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MiR-145 functions as a tumor suppressor by directly targeting histone deacetylase 2 in liver cancer
Authors:Ji Heon Noh  Young Gyoon Chang  Min Gyu Kim  Kwang Hwa Jung  Jeong Kyu Kim  Hyun Jin Bae  Jung Woo Eun  Qingyu Shen  Seung-Jin Kim  So Hee Kwon  Won Sang Park  Jung Young Lee  Suk Woo Nam
Affiliation:1. Lab of Oncogenomics, Department of Pathology, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea;2. Functional RNomics Research Center, The Catholic University of Korea, Seoul, Republic of Korea;3. College of Pharmacy, Yonsei Institute of Pharmaceutical Science, Yonsei University, Incheon 406-840, Republic of Korea
Abstract:
Aberrant regulation of histone deacetylase 2 (HDAC2) plays a pivotal role in the development of hepatocellular carcinoma (HCC), but, the underlying mechanism leading to HDAC2 overexpression is not well understood. We performed microRNA (miRNA) profiling analysis in a subset of HCCs, and identified four down-regulated miRNAs that may target HDAC2 in HCC. Ectopic expression of miRNA mimics evidenced that miR-145 suppresses HDAC2 expression in HCC cells. This treatment repressed cancer cell growth and recapitulated HDAC2 knockdown effects on HCC cells. In conclusion, we suggest that loss or suppression of miR-145 may cause aberrant overexpression of HDAC2 and promote HCC tumorigenesis.
Keywords:MiR-145   HDAC2   Tumor suppressor   Liver cancer
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