Department of Cancer Biology, Beckman Research Institute, City of Hope, Duarte, CA 91010, USA.
Genome Med. 2010 Aug 16;2(8):54. doi: 10.1186/gm175.
The etiology of most human cancers is unknown. Genetic inheritance and environmental factors are thought to have major roles, and for some types of cancer, exposure to carcinogens is a proven mechanism leading to tumorigenesis. Sequencing of entire cancer genomes has not only begun to provide clues regarding functionally relevant mutations, but has also paved the way towards understanding the initial exposures leading to DNA damage, repair and eventually to mutation of specific sequences within a cancer genome. Two recent studies of melanoma and small cell lung cancer exemplify what type of information can be gained from cancer genome sequencing.
大多数人类癌症的病因尚不清楚。遗传和环境因素被认为起着重要作用,对于某些类型的癌症,接触致癌物质是导致肿瘤形成的已知机制。对整个癌症基因组进行测序不仅开始为功能相关突变提供线索,而且为了解导致 DNA 损伤、修复以及最终导致特定癌症基因组序列突变的最初暴露铺平了道路。最近对黑色素瘤和小细胞肺癌的两项研究为例说明了从癌症基因组测序中可以获得哪些信息。