PMID- 34367283 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20220425 IS - 1687-8450 (Print) IS - 1687-8469 (Electronic) IS - 1687-8450 (Linking) VI - 2021 DP - 2021 TI - A Novel Expression Signature from the Perspective of Mesenchymal-Epithelial Transition for Hepatocellular Carcinoma with Regard to Prognosis, Clinicopathological Features, Immune Cell Infiltration, Chemotherapeutic Efficacy, and Immunosuppressive Molecules. PG - 5033416 LID - 10.1155/2021/5033416 [doi] LID - 5033416 AB - PURPOSE: Mesenchymal-epithelial transition (MET), a reverse biological process to epithelial-mesenchymal transition (EMT), is involved in tumor metastasis and invasion. However, the role of MET-related genes (MRGs) in hepatocellular carcinoma (HCC) prognosis remains unclear. METHODS: In this research, we obtained MRGs data and clinical information from public databases. In the TCGA dataset, a prognostic signature for HCC was constructed by the least absolute shrinkage and selection operator (LASSO) method and externally verified using the ICGC dataset. RESULTS: There were 148 differentially expressed MRGs (DEMRGs), out of which 37 MRGs were found associated with overall survival (OS) in the univariate Cox analysis. A novel signature integrating of 5 MRGs was constructed, which split patients into high- and low-risk groups. Kaplan-Meier analysis revealed that high-risk patients had unfavorable OS than those low-risk counterparts. Receiver operating characteristic curve (ROC) showed great performance of this signature in predictive ability. Multivariate Cox analysis confirmed that this signature could independently predict HCC prognosis. The analysis of immune cell infiltration demonstrated that immune status varied differently between high- and low-risk groups. The analysis of clinicopathological characteristics suggested that tumor grade, clinical stage, and T stage were different between risk groups. The analysis between this signature and chemotherapeutic efficacy and immunosuppressive molecules indicated that this signature could serve as a promising predictor. CONCLUSIONS: In conclusion, we constructed and verified a novel signature from the perspective of MET, which was significantly associated with HCC prognosis, clinicopathological features, immune status, chemotherapeutic efficacy, and immunosuppressive biomarkers. CI - Copyright (c) 2021 Lijun Xu and Qing Zheng. FAU - Xu, Lijun AU - Xu L AUID- ORCID: 0000-0001-9515-6128 AD - Key Laboratory of Gastroenterology and Hepatology, Ministry of Health, Inflammatory Bowel Disease Research Center, Shanghai Institute of Digestive Disease, Division of Gastroenterology and Hepatology, Renji Hospital, School of Medicine Shanghai Jiao Tong University, 160# Pu Jian Ave, Shanghai 200127, China. FAU - Zheng, Qing AU - Zheng Q AUID- ORCID: 0000-0001-8742-7629 AD - Key Laboratory of Gastroenterology and Hepatology, Ministry of Health, Inflammatory Bowel Disease Research Center, Shanghai Institute of Digestive Disease, Division of Gastroenterology and Hepatology, Renji Hospital, School of Medicine Shanghai Jiao Tong University, 160# Pu Jian Ave, Shanghai 200127, China. LA - eng PT - Journal Article DEP - 20210728 PL - Egypt TA - J Oncol JT - Journal of oncology JID - 101496537 PMC - PMC8342179 COIS- The authors declare that they have no conflicts of interest. EDAT- 2021/08/10 06:00 MHDA- 2021/08/10 06:01 PMCR- 2021/07/28 CRDT- 2021/08/09 06:31 PHST- 2021/05/06 00:00 [received] PHST- 2021/06/30 00:00 [revised] PHST- 2021/07/14 00:00 [accepted] PHST- 2021/08/09 06:31 [entrez] PHST- 2021/08/10 06:00 [pubmed] PHST- 2021/08/10 06:01 [medline] PHST- 2021/07/28 00:00 [pmc-release] AID - 10.1155/2021/5033416 [doi] PST - epublish SO - J Oncol. 2021 Jul 28;2021:5033416. doi: 10.1155/2021/5033416. eCollection 2021.