| Literature DB >> 32420813 |
Rui Tang1, Jianmei Ji1, Jun Ding1, Jinxin Huang1, Biao Gong1, Xiwen Zhang1, Fu Li1.
Abstract
Myeloma Overexpressed (MYEOV) is closely related to cell growth and differentiation in many cancer types. However, the role of this protein-coding gene in pancreatic ductal adenocarcinoma (PDAC) has rarely been investigated. In this study, we demonstrated that MYEOV was higher expressed in tumor tissues compared with adjacent normal pancreas tissues (ANPTs) both in mRNA and protein levels. We also performed bioinformatic analysis and found high MYEOV expression was positively correlated with tumor differentiation (P = 0.004), lymph node metastasis (P = 0.016) and TNM stage (P = 0.001). Moreover, Kaplan-Meier and Cox proportional-hazards analyses indicated that high MYEOV expression was significantly associated with poor survival in patients with PDAC and that MYEOV was an independent prognostic factor for overall survival in patients with PDAC. Geneset Enrichment Analysis (GSEA) result showed that high expression of MYEOV facilitates glycolysis of tumor cells in PDAC and validated in cellular assays. In conclusion, our results suggest that MYEOV acts as an oncogene in PDAC and can therefore serve as a biomarker for the prognosis of patients with PDAC.Entities:
Keywords: MYEOV; Pancreatic cancer; glycolysis
Year: 2020 PMID: 32420813 PMCID: PMC7469688 DOI: 10.1080/15384101.2020.1757243
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534