Substituted titanocenes induce caspase-dependent apoptosis in human epidermoid carcinoma cells in vitro and exhibit antitumour activity in vivo

被引:56
作者
Bannon, J. H.
Fichtner, I.
O'Neill, A.
Pampillon, C.
Sweeney, N. J.
Strohfeldt, K.
Watson, R. W.
Tacke, M.
Mc Gee, M. M. [1 ]
机构
[1] Univ Coll Dublin, Conway Inst Biomol & Biomed Res, UCD Sch Biomol & Biomed Sci, Dublin 4, Ireland
[2] Max Delbruck Ctr Mol Med, D-13092 Berlin, Germany
[3] Univ Coll Dublin, Conway Inst Biomol & Biomed Res, UCD Sch Med & Med Sci, Dublin 4, Ireland
[4] Univ Coll Dublin, Conway Inst Biomol & Biomed Res, CSCB, UCD Sch Chem & Chem Biol, Dublin 4, Ireland
关键词
titanocene; epidermoid cancer; apoptosis; caspases; chemotherapy; cisplatin;
D O I
10.1038/sj.bjc.6604021
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Titanocene compounds are a novel series of agents that exhibit cytotoxic effects in a variety of human cancer cells in vitro and in vivo. In this study, the antiproliferative activity of two titanocenes (Titanocenes X and Y) was evaluated in human epidermoid cancer cells in vitro. Titanocenes X and Y induce apoptotic cell death in epidermoid cancer cells, with IC50 values that are comparable to cisplatin. Characterisation of the cell death pathway induced by titanocene compounds in A431 cells revealed that apoptosis is preceded by cell cycle arrest and the inhibition of cell proliferation. The induction of apoptosis is dependent on the activation of caspase-3 and -7 but not caspase-8. Furthermore, the antitumour activity of Titanocene Y was tested in an A431 xenograft model of epidermoid cancer. Results indicate that Titanocene Y significantly reduced the growth of A431 xenografts with an antitumour effect similar to cisplatin. These results suggest that titanocenes represent a novel series of promising antitumour agents.
引用
收藏
页码:1234 / 1241
页数:8
相关论文
共 33 条
[1]   Antitumor activity of Titanocene Y against freshly explanted human breast tumor cells and in xenografted MCF-7 tumors in mice [J].
Beckhove, Philipp ;
Oberschmidt, Olaf ;
Hanauske, Axel R. ;
Pampillon, Clara ;
Schirrmacher, Volker ;
Sweeney, Nigel J. ;
Strohfeldt, Katja ;
Tacke, Matthias .
ANTI-CANCER DRUGS, 2007, 18 (03) :311-315
[2]   Cisplatin-induced renal cell apoptosis: Caspase 3-dependent and -independent pathways [J].
Cummings, BS ;
Schnellmann, RG .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2002, 302 (01) :8-17
[3]   Cytotoxicity, DNA strand breakage and DNA-protein crosslinking by a novel transplatinum compound in human A2780 ovarian and MCF-7 breast carcinoma cells [J].
Farrell, N ;
Povirk, LF ;
Dange, Y ;
DeMasters, G ;
Gupta, MS ;
Kohlhagen, G ;
Khan, QA ;
Pommier, Y ;
Gewirtz, DA .
BIOCHEMICAL PHARMACOLOGY, 2004, 68 (05) :857-866
[4]  
FARRELL N, 1999, TOP BIOL INORG CHEM, V1, P99
[5]   Anti-tumor activity of Titanocene Y in xenografted Caki-1 tumors in mice [J].
Fichtner, Iduna ;
Pampillon, Clara ;
Sweeney, Nigel J. ;
Strohfeldt, Katja ;
Tacke, Matthias .
ANTI-CANCER DRUGS, 2006, 17 (03) :333-336
[6]  
GELASCO A, 1999, TOP BIOL INORG CHEM, V1, P1
[7]   Is cisplatin-induced cell death always produced by apoptosis? [J].
Gonzalez, VM ;
Fuertes, MA ;
Alonso, C ;
Perez, JM .
MOLECULAR PHARMACOLOGY, 2001, 59 (04) :657-663
[8]  
HARTL F, 2001, J MOL STRUCT, V559, P331
[9]   Structure, recognition, and processing of cisplatin-DNA adducts [J].
Jamieson, ER ;
Lippard, SJ .
CHEMICAL REVIEWS, 1999, 99 (09) :2467-2498
[10]  
Kasibhatla S, 2003, MOL CANCER THER, V2, P573