J Cancer 2020; 11(8):2222-2233. doi:10.7150/jca.39679 This issue

Research Paper

The Role of MiR-5094 as a Proliferation Suppressor during Cellular Radiation Response via Downregulating STAT5b

Nan Ding1, Junrui Hua1, Jinpeng He1, Dong Lu1, Wenjun Wei1, Yanan Zhang1, Heng Zhou1, Liying Zhang2, Yongqi Liu2, Guangming Zhou3, Jufang Wang1✉

1. Key Laboratory of Space Radiobiology of Gansu Province & Key Laboratory of Heavy Ion Radiation Biology and Medicine of Chinese Academy of Sciences, Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou 730000, China
2. Gansu University of Traditional Chinese Medicine, Lanzhou 730000, China
3. Medical College of Soochow University, Suzhou 215123, China

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Ding N, Hua J, He J, Lu D, Wei W, Zhang Y, Zhou H, Zhang L, Liu Y, Zhou G, Wang J. The Role of MiR-5094 as a Proliferation Suppressor during Cellular Radiation Response via Downregulating STAT5b. J Cancer 2020; 11(8):2222-2233. doi:10.7150/jca.39679. Available from https://www.jcancer.org/v11p2222.htm

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MicroRNAs (miRNAs) play important roles in the regulation of cellular stress responses. We previously uncovered 10 novel human miRNAs which are induced by X-ray irradiation in HeLa cells using Solexa deep sequencing. The most highly expressed new miRNA, miR-5094, was predicted to target STAT5b. This study wonders whether miR-5094 participates in cellular radiation response via STAT5b. Firstly, direct interaction between miRNA-5094 and the STAT5b 3'-UTR was confirmed by luciferase reporter assay. Then, the radiation responsive expression of miR-5094 and STAT5b were measured in HeLa and Jurkat cells, and the expressions of down-stream genes of STAT5b after ionizing radiation (IR) were detected in HeLa cells. At last, the effects of miR-5094 on survival fraction, cell proliferation, cell cycle arrest and apoptosis induced by IR were investigated in HeLa cells, Jurkat cells and human peripheral blood T cells. It was found that up-regulation of miR-5094 by radiation induction or miRNA mimic transfection suppressed expression of STAT5b, and consequently decreased the transcription of down-stream Igf-1 and Bcl-2. Additionally, over expression of miR-5094 resulted in proliferation suppression and knockdown of miR-5094 by miRNA inhibitor after irradiation partially reversed the proliferation suppression induced by miR-5094 in HeLa cells, Jurkat cells and CD4+ T cells. Collectively, our findings demonstrate that up-regulation of miR-5094 down-regulated the expression of STAT5b, thereby suppressing cell proliferation after X-ray irradiation.

Keywords: microRNA, radiation, miR-5094, STAT5b, proliferation