4.5 Article

MicroRNA-328 directly targets p21-activated protein kinase 6 inhibiting prostate cancer proliferation and enhancing docetaxel sensitivity

期刊

MOLECULAR MEDICINE REPORTS
卷 12, 期 5, 页码 7389-7395

出版社

SPANDIDOS PUBL LTD
DOI: 10.3892/mmr.2015.4390

关键词

castration-resistant prostate cancer; proliferation; p21-activated protein kinase 6; microRNA-328; docetaxel

资金

  1. National Natural Science Foundation of China [81370849, 81300472, 81202034]
  2. Natural Science Foundation of Jiangsu Province [BL2013032, BK2012336]
  3. Nanjing City [201201053]
  4. Southeast University [3290002402]
  5. Science Foundation of Ministry of Education of China [20120092120071]
  6. Fundamental Research Funds for the Central Universities
  7. Scientific Research Innovation Project of University in Jiangsu Province [KYLX_0203]

向作者/读者索取更多资源

Prostate cancer (Pca) has one of the highest mortality rates for malignant cancers worldwide. Previous research has demonstrated that numerous genes are aberrantly expressed during Pea onset and development, p21-activated protein kinase 6 (PAK6) is known to be overexpressed in primary and metastatic Pea, however the mechanism of this aberrant expression remains unknown. In the present study, immunohistochemistry demonstrated that PAK6 is overexpressed in castration-resistant Pea (CRPC). Furthermore, PAK6 overexpression was regulated by microRNA (miR)-328. Luciferase reporter assay and western blot analysis indicated that PAK6 was directly targeted by miR-328. Forced expression of miR-328 enhanced docetaxel sensitivity, inhibited cell proliferation and promoted cell apoptosis without affecting the cell cycle. This indicates that miR-328 performs important functions in CRPC progression via PAK6 regulation. This mechanism may be used to enhance the effect of docetaxel.

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