体细胞
生物
癌症
突变
遗传学
基因组
癌细胞
癌症的体细胞进化
种系突变
基因
计算生物学
癌症研究
作者
Iñigo Martincorena,Peter J. Campbell
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2015-09-24
卷期号:349 (6255): 1483-1489
被引量:1129
标识
DOI:10.1126/science.aab4082
摘要
Spontaneously occurring mutations accumulate in somatic cells throughout a person’s lifetime. The majority of these mutations do not have a noticeable effect, but some can alter key cellular functions. Early somatic mutations can cause developmental disorders, whereas the progressive accumulation of mutations throughout life can lead to cancer and contribute to aging. Genome sequencing has revolutionized our understanding of somatic mutation in cancer, providing a detailed view of the mutational processes and genes that drive cancer. Yet, fundamental gaps remain in our knowledge of how normal cells evolve into cancer cells. We briefly summarize a number of the lessons learned over 5 years of cancer genome sequencing and discuss their implications for our understanding of cancer progression and aging.
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