PMID- 29412697 OWN - NLM STAT- MEDLINE DCOM- 20180822 LR - 20211204 IS - 1557-8852 (Electronic) IS - 1084-9785 (Linking) VI - 33 IP - 1 DP - 2018 Feb TI - miR-155 Affects Osteosarcoma MG-63 Cell Autophagy Induced by Adriamycin Through Regulating PTEN-PI3K/AKT/mTOR Signaling Pathway. PG - 32-38 LID - 10.1089/cbr.2017.2306 [doi] AB - OBJECTIVE: Phosphatase and tensin homolog deleted on chromosome 10 (PTEN) plays a positive regulatory role on cell autophagy through inhibiting PI3K/AKT/mammalian target of rapamycin (mTOR) signaling pathway. miR-155 plays a critical role in osteosarcoma occurrence and chemoresistance. Bioinformatics analysis revealed the targeted binding site between miR-155 and the 3'-UTR (untranslated region) of PTEN mRNA. This study investigated the role of miR-155 in regulating osteosarcoma cell autophagy, chemosensitivity to Adriamycin (ADM), and PTEN-PI3K/AKT/mTOR signaling pathway. MATERIALS AND METHODS: Dual luciferase reporter gene assay confirmed the relationship between miR-155 and PTEN. MG-63 cells and drug-resistant MG-63/ADM cells were treated by ADM to compare miR-155, PTEN, p-AKT, p-mTOR, and Beclin-1 expressions. Cell apoptosis was tested by flow cytometry. MG-63/ADM cells were divided into five groups, including anti-miR-NC, anti-miR-155, pSicoR-blank, pSicoR-PTEN, and anti-miR-155+pSicoR-PTEN group. RESULTS: miR-155 targeted suppressed PTEN expression. miR-155, p-AKT, and p-mTOR significantly increased, while PTEN and Beclin-1 obviously reduced in MG-63/ADM cells compared with MG-63 cells. ADM treatment markedly elevated miR-155, p-AKT, and p-mTOR expressions, whereas reduced PTEN level. Beclin-1 was slightly upregulated, and autophagy and apoptosis levels were low. Anti-miR-155 and/or pSicoR-PTEN significantly enhanced PTEN and Beclin-1 expressions, cell apoptosis, and autophagy induced by ADM and declined p-AKT and p-mTOR levels. CONCLUSIONS: miR-155 targeted suppressed PTEN expression, enhanced PI3K/AKT/mTOR signaling pathway, inhibited cell apoptosis and autophagy induced by ADM, and reduced sensitivity to ADM. FAU - Wang, Lin AU - Wang L AD - Department of Orthopedics Institute, Affiliated Dongfeng Hospital, Hubei University of Medicine , Shiyan, China . FAU - Tang, Bing AU - Tang B AD - Department of Orthopedics Institute, Affiliated Dongfeng Hospital, Hubei University of Medicine , Shiyan, China . FAU - Han, Heng AU - Han H AD - Department of Orthopedics Institute, Affiliated Dongfeng Hospital, Hubei University of Medicine , Shiyan, China . FAU - Mao, Dan AU - Mao D AD - Department of Orthopedics Institute, Affiliated Dongfeng Hospital, Hubei University of Medicine , Shiyan, China . FAU - Chen, Jie AU - Chen J AD - Department of Orthopedics Institute, Affiliated Dongfeng Hospital, Hubei University of Medicine , Shiyan, China . FAU - Zeng, Yun AU - Zeng Y AD - Department of Orthopedics Institute, Affiliated Dongfeng Hospital, Hubei University of Medicine , Shiyan, China . FAU - Xiong, Min AU - Xiong M AD - Department of Orthopedics Institute, Affiliated Dongfeng Hospital, Hubei University of Medicine , Shiyan, China . LA - eng PT - Journal Article PT - Retracted Publication DEP - 20180207 PL - United States TA - Cancer Biother Radiopharm JT - Cancer biotherapy & radiopharmaceuticals JID - 9605408 RN - 0 (MIRN155 microRNA, human) RN - 0 (MicroRNAs) RN - 0 (Phosphoinositide-3 Kinase Inhibitors) RN - 80168379AG (Doxorubicin) RN - EC 2.7.1.1 (MTOR protein, human) RN - EC 2.7.11.1 (Proto-Oncogene Proteins c-akt) RN - EC 2.7.11.1 (TOR Serine-Threonine Kinases) RN - EC 3.1.3.67 (PTEN Phosphohydrolase) RN - EC 3.1.3.67 (PTEN protein, human) SB - IM RIN - Cancer Biother Radiopharm. 2021 Sep;36(7):614. PMID: 34357784 MH - Autophagy/drug effects/genetics MH - Bone Neoplasms/drug therapy/genetics/metabolism/pathology MH - Doxorubicin/*pharmacology MH - Humans MH - MicroRNAs/*metabolism MH - Osteosarcoma/drug therapy/genetics/metabolism/pathology MH - PTEN Phosphohydrolase/*metabolism MH - Phosphatidylinositol 3-Kinases/metabolism MH - Phosphoinositide-3 Kinase Inhibitors MH - Proto-Oncogene Proteins c-akt/*metabolism MH - Signal Transduction/drug effects MH - TOR Serine-Threonine Kinases/*metabolism OTO - NOTNLM OT - PTEN-PI3K/AKT/mTOR OT - autophagy OT - miR-155 OT - osteosarcoma EDAT- 2018/02/08 06:00 MHDA- 2018/08/23 06:00 CRDT- 2018/02/08 06:00 PHST- 2018/02/08 06:00 [pubmed] PHST- 2018/08/23 06:00 [medline] PHST- 2018/02/08 06:00 [entrez] AID - 10.1089/cbr.2017.2306 [doi] PST - ppublish SO - Cancer Biother Radiopharm. 2018 Feb;33(1):32-38. doi: 10.1089/cbr.2017.2306. Epub 2018 Feb 7.