Unknown

Dataset Information

0

KCNMA1 cooperating with PTK2 is a novel tumor suppressor in gastric cancer and is associated with disease outcome.


ABSTRACT: Inactivation of tumor suppressor genes by promoter hypermethylation plays a key role in the tumorgenesis. It is necessary to uncover the detailed pattern of whole genome-wide abnormal DNA methylation during the development of gastric cancer (GC).We performed a genome-wide methylation detection using 12 paired of GC tissues and their corresponding normal tissues. Methylation-specific PCR (MSP) and bisulphite sequencing (BSP) were used to measure methylation status of specific CpG site. Based on the bioinformatic analysis, the cell phenotypes and mouse model experiments were constructed to detect effect of the target gene. Using the Kaplan-Meier survival curve, the clinical value of KCNMA1 was assessed in GC patients.The CpG site cg24113782 located at the promoter of KCNMA1 showed the most significant difference, contributing to the commonly silenced KCNMA1in gastric cancer cells and primary GC tissues. The promoter methylation of KCNMA1 was detected in 68.7% (77/112) of tumor tissues, compared with 16.2% (18/112) of normal tissues (P?

SUBMITTER: Ma G 

PROVIDER: S-EPMC5324255 | biostudies-literature | 2017 Feb

REPOSITORIES: biostudies-literature

altmetric image

Publications

KCNMA1 cooperating with PTK2 is a novel tumor suppressor in gastric cancer and is associated with disease outcome.

Ma Gaoxiang G   Liu Hanting H   Hua Qiuhan Q   Wang Meilin M   Du Mulong M   Lin Yadi Y   Ge Yuqiu Y   Gong Weida W   Zhao Qinghong Q   Qiang Fulin F   Tao Guoquan G   Zhang Zhengdong Z   Chu Haiyan H  

Molecular cancer 20170223 1


<h4>Background</h4>Inactivation of tumor suppressor genes by promoter hypermethylation plays a key role in the tumorgenesis. It is necessary to uncover the detailed pattern of whole genome-wide abnormal DNA methylation during the development of gastric cancer (GC).<h4>Method</h4>We performed a genome-wide methylation detection using 12 paired of GC tissues and their corresponding normal tissues. Methylation-specific PCR (MSP) and bisulphite sequencing (BSP) were used to measure methylation statu  ...[more]

Similar Datasets

| S-EPMC5036270 | biostudies-literature
| S-EPMC5540202 | biostudies-literature
| S-EPMC3361457 | biostudies-literature
| S-EPMC3024718 | biostudies-literature
| S-EPMC5409503 | biostudies-literature
| S-EPMC3723650 | biostudies-literature
| S-EPMC3766408 | biostudies-literature
| S-EPMC3775783 | biostudies-literature
| S-EPMC5514911 | biostudies-literature
| S-EPMC8183929 | biostudies-literature