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Ten common genetic variants associated with colorectal cancer risk are not associated with survival after diagnosis

  • Albert Tenesa
  • , Evropi Theodoratou
  • , Farhat V. N. Din
  • , Susan M. Farrington
  • , Roseanne Cetnarskyj
  • , Rebecca A. Barnetson
  • , Mary E. Porteous
  • , Harry Campbell
  • , Malcolm G. Dunlop (Lead / Corresponding author)

    Research output: Contribution to journal › Article › peer-review

    Abstract

    Purpose: To date, genomewide association studies have identified 10 genetic loci associated with colorectal cancer (CRC) susceptibility. We hypothesized that these loci might also affect cancer survival.

    Experimental Design: To determine whether single-nucleotide polymorphisms tagging these 10 loci influenced all-cause and CRC-specific mortality, we prospectively followed survival outcomes for 2,838 Scottish patients recruited soon after a diagnosis of CRC. Survival analysis was conducted using Cox proportional hazard models adjusted for American Joint Committee on Cancer stage, age, and sex.

    Results: None of the single-nucleotide polymorphisms were found to be statistically significantly associated with all-cause or CRC-specific mortality.

    Conclusions: We conclude that none of the 10 common genetic variants thus far shown to be associated with CRC risk are associated with survival from CRC.

    Original languageEnglish
    Pages (from-to)3754-3759
    Number of pages6
    JournalClinical Cancer Research
    Volume16
    Issue number14
    Early online date13 Jul 2010
    DOIs
    Publication statusPublished - Jul 2010

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    ASJC Scopus subject areas

    • Oncology
    • Cancer Research

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