Loni L, Del Tacca M, Danesi R
Interdepartmental Centre of Clinical Pharmacology and Experimental Therapeutics, University of Pisa, Italy.
Br J Cancer. 2001 Nov 16;85(10):1425-31. doi: 10.1054/bjoc.2001.2130.
The variability of tumour responses to chemotherapeutic agents is a topic of major interest in current oncology research. Advances in the knowledge of molecular pathology of cancer make available strategies by which tumour cells can be profiled for their genetic background in order to select anticancer agents that might selectively kill cells in a molecular context that matches the mechanism of action of drugs. The next generation of anticancer treatments might thus be tailored on the basis of the numerous molecular alterations identified in tumour cells of a particular patient. However, to exploit these alterations, it is necessary to understand how they influence the cellular pathways that control the sensitivity or, conversely, resistance to chemotherapeutic agents. The aim of this article is to outline major genetic abnormalities in non-Hodgkin lymphomas that can be used to streamline anticancer drug selection and to underscore the major role of pharmacogenetics, which studies the interactions between genetic background and drug activity, to the prediction of likelihood of response and identification of potential new targets for pharmacological intervention.
肿瘤对化疗药物反应的变异性是当前肿瘤学研究中一个备受关注的话题。癌症分子病理学知识的进展提供了一些策略,通过这些策略可以分析肿瘤细胞的遗传背景,以便选择在与药物作用机制相匹配的分子背景下可能选择性杀死细胞的抗癌药物。因此,下一代抗癌治疗可能会根据在特定患者肿瘤细胞中发现的众多分子改变来量身定制。然而,要利用这些改变,有必要了解它们如何影响控制对化疗药物敏感性或相反地控制耐药性的细胞途径。本文的目的是概述非霍奇金淋巴瘤中的主要基因异常,这些异常可用于简化抗癌药物的选择,并强调药物遗传学(研究遗传背景与药物活性之间相互作用)在预测反应可能性和识别潜在新的药物干预靶点方面的主要作用。