生物
基因沉默
甲基化
癌症研究
DNA甲基化
乳腺癌
抑癌基因
癌症
抑制器
基因
发起人
癌变
遗传学
基因表达
作者
Carolina Álvarez,Teresa Tapia,Valeria Cornejo,Wanda Fernández,Alex Muñoz,Mauricio Camus,Manuel Álvarez,Luigi Devoto,Pilar Carvallo
摘要
Abstract Promoter hypermethylation is gaining strength as one of the main mechanisms through which tumor suppressor genes are silenced during tumor progression. Three tumor suppressor genes are frequently found methylated in their promoter, in concordance with absence of expression, RASSF1A , SLIT2 , and WIF1. In addition, a previous array‐CGH analysis from our group showed that these genes are found in deleted genomic regions observed in hereditary breast cancer tumors. In the present work we analyzed the methylation status of these three tumor suppressor gene promoters in 47 hereditary breast cancer tumors. Promoter methylation status analysis of hereditary breast tumors revealed high methylation frequencies for the three genes (67% RASSF1A , 80% SLIT2 , and 72% WIF1 ). Additionally, the presence of methylated PCR products was associated with absence of protein expression for the three genes and statistically significant for RASSF1A and WIF1 . Interestingly, methylation of all the three genes was found in 4 out of 6 grade I invasive ductal carcinoma tumors. Association between RASSF1A methylation and DCIS tumors was found. These results suggest that silencing of these tumor suppressor genes is an early event in hereditary breast cancer, and could be a marker for pre‐malignant phenotypes. © 2012 Wiley Periodicals, Inc.
科研通智能强力驱动
Strongly Powered by AbleSci AI