Abstract
Background Activation of the ras genes or association with human papillomavirus infection have been extensively studied in colorectal cancer. However, the correlation between K-ras mutations and HPV in colorectal cancer has not been investigated yet. In this study we aimed to investigate the presence of K-ras mutations and their correlation with HPV infection in colon cancer.Methods K-ras mutations were analyzed by a mutagenic PCR assay and digestion with specific restriction enzymes to distinguish the wild-type and mutant codons. HPV infection was analyzed by PCR amplification and hybridization with specific probes by Southern blotting. Stattistical analyses were performed by the chi-square and Fisher's exact testsResults HPV gene fragments were detected in 43 tumors and 17 normal tissue samples. HPV 18 was the prevalent type in the tumor tissue. A mutation at codon 12 of the K-ras gene was present in 31 patients. 56% of the HPV-positive tumors also harbored a K-ras mutation. Codon 13 mutations were not observed. These data indicate that infection with high risk HPV types and mutational activation of the K-ras gene are frequent events in colorectal carcinogenesis.Conclusion Our findings suggest that mutational activation of the K-ras gene is a common event in colon carcinogenesis and that HPV infection may represent an important factor in the development of the premalignant lesions leading to the neoplastic phenotype.
Highlights
Activation of the ras genes or association with human papillomavirus infection have been extensively studied in colorectal cancer
A mutation at codon 12 of the K-ras gene was present in 31 patients. 56% of the human papillomavirus (HPV)-positive tumors harbored a K-ras mutation
Codon 13 mutations were not observed. These data indicate that infection with high risk HPV types and mutational activation of the K-ras gene are frequent events in colorectal carcinogenesis
Summary
Activation of the ras genes or association with human papillomavirus infection have been extensively studied in colorectal cancer. In this study we aimed to investigate the presence of K-ras mutations and their correlation with HPV infection in colon cancer. The ras family of oncogenes (Nras, H-ras and K-ras) encode a small 21-kD protein (p21 ras) involved in the transduction of external stimuli to effector molecules across plasma membranes [2]. This protein has an intrinsic GTPase activity allowing inactivation following signal transduction in the normal cellular environment [2,3]. 90 % of these activating mutations occur in codons 12 and 13 of exon 1 identifying these codons as hot-spot targets [7]
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