Related Experiment Video
Updated: Oct 8, 2025

Complete Laparoscopic Radical Resection of Perihilar Cholangiocarcinoma Type IIIb
Published on: January 17, 2025
The Role of K-Ras and P53 in Biliary Tract Carcinoma
Saara Ahmad1, Bisma Badr2, Asra Khan3
1Department of Biological and Biomedical Sciences, The Aga Khan University, Karachi.
Objective:
To focus mainly on the role of proto-oncogene Ki-ras2 Kirsten rat sarcoma viral oncogene homolog (K-Ras) and tumour-suppressor gene p53 which are among the most commonly mutated genes in biliary tract carcinomas.
Methods:
The systematic review comprised research articles published between 2002 and 2019 on PubMed and Google Scholar databases which were searched using the terms 'TP53', 'K-Ras', 'mutation', 'biliary tract carcinoma', 'cholangiocarcinoma', and 'murine model'. Repetitions, duplicates and irrelevant articles were excluded. No data was retrieved from posters, presentations and symposiums, and experiments involving bile aspirations were also excluded.
Results:
Of the 72 articles reviewed, 11(15.3%) were included. Of them, 3(27.3%) studies, conducted in China, Japan and Taiwan, reported a positive correlation between K-Ras mutation and biliary tract carcinoma. Only 1(9%) study, conducted in China, showed the sole correlation between p53 inactivation and biliary tract carcinoma. Also, 4(36.4%) studies, conducted in China, Japan and Europe, showed a positive association of both K-Ras mutation and p53 inactivation with biliary tract carcinoma.
Conclusions:
K-Ras and p53 mutation both contribute to biliary tract carcinoma. K-Ras mutation, however, has a much higher frequency compared to p53 inactivation in such cancers.
Insights
K-Ras and p53 mutations are common in biliary tract carcinomas. K-Ras mutations occur more frequently than p53 inactivation in these cancers.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Biliary tract carcinomas (BTCs) are aggressive cancers with limited treatment options.
- Proto-oncogene K-Ras (Kirsten rat sarcoma viral oncogene homolog) and tumor suppressor gene p53 are frequently mutated in various cancers.
- Understanding the specific roles of K-Ras and p53 mutations in BTC pathogenesis is crucial for developing targeted therapies.
Approach:
- A systematic review of research articles published between 2002 and 2019 was conducted.
- PubMed and Google Scholar databases were searched using keywords related to K-Ras, p53, mutation, and biliary tract carcinoma.
- Articles were screened for relevance, excluding duplicates, irrelevant studies, posters, presentations, symposiums, and experiments involving bile aspirations.
Key Points:
- Out of 72 reviewed articles, 11 met the inclusion criteria for this systematic review.
- Three studies reported a positive correlation between K-Ras mutations and BTC.
- One study indicated a correlation between p53 inactivation and BTC, while four studies associated both K-Ras mutations and p53 inactivation with BTC.
Conclusions:
- Both K-Ras mutations and p53 inactivation play a role in the development of biliary tract carcinomas.
- K-Ras mutations are observed with a significantly higher frequency compared to p53 inactivation in BTC.
- Further research into the specific mechanisms and therapeutic targeting of these mutations in BTC is warranted.
More Related Videos
28:15Deficient Pms2, ERCC1, Ku86, CcOI in Field Defects During Progression to Colon Cancer
Published on: July 28, 2010
06:51Utilizing 18F-FDG PET/CT Imaging and Quantitative Histology to Measure Dynamic Changes in the Glucose Metabolism in Mouse Models of Lung Cancer
Published on: July 21, 2018
Related Concept Videos
The Ras Gene
Ras is a...
Abnormal Proliferation
The Retinoblastoma Gene
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
Negative Regulator Molecules
DNA Damage can Stall the Cell Cycle
Tumor Progression
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...