4.5 Article

miR-135a-5p inhibits tumor invasion by targeting ANGPT2 in gallbladder cancer

期刊

MOLECULAR MEDICINE REPORTS
卷 24, 期 1, 页码 -

出版社

SPANDIDOS PUBL LTD
DOI: 10.3892/mmr.2021.12167

关键词

gallbladder cancer; microRNA-135a-5p; angiopoietin-2

资金

  1. Health Science and Technology Project of Shanghai Pudong New Area Health Commission [PW2020A-33]
  2. Pudong New Area Key Specialty of Thyroid [PWZzk2017-21]
  3. 'Postgraduate Innovation Training Special Project' of Shanghai University of Traditional Chinese Medicine [Y2021023]

向作者/读者索取更多资源

The study found that miR-135a-5p plays a regulatory role in GBC by targeting ANGPT2, inhibiting cell proliferation and invasion. It suggests miR-135a-5p could be a potential biomarker for GBC progression and a target for therapeutic intervention in GBC.
Gallbladder cancer (GBC) is the most aggressive cancer type in the biliary tract, and our previous studies observed that microRNA (miR)-135a-5p expression was downregulated in GBC tissues. However, few studies have focused on the mechanism of action of the miR-135a-5p target genes in GBC. The present study aimed to investigate the regulatory role of miR-135a-5p signaling in GBC. The present study found that miR-135a-5p expression was downregulated in GBC tissue, as detected by immunohistochemistry and reverse transcription-quantitative PCR. In addition, overexpression of miR-135a-5p significantly inhibited the proliferation and migration of GBC-SD cells. Using a luciferase activity assay, it was identified that angiopoietin-2 (ANGPT2) was a potential target gene of miR-135a-5p in GBC. Knockdown of ANGPT2 expression significantly inhibited the proliferation and invasion of GBC-SD cells. In conclusion, the present results suggested that miR-135a-5p affected GBC cell proliferation and invasion by targeting ANGPT2. Moreover, miR-135a-5p may be a potential biomarker for GBC progression and a potential target for GBC therapeutic intervention.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据