Mutation patterns and prognostic analysis of BRAF/KRAS/PIK3CA in colorectal cancer

Chengfeng Wang1, Diling Pan2

  • 1Department of Gastrointestinal Surgery, Affiliated people's Hospital (Fujian Provincial People's Hospital), Fujian University of Traditional Chinese Medicine, Fujian, China.

Abstract

Insights

Colorectal cancer patient survival is linked to specific gene mutations in B-Raf Proto-Oncogene (BRAF), KRAS Proto-Oncogene (KRAS), and Phosphatidylinositol-4,5-Bisphosphate 3-Kinase Catalytic Subunit Alpha (PIK3CA). These mutation patterns, not clinicopathological features, predict patient outcomes.

Area of Science:

  • Oncology
  • Molecular Biology
  • Genetics

Background:

  • Colorectal cancer (CRC) is characterized by aberrant gene expression and signaling pathways.
  • Mutations in B-Raf Proto-Oncogene (BRAF), KRAS Proto-Oncogene (KRAS), and Phosphatidylinositol-4,5-Bisphosphate 3-Kinase Catalytic Subunit Alpha (PIK3CA) are common in CRC.

Purpose of the Study:

  • To investigate the relationship between BRAF, KRAS, and PIK3CA mutations and the clinicopathologic features and prognosis of colorectal cancer patients.

Main Methods:

  • 150 colorectal cancer patients were grouped by BRAF, KRAS, and PIK3CA mutation patterns.
  • Chi-square test analyzed associations with clinicopathological factors.
  • Kaplan-Meier curves and Cox regression assessed survival impact.

Main Results:

  • BRAF, KRAS, and PIK3CA mutations showed no association with age, sex, or alcoholism.
  • Overall survival rate was significantly associated with gene mutation patterns.
  • Patients with KRAS+/PIK3CA-/BRAF- or KRAS-/PIK3CA-/BRAF+ mutations had better prognoses than KRAS+/PIK3CA+/BRAF- patients.

Conclusions:

  • BRAF, KRAS, and PIK3CA mutant patterns are independent of general and clinicopathological features in colorectal cancer.
  • Gene mutation patterns serve as significant prognostic factors for colorectal cancer.

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