PMID- 28346809 OWN - NLM STAT- MEDLINE DCOM- 20170619 LR - 20220408 IS - 1551-4005 (Electronic) IS - 1538-4101 (Print) IS - 1551-4005 (Linking) VI - 16 IP - 6 DP - 2017 Mar 19 TI - MALAT1 promotes osteosarcoma development by regulation of HMGB1 via miR-142-3p and miR-129-5p. PG - 578-587 LID - 10.1080/15384101.2017.1288324 [doi] AB - Recently, emerging evidence has demonstrated that metastasis-associated lung adenocarcinoma transcript 1 (MALAT1), a long non-coding RNAs (lncRNAs), contributes to the initiation and development of tumors, including osteosarcoma (OS). Multiple studies have suggested an oncogenic role of MALAT1 and high-mobility group protein B1 (HMGB1) in OS tumorigenesis and metastasis, but the effects and mechanisms are not unanimous. Here, we showed that MALAT1 and HMGB1 were significantly increased in human OS cell lines and knockdown of MALAT1 reduced HMGB1 expression. By using online tools, we screen out 2 candidate miRNAs, miR-142-3p and miR-129-5p which may be associated with both MALAT1 and HMGB1. Luciferase reporter assay revealed a direct interaction between the 2 miRNAs and MALAT1, respectively, via a putative binding site within MALAT1. Meanwhile, both the 2 miRNAs could bind to HMGB1 3'-untranslated region (3'-UTR) and regulate HMGB1 expression. Moreover, knockdown of MALAT1 decreased HMGB1 expression, inhibited OS cell growth and promoted apoptosis, while miR-142-3p and miR-129-5p inhibitor partly restored the inhibitory effect of MALAT1 knockdown on HMGB1 expression, OS cell growth and the promotion of apoptosis. In OS tissues, the expression of MALAT1 and HMGB1 was upregulated while the expression of miR-142-3p and miR-129-5p was downregulated. Together, our results support a MALAT1/miR-142-3p/miR-129-5p/HMGB1 axis in OS cell proliferation and tumor progression. MALAT1 promoted OS cell growth through inhibition of miR-142-3p or miR-129-5p and by targeting HMGB1. FAU - Liu, Ke AU - Liu K AD - a Department of Ophthalmology , The Second Xiangya Hospital, Central South University , Changsha , Hunan , P.R. China. FAU - Huang, Jun AU - Huang J AD - b Department of Orthopaedics , The Second Xiangya Hospital, Central South University , Changsha , Hunan , P.R. China. FAU - Ni, Jiangdong AU - Ni J AD - b Department of Orthopaedics , The Second Xiangya Hospital, Central South University , Changsha , Hunan , P.R. China. FAU - Song, Deye AU - Song D AD - b Department of Orthopaedics , The Second Xiangya Hospital, Central South University , Changsha , Hunan , P.R. China. FAU - Ding, Muliang AU - Ding M AD - b Department of Orthopaedics , The Second Xiangya Hospital, Central South University , Changsha , Hunan , P.R. China. FAU - Wang, Junjie AU - Wang J AD - b Department of Orthopaedics , The Second Xiangya Hospital, Central South University , Changsha , Hunan , P.R. China. FAU - Huang, Xianzhe AU - Huang X AD - b Department of Orthopaedics , The Second Xiangya Hospital, Central South University , Changsha , Hunan , P.R. China. FAU - Li, Wenzhao AU - Li W AD - b Department of Orthopaedics , The Second Xiangya Hospital, Central South University , Changsha , Hunan , P.R. China. LA - eng PT - Journal Article DEP - 20170210 PL - United States TA - Cell Cycle JT - Cell cycle (Georgetown, Tex.) JID - 101137841 RN - 0 (3' Untranslated Regions) RN - 0 (HMGB1 Protein) RN - 0 (MALAT1 long non-coding RNA, human) RN - 0 (MIRN142 microRNA, human) RN - 0 (MicroRNAs) RN - 0 (Mirn129 microRNA, human) RN - 0 (RNA, Long Noncoding) SB - IM MH - 3' Untranslated Regions/genetics MH - Apoptosis/genetics MH - Base Sequence MH - Bone Neoplasms/*pathology MH - Carcinogenesis/*genetics MH - Cell Line, Tumor MH - Cell Proliferation/genetics MH - Gene Expression Regulation, Neoplastic MH - HMGB1 Protein/*genetics/metabolism MH - Humans MH - MicroRNAs/*genetics/metabolism MH - Osteosarcoma/*genetics/*pathology MH - RNA, Long Noncoding/genetics/*metabolism PMC - PMC5384591 OTO - NOTNLM OT - HMGB1 OT - lncRNA-MALAT1 OT - miR-129-5p OT - miR-142-3p OT - osteosarcoma EDAT- 2017/03/28 06:00 MHDA- 2017/06/20 06:00 PMCR- 2018/02/10 CRDT- 2017/03/28 06:00 PHST- 2017/03/28 06:00 [entrez] PHST- 2017/03/28 06:00 [pubmed] PHST- 2017/06/20 06:00 [medline] PHST- 2018/02/10 00:00 [pmc-release] AID - 1288324 [pii] AID - 10.1080/15384101.2017.1288324 [doi] PST - ppublish SO - Cell Cycle. 2017 Mar 19;16(6):578-587. doi: 10.1080/15384101.2017.1288324. Epub 2017 Feb 10.