PMID- 32862616 OWN - NLM STAT- MEDLINE DCOM- 20210209 LR - 20210209 IS - 2241-6293 (Electronic) IS - 1107-0625 (Linking) VI - 25 IP - 3 DP - 2020 May-Jun TI - Research on mechanism of miR-130a in regulating autophagy of bladder cancer cells through CYLD. PG - 1636-1642 AB - PURPOSE: The study aimed to explore the regulatory mechanism of micro ribonucleic acid (miR)-130a in the autophagy of bladder cancer cells through cylindromatosis (CYLD). METHODS: Human bladder cancer T24 cell line was used as the objects of the study. After miR-130a was knocked down using small-interfering RNA (siRNA) in T24 cell line, the changes in expressions of miR-130a and CYLD in each group were detected via quantitative reverse transcription-polymerase chain reaction (qRT-PCR). The cell proliferation in each group was detected using cell counting kit-8 (CCK8) assay and flow cytometry. The changes in mRNA and protein levels of microtubule-associated protein 1 light chain 3 (LC3) and Beclin1 were determined using qRT-PCR and Western blotting. The autolysosomes were detected through acridine orange (AO)/ethidium staining bromide (ER) staining. Moreover, CYLD was knocked down using siRNA, and then the changes in mRNA expressions of miR-130a, LC3 and Beclin1 in each group were detected through qRT-PCR. RESULTS: After interference in miR-130a with siRNA, miR-130a-siRNA group had a significantly lower mRNA expression of miR-130a compared with NC-siRNA group and a significantly higher mRNA expression of CYLD (p<0.05), obviously inhibited cell proliferation (p<0.05), and decreased significantly mRNA and protein expressions of LC3 showing Beclin1 (p<0.05), and an evidently smaller number of autolysosomes. After knockdown of CYLD using siRNA, the mRNA expression of miR-130a had no significant changes (p>0.05), while the mRNA expressions of LC3 and Beclin1 declined significantly in CYLD-siRNA group compared with those in NC-siRNA group (p<0.05). CONCLUSION: MiR-130 can promote the autophagy of bladder cancer cells through regulating CYLD, thus facilitating the proliferation of tumor cells. FAU - Dai, Haitao AU - Dai H AD - Department of Urology, the first People's Hospital of Jingzhou (The First Affiliated Hospital of Yangtze University), Jingzhou, Hubei 434000, P.R. China. FAU - Liu, Changmao AU - Liu C FAU - Liu, Yuanhua AU - Liu Y FAU - Zhang, Zhong AU - Zhang Z FAU - Peng, Changwei AU - Peng C FAU - Wang, Zhongyu AU - Wang Z FAU - Zheng, Jiang AU - Zheng J FAU - Li, Chenglong AU - Li C FAU - Yu, Weimin AU - Yu W FAU - Cheng, Fan AU - Cheng F LA - eng PT - Journal Article PL - Cyprus TA - J BUON JT - Journal of B.U.ON. : official journal of the Balkan Union of Oncology JID - 100883428 RN - 0 (MIRN130 microRNA, human) RN - 0 (MicroRNAs) RN - 0 (RNA, Messenger) RN - 0 (RNA, Small Interfering) RN - EC 3.4.19.12 (CYLD protein, human) RN - EC 3.4.19.12 (Deubiquitinating Enzyme CYLD) SB - IM MH - Apoptosis/genetics MH - Autophagy/*genetics MH - Cell Line, Tumor MH - Cell Proliferation/genetics MH - Deubiquitinating Enzyme CYLD/*genetics MH - Gene Expression Regulation, Neoplastic/genetics MH - Humans MH - MicroRNAs/*genetics MH - RNA, Messenger/genetics MH - RNA, Small Interfering/genetics MH - Urinary Bladder Neoplasms/*genetics/pathology EDAT- 2020/08/31 06:00 MHDA- 2021/02/10 06:00 CRDT- 2020/08/31 06:00 PHST- 2020/08/31 06:00 [entrez] PHST- 2020/08/31 06:00 [pubmed] PHST- 2021/02/10 06:00 [medline] PST - ppublish SO - J BUON. 2020 May-Jun;25(3):1636-1642.