메뉴 건너뛰기




Volumn 237, Issue 1, 2006, Pages 143-154

SK-7041, a new histone deacetylase inhibitor, induces G2-M cell cycle arrest and apoptosis in pancreatic cancer cell lines

Author keywords

Apoptosis; Cell cycle; Histone deacetylase inhibitor; Pancreatic cancer; SK 7041

Indexed keywords

CYCLIN B1; CYCLIN D2; HISTONE DEACETYLASE INHIBITOR; HYDROXAMIC ACID; N (2 AMINOPHENYL) 4 (3 PYRIDINYLMETHOXYCARBONYLAMINOMETHYL)BENZAMIDE; PROTEIN BAK; PROTEIN BAX; PROTEIN BCL 2; PROTEIN BCL XL; PROTEIN MCL 1; PROTEIN P21; SK 7041; TRICHOSTATIN A; UNCLASSIFIED DRUG;

EID: 33646533106     PISSN: 03043835     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.canlet.2005.05.040     Document Type: Article
Times cited : (38)

References (30)
  • 1
    • 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. Histone deacetylase inhibitor selectively induces p21WAF1 expression and gene-associated histone acetylation. Proc. Natl Acad. Sci. USA 97 (2000) 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
  • 3
    • 0036527775 scopus 로고    scopus 로고
    • Histone-deacetylase inhibitors: novel drugs for the treatment of cancer
    • Johnstone R.W. Histone-deacetylase inhibitors: novel drugs for the treatment of cancer. Nat. Rev. Drug Discov. 1 (2001) 287-299
    • (2001) Nat. Rev. Drug Discov. , vol.1 , pp. 287-299
    • Johnstone, R.W.1
  • 4
    • 0034086168 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors trigger a G2 checkpoint in normal cells that is defective in tumor cells
    • Qiu L., Burgess A., Fairlie D.P., Leonard H., Parsons P.G., and Gabrielli B.G. Histone deacetylase inhibitors trigger a G2 checkpoint in normal cells that is defective in tumor cells. Mol. Biol. Cell 11 (2000) 2069-2083
    • (2000) Mol. Biol. Cell , vol.11 , pp. 2069-2083
    • Qiu, L.1    Burgess, A.2    Fairlie, D.P.3    Leonard, H.4    Parsons, P.G.5    Gabrielli, B.G.6
  • 5
    • 0141954051 scopus 로고    scopus 로고
    • an inhibitor of histone deacetylases, strongly suppresses growth of pancreatic adenocarcinoma cells
    • Donadelli M., Costanzo C., Faggioli L., Scupoli M.T., Moore P.S., Bassi C., et al. an inhibitor of histone deacetylases, strongly suppresses growth of pancreatic adenocarcinoma cells. Mol. Carcinog. 38 (2003) 59-69
    • (2003) Mol. Carcinog. , vol.38 , pp. 59-69
    • Donadelli, M.1    Costanzo, C.2    Faggioli, L.3    Scupoli, M.T.4    Moore, P.S.5    Bassi, C.6
  • 6
    • 0033551152 scopus 로고    scopus 로고
    • A synthetic inhibitor of histone deacetylase, MS-27-275, with marked in vivo antitumor activity against human tumors
    • Saito A., Yamashita T., Mariko Y., Nosaka Y., Tsuchiya K., Ando T., et al. A synthetic inhibitor of histone deacetylase, MS-27-275, with marked in vivo antitumor activity against human tumors. Proc. Natl Acad. Sci. USA 96 (1996) 4592-4597
    • (1996) Proc. Natl Acad. Sci. USA , vol.96 , pp. 4592-4597
    • Saito, A.1    Yamashita, T.2    Mariko, Y.3    Nosaka, Y.4    Tsuchiya, K.5    Ando, T.6
  • 7
    • 10744229506 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 3-(4-substituted-phenyl)-N-hydroxy-2-propenamides, a new class of histone deacetylase inhibitors
    • Kim D.K., Lee J.Y., Kim J.S., Ryu J.H., Choi J.Y., Lee J.W., et al. Synthesis and biological evaluation of 3-(4-substituted-phenyl)-N-hydroxy-2-propenamides, a new class of histone deacetylase inhibitors. J. Med. Chem. 46 (2003) 5745-5751
    • (2003) J. Med. Chem. , vol.46 , pp. 5745-5751
    • Kim, D.K.1    Lee, J.Y.2    Kim, J.S.3    Ryu, J.H.4    Choi, J.Y.5    Lee, J.W.6
  • 8
    • 4143101371 scopus 로고    scopus 로고
    • Class I histone deacetylase-selective novel synthetic inhibitors potently inhibit human tumor proliferation
    • Park J.H., Jung Y., Kim T.Y., Kim S.G., Jong H.S., Lee J.W., et al. Class I histone deacetylase-selective novel synthetic inhibitors potently inhibit human tumor proliferation. Clin. Cancer Res. 10 (2004) 5271-5281
    • (2004) Clin. Cancer Res. , vol.10 , pp. 5271-5281
    • Park, J.H.1    Jung, Y.2    Kim, T.Y.3    Kim, S.G.4    Jong, H.S.5    Lee, J.W.6
  • 9
    • 0141954051 scopus 로고    scopus 로고
    • an inhibitor of histone deacetylases, strongly suppresses growth of pancreatic adenocarcinoma cells
    • Donadelli M., Costanzo C., Faggioli L., Scupoli M.T., Moore P.S., Bassi C., et al. an inhibitor of histone deacetylases, strongly suppresses growth of pancreatic adenocarcinoma cells. Mol. Carcinog. 38 (2003) 59-69
    • (2003) Mol. Carcinog. , vol.38 , pp. 59-69
    • Donadelli, M.1    Costanzo, C.2    Faggioli, L.3    Scupoli, M.T.4    Moore, P.S.5    Bassi, C.6
  • 10
    • 6044264858 scopus 로고    scopus 로고
    • FR901228, a novel histone deacetylase inhibitor, induces cell cycle arrest and subsequent apoptosis in refractory human pancreatic cancer cells
    • Sato N., Ohta T., Kitagawa H., Kayahara M., Ninomiya I., Fushida S., et al. FR901228, a novel histone deacetylase inhibitor, induces cell cycle arrest and subsequent apoptosis in refractory human pancreatic cancer cells. Int. J. Oncol. 24 (2004) 679-685
    • (2004) Int. J. Oncol. , vol.24 , pp. 679-685
    • Sato, N.1    Ohta, T.2    Kitagawa, H.3    Kayahara, M.4    Ninomiya, I.5    Fushida, S.6
  • 11
    • 0035328528 scopus 로고    scopus 로고
    • The histone deacetylase inhibitor, CBHA, inhibits growth of human neuroblastoma xenografts in vivo, alone and synergistically with all-trans retinoic acid
    • Coffey D.C., Kutko M.C., Glick R.D., Butler L.M., Heller G., Rifkind R.A., et al. The histone deacetylase inhibitor, CBHA, inhibits growth of human neuroblastoma xenografts in vivo, alone and synergistically with all-trans retinoic acid. Cancer Res. 61 (2001) 3591-3594
    • (2001) Cancer Res. , vol.61 , pp. 3591-3594
    • Coffey, D.C.1    Kutko, M.C.2    Glick, R.D.3    Butler, L.M.4    Heller, G.5    Rifkind, R.A.6
  • 12
    • 0036301281 scopus 로고    scopus 로고
    • Phase I trial of the histone deacetylase inhibitor, depsipeptide (FR901228, NSC 630176), in patients with refractory neoplasm
    • Sandor V., Bakke S., Robey R.W., Kang M.H., Blagosklonny M.V., Bender J., et al. Phase I trial of the histone deacetylase inhibitor, depsipeptide (FR901228, NSC 630176), in patients with refractory neoplasm. Clin. Cancer Res. 8 (2002) 718-728
    • (2002) Clin. Cancer Res. , vol.8 , pp. 718-728
    • Sandor, V.1    Bakke, S.2    Robey, R.W.3    Kang, M.H.4    Blagosklonny, M.V.5    Bender, J.6
  • 13
    • 0034665124 scopus 로고    scopus 로고
    • Suberoylanilide hydroxamic acid, an inhibitor of histone deacetylase, 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., et al. Suberoylanilide hydroxamic acid, an inhibitor of histone deacetylase, suppresses the growth of prostate cancer cells in vitro and in vivo. Cancer Res. 60 (2000) 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
  • 14
    • 0037130244 scopus 로고    scopus 로고
    • Structure-activity relationships on phenylalanine-containing inhibitors of histone deacetylase: in vitro enzyme inhibition, induction of differentiation, and inhibition of proliferation in Friend leukemic cells
    • Wittich S., Scherf H., Xie C., Brosch G., Loidl P., Gerhauser C., et al. Structure-activity relationships on phenylalanine-containing inhibitors of histone deacetylase: in vitro enzyme inhibition, induction of differentiation, and inhibition of proliferation in Friend leukemic cells. J. Med. Chem. 45 (2002) 3296-3309
    • (2002) J. Med. Chem. , vol.45 , pp. 3296-3309
    • Wittich, S.1    Scherf, H.2    Xie, C.3    Brosch, G.4    Loidl, P.5    Gerhauser, C.6
  • 15
    • 0033562343 scopus 로고    scopus 로고
    • Both Sp1 and Sp3 are responsible for p21waf1 promoter activity induced by histone deacetylase inhibitor in NIH3T3 cells
    • Xiao H., Hasegawa T., and Isobe K. Both Sp1 and Sp3 are responsible for p21waf1 promoter activity induced by histone deacetylase inhibitor in NIH3T3 cells. J. Cell. Biochem. 73 (1999) 291-302
    • (1999) J. Cell. Biochem. , vol.73 , pp. 291-302
    • Xiao, H.1    Hasegawa, T.2    Isobe, K.3
  • 16
    • 0037455825 scopus 로고    scopus 로고
    • Histone deacetylase inhibitor trichostatin A induces cell-cycle arrest/apoptosis and hepatocyte differentiation in human hepatoma cells
    • Yamashita Y., Shimada M., Harimoto N., Rikimaru T., Shirabe K., Tanaka S., et al. Histone deacetylase inhibitor trichostatin A induces cell-cycle arrest/apoptosis and hepatocyte differentiation in human hepatoma cells. Int. J. Cancer 103 (2003) 572-576
    • (2003) Int. J. Cancer , vol.103 , pp. 572-576
    • Yamashita, Y.1    Shimada, M.2    Harimoto, N.3    Rikimaru, T.4    Shirabe, K.5    Tanaka, S.6
  • 19
    • 0025246110 scopus 로고
    • Universal control mechanism regulating onset of M-phase
    • Nurse P. Universal control mechanism regulating onset of M-phase. Nature 344 (1990) 503-508
    • (1990) Nature , vol.344 , pp. 503-508
    • Nurse, P.1
  • 20
    • 0033558850 scopus 로고    scopus 로고
    • Sodium butyrate induces G2 arrest in the human breast cancer cells MDA-MB-231 and renders them competent for DNA rereplication
    • Lallemand F., Courilleau D., Buquet-Fagot C., Atfi A., and Montagne M.N. Sodium butyrate induces G2 arrest in the human breast cancer cells MDA-MB-231 and renders them competent for DNA rereplication. Cell Res. 247 (1999) 432-440
    • (1999) Cell Res. , vol.247 , pp. 432-440
    • Lallemand, F.1    Courilleau, D.2    Buquet-Fagot, C.3    Atfi, A.4    Montagne, M.N.5
  • 21
    • 0028171292 scopus 로고
    • G1 phase progression: cycling on cue
    • Sherr C.J. G1 phase progression: cycling on cue. Cell 79 (1994) 551-555
    • (1994) Cell , vol.79 , pp. 551-555
    • Sherr, C.J.1
  • 22
    • 0031843167 scopus 로고    scopus 로고
    • Increased expression of cyclin D2 during multiple states of growth arrest in primary and established cells
    • Meyyappan M., Wong H., Hull C., and Riabowol K.T. Increased expression of cyclin D2 during multiple states of growth arrest in primary and established cells. Mol. Cell. Biol. 18 (1998) 3163-3172
    • (1998) Mol. Cell. Biol. , vol.18 , pp. 3163-3172
    • Meyyappan, M.1    Wong, H.2    Hull, C.3    Riabowol, K.T.4
  • 23
    • 0037389979 scopus 로고    scopus 로고
    • Methylation of cyclin D2 is observed frequently in pancreatic cancer but is also an age-related phenomenon in gastrointestinal tissues
    • Matsubayashi H., Sato N., Fukushima N., Yeo C.J., Walter K.M., Brune K., et al. Methylation of cyclin D2 is observed frequently in pancreatic cancer but is also an age-related phenomenon in gastrointestinal tissues. Clin. Cancer Res. 9 (2003) 1446-1452
    • (2003) Clin. Cancer Res. , vol.9 , pp. 1446-1452
    • Matsubayashi, H.1    Sato, N.2    Fukushima, N.3    Yeo, C.J.4    Walter, K.M.5    Brune, K.6
  • 24
    • 0030809026 scopus 로고    scopus 로고
    • Bcl-2 and bak may play a pivotal role in sodium butyrate-induced apoptosis in colonic epithelial cells; however overexpression of bcl-2 does not protect against bak-mediated apoptosis
    • Hague A., Diaz G.D., Hicks D.J., Krajewski S., Reed J.C., and Paraskeva C. Bcl-2 and bak may play a pivotal role in sodium butyrate-induced apoptosis in colonic epithelial cells; however overexpression of bcl-2 does not protect against bak-mediated apoptosis. Int. J. Cancer 72 (1997) 898-905
    • (1997) Int. J. Cancer , vol.72 , pp. 898-905
    • Hague, A.1    Diaz, G.D.2    Hicks, D.J.3    Krajewski, S.4    Reed, J.C.5    Paraskeva, C.6
  • 25
    • 0035184066 scopus 로고    scopus 로고
    • Histone deacetylase inhibitor down regulation of bcl-xl gene expression leads to apoptotic cell death in mesothelioma
    • Cao X.X., Mohuiddin I., Ece F., McConkey D.J., and Smythe W.R. Histone deacetylase inhibitor down regulation of bcl-xl gene expression leads to apoptotic cell death in mesothelioma. Am. J. Respir. Cell. Mol. Biol. 25 (2001) 562-568
    • (2001) Am. J. Respir. Cell. Mol. Biol. , vol.25 , pp. 562-568
    • Cao, X.X.1    Mohuiddin, I.2    Ece, F.3    McConkey, D.J.4    Smythe, W.R.5
  • 26
    • 0034775318 scopus 로고    scopus 로고
    • Inhibition of histone deacetylase activity enhances Fas receptor-mediated apoptosis in leukemic lymphoblasts
    • Bernhard D., Skvortsov S., Tinhofer I., Hubl H., Greil R., Csordas A., et al. Inhibition of histone deacetylase activity enhances Fas receptor-mediated apoptosis in leukemic lymphoblasts. Cell Death Differ. 8 (2001) 1014-1021
    • (2001) Cell Death Differ. , vol.8 , pp. 1014-1021
    • Bernhard, D.1    Skvortsov, S.2    Tinhofer, I.3    Hubl, H.4    Greil, R.5    Csordas, A.6
  • 27
    • 4444239987 scopus 로고    scopus 로고
    • The histone deacetylase inhibitor suberic bishydroxamate regulates the expression of multiple apoptotic mediators and induces mitochondria-dependent apoptosis of melanoma cells
    • Zhang X.D., Gillespie S.K., Borrow J.M., and Hersey P. The histone deacetylase inhibitor suberic bishydroxamate regulates the expression of multiple apoptotic mediators and induces mitochondria-dependent apoptosis of melanoma cells. Mol. Cancer Ther. 3 (2004) 425-435
    • (2004) Mol. Cancer Ther. , vol.3 , pp. 425-435
    • Zhang, X.D.1    Gillespie, S.K.2    Borrow, J.M.3    Hersey, P.4
  • 28
    • 9444238027 scopus 로고    scopus 로고
    • The histone deacetylase inhibitor FR901228 induces caspase-dependent apoptosis via the mitochondrial pathway in small cell lung cancer cells
    • Doi S., Soda H., Oka M., Tsurutani J., Kitazaki T., Nakamura Y., et al. The histone deacetylase inhibitor FR901228 induces caspase-dependent apoptosis via the mitochondrial pathway in small cell lung cancer cells. Mol. Cancer Ther. 3 (2004) 1397-1402
    • (2004) Mol. Cancer Ther. , vol.3 , pp. 1397-1402
    • Doi, S.1    Soda, H.2    Oka, M.3    Tsurutani, J.4    Kitazaki, T.5    Nakamura, Y.6
  • 29
    • 0036171675 scopus 로고    scopus 로고
    • The histone-deacetylase inhibitor Trichostatin A blocks proliferation and triggers apoptotic programs in hepatoma cells
    • Herold C., Ganslmayer M., Ocker M., Hermann M., Geerts A., Hahn E.G., et al. The histone-deacetylase inhibitor Trichostatin A blocks proliferation and triggers apoptotic programs in hepatoma cells. J. Hepatol. 36 (2002) 233-240
    • (2002) J. Hepatol. , vol.36 , pp. 233-240
    • Herold, C.1    Ganslmayer, M.2    Ocker, M.3    Hermann, M.4    Geerts, A.5    Hahn, E.G.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.