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Volumn 20, Issue 3, 2012, Pages 313-319

Anti-cancer effect of IN-2001 in MDA-MB-231 human breast cancer

Author keywords

HDAC; IN 2001; MDA MB 231

Indexed keywords

3 (4 DIMETHYLAMINOPHENYL) N HYDROXY 2 PROPENAMIDE; CYCLIN D1; CYCLIN D2; CYCLIN DEPENDENT KINASE INHIBITOR 1; CYCLIN DEPENDENT KINASE INHIBITOR 1B; HISTONE DEACETYLASE; HISTONE DEACETYLASE INHIBITOR; IN 2001; TRICHOSTATIN A; UNCLASSIFIED DRUG; VORINOSTAT;

EID: 84862664156     PISSN: 19769148     EISSN: 20054483     Source Type: Journal    
DOI: 10.4062/biomolther.2012.20.3.313     Document Type: Article
Times cited : (5)

References (36)
  • 1
    • 0032499756 scopus 로고    scopus 로고
    • P21(WAF1) is required for butyrate-mediated growth inhibition of human colon cancer cells
    • Archer, S. Y., Meng, S., Shei, A. and Hodin, R. A. (1998) p21(WAF1) is required for butyrate-mediated growth inhibition of human colon cancer cells. Proc. Natl. Acad. Sci. USA 95, 6791-6796.
    • (1998) Proc. Natl. Acad. Sci. USA , vol.95 , pp. 6791-6796
    • Archer, S.Y.1    Meng, S.2    Shei, A.3    Hodin, R.A.4
  • 2
    • 0642336667 scopus 로고    scopus 로고
    • Antiproliferative signalling by 1,25(OH)2D3 in prostate and breast cancer is suppressed by a mechanism involving histone deacetylation
    • Banwell, C. M., Singh, R., Stewart, P. M., Uskokovic, M. R. and Campbell, M. J. (2003) Antiproliferative signalling by 1,25(OH)2D3 in prostate and breast cancer is suppressed by a mechanism involving histone deacetylation. Recent Results Cancer Res. 164, 83-98.
    • (2003) Recent Results Cancer Res , vol.164 , pp. 83-98
    • Banwell, C.M.1    Singh, R.2    Stewart, P.M.3    Uskokovic, M.R.4    Campbell, M.J.5
  • 3
    • 0034141972 scopus 로고    scopus 로고
    • CREB-binding protein and p300: Molecular integrators of hematopoietic transcription
    • Blobel, G. A. (2000) CREB-binding protein and p300: molecular integrators of hematopoietic transcription. Blood 95, 745-755.
    • (2000) Blood , vol.95 , pp. 745-755
    • Blobel, G.A.1
  • 4
    • 1842483852 scopus 로고    scopus 로고
    • Inactivation of the Wip1 phosphatase inhibits mammary tumorigenesis through p38 MAPK-mediated activation of the p16(Ink4a)-p19(Arf) pathway
    • Bulavin, D. V., Phillips, C., Nannenga, B., Timofeev, O., Donehower, L. A., Anderson, C. W., Appella, E. and Fornace, A. J. Jr. (2004) Inactivation of the Wip1 phosphatase inhibits mammary tumorigenesis through p38 MAPK-mediated activation of the p16(Ink4a)-p19(Arf) pathway. Nat. Genet. 36, 343-350.
    • (2004) Nat. Genet , vol.36 , pp. 343-350
    • Bulavin, D.V.1    Phillips, C.2    Nannenga, B.3    Timofeev, O.4    Donehower, L.A.5    Anderson, C.W.6    Appella, E.7    Fornace Jr., A.J.8
  • 5
    • 0034665124 scopus 로고    scopus 로고
    • Suberoylanilide hydroxamic acid, an inhibitor of histonedeacetylase, suppresses the growth of prostate cancer cells in vitro and in vivo
    • Butler, L. M., Agus, D. B., Scher, H. I., Higgins, B., Rose, A., Cordon- Cardo, C., Thaler, H. T., Rifkind, R. A., Marks, P. A. and Richon, V. M. (2000a) Suberoylanilide hydroxamic acid, an inhibitor of histonedeacetylase, suppresses the growth of prostate cancer cells in vitro and in vivo. Cancer Res. 60, 5165-5170.
    • (2000) Cancer Res , vol.60 , pp. 5165-5170
    • Butler, L.M.1    Agus, D.B.2    Scher, H.I.3    Higgins, B.4    Rose, A.5    Cordon- cardo, C.6    Thaler, H.T.7    Rifkind, R.A.8    Marks, P.A.9    Richon, V.M.10
  • 6
    • 0008518619 scopus 로고    scopus 로고
    • Hybrid polar inhibitors of histone deacetylase suppress the growth of the CWR22 human prostate cancer xenograft
    • Butler, L. M., Higgins, B., Fox, W. D., Agus, D. B., Cordon-Cardo, C. and Scher, H. J. (2000b) Hybrid polar inhibitors of histone deacetylase suppress the growth of the CWR22 human prostate cancer xenograft. Proc. Am. Assoc. Cancer Res. 41, 289.
    • (2000) Proc. Am. Assoc. Cancer Res , vol.41 , pp. 289
    • Butler, L.M.1    Higgins, B.2    Fox, W.D.3    Agus, D.B.4    Cordon-Cardo, C.5    Scher, H.J.6
  • 9
    • 0034045040 scopus 로고    scopus 로고
    • Histone deacetylases, transcriptional control, and cancer
    • Cress, W. D. and Seto, E. (2000) Histone deacetylases, transcriptional control, and cancer. J. Cell Physiol. 184, 1-16.
    • (2000) J. Cell Physiol , vol.184 , pp. 1-16
    • Cress, W.D.1    Seto, E.2
  • 10
    • 0032516221 scopus 로고    scopus 로고
    • Histone deacetylase associated with mSin3A mediates repression by the acute promyelocytic leukemia-associated PLZF protein
    • David, G., Alland, L., Hong, S. H., Wong, C. W., DePinho, R. A. and Dejean, A. (1998) Histone deacetylase associated with mSin3A mediates repression by the acute promyelocytic leukemia-associated PLZF protein. Oncogene 16, 2549-2556.
    • (1998) Oncogene , vol.16 , pp. 2549-2556
    • David, G.1    Alland, L.2    Hong, S.H.3    Wong, C.W.4    Depinho, R.A.5    Dejean, A.6
  • 11
    • 0033740191 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors decrease proliferation and modulate cell cycle gene expression in normal mammary epithelial cells
    • Davis, T., Kennedy, C., Chiew, Y. E., Clarke, C. L. and deFazio, A. (2000) Histone deacetylase inhibitors decrease proliferation and modulate cell cycle gene expression in normal mammary epithelial cells. Clin. Cancer Res. 6, 4334-4342.
    • (2000) Clin. Cancer Res , vol.6 , pp. 4334-4342
    • Davis, T.1    Kennedy, C.2    Chiew, Y.E.3    Clarke, C.L.4    Defazio, A.5
  • 15
    • 0035833338 scopus 로고    scopus 로고
    • Inhibitors of histone deacetylasearrest cell cycle and induce apoptosis in cervical carcinoma cells circumventing human papillomavirus oncogene expression
    • Finzer, P., Kuntzen, C., Soto, U., zur Hausen, H. and Rösl, F. (2001) Inhibitors of histone deacetylasearrest cell cycle and induce apoptosis in cervical carcinoma cells circumventing human papillomavirus oncogene expression. Oncogene 20, 4768-4776.
    • (2001) Oncogene , vol.20 , pp. 4768-4776
    • Finzer, P.1    Kuntzen, C.2    Soto, U.3    Zur, H.H.4    Rösl, F.5
  • 17
    • 0035793107 scopus 로고    scopus 로고
    • Potent histone deacetylase inhibitors built from trichostatin A and cyclic tetrapeptide antibiotics including trapoxin
    • Furumai, R., Komatsu, Y., Nishino, N., Khochbin, S., Yoshida, M. and Horinouchi, S. (2001) Potent histone deacetylase inhibitors built from trichostatin A and cyclic tetrapeptide antibiotics including trapoxin. Proc. Natl. Acad. Sci. USA 98, 87-92.
    • (2001) Proc. Natl. Acad. Sci. USA , vol.98 , pp. 87-92
    • Furumai, R.1    Komatsu, Y.2    Nishino, N.3    Khochbin, S.4    Yoshida, M.5    Horinouchi, S.6
  • 18
    • 0042905956 scopus 로고    scopus 로고
    • Gene expression profi ling of multiple histone deacetylase (HDAC) inhibitors: Defi ning a common gene set produced by HDAC inhibition in T24 and MDA carcinoma cell lines
    • Glaser, K. B., Staver, M. J., Waring, J. F., Stender, J., Ulrich, R. G. and Davidsen,S. K. (2003) Gene expression profi ling of multiple histone deacetylase (HDAC) inhibitors: defi ning a common gene set produced by HDAC inhibition in T24 and MDA carcinoma cell lines. Mol. Cancer Ther. 2, 151-163.
    • (2003) Mol. Cancer Ther , vol.2 , pp. 151-163
    • Glaser, K.B.1    Staver, M.J.2    Waring, J.F.3    Stender, J.4    Ulrich, R.G.5
  • 20
    • 0035862199 scopus 로고    scopus 로고
    • The human histone deacetylase family
    • Gray, S. G. and Ekström, T. J. (2001) The human histone deacetylase family. Exp. Cell Res. 262, 75-83.
    • (2001) Exp. Cell Res , vol.262 , pp. 75-83
    • Gray, S.G.1    Ekström, T.J.2
  • 21
    • 0030798245 scopus 로고    scopus 로고
    • Histone acetylation in chromatin structure and transcription
    • Grunstein, M. (1997) Histone acetylation in chromatin structure and transcription. Nature 389, 349-352.
    • (1997) Nature , vol.389 , pp. 349-352
    • Grunstein, M.1
  • 22
    • 0842277812 scopus 로고    scopus 로고
    • Histone deacetylase (HDAC) inhibitor activation of p21WAF1 involves changes in promoter-associated proteins, including HDAC1
    • Gui, C. Y., Ngo, L., Xu, W. S., Richon, V. M. and Marks, P. A. (2004) Histone deacetylase (HDAC) inhibitor activation of p21WAF1 involves changes in promoter-associated proteins, including HDAC1. Proc. Natl. Acad. Sci. USA 101, 1241-1246.
    • (2004) Proc. Natl. Acad. Sci. USA , vol.101 , pp. 1241-1246
    • Gui, C.Y.1    Ngo, L.2    Xu, W.S.3    Richon, V.M.4    Marks, P.A.5
  • 23
    • 0036527775 scopus 로고    scopus 로고
    • Histone-deacetylase inhibitors: Novel drugs for the treatment of cancer
    • Johnstone, R. W. (2002) Histone-deacetylase inhibitors: novel drugs for the treatment of cancer. Nat. Rev. Drug. Discov. 1, 287-299.
    • (2002) Nat. Rev. Drug. Discov , vol.1 , pp. 287-299
    • Johnstone, R.W.1
  • 24
    • 0041347519 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors in cancer therapy: Is transcription the primary target?
    • Johnstone, R. W. and Licht, J.D. (2003) Histone deacetylase inhibitors in cancer therapy: is transcription the primary target? Cancer Cell 4, 13-18.
    • (2003) Cancer Cell , vol.4 , pp. 13-18
    • Johnstone, R.W.1    Licht, J.D.2
  • 25
    • 0034654011 scopus 로고    scopus 로고
    • Acetylation: A regulatory modifi cation to rival phosphorylation?
    • Kouzarides, T. (2000) Acetylation: a regulatory modifi cation to rival phosphorylation? EMBO J. 19, 1176-1179.
    • (2000) EMBO J , vol.19 , pp. 1176-1179
    • Kouzarides, T.1
  • 28
    • 0032989027 scopus 로고    scopus 로고
    • Anti-tumouractivity in vitro and in vivo of selective differentiating agents containing hydroxamate
    • Qui, L., Kelso, M. J., Hansen, C., West, M. L., Fairlie, D. P. and Parson, P. G. (1999) Anti-tumouractivity in vitro and in vivo of selective differentiating agents containing hydroxamate. Br. J. Cancer 80, 1252-1258.
    • (1999) Br. J. Cancer , vol.80 , pp. 1252-1258
    • Qui, L.1    Kelso, M.J.2    Hansen, C.3    West, M.L.4    Fairlie, D.P.5    Parson, P.G.6
  • 29
    • 0029153609 scopus 로고
    • Kip/ Cip and Ink4 Cdk inhibitors cooperate to induce cell cycle arrest in response to TGF-beta
    • Reynisdóttir, I., Polyak, K., Iavarone, A. and Massagué, J. (1995) Kip/ Cip and Ink4 Cdk inhibitors cooperate to induce cell cycle arrest in response to TGF-beta. Genes Dev. 9, 1831-1845.
    • (1995) Genes Dev , vol.9 , pp. 1831-1845
    • Reynisdóttir, I.1    Polyak, K.2    Iavarone, A.3    Massagué, J.4
  • 30
    • 0034730127 scopus 로고    scopus 로고
    • Histone deacetylase inhibitor selectively induces p21WAF1 expression and gene-associated histone acetylation
    • Richon, V. M., Sandhoff, T. W., Rifkind, R. A. and Marks, P. A. (2000) Histone deacetylase inhibitor selectively induces p21WAF1 expression and gene-associated histone acetylation. Proc. Natl. Acad. Sci. USA 97, 10014-10019.
    • (2000) Proc. Natl. Acad. Sci. USA , vol.97 , pp. 10014-10019
    • Richon, V.M.1    Sandhoff, T.W.2    Rifkind, R.A.3    Marks, P.A.4
  • 31
    • 0035406174 scopus 로고    scopus 로고
    • Evidence of a functional role forthe cyclin-dependent kinase-inhibitor p21WAF1/CIP1/MDA6 in promoting differentiation and preventing mitochondrial dysfunction and apoptosis induced by sodium butyrate in human myelomonocytic leukemia cells (U937)
    • Rosato, R. R., Wang, Z., Gopalkrishnan, R. V., Fisher, P. B. and Grant, S. (2001) Evidence of a functional role forthe cyclin-dependent kinase-inhibitor p21WAF1/CIP1/MDA6 in promoting differentiation and preventing mitochondrial dysfunction and apoptosis induced by sodium butyrate in human myelomonocytic leukemia cells (U937). Int. J. Oncol. 19, 181-191.
    • (2001) Int. J. Oncol , vol.19 , pp. 181-191
    • Rosato, R.R.1    Wang, Z.2    Gopalkrishnan, R.V.3    Fisher, P.B.4    Grant, S.5
  • 33
    • 0032030770 scopus 로고    scopus 로고
    • Histone acetylation and transcriptional regulatory mechanisms
    • Struhl, K. (1998) Histone acetylation and transcriptional regulatory mechanisms. Genes Dev. 12, 599-606.
    • (1998) Genes Dev , vol.12 , pp. 599-606
    • Struhl, K.1
  • 34
    • 0034901985 scopus 로고    scopus 로고
    • Trichostatin A is a histone deacetylase inhibitor with potent antitumor activity against breast cancer in vivo
    • Vigushin, D. M., Ali, S., Pace, P. E., Mirsaidi, N., Ito, K., Adcock, I. and Coombes, R. C. (2001) Trichostatin A is a histone deacetylase inhibitor with potent antitumor activity against breast cancer in vivo. Clin. Cancer Res. 7, 971-976.
    • (2001) Clin. Cancer Res , vol.7 , pp. 971-976
    • Vigushin, D.M.1    Ali, S.2    Pace, P.E.3    Mirsaidi, N.4    Ito, K.5    Adcock, I.6    Coombes, R.C.7
  • 35
    • 0036176617 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors in cancer treatment
    • Vigushin, D. M. and Coombes, R. C. (2002) Histone deacetylase inhibitors in cancer treatment. Anticancer Drugs 13, 1-13.
    • (2002) Anticancer Drugs , vol.13 , pp. 1-13
    • Vigushin, D.M.1    Coombes, R.C.2
  • 36
    • 4544323749 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors: Understanding a new wave of anticancer agents
    • Villar-Garea, A. and Esteller, M. (2004) Histone deacetylase inhibitors: understanding a new wave of anticancer agents. Int. J. Cancer 112, 171-178.
    • (2004) Int. J. Cancer , vol.112 , pp. 171-178
    • Villar-Garea, A.1    Esteller, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.