Influence of methylated p15 INK4b and p16 INK4a genes on clinicopathological features in colorectal cancer
Autor: | Mutsuo Sasaki, Gen Yoshiya, Atsushi Ishiguro, Takenori Takahata, Akihiro Munakata, Masato Saito, Yoshihiro Tamura |
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Rok vydání: | 2006 |
Předmět: | |
Zdroj: | Journal of Gastroenterology and Hepatology. 21:1334-1339 |
ISSN: | 1440-1746 0815-9319 |
DOI: | 10.1111/j.1440-1746.2006.04137.x |
Popis: | Background and Aim: Genetic silencing by promoter methylation has attracted attention in the carcinogenesis of colorectal cancer. Methylation of the p16 INK4a gene has been found in primary colorectal cancer. Although the p15 INK4b gene displays high homology to the p16 INK4a gene in the amino acid sequence, methylation of p15 INK4b has not been fully studied. We investigated p15 INK4b methylation status in patients with colorectal cancer to verify the association between the methylation of p15 INK4b and clinicopathological features compared with p16 INK4a . Methods: DNA samples from the tissues of primary colorectal cancer and corresponding adjacent normal colon mucosa were obtained from surgical resections of 88 patients (47 males and 41 females, aged 29-83 years). Methylation-specific polymerase chain reaction was used to analyze p15 INK4b and p16 INK4a methylation status after bisulfite modification. Cumulative survival rates (mean follow-up period: 53.2 months) were calculated by the Kaplan-Meier analysis. Results: Methylations of p15 INK4b and p16 INK4a genes were detected in 23 (26.1%) and 20 (22.7%) colorectal cancers, respectively. Methylation of p15 INK4b was not associated with any clinicopathological features. Compared with normal mucosa, the methylation of p15 INK4b was more prominent in tumor tissue (P < 0.001). Reverse transcription-polymerase chain reaction (RT-PCR) revealed that p15 INK4b methylaton decreased mRNA expression. Kaplan-Meier analysis showed that patients with stage I-II had a significant difference in survival rate between those with and without methylated p15 INK4b (P = 0.018). Conclusions: Our results suggest that methylation of the p15 INK4b gene contributes to the process of carcinogenesis in colorectal cancer as well as p16 INK4a and is useful as a prognostic factor in the early stage. |
Databáze: | OpenAIRE |
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