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Mutant allele‐specific imbalance modulates prognostic impact of KRAS mutations in colorectal adenocarcinoma and is associated with worse overall survival
Author(s) -
Hartman D. J.,
Davison J. M.,
Foxwell T. J.,
Nikiforova M. N.,
Chiosea S. I.
Publication year - 2012
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.27461
Subject(s) - kras , hazard ratio , colorectal cancer , biology , odds ratio , mutation , chromosome , adenocarcinoma , oncology , allele , cancer research , medicine , confidence interval , genetics , gene , cancer
The prognostic impact of distinct KRAS mutations in colorectal carcinomas is not fully characterized. We hypothesized that the prognostic impact of KRAS mutations is modulated by KRAS mutant allele‐specific imbalance (MASI). KRAS MASI was assessed by sequencing electropherograms in KRAS ‐mutated colorectal carcinomas ( N = 394, prospectively tested). The mechanism of KRAS MASI was studied by fluorescence in situ hybridization (FISH; N = 50). FISH showed that KRAS MASI developed by chromosome 12 hyperploidy (9/18, 50%) or KRAS amplification (1/18, 5.5%). KRAS MASI was more common in tumors with KRAS codon 13 than with codon 12 mutations [24/81, 30% vs . 54/313, 17%; odds ratio (OR), 2.0, 95% confidence interval (CI), 1.2–3.5; p = 0.01]. KRAS MASI was correlated with overall survival ( N = 358, median follow‐up = 21 months). In a multivariate analysis, KRAS codon 13 MASI was an independent adverse prognostic factor (compared to codon 13 mutants without MASI combined with all codon 12 mutants; adjusted hazard ratio, 2.2, 95% CI: 1.2–3.9; p = 0.01). KRAS MASI arises through chromosome 12 hyperploidy or KRAS amplification and, when affects KRAS codon 13, is associated with worse overall survival.