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RAS mutations in human cancers: Roles in precision medicine

期刊

SEMINARS IN CANCER BIOLOGY
卷 59, 期 -, 页码 23-35

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.semcancer.2019.06.007

关键词

Mutation; Precision medicine; Oncogene; HRAS; KRAS; NRAS; Cancer; Personalized medicine

类别

资金

  1. Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan [06044072]
  2. Japan Society for the Promotion of Sciences [257132]
  3. National Institute of Health (NIH), U.S.A. [CA22701]
  4. Government of Japan
  5. Grants-in-Aid for Scientific Research [06044072] Funding Source: KAKEN

向作者/读者索取更多资源

Ras proteins play a crucial role as a central component of the cellular networks controlling a variety of signaling pathways that regulate growth, proliferation, survival, differentiation, adhesion, cytoskeletal rearrangements and motility of a cell. Almost, 4 decades passed since Ras research was started and ras genes were originally discovered as retroviral oncogenes. Later on, mutations of the human RAS genes were linked to tumorigenesis. Genetic analyses found that RAS is one of the most deregulated oncogenes in human cancers. In this review, we summarize the pioneering works which allowed the discovery of RAS oncogenes, the finding of frequent mutations of RAS in various human cancers, the role of these mutations in tumorigenesis and mutation-activated signaling networks. We further describe the importance of RAS mutations in personalized or precision medicine particularly in molecular targeted therapy, as well as their use as diagnostic and prognostic markers as therapeutic determinants in human cancers.

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