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Published on: March 1, 2024
KRAS and BRAF mutations in prostate carcinomas of Chinese patients
Yanying Shen1, Yachao Lu, Xiaolu Yin
1Department of Pathology, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, 200127, China.
Abstract:
Aberrance in the RAS/RAF/MEK/MAPK pathway is reportedly important in many tumor types, including prostate carcinoma. Continuous activation of the pathway can be caused by mutations of upstream targets such as KRAS and BRAF. However, rates of KRAS and BRAF mutations in prostate carcinoma are reported to vary in different populations. To date, there has been no such report in Chinese patients. In this study, we examined 121 samples of prostate carcinoma in Chinese subjects for mutations at codons 12 and 13 of KRAS and codon 600 of BRAF by means of the mutant-enriched polymerase chain reaction-coupled sequencing method. The identified KRAS and BRAF mutations were analyzed for association with tumor differentiation and clinical stage. The result showed that KRAS mutations were detected in 9.1% (11 of 121) of prostate carcinomas, while no BRAF mutation was found in any case studied. No association was found between KRAS mutation and clinicopathological characteristics of the tumors. Our study suggests that mutations of KRAS, not BRAF, may play a role in the pathogenesis of prostate carcinoma in Chinese patients.
Insights
RAS/RAF/MEK/MAPK pathway mutations, specifically KRAS, are implicated in prostate cancer. This study found KRAS mutations in 9.1% of Chinese prostate carcinoma patients, but no BRAF mutations, suggesting KRAS
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- The RAS/RAF/MEK/MAPK pathway is crucial in various cancers, including prostate carcinoma.
- Mutations in KRAS and BRAF can lead to pathway overactivation, but their prevalence varies geographically.
- Previous studies have not reported on KRAS and BRAF mutation status in Chinese prostate carcinoma patients.
Purpose of the Study:
- To investigate the frequency of KRAS and BRAF mutations in Chinese prostate carcinoma patients.
- To analyze the association between identified mutations and clinicopathological features.
- To determine the role of KRAS and BRAF mutations in the pathogenesis of prostate cancer in this population.
Main Methods:
- Analysis of 121 prostate carcinoma samples from Chinese subjects.
- Utilized mutant-enriched polymerase chain reaction-coupled sequencing.
- Targeted sequencing of KRAS codons 12 and 13, and BRAF codon 600.
Main Results:
- KRAS mutations were identified in 9.1% (11/121) of the prostate carcinoma samples.
- No BRAF mutations were detected in any of the studied cases.
- No significant association was found between KRAS mutations and tumor differentiation or clinical stage.
Conclusions:
- KRAS mutations, but not BRAF mutations, appear to be involved in the development of prostate carcinoma in the Chinese population.
- These findings contribute to understanding the molecular landscape of prostate cancer in specific ethnic groups.
- Further research may explore therapeutic strategies targeting the RAS/RAF/MEK/MAPK pathway in Chinese prostate cancer patients.
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