Kinase inhibitors and uses thereof

Patent metadata

Field	Value
Publication number	US-9447158-B2
Application number	US-201414258418-A
Country	US
Kind code	B2
Filing date	Apr 22, 2014
Priority date	Jan 10, 2007
Publication date	Sep 20, 2016
Grant date	Sep 20, 2016

Abstract

The present invention relates to kinase inhibiting compositions and uses thereof. The invention further provides isolated kinase inhibiting peptides and uses thereof for inhibiting hyperplasia, for inhibiting the growth of neoplasms, and for inducing programmed cell death in a cell population.

First claim

What is claimed is:

1. A method for inhibiting a kinase activity of a kinase enzyme, the method comprising the step of providing a kinase inhibiting composition,
wherein the amino acid sequence of the kinase inhibiting peptide is WLRRIKAWLRRIKALARQLGVAA [SEQ ID NO: 113], and
wherein the kinase enzyme contacts the kinase inhibiting composition, wherein the activity of the kinase enzyme is inhibited, and wherein the kinase enzyme is selected from the group consisting of: Ab 1, Akt/PKB, AMPK, Arg, Ask, Aurora-A, Axl, Blk, Bmx, Brk, BTK, CaMKI, CaMKIδ, CaMKIIβ, CaMKIγ, CaMKI1β, Casein Kinase, Cdk, CDK9/cyclin, CKly1, CKly2, CKly3, Ck1δ, CK2α, CK2, CHK, CDK1/cyclinB, CHK1, CHK2 mutants, CK1δ, CK2, c-Kit, CLK2, CLK3, Cott, Csk, DAPK1, DCAMKL2, DDR, DYRK2, EGFR, Ephs, EphA2, FAK, Fer, Fes/Fps, FGFR, FGFR1, Fgr, Fit, Flt3, Flt4, Fms/CSF-1 R, Fyn, GRK5, GRK6, GRK7, GSK, GSK3, Hck, HER/ErbB, HIPK1, HIPK2, HIPK3, IGF-1R, ICF IR, IKK, Insulin R, IRAK, IRAK1, IRAK4, JAK, JAK1, JAK2, JAK3, JNK/SAPK, KDR, Lck, LIMK, LIMK1, LOK, Lyn, MAPK, MAPK1, MAPKAP Kinase, MEK, MEK1, MELK, Met, Mer, MINK, MKK, MLCK, MLK1, MRCKa, MSK1, MST, MST3, NEK, NEK3, NEK9, PDGFR, PDGFRα, PDGFRβ, PDK, PhKγ2, PI 3-Kinase, PIM, Pim-1, Pim-2, Pim-3, PKC, PKCβ1, PKCδ, PKD2, PKR, PKA, PKBβ, PKCβI, PKG1, PKG1α, PKG1β, PLK, PRAK, PTK5, Pyk, Raf, Rct, RIPK2, ROK/ROCK, ROCK-I, Ron, Ros, Rse, Rsk4, Rsk/MAPKAP Kinase, S6 Kinase, Rsk2, SAPK2a, SGK, c-Src, Src(1-530), Src, Syk, TAK1, TA01, TAO2, TBK, Tie2/TEK, TLK2, Trk, TSSK2, TrkA, Txk, ULK3, Ulk2, VRK2, WEE, Yes, ZAP-70 and ZIPK.

2. A method for inhibiting a kinase activity of a kinase enzyme, the method comprising the step of providing a kinase inhibiting composition,
wherein the kinase inhibiting peptide is HRRIKAWLKKIKALARQLGVAA [SEQ ID NO: 166], and
wherein the kinase enzyme contacts the kinase inhibiting composition, wherein the activity of the kinase enzyme is inhibited, and wherein the kinase enzyme is selected from the group consisting of: Ab 1, Akt/PKB, AMPK, Arg, Ask, Aurora-A, Axl, Blk, Bmx, Brk, BTK, CaMKI, CaMKIδ, CaMKIIβ, CaMKIIγ, CaMKI1β, Casein Kinase, Cdk, CDK9/cyclin, CKly1, CKly2, CKly3, Ck1δ, CK2α, CK2, CHK, CDK1/cyclinB, CHK1, CHK2 mutants, CK1δ, CK2, c-Kit, CLK2, CLK3, Cott, Csk, DAPK1, DCAMKL2, DDR, DYRK2, EGFR, Ephs, EphA2, FAK, Fer, Fes/Fps, FGFR, FGFR1, Fgr, Fit, Flt3, Flt4, Fms/CSF-1 R, Fyn, GRK5, GRK6, GRK7, GSK, GSK3, Hck, HER/ErbB, HIPK1, HIPK2, HIPK3, IGF-1R, ICF IR, IKK, Insulin R, IRAK, IRAK1, IRAK4, JAK, JAK1, JAK2, JAK3, JNK/SAPK, KDR, Lck, LIMK, LIMK1, LOK, Lyn, MAPK, MAPK1, MAPKAP Kinase, MEK, MEK1, MELK, Met, Mer, MINK, MKK, MLCK, MLK1, MRCKa, MSK1, MST, MST3, NEK, NEK3, NEK9, PDGFR, PDGFRα, PDGFRβ, PDK, PhKγ2, PI 3-Kinase, PIM, Pim-1, Pim-2, Pim-3, PKC, PKCβ1, PKCδ, PKD2, PKR, PKA, PKBβ, PKCβI, PKG1, PKG1α, PKG1β, PLK, PRAK, PTK5, Pyk, Raf, Rct, RIPK2, ROK/ROCK, ROCK-I, Ron, Ros, Rse, Rsk4, Rsk/MAPKAP Kinase, S6 Kinase, Rsk2, SAPK2a, SGK, c-Src, Src(1-530), Src, Syk, TAK1, TA01, TAO2, TBK, Tie2/TEK, TLK2, Trk, TSSK2, TrkA, Txk, ULK3, Ulk2, VRK2, WEE, Yes, ZAP-70 and ZIPK.

3. A method for inhibiting hyperplasia in a cell population, the method comprising the step of providing a therapeutically effective amount of a kinase inhibiting composition to a subject in need thereof,
wherein the kinase inhibiting composition comprises an inhibitory amount of a kinase inhibiting peptide,
wherein the kinase inhibiting peptide inhibits a kinase activity of a kinase enzyme, wherein the kinase enzyme is selected from the group consisting of: Ab I, Akt/PKB, AMPK, Arg, Ask, Aurora-A, Axl, Blk, Bmx, Brk, BTK, CaMKI, CaMKIδ, CaMKIIβ, CaMKIIγ, CaMKI1β, Casein Kinase, Cdk, CDK9/cyclin, CKly1, CKly2, CKly3, Ck1δ, CK2α, CK2, CHK, CDK1/cyclinB, CHK1, CHK2 mutants, CK1δ, CK2, c-Kit, CLK2, CLK3, Cott, Csk, DAPK1, DCAMKL2, DDR, DYRK2, EGFR, Ephs, EphA2, FAK, Fer, Fes/Fps, FGFR, FGFR1, Fgr, Fit, Flt3, Flt4, Fms/CSF-1 R, Fyn, GRK5, GRK6, GRK7, GSK, GSK3, Hck, HER/ErbB, HIPK1, HIPK2, HIPK3, IGF-1R, ICF IR, IKK, Insulin R, IRAK, IRAK1, IRAK4, JAK, JAK1, JAK2, JAK3, JNK/SAPK, KDR, Lck, LIMK, LIMK1, LOK, Lyn, MAPK, MAPK1, MAPKAP Kinase, MEK, MEK1, MELK, Met, Mer, MINK, MKK, MLCK, MLK1, MRCKa, MSK1, MST, MST3, NEK, NEK3, NEK9, PDGFR, PDGFRα, PDGFRβ, PDK, PhKγ2, PI 3-Kinase, PIM, Pim-1, Pim-2, Pim-3, PKC, PKCβ1, PKCδ, PKD2, PKR, PKA, PKBβ, PKCβI, PKG1, PKG1α, PKG1β, PLK, PRAK, PTK5, Pyk, Raf, Rct, RIPK2, ROK/ROCK, ROCK-I, Ron, Ros, Rse, Rsk4, Rsk/MAPKAP Kinase, S6Kinase, Rsk2, SAPK2a, SGK, c-Src, Src(1-530), Src, Syk, TAK1, TAO1, TAO2, TBK, Tie2/TEK, TLK2, Trk, TSSK2, TrkA, Txk, ULK3, U1k2, VRK2, WEE, Yes, ZAP-70 and ZIPK,
wherein the kinase inhibiting peptide is YARAAARQARAKALARQLGVAA [SEQ ID NO: 106], wherein at least one hyperplastic cell contacts the kinase inhibiting composition, and wherein the hyperplasia of the at least one hyperplastic cell is inhibited.

4. A method for inhibiting growth of a neoplasm, the method comprising the step of providing a therapeutically effective amount of a kinase inhibiting composition to a subject in need thereof,
wherein the kinase inhibiting composition comprises an inhibitory amount of a kinase inhibiting peptide,
wherein the kinase inhibiting peptide inhibits a kinase activity of a kinase enzyme, wherein the kinase enzyme is selected from the group consisting of: Ab 1, Akt/PKB, AMPK, Arg, Ask, Aurora-A, Axl, Blk, Bmx, Brk, BTK, CaMKI, CaMKIδ, CaMKIIβ, CaMKIIγ, CaMKI1β, Casein Kinase, Cdk, CDK9/cyclin, CKly1, CKly2, CKly3, Ck1δ, CK2α, CK2, CHK, CDK1/cyclinB, CHK1, CHK2 mutants, CK1δ, CK2, c-Kit, CLK2, CLK3, Cott, Csk, DAPK1, DCAMKL2, DDR, DYRK2, EGFR, Ephs, EphA2, FAK, Fer, Fes/Fps, FGFR, FGFR1, Fgr, Fit, Flt3, Flt4, Fms/CSF-1 R, Fyn, GRK5, GRK6, GRK7, GSK, GSK3, Hck, HER/ErbB, HIPK1, HIPK2, HIPK3, IGF-1R, ICF IR, IKK, Insulin R, IRAK, IRAK1, IRAK4, JAK, JAK1, JAK2, JAK3, JNK/SAPK, KDR, Lck, LIMK, LIMK1, LOK, Lyn, MAPK, MAPK1, MAPKAP Kinase, MEK, MEK1, MELK, Met, Mer, MINK, MKK, MLCK, MLK1, MRCKa, MSK1, MST, MST3, NEK, NEK3, NEK9, PDGFR, PDGFRα, PDGFRβ, PDK, PhKγ2, PI 3-Kinase, PIM, Pim-1, Pim-2, Pim-3, PKC, PKCβ1, PKCδ, PKD2, PKR, PKA, PKBβ, PKCβI, PKG1, PKG1α, PKG1β, PLK, PRAK, PTK5, Pyk, Raf, Rct, RIPK2, ROK/ROCK, ROCK-I, Ron, Ros, Rse, Rsk4, Rsk/MAPKAP Kinase, S6Kinase, Rsk2, SAPK2a, SGK, c-Src, Src(1-530), Src, Syk, TAK1, TAO1, TAO2, TBK, Tie2/TEK, TLK2, Trk, TSSK2, TrkA, Txk, ULK3, Ulk2, VRK2, WEE, Yes, ZAP-70 and ZIPK,
wherein the amino acid sequence of the kinase inhibiting peptide is selected from the group consisting of FAKLAARLYRKALARQLGVAA [SEQ ID NO: 163] and HRRIKAWLKKIKALARQLGVAA [SEQ ID NO: 166], wherein the kinase inhibiting composition contacts the neoplasm, and wherein growth of the neoplasm is inhibited.

5. The method according to claim 4 , wherein the neoplasm is a carcinoma.

6. The method according to claim 4 , wherein the neoplasm is selected from the group consisting of a breast cancer, a central nervous system cancer, a colon cancer, a pancreatic cancer, a prostate cancer, and a lung cancer.

7. The method according to claim 4 , wherein the kinase inhibiting peptide is HRRIKAWLKKIKALARQLGVAA [SEQ ID NO: 166].

8. The method according to claim 4 , wherein the kinase inhibiting peptide is FAKLAARLYRKALARQLGVAA [SEQ ID NO: 163].

9. A method for inducing programmed cell death in a cell population, the method comprising the step of providing a kinase inhibiting composition,
wherein the kinase inhibiting composition comprises an inhibitory amount of a kinase inhibiting peptide,
wherein the kinase inhibiting peptide inhibits a kinase activity of a kinase enzyme, wherein the kinase enzyme is selected from the group consisting of: Ab 1, Akt/PKB, AMPK, Arg, Ask, Aurora-A, Axl, Blk, Bmx, Brk, BTK, CaMKI, CaMKIδ, CaMKIIβ, CaMKIIγ, CaMKI1β, Casein Kinase, Cdk, CDK9/cyclin, CKly1, CKly2, CKly3

Assignees

• Purdue Research Foundation

Inventors

• Panitch Alyssa
• Seal Brandon
• Ward Brian

Classifications

• A61P43/00

  Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

• C07K14/4703

  Inhibitors; Suppressors · CPC title

• A61K38/16

  Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof {(enzyme inhibitors A61K38/005)} · CPC title

• C07K7/06

  having 5 to 11 amino acids · CPC title

• C07K14/4747 Primary

  Apoptosis related proteins · CPC title