Hypoxia-induced microRNA-10b-3p promotes esophageal squamous cell carcinoma growth and metastasis by targeting TSGA10
Author(s) -
Qiang Zhang,
Jingjing Zhang,
Zhanzhao Fu,
Lixin Dong,
Yong Tang,
Chunlei Xu,
Haifeng Wang,
Tao Zhang,
Yue Wu,
Chao Dong,
Shasha Shao,
Guangxia Wang
Publication year - 2019
Publication title -
aging
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.473
H-Index - 90
ISSN - 1945-4589
DOI - 10.18632/aging.102462
Subject(s) - microrna , hypoxia (environmental) , metastasis , cancer research , cell growth , biology , cell , in vivo , esophageal cancer , esophageal squamous cell carcinoma , carcinoma , cancer , medicine , gene , chemistry , genetics , organic chemistry , oxygen , biochemistry , microbiology and biotechnology
Evidence has shown that hypoxia promotes esophageal squamous cell carcinoma (ESCC) growth and metastasis, but the molecular mechanisms underlying that response remain poorly understood. MicroRNAs (miRNAs) are post-transcriptional regulators that participate in various cancer-related processes. Here, we demonstrated that hypoxia along with hypoxia-inducible factor 1α significantly increased expression of miR-10b-3p. Inhibition of miR-10b-3p weakened the effects of hypoxia on ESCC cell proliferation, migration and invasion, while miR-10b-3p overexpression had the opposite effects. Mechanistically, miR-10b-3p acted as cancer-promoting gene by targeting testis specific 10. Using a xenograft model, we observed that administration of miR-10b-3p agomir to tumors enhanced their growth and metastasis in vivo. These findings verified the potent regulatory role played by hypoxia-induced miR-10b-3p expression in ESCC progression. These results suggest that miR-10b-3p may be a useful therapeutic target for treating ESCC.
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