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MIER3在结直肠癌中的表达及其相关蛋白的生物信息学分析

宋文 彭曼 段世玉 林创 徐琼 周军

南方医科大学学报2017,Vol.37Issue(8):1040-1046,7.
南方医科大学学报2017,Vol.37Issue(8):1040-1046,7.DOI:10.3969/j.issn.1673-4254.2017.08.07

MIER3在结直肠癌中的表达及其相关蛋白的生物信息学分析

Expression of MIER3 in colorectal cancer and bioinformatic analysis of MIER3-interacting proteins

宋文 1彭曼 2段世玉 3林创 1徐琼 1周军3

作者信息

  • 1. 南方医科大学南方医院病理科,广东 广州 510515
  • 2. 南方医科大学放疗科,广东 广州 510515
  • 3. 南方医科大学基础医学院病理学系,广东 广州 510515
  • 折叠

摘要

Abstract

Objective To explore role of MIER3 gene in the development and progression of human colorectal carcinoma (CRC) and analyze the proteins that interact with MIER3 using bioinformatic techniques. Methods MIER3 mRNA and protein expressions were detected in 8 CRC biopsy samples and paired adjacent tissues using real-time PCR and Western blotting. A recombinant eukaryotic expression vector pcDNA3-MIER3 was constructed and its effect on the proliferation and invasion of CRC cells were tested using CCK8 assay and Transwell migration assay. Bioinformatic methods were used to predict and analyze MIER3-interacting proteins. Results MIER3 was obviously down-regulated in the 8 CRC tissues as compared with the paired adjacent tissues. In human CRC cell line DLD1, MIER3 overexpression induced by transfection of the cells with pcDNA3-MIER3 significantly inhibited the cell proliferation and suppressed cell invasiveness in vitro. Bioinformatics analyses indicated that NAT9 was a potential MIER3-interacting protein and MIER3 was probably associated with tumor susceptibility. Conclusion MIER3, which is obviously down-regulated in CRC tissues, is closely associated with the proliferation and invasion of CRC, and NAT9 protein is a probable MIER3-interacting protein.

关键词

MIER3/增殖/侵袭/生物信息学

Key words

MIER3/proliferation/invasion/bioinformatics

引用本文复制引用

宋文,彭曼,段世玉,林创,徐琼,周军..MIER3在结直肠癌中的表达及其相关蛋白的生物信息学分析[J].南方医科大学学报,2017,37(8):1040-1046,7.

基金项目

国家自然科学基金(81272763,81672466) (81272763,81672466)

广东省自然科学基金(2014A030313286) Supported by National Natural Science Foundation of China (81272763, 81672466). (2014A030313286)

南方医科大学学报

OA北大核心CSCDCSTPCDMEDLINE

1673-4254

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