Federal State Budget Institution «Rostov Research Oncologic Institute», Rostov-on-Don, the Russian Federation
*Corresponding author: Natalia V. Soldatkina. PhD, Rostov Research Oncological Institute Rostov-on-Don, the Russian Federation. E-mail: snv-rnioi@yandex.ru
Published: March 25, 2015. DOI: 10.21103/Article5(1)_CR2
The aim of this study was to investigate the frequency and spectrum of KRAS mutations in men and women with colorectal cancer (CRC), and an impact of KRAS-mutation status on the clinical and morphological features of CRC. The study included 303 patients (168/55.4% women and 135/44.6% men) with CRC T2-4N0-2M0-1. We defined 7 KRAS SNP-mutations (G12D, G12A, G12R, G12C, G12S, G12V and G13D) located within codons 12 and 13 using Bio-Rad real-time thermal cyclers CFX96 and Real-Time-PCR- KRAS-7M Kit. The frequency of KRAS mutations was 35.6% in the CRC patients with a predominant presence of G>A transitions. The KRAS codon 12 and 13 mutations are predictive of poor prognosis The KRAS-mutated CRC has clinical features in view of the gender differences. KRAS-mutation status is a promising predictive biomarker of personalized treatment.
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Int J Biomed. 2015; 5(1):11-15. © 2015 International Medical Research and Development Corporation. All rights reserved.