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Mutation patterns and prognostic analysis of BRAF/KRAS/PIK3CA in colorectal cancer
1Department of Gastrointestinal Surgery, Affiliated people's Hospital (Fujian Provincial People's Hospital), Fujian University of Traditional Chinese Medicine, Fujian, China.
Background And Objective:
Aberrant gene expression and abnormal signaling pathways often occur in patients with colorectal cancer, in which mutations in B-Raf Proto-Oncogene (BRAF), KRAS Proto-Oncogene (KRAS), and Phosphatidylinositol-4,5-Bisphosphate 3-Kinase Catalytic Subunit Alpha (PIK3CA) are quite common. In this study, the relationship between BRAF, KRAS, and PIK3CA mutations and clinicopathologic features and prognosis of colorectal cancer patients was investigated.
Methods:
One hundred and fifty patients with colorectal cancer admitted to Affiliated people's Hospital (Fujian Provincial People's Hospital), Fujian University of Traditional Chinese Medicine were collected and grouped according to the mutation patterns of BRAF, KRAS, and PIK3CA. The association between BRAF, KRAS, and PIK3CA mutations and pathological factors (age, sex, etc.) was analyzed using the Chi-square test. Subsequently, survival analysis was performed to screen the impact factors of overall survival time by Kaplan-Meier (K-M) curve, and Cox regression model was established for the selected factors.
Results:
BRAF, KRAS, and PIK3CA mutations were not associated with age, sex, and alcoholism. K-M curve and log-rank test results demonstrated that among the factors included in this study, overall survival rate of colorectal cancer patients was only associated with mutation factors. The prognosis of KRAS+/PIK3CA-/BRAF-mutant and KRAS-/PIK3CA-/BRAF+mutant patients was better than that of KRAS+/PIK3CA+/BRAF-mutant patients.
Conclusion:
The mutant patterns of BRAF, KRAS, and PIK3CA were not related to the general and clinicopathological features of patients. The mutant pattern could be used as an independent prognostic factor for colorectal cancer.
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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