Amplified genes as therapeutic targets in cancer

Mark Basik , Natasha J. Caplen , Olli-P. Kallioniemi , Spyro Mousses
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引用次数: 2

Abstract

The most effective targeted cancer therapies have arisen from research into genetically altered oncogenes, including BCR-ABL, HER2, RAS and EGFR. Recent advances in cancer genetics have identified many regions of the genome that undergo amplification (increase in copy number) but, in most cases, the key oncogenic targets driving the growth and survival of cancer cells remain unknown. In this review, we discuss high-throughput technologies for the discovery of putative oncogenes, and clinical and functional validation of these genes as targets for therapy. New technologies in translational genomics facilitate the identification, validation and prioritization of candidate molecular targets for anti-cancer therapy.

扩增基因作为癌症治疗靶点
最有效的靶向癌症治疗方法来自对基因改变癌基因的研究,包括BCR-ABL、HER2、RAS和EGFR。癌症遗传学的最新进展已经确定了基因组的许多区域经历扩增(拷贝数增加),但在大多数情况下,驱动癌细胞生长和存活的关键致癌靶点仍然未知。在这篇综述中,我们讨论了用于发现推定致癌基因的高通量技术,以及这些基因作为治疗靶点的临床和功能验证。翻译基因组学的新技术促进了抗癌治疗候选分子靶点的鉴定、验证和优先排序。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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