Suppr超能文献

[MIER3在结直肠癌中的表达及MIER3相互作用蛋白的生物信息学分析]

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

作者信息

Song Wen, Peng Man, Duan Shi-Yu, Lin Chuang, Xu Qiong, Zhou Jun

机构信息

Department of Pathology, Nanfang Hospital1, Department of Radiotherapy, Nanfang Hospital2, Department of Pathology, School of Basic Medical Sciences3, Southern Medical University, Guangzhou 510515, China. E-mail:

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2017 Aug 20;37(8):1040-1046. doi: 10.3969/j.issn.1673-4254.2017.08.07.

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.

摘要

目的

探讨MIER3基因在人类结直肠癌(CRC)发生发展及进程中的作用,并运用生物信息学技术分析与MIER3相互作用的蛋白质。

方法

采用实时定量PCR和蛋白质免疫印迹法检测8例CRC活检样本及其配对的癌旁组织中MIER3 mRNA和蛋白质的表达。构建重组真核表达载体pcDNA3-MIER3,运用CCK8法和Transwell迁移实验检测其对CRC细胞增殖和侵袭的影响。采用生物信息学方法预测和分析与MIER3相互作用的蛋白质。

结果

与配对的癌旁组织相比,8例CRC组织中MIER3明显下调。在人CRC细胞系DLD1中,用pcDNA3-MIER3转染细胞诱导MIER3过表达,显著抑制细胞增殖并在体外抑制细胞侵袭性。生物信息学分析表明NAT9是一种潜在的与MIER3相互作用的蛋白质,且MIER3可能与肿瘤易感性相关。

结论

MIER3在CRC组织中明显下调,与CRC的增殖和侵袭密切相关,NAT9蛋白可能是与MIER3相互作用的蛋白质。

相似文献

本文引用的文献

2
Differential HDAC1 and 2 Recruitment by Members of the MIER Family.MIER家族成员对HDAC1和HDAC2的差异性招募
PLoS One. 2017 Jan 3;12(1):e0169338. doi: 10.1371/journal.pone.0169338. eCollection 2017.
5
RAS and BRAF in metastatic colorectal cancer management.RAS和BRAF在转移性结直肠癌治疗中的作用
J Gastrointest Oncol. 2016 Oct;7(5):687-704. doi: 10.21037/jgo.2016.06.12.
8
Cancer statistics in China, 2015.《中国癌症统计数据 2015》
CA Cancer J Clin. 2016 Mar-Apr;66(2):115-32. doi: 10.3322/caac.21338. Epub 2016 Jan 25.
10
Towards an understanding of the structure and function of MTA1.迈向对MTA1结构与功能的理解
Cancer Metastasis Rev. 2014 Dec;33(4):857-67. doi: 10.1007/s10555-014-9513-5.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验