limb using 0.014 inch guidewire (Hi-torque floppy II) under fluoroscopicguidance.
- the tip of catheter is positioned in the internal iliac artery at the livel of the interspace between the seventh lumbar and the first sacral vertebrae.
- nonionic contrast media Isovue-370, Squibb Diagnostics, New Brunswick, New Jersey
- an automated angiographic injector Medrad, Pittsburgh, Pennsylvania
- Serial angiographic images (1 per second for 10 seconds) are then recorded on 105-mm spot film.
- Morphometric angiographic analysis of collateral vessel development is performed using a grid overlay comprised of 2.5 -mm circles arranged in rows spaced 5 mm apart. The overlay is applied to the 4- second angiogram recorded at the level of the medial thigh.
- a defined area is chosen in which the number of contrast-opacified arteries crossing over circles as well as the total number of circles encompassing the medial thigh area are counted in single blind fashion.
- An angiographic score is calculated for each film as the ratio of crossing opacified arteries divided by the total number of circles in the defined area of the ischemic thigh.
- a 0.018-inch guidewire with a 12-MHz piezoelectric transducer at the distal tip (FloMap: Cardiometrics, Mountainview, California) is used to measure blood flow velocity (Takeshita et al, 1996).
- the Doppler wire records a real-time spectral analysis of the Doppler signal from which the average peak velocity (APV, temporal average fo the instantaneous peak velocity waveform) is calculated and displayed on line.
- the wire is advanced through the 3 Fr. infusion catheter positioned at the origin of the common iliac artery to the proximal segment of the internal iliac artery supplying the ischemic limb. A stabilized velocity of 2 minutes before recording resting APV is required.
- the 3 Fr. infusion catheter is redirected to the proximal segment of the internal iliac artery of the ischemic limb, and selective internal iliac angiography is performed as described.
- the angiographic luminal diameter of the internal iliac artery in the ischemic limb and of the external artery in the normal limb are determined using an automated edge-detection system (Quantum 20001; QCS, Ann Arbor Michigan) as described.
- the film selected for analysis is scanned with a high resolution video camera, and the signal produced by the video camera is digitized and displayed on a video monitor (Laser Scan; ImageComm, Santa Clara, California).
- Center lines are traced manually for a 10-mm segment beginning immediately distal to the tip of the Doppler wire.
- the contours are subsequently detected automatically on the basis of the weighted sum of first and second derivative functions applied to the digitized brightness information.
- the vascular diameter is then measured at the site of the Doppler sample volume (5 mm distal to the wire tip).
- Cross Sectional area is calculated assuming a cirular lumen.
- the mean velocity is estimated as 0.5 X APV by assuming a time-averaged parabolic velocity profile across the vessel. Angiographic luminal diameter measurements from the angiogram recorded immediately before Doppler recording are used for calculation of rest and maximum flow.
- the effect of survivin gene transfer upon anatomic evidence of collateral artery formation is further examined by identifying capillaries in light microscopic sections taken from the ischemic hindlimbs (Takeshita et al. 1996). Tissue specimens are obtained as transverse sections from the ischemic hindlimbs at the time of death (Day 30 posttransfection). Muscle samples are embedded in optimal cutting temperature compound (Miles, Elkhart, Indiana) and snap-frozen in liquid nitrogen. Multiple frozen sections (5 ⁇ m in thickness) are then cut from each specimen on a cryostat (Miles) so that the muscle fibers are oriented in a transverse fashion, and two sections are then placed on glass slides.
- optimal cutting temperature compound Miles, Elkhart, Indiana
- Tissue sections are stained for alkaline phosphatase using an indoxyl- tetrazolium method to detect capillary endothelial cells (Takeshita et al. 1996) and then counterstained with eosin.
- capillaries identified at necropsy are evaluated in relation to muscle fibers; a total number of 20 different fields is randomly selected and the number of capillaries and muscle fibers are counted under a 20X objective to determine the capillary to muscle fiber ratio.
- Tissue sections are systematically retrieved from gonads, liver, heart, lung , brain, and contralateral (nontransfected) lower limb skeletal muscle and examined by light microscopy for evidence of neoangiogenesis as well as evidence of immune-related inflammtory cell infiltrates.
- tissue sections are harvested on Day 30 from the site of gene transfer in a number of rabbits selected at random. These included a few transfected with phSurvivin and a few transfected with LacZ.
- the site of gene transfer is identified by the fact that gene transfer is performed at the origin of the internal iliac artery; accordingly, an arterial segment approximately 5 mm in length is retrieved from the origin of this artery just distal to the bifurcation of the common iliac artery.
- the section is stained with hematoxylin and eoxin and then morphometrically evaluated by light microscopy for intimal and medial thickness, from which the intima to media ratio is derived (Takeshita et al, 1996).
- Plasmid phSurvivin consists of a eucaryotic pUC 118 expression vector into wliich cDNA encoding survivin has been inserted. A 763 basepair cytomegalovirus promoter/enhancer is used to drive Survivin expression.
- the PUC 118 vector includes an SV40 polyadenylation sequence, an Escherichia coli origin of replication, and the ⁇ - lactamase gene for ampicillin resistance.
- the plasmid is prepared from cultures of phSurvivin transformed E coli, purified with a Qiagen-tip 2500 column, precipitated with isopropanol washed with 70% ethanol, and dried on a Speed Vac.
- the purified plasmid is reconstituted in sterile saline, stored in vials, and pooled for quality control analyses (absorbance at wavelengths of 260 and 280 nm to document ratio between 1.75 and 1.85; limulus amoebocyte lysate gel-clot assay [Bio-Whittaker] to establish bacterial endotoxin levels below 5 endotoxin units per kg bodyweight; microbial cultures; southern blot for level of contaminating genomic E coli DNA; and ethidium bomide staining after agarose- gel electrophoresis to confirm that over 90% of the nucleic acid was in the closed, circular supercoiled form).
- the survivin coding region from each pooled batch is resequenced (Applied Biosystem 373 A). Percutaneous Arterial Gene Transfer .
- Arterial gene transfer is performed on a patient with an ischemic leg.
- Arterial gene transfer is done with a hydrogel-coated balloon-angioplasty-catheter (Boston Scientific).
- a sterile pipette is used to apply 2000 g plasmid DNA at 10.3 ⁇ g/ ⁇ l in 194.2 ⁇ l sterile saline to external hydrogel coat of the inflated angioplasty balloon.
- the balloon is deflated, retracted into a protective sheath reinflated to 2280 mm Hg, and advanced along with the sheath over a 45.7 mm guidewire under floroscopic guidance to the site of gene transfer.
- the balloon is then deflated, the sheath retracted, and the balloon reinflated at nominal pressures for 4-5 min.
- the balloon is deflated, all catheters and wires removed, and a final angiogram recorded to ensure satisfactory patency of the site.
- Intravascular ultrasound is done immediately before gene transfer to show that the intended site, the distal popliteal artery is free of atherosclerotic plaque that might compromise transfection efficiency (Isner et al, 1996). Repeat ultrasound at 4 weeks and 12 weeks after gene transfer is done to ensure that there is no neointimal thickening resulting from inflation of the hydrogel-coated angioplasty-balloon-catheter.
- Digital substraction angiography is performed 4 weeks after gene therapy, and magnetic resonance angiography is performed 4 and 12 weeks after gene therapy. Both are performed to detect gene transfer promoted angiogenesis.
- vascular homeostasis during inflammation, immune response and transplant accommodation depends on the ability of endothelial cells (EC) to continuously counteract a cellular suicide program, i.e. apoptosis (Karsan et al, 1996).
- apoptosis a cellular suicide program
- This process involves a sequential cascade activation of intracellular cysteine proteases, i.e., caspases, initiated by ligation of cell surface death receptors or by cytoplasmic assembly of cell death initiators, i.e., apoptosome, after mitochondrial damage (Hengartner, 2000).
- Inhibition of EC apoptosis is also an obligatory prerequisite of angiogenesis, in which multiple receptor-ligand interactions at the EC surface stimulate proliferation, migration and remodeling of EC to generate new vascular networks (Risau, 1997).
- antibody or adeno viral targeting of critical angiogenesis regulators including vascular endothelial cell growth factor (VEGF) (Alon et al, 1995; Yuan et al, 1996), or the angiopoietin-1 (Ang-1) receptor, Tie-2 (Lin et al, 1998), resulted in involution of vascular networks accompanied by morphological and biochemical hallmarks of EC apoptosis.
- angiogenesis has been associated with de novo expression of an heterogeneous set of anti-apoptotic "protective genes" in the endothelium (Bach et al, 1997), some of which become induced via NF- ⁇ B signaling (Stehlik et al, 1998).
- stimulation of EC angiogenesis by VEGF or Ang-1 resulted in up-regulation of anti- apoptotic bcl-2 and Al molecules (Gerber et al, 1998a; Nor et al, 1999) and expression of Inhibitor of Apoptosis (IAP) proteins (Devereaux et al, 1999), survivin and XIAP (O'Connor et al, 2000a; Tran et al, 1999; Papapetropoulos et al, 2000).
- IAP Inhibitor of Apoptosis
- an antisense targeting strategy was used to identify the relative contribution of survivin to the anti-apoptotic function of VEGF in endothelium.
- Human umbilical vein EC were maintained in Ml 99 medium containing 20% fetal calf serum (FCS), 50 ⁇ g/ml endothelial cell growth supplement (ECGS), 100 ⁇ g/ml heparin, 100 ⁇ g/ml penicillin, and 100 ⁇ g/ml streptomycin (all from Life Technologies, Grand Island, NY) in 5% CO2 at 37°C, as described by O"Connor et al. (2000).
- Subconfluenf EC were rendered quiescent by a 18 h culture in Ml 99 plus 0.1% FCS. Cells were detached with 0.05% trypsin/0.02% EDTA, seeded in C6-well plates (Costar Corp., New Bedford, MA), grown to 70% confluency, and used between passages 2 and 3. Antisense Gene Targeting.
- Protein-normalized aliquots of cell extracts were electrophoresed on SDS polyacrylamide gradient gels, transferred to nylon membranes (Millipore Corp.) for 1 h at 1 A, and immunoblotted with 2 ⁇ g/ml of a rabbit antibody to survivin or a mouse monoclonal antibody to bcl-2 (Transduction Laboratories, CA) followed by chemiluminescence (Amersham, Arlington Heights, IL) and autoradiography. Samples were sequentially analyzed by Western blotting with a mouse antibody to ⁇ -actin to confirm equivalent protein loading.
- a survivin antisense oligonucleotide with the sequence 5'-TGTGCTATTCTGTGAATT-3' was characterized previously for its ability to suppress endogenous survivin mRNA expression in T24 bladder and HeLa epithelial carcinoma cells (Li et al, 1999b).
- a scrambled oligonucleotide with the sequence 5'TAAGCTGTTCTATGTGTT-3' was used as a control, and also characterized in previous cell culture assays (Li et al, 1999b). Oligonucleotides were synthesized with uniform phosphorothioate linkages, and underlined nucleosides correspond to 2'-O-methoxyethyl nucleosides.
- Antisense oligonucleotides to platelet- endothelial cell adhesion molecule-1 (PECAM-1, CD31), lymphocyte function- associated molecule-3 (LFA-3, CD58) and intercellular adhesion molecule-1 (ICAM-1, CD54) were synthesized as described above and characterized in previous studies (Baker et al, 1997).
- increasing concentrations of control scrambled or the various antisense oligonucleotide 50-500 nM were mixed with 1 ml of OPTI-MEM and 6 ⁇ l Lipofectin according to manufacturer instructions (Life Technologies, MD), and incubated with serum-starved EC for 8 h.
- transfection medium was replaced with M199 plus 0.1% FCS for an additional 18 h followed by VEGF stimulation for 24 h.
- Transfection efficiency was monitored by fluorescence microscopy using FITC-conjugated oligonucleotides and was always >85%.
- EC were transfected with control or the survivin antisense oligonucleotide, harvested after a 24 h culture at 37°C and total RNA was extracted using the Quiagen Rneasy reagent, according to the manufacturer's recommendations.
- RNA samples were separated on 1% agarose-formaldehyde gels, transferred to Hybond nylon membranes and hybridized with a 32 P-random primed labeled survivin cDNA with visualization of radioactive bands by autoradiography.
- Northern blots were re-probed with random primed 32 P-labeled human G3PDH cDNA to confirm equal loading of the various RNA samples.
- EC were transfected with increasing concentrations of control or the various antisense oligonucleotides, stimulated with 50 ng/ml VEGF for 16 h at 37°C, and incubated in the presence of 25 ⁇ M C-6 ceramide or the combination of TNF ⁇ (10 ng/ml Endogen, Woburn, MA) plus cycloheximide (10 ⁇ g/ml, Sigma) for an additional 12 h at 37°C.
- TNF ⁇ 10 ng/ml Endogen, Woburn, MA
- cycloheximide 10 ⁇ g/ml, Sigma
- EC floaters plus attached cells
- EC floaters plus attached cells
- EC floaters plus attached cells
- EC were harvested, fixed in 70% ethanol, stained with 10 ⁇ g/ml propidium iodide plus 100 ⁇ g/ml RNase A and 0.05% Triton X-100 in phosphate-buffered saline, pH 7.4, and analyzed for DNA content by flow cytometry, as described (O'Connor et al, 2000).
- transfected EC stimulated with VEGF and incubated with C-6 ceramide for 12 h at 37°C were harvested, washed in PBS, pH 7.4, and fixed in 4% paraformaldehyde containing 0.25% Triton X-100 for 10 min at 22°C.
- Cell nuclei were stained with 6.5 ⁇ g/ml 4,6- diamidino-2-phenylindole (DAPI, Sigma), 16% polyvinyl alcohol (Air Products and Chemicals, Allentown, PA), and 40% glycerol. Cells were independently scored for morphologic signs of apoptosis (chromatin condensation, DNA fragmentation) using a Zeiss fluorescent microscope.
- DAPI 4,6- diamidino-2-phenylindole
- Polyvinyl alcohol Air Products and Chemicals, Allentown, PA
- glycerol 40% glycerol.
- transfected EC treated with VEGF plus ceramide were lysed in 0.25% Triton X-100, 10 mM KC1, 1.5 mM MgC12, 1 mM EDTA, 1 mM DTT, 20 mM HEPES plus protease inhibitors.
- Protein-normalized aliquots of the various cell extracts were separated by SDS gel electrophoresis, transferred to nylon membranes (Millipore Corp.), and immunoblotted with a 1 :5000 dilution of a rabbit antibody to caspase 3 (Transduction Laboratories), or a 1 : 1000 dilution of a mouse antibody to Poly-ADP ribose polymerase (PARP, Pharmingen, San Diego, CA) followed by chemiluminescence (Amersham, Arlington Heights, IL).
- PARP Poly-ADP ribose polymerase
- Migration assays were performed using a Boyden chamber (Neuroprobe; Morales-Ruiz et al, 2000). Briefly, quiescent EC were transfected with control or the survivin antisense oligonucleotide, stimulated with VEGF, and detached using 0.05%> trypsin and 0.53 mM EDTA. Twenty thousand cells were suspended in Ml 99 medium containing 0.1% BSA and added to the lower chamber. Polycarbonate filters (8- ⁇ m diameter) were coated with 100 ⁇ g/ml type I collagen. The top half of the chamber was attached and the chamber was incubated in an inverted position at 37°C for 2 h.
- VEGF vascular endothelial growth factor
- SPP-1 D-erythro-sphyngosine-1- phosphate
- EC-collagen mixture Ten drops (0.1 ml each) of the EC-collagen mixture were added to a 35-mm plate. Plates were placed in a humidified incubator at 37°C, and the EC-collagen mixtures were allowed to gel for 10 min, after which 3 ml of Ml 99 medium containing 20% FCS, 50 ⁇ g/ml ECGS, 100 ⁇ g/ml heparin, 100 ⁇ g/ml penicillin, and 100 ⁇ g/ml streptomycin were added to each plate. EC were allowed to form capillary-like vascular tubes over a 24-h incubation in the presence of 16 nM phorbol myristate acetate (PMA, Sigma).
- PMA 16 nM phorbol myristate acetate
- EC were washed three times in phosphate buffered saline (PBS), pH 7.2, and supplemented with fresh Ml 99 growth medium in the presence or in the absence of 50 ng/ml VEGF.
- PBS phosphate buffered saline
- the cultures were examined by phase-contrast microscopy for the presence of capillary-like vascular tubes during additional 48 h incubation at 37°C as described (Papapetropoulos et al, 1999).
- Antisense Targeting of Survivin Suppresses the Anti- Apoptotic Function of VEGF in EC.
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Gastroenterology & Hepatology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Toxicology (AREA)
- Zoology (AREA)
- Heart & Thoracic Surgery (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Cardiology (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Materials For Medical Uses (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Abstract
Description
Claims
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US17299199P | 1999-12-21 | 1999-12-21 | |
US172991P | 1999-12-21 | ||
PCT/US2000/034663 WO2001046455A2 (en) | 1999-12-21 | 2000-12-21 | Survivin promotion of angiogenesis |
Publications (2)
Publication Number | Publication Date |
---|---|
EP1242050A2 true EP1242050A2 (en) | 2002-09-25 |
EP1242050A4 EP1242050A4 (en) | 2004-05-26 |
Family
ID=22630045
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP00990262A Withdrawn EP1242050A4 (en) | 1999-12-21 | 2000-12-21 | Survivin promotion of angiogenesis |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP1242050A4 (en) |
JP (1) | JP2003529554A (en) |
AU (1) | AU2730801A (en) |
CA (1) | CA2393646A1 (en) |
MX (1) | MXPA02006167A (en) |
WO (1) | WO2001046455A2 (en) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE60037938T2 (en) | 1999-02-26 | 2009-01-29 | The University Of British Columbia, Vancouver | ANTISENSE THERAPY FOR TRPM-2 |
US6900187B2 (en) | 1999-02-26 | 2005-05-31 | The University Of British Columbia | TRPM-2 antisense therapy using an oligonucleotide having 2′-O-(2-methoxy)ethyl modifications |
US7569551B2 (en) | 2000-02-25 | 2009-08-04 | The University Of British Columbia | Chemo- and radiation-sensitization of cancer by antisense TRPM-2 oligodeoxynucleotides |
AU2001275707A1 (en) * | 2000-07-26 | 2002-02-05 | Cambridge University Technical Services Limited | Use of panaxatriol for stimulation angiogenesis |
NZ533126A (en) | 2002-01-17 | 2006-04-28 | Univ British Columbia | Bispecific antisense oligonucleotides that inhibit IGFBP-2 and IGFBP-5 and methods of using same |
US7285541B2 (en) | 2002-08-21 | 2007-10-23 | The University Of British Columbia | Treatment of melanoma by reduction in clusterin levels |
US7713738B2 (en) | 2003-02-10 | 2010-05-11 | Enzon Pharmaceuticals, Inc. | Oligomeric compounds for the modulation of survivin expression |
EP1615943A4 (en) * | 2003-04-18 | 2006-08-16 | Univ Pennsylvania | Compositions and methods for sirna inhibition of angiopoietin 1 and 2 and their receptor tie2 |
US8710020B2 (en) | 2004-04-02 | 2014-04-29 | The University Of British Columbia | Clusterin antisense therapy for treatment of cancer |
WO2006050732A2 (en) | 2004-11-09 | 2006-05-18 | Santaris Pharma A/S | Lna oligonucleotides and the treatment of cancer |
WO2009043104A1 (en) * | 2007-10-04 | 2009-04-09 | Bionomics Limited | Markers of endothelial cells and uses thereof |
FR2932086A1 (en) * | 2008-06-06 | 2009-12-11 | Lvmh Rech | ANTI-AGE COSMETIC CARE METHOD BY STIMULATING THE EXPRESSION OF SURVIVAL |
US9279750B2 (en) | 2013-03-15 | 2016-03-08 | Iris International, Inc. | Method and composition for staining and sample processing |
AU2016318158B2 (en) * | 2015-09-04 | 2022-09-15 | Health Research, Inc. | Anti-survivin antibodies for cancer therapy |
-
2000
- 2000-12-21 WO PCT/US2000/034663 patent/WO2001046455A2/en not_active Application Discontinuation
- 2000-12-21 CA CA002393646A patent/CA2393646A1/en not_active Abandoned
- 2000-12-21 AU AU27308/01A patent/AU2730801A/en not_active Abandoned
- 2000-12-21 JP JP2001546951A patent/JP2003529554A/en active Pending
- 2000-12-21 EP EP00990262A patent/EP1242050A4/en not_active Withdrawn
- 2000-12-21 MX MXPA02006167A patent/MXPA02006167A/en unknown
Non-Patent Citations (4)
Title |
---|
FUJIKAWA KOSHI ET AL: "Role of PI 3-kinase in angiopoietin-1-mediated migration and attachment-dependent survival of endothelial cells" EXPERIMENTAL CELL RESEARCH, vol. 253, no. 2, 15 December 1999 (1999-12-15), pages 663-672, XP002275040 ISSN: 0014-4827 * |
FUJIO Y ET AL: "Akt mediates cytoprotection of endothelial cells by vascular endothelial growth factor in an anchorage-dependent manner" JOURNAL OF BIOLOGICAL CHEMISTRY, AMERICAN SOCIETY OF BIOLOGICAL CHEMISTS, BALTIMORE, MD, US, vol. 274, no. 23, April 1999 (1999-04), pages 16349-16354, XP002136061 ISSN: 0021-9258 * |
LI F ET AL: "PLEIOTROPIC CELL-DIVISION DEFECTS AND APOPTOSIS INDUCED BY INTERFERENCE WITH SURVIVIN FUNCTION" NATURE CELL BIOLOGY, MACMILLAN PUBLISHERS, GB, vol. 1, December 1999 (1999-12), pages 461-466, XP001034788 ISSN: 1465-7392 * |
See also references of WO0146455A2 * |
Also Published As
Publication number | Publication date |
---|---|
AU2730801A (en) | 2001-07-03 |
WO2001046455A2 (en) | 2001-06-28 |
CA2393646A1 (en) | 2001-06-28 |
EP1242050A4 (en) | 2004-05-26 |
JP2003529554A (en) | 2003-10-07 |
WO2001046455A3 (en) | 2002-05-10 |
MXPA02006167A (en) | 2004-02-26 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5863904A (en) | Methods for treating cancers and restenosis with P21 | |
Nikol et al. | Molecular biology and post-angioplasty restenosis | |
KR100304033B1 (en) | Pharmaceutical composition for the treatment of cell proliferative diseases | |
US5851521A (en) | Viral vectors and their use for treating hyperproliferative disorders, in particular restenosis | |
EP1766768B1 (en) | Use of lacritin in promoting ocular cell survival | |
WO2001046455A2 (en) | Survivin promotion of angiogenesis | |
US20030144240A1 (en) | Antisense strategy to modulate estrogen receptor response (ER alpha and/or ER beta) | |
JP2009148293A (en) | Peptide antagonist of vascular endothelial growth factor | |
JPH11503911A (en) | Arteriovenous and venous transplantation therapy: methods and compositions | |
US6458590B1 (en) | Methods and compositions for treatment of restenosis | |
Han et al. | Potential anti-angiogenic role of Slit2 in corneal neovascularization | |
Rosenberg | Vascular smooth muscle cell proliferation: basic investigations and new therapeutic approaches | |
US20080045474A1 (en) | Method for treatment of invasive cells | |
EP1255829B1 (en) | Inhibitor of hepatocyte growth factor activator for use in modulation of angiogenesis and cardiovascularization | |
US8227412B2 (en) | Bioactive parstatin peptides and methods of use | |
US7105656B2 (en) | Compositions and methods for treating hematologic malignancies and multiple drug resistance | |
US20020164624A1 (en) | VEGF-D expression in brain cancer | |
JP2022509445A (en) | Compositions and Methods for Treating or Preventing Fibrosis | |
JP2004506595A (en) | Promotion or inhibition of angiogenesis and cardiovascularization | |
US20090048158A1 (en) | Insulin-Like Growth Factor Binding Protein-4 Compounds and Methods for Inhibiting Angiogenesis and Tumor Growth in Mammalian Cells | |
JP2003512442A (en) | Cancer Treatment | |
US20040023915A1 (en) | Tocopherol associated protein and uses thereof | |
Klocke et al. | Recently patented applications of homologous cellular and extracellular agents as therapeutics or targets for the prevention of restenosis post-angioplasty | |
WO2005034978A2 (en) | MEDICAL USE OF IKKϵ OR OF INHIBITORS THEREOF | |
JP2007291009A (en) | Agent for inhibiting intimal thickening |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 20020618 |
|
AK | Designated contracting states |
Kind code of ref document: A2 Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR |
|
AX | Request for extension of the european patent |
Free format text: AL;LT;LV;MK;RO;SI |
|
RIC1 | Information provided on ipc code assigned before grant |
Ipc: 7A 61K 48/00 B Ipc: 7A 61K 31/713 B Ipc: 7A 61K 38/17 B Ipc: 7C 12N 15/12 B Ipc: 7C 07K 14/515 B Ipc: 7A 61K 31/711 B Ipc: 7C 07K 14/47 A |
|
A4 | Supplementary search report drawn up and despatched |
Effective date: 20040416 |
|
17Q | First examination report despatched |
Effective date: 20050322 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
|
18D | Application deemed to be withdrawn |
Effective date: 20051002 |