paperKB
coga / coga-kb
Help
Sign in

Chunk #17 — Results — Identification of somatic mutations in cancer samples

Source
Detection of low prevalence somatic mutations in solid tumors with ultra-deep targeted sequencing.
Embedded
yes

Text

In the primary breast cancer sample, we identified a single somatic mutation (HRAS-G12V) by UDT-Seq (Table 1; Table S8 in Additional file 2). HRAS-G12V (prevalence 51%) is a common activating mutation in bladder cancer [18], and its role in breast cancer has not been described. HRAS-G12V is homologous to the KRAS-G12D mutation and similarly may be important in the development of resistance to tyrosine kinase targeting agents [16]. This mutation was also identified in the matching xenograft sample at a similar prevalence (48%), suggesting its importance for breast cancer growth and proliferation.