1] Section of Oncology, Institute of Medicine, University of Bergen, Bergen, Norway [2] Department of Oncology, Haukeland University Hospital, Bergen, Norway.
Oncogene. 2013 Nov 14;32(46):5315-30. doi: 10.1038/onc.2013.48. Epub 2013 Mar 11.
Although new agents are implemented to cancer therapy, we lack fundamental understandings of the mechanisms of chemoresistance, the main obstacle to cure in cancer. Here we review clinical evidence linking molecular defects to drug resistance across different tumour forms and discuss contemporary experimental evidence exploring these mechanisms. Although evidence, in general, is sparse and fragmentary, merging knowledge links drug resistance, and also sensitivity, to defects in functional pathways having a key role in cell growth arrest or death and DNA repair. As these pathways may act in concert, there is a need to explore multiple mechanisms in parallel. Taking advantage of massive parallel sequencing and other novel high-throughput technologies and base research on biological hypotheses, we now have the possibility to characterize functional defects related to these key pathways and to design a new generation of studies identifying the mechanisms controlling resistance to different treatment regimens in different tumour forms.
尽管新的药物已经被应用于癌症治疗,但是我们对癌症治疗的主要障碍——化疗耐药的机制仍然缺乏基本的了解。在这里,我们回顾了将分子缺陷与不同肿瘤类型的耐药性联系起来的临床证据,并讨论了探索这些机制的当代实验证据。尽管一般来说,证据是稀疏和零碎的,但将知识融合在一起将耐药性和敏感性与在细胞生长停滞或死亡和 DNA 修复中起关键作用的功能途径的缺陷联系起来。由于这些途径可能协同作用,因此需要并行探索多种机制。利用大规模平行测序和其他新型高通量技术以及基于生物学假设的基础研究,我们现在有可能描述与这些关键途径相关的功能缺陷,并设计新一代的研究,以确定不同肿瘤类型中不同治疗方案耐药性的控制机制。