KRAS mutation, KRAS-LCS6 polymorphism, and non-small cell lung cancer

H. H. Nelson, B. C. Christensen, S. L. Plaza, J. K. Wiencke, C. J. Marsit, K. T. Kelsey

Research output: Contribution to journalArticlepeer-review

47 Scopus citations

Abstract

The let-7 family of microRNAs are important regulatory molecules in lung cancer. One downstream target of let-7 is the RAS gene family, including KRAS, an important oncogene in the etiology and clinical outcome of lung adenocarcinoma. Recently, a SNP in the let-7 binding region of the KRAS 3' UTR was identified (termed LCS6). This functional polymorphism alters let-7 binding, resulting in both increased KRAS expression and decreased let-7 exposure. Further, this SNP has been reported as a risk trait for lung cancer among low-moderate smokers. Given the functionality of LCS6, we tested the hypothesis that this SNP is associated with the occurrence of KRAS mutation as well as patient survival. Here, we report there is no association between the LCS6 KRAS polymorphism and KRAS mutation. Further, we find no association between the LCS6 polymorphism and lung cancer survival. These unexpected findings imply that this newly reported KRAS LCS6 polymorphism will have limited clinical utility for NSCLC.

Original languageEnglish (US)
Pages (from-to)51-53
Number of pages3
JournalLung Cancer
Volume69
Issue number1
DOIs
StatePublished - Jul 2010

Bibliographical note

Funding Information:
This work was supported by NIH grant P30 CA-077598 .

Keywords

  • Adenocarcinoma
  • KRAS
  • LCS6
  • Let-7
  • Lung cancer
  • MiRNA

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