PMID- 32640423 OWN - NLM STAT- MEDLINE DCOM- 20210308 LR - 20210308 IS - 1945-4589 (Electronic) IS - 1945-4589 (Linking) VI - 12 IP - 13 DP - 2020 Jul 8 TI - TRIM29 mediates lung squamous cell carcinoma cell metastasis by regulating autophagic degradation of E-cadherin. PG - 13488-13501 LID - 10.18632/aging.103451 [doi] AB - Lung squamous cell carcinoma (LSCC) is the most common histological type of primary lung cancer. In this study, we had tested the biological role of TRIM29 in LSCC cells. TRIM29 abundance, the relationships between TRIM29 and E-cadherin and autophagy degradation related proteins in clinical tissues and six cell lines were studied with quantitative real-time PCR test (qRT-PCR) and western blot. TRIM29 overexpression treated HTB-182 cells and knockdown treated NCL-H1915 cells was used for studying cell proliferation, colony formation, migration, invasion, and the expression of epithelial mesenchymal transformation (EMT) associated biomarkers. The relationships between TRIM29 and BECN1 were investigated with western blot. TRIM29 was profoundly overexpressed in LSCC tissues and cells compared with human normal bronchial epithelial cells (HNBE). High TRIM29 expression was closely related to overall survival (OS). TRIM29 overexpression and knockdown affected LSCC activity and the expression of EMT associated biomarkers. TRIM29 can regulate the degradation of E-cadherin and autophagy of LSCC through BECN1 gene, and promote autophagy in HTB-182 and NCL-H1915 cells. Our results revealed that TRIM29 could promote the proliferation, migration, and invasion of LSCC via E-cadherin autophagy degradation. The results are useful for further study in LSCC. FAU - Xu, Weifeng AU - Xu W AD - Department of Medical Oncology, The Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou 450008, Henan, P.R. China. FAU - Chen, Beibei AU - Chen B AD - Department of Medical Oncology, The Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou 450008, Henan, P.R. China. FAU - Ke, Dianshan AU - Ke D AD - Department of Cell Biology, Southern Medical University, Guangzhou 510515, Guangdong, China. FAU - Chen, Xiaobing AU - Chen X AD - Department of Medical Oncology, The Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou 450008, Henan, P.R. China. LA - eng PT - Journal Article PT - Observational Study DEP - 20200708 PL - United States TA - Aging (Albany NY) JT - Aging JID - 101508617 RN - 0 (Antigens, CD) RN - 0 (CDH1 protein, human) RN - 0 (Cadherins) RN - 0 (DNA-Binding Proteins) RN - 0 (TRIM29 protein, human) RN - 0 (Transcription Factors) SB - IM EIN - Aging (Albany NY). 2020 Jul 30;12(14):15183. PMID: 32756016 MH - Antigens, CD/*metabolism MH - Autophagy/*genetics MH - Cadherins/*metabolism MH - Carcinoma, Squamous Cell/genetics/mortality/*secondary MH - Cell Line, Tumor MH - Cell Movement/genetics MH - Cell Proliferation/genetics MH - DNA-Binding Proteins/genetics/*metabolism MH - Datasets as Topic MH - Epithelial-Mesenchymal Transition/genetics MH - Gene Expression Regulation, Neoplastic MH - Gene Knockdown Techniques MH - Humans MH - Kaplan-Meier Estimate MH - Lung/pathology MH - Lung Neoplasms/genetics/mortality/*pathology MH - Neoplasm Invasiveness/genetics MH - Proteolysis MH - Transcription Factors/genetics/*metabolism PMC - PMC7377877 OTO - NOTNLM OT - EMT OT - HNBE OT - LSCC OT - OS OT - TRIM29 COIS- CONFLICTS OF INTEREST: Authors declare no conflicts of interest. EDAT- 2020/07/09 06:00 MHDA- 2021/03/09 06:00 PMCR- 2020/07/15 CRDT- 2020/07/09 06:00 PHST- 2019/12/21 00:00 [received] PHST- 2020/05/01 00:00 [accepted] PHST- 2020/07/09 06:00 [pubmed] PHST- 2021/03/09 06:00 [medline] PHST- 2020/07/09 06:00 [entrez] PHST- 2020/07/15 00:00 [pmc-release] AID - 103451 [pii] AID - 10.18632/aging.103451 [doi] PST - ppublish SO - Aging (Albany NY). 2020 Jul 8;12(13):13488-13501. doi: 10.18632/aging.103451. Epub 2020 Jul 8.