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Clinicopathological Evaluation of KRAS Mutations and Their Relationship with P21 Immunohistochemical Expression in Colorectal Carcinoma
Abstract
Purpose: This study aims to evaluate the clinicopathological significance of KRAS mutations and the immunohistochemical expression of p21 in colorectal carcinoma (CRC), and to explore their correlation with various pathological parameters.
Materials and Methods: A total of 30 metastatic CRC cases diagnosed and/or treated at Ankara Oncology Training and Research Hospital were retrospectively analyzed. KRAS mutation analysis was conducted using pyrosequencing, and p21 expression was evaluated via immunohistochemistry. Associations between KRAS mutation status, p21 expression, and clinicopathological variables including tumor grade, size, invasion depth, and lymph node status were statistically analyzed.
Results: KRAS mutations were identified in 15 (50%) of the cases, with codon 12 mutations being the most frequent. p21 nuclear expression was observed more commonly in KRAS mutant tumors. A significant association was found between p21 expression and pathological tumor invasion depth. No significant correlation was detected between KRAS mutations and tumor localization, grade, or other parameters.
Conclusion: KRAS mutations, particularly at codon 12, are common in CRC and may influence p21 expression. The findings suggest a potential link between KRAS mutation and the molecular regulation of p21, warranting further investigation in larger cohorts.
Keywords
References
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Details
Primary Language
English
Subjects
Pathology, Cancer Genetics, Predictive and Prognostic Markers
Journal Section
Research Article
Early Pub Date
November 7, 2025
Publication Date
October 10, 2025
Submission Date
August 4, 2025
Acceptance Date
October 10, 2025
Published in Issue
Year 2025 Volume: 6 Number: 3
APA
Çelik, B., & Kandemir, O. (2025). Clinicopathological Evaluation of KRAS Mutations and Their Relationship with P21 Immunohistochemical Expression in Colorectal Carcinoma. Experimental and Applied Medical Science, 6(3), 269-278. https://doi.org/10.46871/eams.1757628
AMA
1.Çelik B, Kandemir O. Clinicopathological Evaluation of KRAS Mutations and Their Relationship with P21 Immunohistochemical Expression in Colorectal Carcinoma. Exp Appl Med Sci. 2025;6(3):269-278. doi:10.46871/eams.1757628
Chicago
Çelik, Burçin, and Olcay Kandemir. 2025. “Clinicopathological Evaluation of KRAS Mutations and Their Relationship With P21 Immunohistochemical Expression in Colorectal Carcinoma”. Experimental and Applied Medical Science 6 (3): 269-78. https://doi.org/10.46871/eams.1757628.
EndNote
Çelik B, Kandemir O (October 1, 2025) Clinicopathological Evaluation of KRAS Mutations and Their Relationship with P21 Immunohistochemical Expression in Colorectal Carcinoma. Experimental and Applied Medical Science 6 3 269–278.
IEEE
[1]B. Çelik and O. Kandemir, “Clinicopathological Evaluation of KRAS Mutations and Their Relationship with P21 Immunohistochemical Expression in Colorectal Carcinoma”, Exp Appl Med Sci, vol. 6, no. 3, pp. 269–278, Oct. 2025, doi: 10.46871/eams.1757628.
ISNAD
Çelik, Burçin - Kandemir, Olcay. “Clinicopathological Evaluation of KRAS Mutations and Their Relationship With P21 Immunohistochemical Expression in Colorectal Carcinoma”. Experimental and Applied Medical Science 6/3 (October 1, 2025): 269-278. https://doi.org/10.46871/eams.1757628.
JAMA
1.Çelik B, Kandemir O. Clinicopathological Evaluation of KRAS Mutations and Their Relationship with P21 Immunohistochemical Expression in Colorectal Carcinoma. Exp Appl Med Sci. 2025;6:269–278.
MLA
Çelik, Burçin, and Olcay Kandemir. “Clinicopathological Evaluation of KRAS Mutations and Their Relationship With P21 Immunohistochemical Expression in Colorectal Carcinoma”. Experimental and Applied Medical Science, vol. 6, no. 3, Oct. 2025, pp. 269-78, doi:10.46871/eams.1757628.
Vancouver
1.Burçin Çelik, Olcay Kandemir. Clinicopathological Evaluation of KRAS Mutations and Their Relationship with P21 Immunohistochemical Expression in Colorectal Carcinoma. Exp Appl Med Sci. 2025 Oct. 1;6(3):269-78. doi:10.46871/eams.1757628