Unknown

Dataset Information

0

Recent progress in the study of methylated tumor suppressor genes in gastric cancer.


ABSTRACT: Gastric cancer is one of the most common malignancies and a leading cause of cancer mortality worldwide. The pathogenesis mechanisms of gastric cancer are still not fully clear. Inactivation of tumor suppressor genes and activation of oncogenes caused by genetic and epigenetic alterations are known to play significant roles in carcinogenesis. Accumulating evidence has shown that epigenetic silencing of the tumor suppressor genes, particularly caused by hypermethylation of CpG islands in promoters, is critical to carcinogenesis and metastasis. Here, we review the recent progress in the study of methylations of tumor suppressor genes involved in the pathogenesis of gastric cancer. We also briefly describe the mechanisms that induce tumor suppressor gene methylation and the status of translating these molecular mechanisms into clinical applications.

SUBMITTER: Hu XT 

PROVIDER: S-EPMC3845584 | biostudies-literature | 2013 Jan

REPOSITORIES: biostudies-literature

altmetric image

Publications

Recent progress in the study of methylated tumor suppressor genes in gastric cancer.

Hu Xiao-Tong XT   He Chao C  

Chinese journal of cancer 20111104 1


Gastric cancer is one of the most common malignancies and a leading cause of cancer mortality worldwide. The pathogenesis mechanisms of gastric cancer are still not fully clear. Inactivation of tumor suppressor genes and activation of oncogenes caused by genetic and epigenetic alterations are known to play significant roles in carcinogenesis. Accumulating evidence has shown that epigenetic silencing of the tumor suppressor genes, particularly caused by hypermethylation of CpG islands in promoter  ...[more]

Similar Datasets

| S-EPMC2955155 | biostudies-literature
| S-EPMC2914707 | biostudies-literature
| S-EPMC8183929 | biostudies-literature
| S-EPMC8207056 | biostudies-literature
| S-EPMC3769458 | biostudies-literature
| S-EPMC3824540 | biostudies-other
| S-EPMC4041902 | biostudies-other
| S-EPMC6411624 | biostudies-literature