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Erschienen in: Tumor Biology 2/2016

07.09.2015 | Original Article

MiR-378 suppresses prostate cancer cell growth through downregulation of MAPK1 in vitro and in vivo

verfasst von: Qi-guang Chen, Wei Zhou, Tao Han, Shu-qi Du, Zhen-hua Li, Zhe Zhang, Guang-yi Shan, Chui-ze Kong

Erschienen in: Tumor Biology | Ausgabe 2/2016

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Abstract

Prostate cancer is one of the biggest health problems for the aging male. To the present, the roles of dysregulated microRNAs in prostate cancer are still unclear. Here, we evaluated the anti-proliferative role of miR-378 in prostate cancer. And, we found that the expression of miR-378 was significantly downregulated in clinical prostate cancer tissues. In vitro assay suggested that overexpression of miR-378-suppressed prostate cancer cell migration and invasion promoted cell apoptosis. Furthermore, we identified and validated MAPK1 as a direct target of miR-378. Ectopic expression of MAPK1 rescues miR-378-suppressed cell migration and invasion. In vivo assay demonstrated that the stably miR-378-overexpressed prostate cancer cells displayed a significantly reduction in tumor growth. Taken together, our data suggested that miR-378 may act as a potential therapeutic target against human prostate cancer.
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Metadaten
Titel
MiR-378 suppresses prostate cancer cell growth through downregulation of MAPK1 in vitro and in vivo
verfasst von
Qi-guang Chen
Wei Zhou
Tao Han
Shu-qi Du
Zhen-hua Li
Zhe Zhang
Guang-yi Shan
Chui-ze Kong
Publikationsdatum
07.09.2015
Verlag
Springer Netherlands
Erschienen in
Tumor Biology / Ausgabe 2/2016
Print ISSN: 1010-4283
Elektronische ISSN: 1423-0380
DOI
https://doi.org/10.1007/s13277-015-3996-8

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