Extreme sensitivity to Yondelis® (Trabectedin, ET-743) in low passaged sarcoma cell lines correlates with mutated p53

被引:33
作者
Moneo, Victoria
Serelde, Beatriz G.
Fominaya, Jess
Leal, Juan F. M.
Blanco-Aparicio, Carmen
Romero, Lourdes
Sanchez-Beato, Margarita
Cigudosa, Juan C.
Tercero, Juan C.
Piris, Miguel A.
Jimeno, Jose
Carnero, Amancio
机构
[1] CNIO, Expt Therapeut Programme, Madrid 28029, Spain
[2] Mol Pathol Programme, Madrid, Spain
[3] Spanish Natl Canc Ctr CNIO, Biotechnol Programme, Madrid, Spain
[4] Pharmamar R&D Madrid, Madrid, Spain
关键词
Trabectedin; ET-743; p53; sarcoma;
D O I
10.1002/jcb.21073
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Yondelis(R) (Trabectedin, ET-743) is a marine anticancer agent currently in Phase II/III development in patients with advanced pretreated Soft tissue sarcoma. In the present study, we generated a panel of low passaged tumor cell lines from samples explanted from chemonaive sarcoma patients with different turner types. We assessed in vitro sensitivity/resistance to Trabectedin and doxorubicin in a panel of sarcoma cell lines and examined the correlation between molecular alterations in DNA repair genes and sensitivity to Trabectedin. We treated cell lines with Trabectedin and doxorubicin in both 96-h and clonogenic assays. In both assays, well-defined groups of resistant and sensitive cell lines were observed. Resistance to Trabectedin did not correlate with resistance to doxorubicin, indicating that the two drugs may have different mechanisms of resistance. p53 mutations and deletions correlated with extreme sensitivity (IC50 < 1 nM) to Trabectedin (P < 0.01). In a pair of isogenic cell lines differing only in the presence or absence of wildtype p53, the absence of P53 rendered cells threefold more sensitive to Trabectedin.
引用
收藏
页码:339 / 348
页数:10
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