PMID- 33821684 OWN - NLM STAT- MEDLINE DCOM- 20211117 LR - 20211117 IS - 1555-3892 (Electronic) IS - 0963-6897 (Print) IS - 0963-6897 (Linking) VI - 30 DP - 2021 Jan-Dec TI - LncRNA MNX1-AS1 Contributes to Laryngeal Squamous Cell Carcinoma Growth and Migration by Regulating mir-744-5p/bcl9/beta-Catenin Axis. PG - 9636897211005682 LID - 10.1177/09636897211005682 [doi] LID - 09636897211005682 AB - Increasing evidence has indicated that long noncoding RNAs (lncRNAs) are involved in the progression of laryngeal squamous cell carcinoma (LSCC). Here, we aimed to disclose the role of MNX1-AS1 in LSCC progression, and explore whether MNX1-AS1 participates in LSCC progression via targeting miR-744-5p to active BCL9/beta-catenin signaling. Sixty-five human LSCC tissues and the paracancerous normal tissues were recruited to determine the levels of MNX1-AS1, miR-744-5p and BCL9 using qRT-PCR. The interaction of miR-744-5p and MNX1-AS1/BCL9 was determined by using the RNA immunoprecipitation (RIP) assay and/or luciferase gene reporter assay. Cell viability, in vivo tumor formation, invasion and migration abilities were detected by MTT, Xenograft models and Transwell assays. MNX1-AS1 level was increased significantly in human LSCC tissues as compared with the normal tissues, which showed a positive correlation with BCL9 level while a negative correlation with miR-744-5p level. High level of MNX1-AS1 predicted a poor prognosis and an advanced clinical process in LSCC patients. miR-744-5p targeted upregulation weakened the luciferase activity of MNX1-AS1 and /BCL9, and downregulated their expression levels-wt, while showed no effect when the binding sites were mutated. Knockdown of MNX1-AS1 markedly weakened cell viability, migration, and invasion abilities, while BCL9 overexpression abolished these tendencies. In addition, MNX1-AS1 downregulation induced decreases in tumor volumes and weights in vivo, accompanied by reductions in BCL9, Ki-67 and beta-catenin expression and an increase in miR-744-5p expression. Collectively, this study reveals that MNX1-AS1 contributes to cell growth and migration by regulating miR-744-5p/BCL9/beta-catenin axis in LSCC. FAU - Ma, Bingliang AU - Ma B AD - Department of Otolaryngology, the First Affiliated Hospital, Huzhou University, the First People's Hospital of Huzhou, Huzhou City, Zhejiang Province, China. FAU - Ren, Gang AU - Ren G AUID- ORCID: 0000-0002-0107-0524 AD - Department of Otolaryngology, the First Affiliated Hospital, Huzhou University, the First People's Hospital of Huzhou, Huzhou City, Zhejiang Province, China. FAU - Xu, Jue AU - Xu J AD - Department of Otolaryngology, the First Affiliated Hospital, Huzhou University, the First People's Hospital of Huzhou, Huzhou City, Zhejiang Province, China. FAU - Yin, Chenyi AU - Yin C AD - Department of Otolaryngology, the First Affiliated Hospital, Huzhou University, the First People's Hospital of Huzhou, Huzhou City, Zhejiang Province, China. FAU - Shi, Yuye AU - Shi Y AD - Department of Surgical Anesthesiology, the First Affiliated Hospital, Huzhou University, the First People's Hospital of Huzhou, Huzhou City, Zhejiang Province, China. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - Cell Transplant JT - Cell transplantation JID - 9208854 RN - 0 (MIRN744 microRNA, mouse) RN - 0 (MicroRNAs) RN - 0 (RNA, Long Noncoding) RN - 0 (beta Catenin) SB - IM MH - Animals MH - Carcinoma, Squamous Cell/*genetics/pathology MH - Cell Line, Tumor MH - Cell Movement MH - Cell Proliferation MH - Disease Models, Animal MH - Humans MH - Laryngeal Neoplasms/*genetics/pathology MH - Male MH - Mice MH - Mice, Nude MH - MicroRNAs/*metabolism MH - RNA, Long Noncoding/*metabolism MH - Up-Regulation MH - beta Catenin/*metabolism PMC - PMC8033468 OTO - NOTNLM OT - BCL9 OT - MNX1-AS1 OT - cell growth OT - laryngeal squamous cell carcinoma OT - miR-744-5p COIS- Declaration of Conflicting Interests: The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article. EDAT- 2021/04/07 06:00 MHDA- 2021/11/18 06:00 PMCR- 2021/04/06 CRDT- 2021/04/06 12:18 PHST- 2021/04/06 12:18 [entrez] PHST- 2021/04/07 06:00 [pubmed] PHST- 2021/11/18 06:00 [medline] PHST- 2021/04/06 00:00 [pmc-release] AID - 10.1177_09636897211005682 [pii] AID - 10.1177/09636897211005682 [doi] PST - ppublish SO - Cell Transplant. 2021 Jan-Dec;30:9636897211005682. doi: 10.1177/09636897211005682.