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首页|期刊导航|癌变·畸变·突变|SOX30基因调控桥粒基因DSC3抑制肺腺癌的增殖与迁移

SOX30基因调控桥粒基因DSC3抑制肺腺癌的增殖与迁移

马帮靖 郝翔麟 韩飞 陈洪强 刘晋祎 曹佳 张爱华

癌变·畸变·突变2018,Vol.30Issue(3):165-170,175,7.
癌变·畸变·突变2018,Vol.30Issue(3):165-170,175,7.DOI:10.3969/j.issn.1004-616x.2018.03.001

SOX30基因调控桥粒基因DSC3抑制肺腺癌的增殖与迁移

Inhibition of proliferation and migration of lung adenocarcinoma cells by SOX30 gene via regulation of DSC3 gene

马帮靖 1郝翔麟 2韩飞 2陈洪强 2刘晋祎 2曹佳 2张爱华1

作者信息

  • 1. 贵州医科大学公共卫生学院毒理教研室,贵州贵阳550004
  • 2. 陆军军医大学军事预防医学系毒理学研究所,重庆400038
  • 折叠

摘要

Abstract

OBJECTIVE:To investigate interactions between SOX30 and DSC3 genes and their roles in the development of lung adenocarcinoma.METHODS:The GO enrichment analysis was used to screen possible downstream genes and pathways of SOX30 transcriptional regulation.The JASPAR database was used to predict the SOX30 transcription binding sites in the promoter region of DSC3.Expression data of SOX30 and DSC3 were downloaded from the TCGA database,and their relationships were evaluated using the Spearman rank correlation analysis.The reverse transcription-PCR was used to measure the mRNA levels of DSC3 in A549-SOX30+DSC3 miRNA stably transfected cells and the lung tissues of SOX30+/+,SOX30+/-and SOX30-/-mice.The colony formation and wound healing assays were used to confirm whether the inhibition of the proliferation and migration of SOX30 in A549 cells depended on the expression of DSC3 or not.RESULTS:The GO enrichment analysis shows the function of SOX30 gene was significantly related to the cell junction proteins,such as focal adhesion,anchoring junction,and adhesion junction.And several SOX30 binding sites were found in the promoter region of DSC3.Furthermore,expression of DSC3 was in positive correlation with that of SOX30 in human lung adenocarcinoma(r=0.154,P=0.000).In addition,the ectopic expression of SOX30 in A549 cell lines dramatically increased DSC3 mRNA level (P<0.05),and knockout of SOX30 significantly decreased DSC3 mRNA level in lung tissues of SOX30-/-mice (P<0.05).In addition,knockdown of DSC3 attenuated the inhibition effects of SOX30 on proliferation and migration in A549 cells (P<0.05).CONCLUSION:SOX30 was a critical transcription factor in the expression regulation of DSC3,and DSC3 was an important downstream gene of SOX30.Therefore,SOX30-DSC3 may play an important role in the development of lung adenocarcinoma.

关键词

SOX30/DSC3/肺癌/调控/增殖/迁移

Key words

SOX30/DCS3/lung cancer/regulation/proliferation/migration

分类

医药卫生

引用本文复制引用

马帮靖,郝翔麟,韩飞,陈洪强,刘晋祎,曹佳,张爱华..SOX30基因调控桥粒基因DSC3抑制肺腺癌的增殖与迁移[J].癌变·畸变·突变,2018,30(3):165-170,175,7.

基金项目

国家自然科学基金(81773461) (81773461)

癌变·畸变·突变

OACSTPCD

1004-616X

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