Comparison of two different screening methods for the KRAS mutation in colorectal cancer

Clin Lab. 2010;56(5-6):175-86.

Abstract

Background: To compare high resolution melting (HRM) and primer extension (PE) for mutation screening of KRAS codons 12 and 13.

Methods: DNA samples were isolated from 60 colorectal cancer (CRC) patients. HRM and primer extension analyses were used for mutation screening of KRAS codons 12 and 13.

Results: Both methods can detect KRAS mutations in a DNA mixture containing as little as 5% mutant DNA. The concordant rate between the two methods was 100%. HRM analysis is able to distinguish mutant from wild type, however, it is unable to detect the actual base change. PE analysis needs more procedures, is time-consuming and slightly more expensive but it is able to detect the precise mutation.

Conclusions: This study showed that HRM is a reliable screening method to identify mutations in the KRAS gene, and the PE can be used as a diagnostic method to accurately pinpoint the nature of mutations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / genetics*
  • Adenocarcinoma / pathology
  • Base Sequence
  • Cell Line, Tumor
  • Codon / genetics
  • Colorectal Neoplasms / genetics*
  • Colorectal Neoplasms / pathology
  • DNA Mutational Analysis / methods
  • DNA Primers
  • DNA, Neoplasm / genetics
  • DNA, Neoplasm / isolation & purification
  • Guanine
  • Humans
  • Mass Screening / methods
  • Mutation*
  • Nucleic Acid Denaturation / genetics
  • Polymorphism, Single Nucleotide
  • Proto-Oncogene Proteins / genetics*
  • Proto-Oncogene Proteins p21(ras)
  • Sequence Deletion
  • Thymine
  • ras Proteins / genetics*

Substances

  • Codon
  • DNA Primers
  • DNA, Neoplasm
  • KRAS protein, human
  • Proto-Oncogene Proteins
  • Guanine
  • Proto-Oncogene Proteins p21(ras)
  • ras Proteins
  • Thymine