4.3 Article

miR-93/miR-106b/miR-375-CIC-CRABP1: a novel regulatory axis in prostate cancer progression

期刊

ONCOTARGET
卷 6, 期 27, 页码 23533-23547

出版社

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.4372

关键词

prostate cancer; capicua; ETV5; CRABP1; microRNA

资金

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Korean Ministry of Science, ICT and Future Planning [NRF-2012R1A1A1005631, NRF-2015R1A1A1A05001401, NRF-2013R1A1A2063089]
  2. POSTECH Basic Science Research Institute [4.0010906.01]
  3. TJ Park Science Fellowship of POSCO TJ Park Foundation
  4. BK21 Plus Program (Program of Bio-Molecular Function, POSTECH)

向作者/读者索取更多资源

Capicua (CIC) has been implicated in pathogenesis of spinocerebellar ataxia type-1 (SCA1) neurodegenerative disease and some types of cancer; however, the role of CIC in prostate cancer remains unknown. Here we show that CIC suppresses prostate cancer progression. CIC expression was markedly decreased in human prostatic carcinoma. CIC overexpression suppressed prostate cancer cell proliferation, invasion, and migration, whereas CIC RNAi exerted opposite effects. We found that knock-down of CIC derepresses expression of ETV5 and CRABP1 in LNCaP and PC-3 cells, respectively, thereby promoting cell proliferation and invasion. We also discovered that miR-93, miR-106b, and miR-375, which are known to be frequently overexpressed in prostate cancer patients, cooperatively down-regulate CIC levels to promote cancer progression. Altogether, we suggest miR-93/miR-106b/miR-375-CIC-CRABP1 as a novel key regulatory axis in prostate cancer progression.

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