PMID- 35236250 OWN - NLM STAT- MEDLINE DCOM- 20220408 LR - 20220606 IS - 2165-5987 (Electronic) IS - 2165-5979 (Print) IS - 2165-5979 (Linking) VI - 13 IP - 3 DP - 2022 Mar TI - Circular RNA ZNF609 promotes laryngeal squamous cell carcinoma progression by upregulating epidermal growth factor receptor via sponging microRNA-134-5p. PG - 6929-6941 LID - 10.1080/21655979.2022.2034703 [doi] AB - Emerging evidence has revealed that aberrantly expressed circular RNAs (circRNAs) play vital roles in tumorigenesis and progression of diverse human malignancies. CircZNF609 was found to be involved in hepatocellular carcinoma, but the role and underlying mechanism of circZNF609 in laryngeal squamous cell carcinoma (LSCC) remain unclear. This study aimed to explore the molecular mechanism of circZNF609 in LSCC. qRT-qPCR was performed to detect the expression of circZNF609 and microRNA-134-5p (miR-134-5p) in LSCC. Colony formation assay, CCK-8 assay, BrdU incorporation assay, clone formation assay, transwell invasion assay and Western blot analysis were performed to evaluate LSCC cell proliferation, as well as the expression of proliferating cell nuclear antigen (PCNA) and MMP-2. Luciferase reporter assay, target gene prediction and screening were used to validate downstream target genes of circZNF609 and miR-134-5p. EGFR expression was detected by Western blot analysis and RT-qPCR. Nude mice were used to detect tumor changes. CircZNF609 was upregulated in LSCC and associated with poor survival of LSCC patients. Knockdown of circZNF609 inhibited LSCC proliferation, invasion and the expression of PCNA and matrix matalloproteinases-2 (MMP-2). CircZNF609 can regulate miR-134-5p to upregulate epidermal growth factor receptor (EGFR). In addition, knockdown of EGFR or overexpression of miR-134-5p could reverse the tumor-promoting effects of circZNF609 in LSCC. In LSCC tissues, circZNF609 was negatively correlated with miR-134-5p and positively correlated with EGFR. CircZNF609 promotes the progression of LSCC via the miR-134-5p/EGFR axis, which might be the therapeutic target of LSCC. FAU - Yin, Xiaoyan AU - Yin X AD - Department of Otolaryngology, Head & Neck Surgery, The Second Hospital of Hebei Medical University, PR. China. FAU - Wang, Jingmiao AU - Wang J AD - Department of Otolaryngology, Head & Neck Surgery, The Second Hospital of Hebei Medical University, PR. China. FAU - Shan, Chunguang AU - Shan C AD - Department of Otolaryngology, Head & Neck Surgery, The Second Hospital of Hebei Medical University, PR. China. FAU - Jia, Qiaojing AU - Jia Q AD - Department of Otolaryngology, Head & Neck Surgery, The Second Hospital of Hebei Medical University, PR. China. FAU - Bian, Yanrui AU - Bian Y AD - Department of Otolaryngology, Head & Neck Surgery, The Second Hospital of Hebei Medical University, PR. China. FAU - Zhang, Haizhong AU - Zhang H AUID- ORCID: 0000-0002-0836-180X AD - Department of Otolaryngology, Head & Neck Surgery, The Second Hospital of Hebei Medical University, PR. China. LA - eng PT - Journal Article PL - United States TA - Bioengineered JT - Bioengineered JID - 101581063 RN - 0 (MIRN134 microRNA, human) RN - 0 (MicroRNAs) RN - 0 (Proliferating Cell Nuclear Antigen) RN - 0 (RNA, Circular) RN - EC 2.7.10.1 (ErbB Receptors) RN - EC 3.4.24.24 (Matrix Metalloproteinase 2) SB - IM MH - Animals MH - Cell Line, Tumor MH - Cell Proliferation/genetics MH - ErbB Receptors/genetics/metabolism MH - Gene Expression Regulation, Neoplastic MH - *Head and Neck Neoplasms/genetics MH - Humans MH - *Laryngeal Neoplasms/genetics/metabolism/pathology MH - *Liver Neoplasms/genetics MH - Matrix Metalloproteinase 2/genetics MH - Mice MH - Mice, Nude MH - *MicroRNAs/genetics/metabolism MH - Proliferating Cell Nuclear Antigen/genetics/metabolism MH - RNA, Circular/genetics MH - Squamous Cell Carcinoma of Head and Neck/genetics PMC - PMC8973624 OTO - NOTNLM OT - CircRNAs OT - EGFR OT - ZNF609 OT - laryngeal squamous cell carcinoma OT - miR-134-5p COIS- No potential conflict of interest was reported by the author(s). EDAT- 2022/03/04 06:00 MHDA- 2022/04/09 06:00 PMCR- 2022/03/02 CRDT- 2022/03/03 05:30 PHST- 2022/03/03 05:30 [entrez] PHST- 2022/03/04 06:00 [pubmed] PHST- 2022/04/09 06:00 [medline] PHST- 2022/03/02 00:00 [pmc-release] AID - 2034703 [pii] AID - 10.1080/21655979.2022.2034703 [doi] PST - ppublish SO - Bioengineered. 2022 Mar;13(3):6929-6941. doi: 10.1080/21655979.2022.2034703.