A novel charges trinuclear platinum complex effective against cisplatin-resistant tumours: hypersensitivity of p53-mutant human tumour xenografts

被引:119
作者
Pratesi, G
Perego, P
Polizzi, D
Righetti, SC
Supino, R
Caserini, C
Manzotti, C
Giuliani, FC
Pezzoni, G
Tognella, S
Spinelli, S
Farrell, N
Zunino, F
机构
[1] Ist Nazl Studio & Cura Tumori, I-20133 Milan, Italy
[2] Boehringer Mannheim Italia SPA, I-20052 Monza, Milan, Italy
[3] Univ Vermont, Dept Chem, Burlington, VT 05405 USA
[4] Univ Vermont, Vermont Canc Ctr, Burlington, VT 05405 USA
关键词
multinuclear platinum complex; cisplatin; drug resistance; p53; mutation;
D O I
10.1038/sj.bjc.6690620
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Multinuclear platinum compounds were rationally designed to bind to DNA in a different manner from that of cisplatin and its mononuclear analogues. A triplatinum compound of the series (BBR 3464) was selected for preclinical development, since, in spite of its charged nature, it was very potent as cytotoxic agent and effective against cisplatin-resistant tumour cells. Anti-tumour efficacy studies were performed in a panel of human tumour xenografts refractory or poorly responsive to cisplatin. The novel platinum compound exhibited efficacy in all tested tumours and an impressive efficacy (including complete tumour regressions) was displayed in two lung carcinoma models, CaLu-3 and POCS. Surprisingly, BBR 3464 showed a superior activity against p53-mutant tumours as compared to those carrying the wild-type gene;The involvement of p53 in tumour response was investigated in an osteosarcoma cell line, SAGS, which is null for p53 and is highly sensitive to BBR 3464, and in the same cells following introduction-of the wild-type p53 gene. Thus the pattern of cellular response was investigated in a panel of human tumour cells with a different p53 gene status. The results showed that the transfer of functional p53 resulted in a marked (tenfold) reduction of cellular chemosensitivity to the multinuclear platinum complex but ina moderate sensitization to cisplatin. In addition, in contrast to cisplatin, the triplatinum complex was very effective as an inducer of apoptosis in a lung carcinoma cell line carrying mutant p53. The peculiar pattern of anti-tumour activity of the triplatinum complex and its ability to induce p53-independent cell death may have relevant pharmacological implications, since p53, a critical protein involved in DNA repair and induction of apoptosis by conventional DMA-damaging agents, is defective in several human tumours. We suggest that the peculiar DNA binding, properties of the triplatinum complex may contribute to the striking profile of anti-tumour efficacy. Taken together, the available information supports that anti-tumour activity of the novel compound is mediated by a mechanism-different from that of conventional platinum complexes, and compounds of this series could represent a new class of promising anti-tumour agents.
引用
收藏
页码:1912 / 1919
页数:8
相关论文
共 30 条
[1]   Dominant-negative p53 mutations selected in yeast hit cancer hot spots [J].
Brachmann, RK ;
Vidal, M ;
Boeke, JD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (09) :4091-4095
[2]  
Caserini C, 1997, CLIN CANCER RES, V3, P955
[3]  
CHU G, 1994, J BIOL CHEM, V269, P787
[4]   Cisplatin resistance and DNA repair [J].
Crul, M ;
Schellens, JHM ;
Beijnen, JH ;
Maliepaard, M .
CANCER TREATMENT REVIEWS, 1997, 23 (5-6) :341-366
[6]   NONCLASSICAL PLATINUM ANTITUMOR AGENTS - PERSPECTIVES FOR DESIGN AND DEVELOPMENT OF NEW DRUGS COMPLEMENTARY TO CISPLATIN [J].
FARRELL, N .
CANCER INVESTIGATION, 1993, 11 (05) :578-589
[7]  
Farrell N., 1997, Proceedings of the American Association for Cancer Research Annual Meeting, V38, P310
[8]   EFFECTS OF GEOMETRIC ISOMERISM AND LIGAND SUBSTITUTION IN BIFUNCTIONAL DINUCLEAR PLATINUM COMPLEXES ON BINDING-PROPERTIES AND CONFORMATIONAL-CHANGES IN DNA [J].
FARRELL, N ;
APPLETON, TG ;
QU, Y ;
ROBERTS, JD ;
FONTES, APS ;
SKOV, KA ;
WU, P ;
ZOU, Y .
BIOCHEMISTRY, 1995, 34 (47) :15480-15486
[9]   DNA-BINDING AND CHEMISTRY OF DINUCLEAR PLATINUM COMPLEXES [J].
FARRELL, N .
COMMENTS ON INORGANIC CHEMISTRY, 1995, 16 (06) :373-389
[10]  
Farrell N., 1996, Advances in DNA Sequence-Specific Agents, V2, P216, DOI [10.1016/S1067-568X(96)80010-7, DOI 10.1016/S1067-568X(96)80010-7]