Rapid identification of somatic mutations in colorectal and breast cancer tissues using mismatch repair detection (MRD)

✍ Scribed by Steven Bentivegna; Jianbiao Zheng; Eugeni Namsaraev; Victoria E.H. Carlton; Adam Pavlicek; Martin Moorhead; Farooq Siddiqui; Zhiyong Wang; Liana Lee; James S. Ireland; Kent Suyenaga; Thomas D. Willis; Malek Faham; Albert B. Seymour

• Publisher: John Wiley and Sons
• Year: 2008
• Tongue: English
• Weight: 367 KB
• Volume: 29
• Category: Article
• ISSN: 1059-7794
• DOI: 10.1002/humu.20672

✦ Synopsis

Communicated by Richard Wooster

Mismatch repair detection (MRD) was used to screen 93 matched tumor-normal sample pairs and 22 cell lines for somatic mutations in 30 cancer relevant genes. Using a starting amount of only 150 ng of genomic DNA, we screened 102 kb of sequence for somatic mutations in colon and breast cancer. A total of 152 somatic mutations were discovered, encompassing previously reported mutations, such as BRAF V600E and KRAS G12S, G12V, and G13D, as well as novel mutations, including some in genes in which somatic mutations have not previously been reported, such as MAP2K1 and MAP2K2. The distribution of mutations ranged widely within and across tumor types. The functional significance of many of these mutations is not understood, with patterns of selection only evident in KRAS and BRAF in colon cancer. These results present a novel approach to high-throughput mutation screening using small amounts of starting material and reveal a mutation spectrum across 30 genes in a large cohort of breast and colorectal cancers.