Promoter hypermethylation of tumor-related genes in peritoneal lavage and the prognosis of patients with colorectal cancer
Autor: | Fumio Konishi, Yutaka J. Kawamura, Osamu Takata, Koichi Suzuki, Hidenori Kamiyama, Hiroshi Noda |
---|---|
Rok vydání: | 2009 |
Předmět: |
Adult
Male Colorectal cancer Polymerase Chain Reaction CDH1 law.invention CDKN2A law Humans Medicine Promoter Regions Genetic Therapeutic Irrigation Polymerase chain reaction Aged Aged 80 and over biology business.industry Peritoneal fluid General Medicine Methylation DNA Methylation Middle Aged Prognosis medicine.disease digestive system diseases Oncology Cancer cell DNA methylation biology.protein Cancer research Female Surgery Peritoneum Colorectal Neoplasms business |
Zdroj: | Journal of Surgical Oncology. 100:69-74 |
ISSN: | 1096-9098 0022-4790 |
DOI: | 10.1002/jso.21291 |
Popis: | Background and Objectives The predictive value of free cancer cells in the peritoneal fluid of patients with colorectal cancer (CRC) remain to be elucidated. The aim of this study was to determine the prognostic relevance of the methylation of tumor-related genes detected in the peritoneal lavage fluid (PLF) of patients undergoing a resection for CRC. Methods The promoter methylation pattern of four target genes, CDH1, CDKN2A (p16), MGMT, and APC, was examined in 51 primary CRC and corresponding matched PLF DNA. The relative methylation levels of these genes in primary CRC tissue and paired PLF were assessed by quantitative methylation-specific polymerase chain reaction (QMSP). Results An aberrant methylation of at least one gene was found in 45 of 51 (88%) primary tumors. In matched PLF specimens, the frequencies of aberrant promoter methylation detected for each marker were 16% for CDH1, 2% for p16, 4% for MGMT and 24% for APC. Patients with PLF demonstrating the methylation of more than one of these four target genes demonstrated significantly shorter relapse-free survival. Conclusions These findings suggest that disseminated tumor cells in PLF detected by QMSP may correlate with the postoperative clinical course of patients undergoing curative surgery for CRC. J. Surg. Oncol. 2009;100:69–74. © 2009 Wiley-Liss, Inc. |
Databáze: | OpenAIRE |
Externí odkaz: |