| Literature DB >> 33436941 |
Wenjuan Zha1, Xiaomin Li1, Xiaowei Tie1, Yao Xing1, Hao Li2, Fei Gao3, Ting Ye2, Wangqi Du2, Rui Chen4, Yangchen Liu5.
Abstract
The long noncoding RNASBF2-AS1 can promote the occurrence and development of many kinds of tumours, but its role in oesophageal squamous cell carcinoma (ESCC) is unknown. We found that SBF2-AS1 was up-regulated in ESCC, and its expression was positively correlated with tumor size (P = 0.0001), but was not related to gender, age, TNM stage, histological grade, and lymphnode metastasis (P > 0.05). It was further found that the higher the expression of SBF2-AS1, the lower the survival rate. COX multivariate analysis showed that the expression of SBF2-AS1 was an independent prognostic factor. Functional experiments show that inhibition of SBF2-AS1 can inhibit the proliferation of ESCC through in vivo and in vitro, and overexpression of SBF2-AS1 can promote the proliferation of ESCC and inhibit its apoptosis. In mechanism, SBF2-AS1/miR-338-3P, miR-362-3P/E2F1 axis are involved in the regulation of ESCC growth. In general, SBF2-AS1 may be used as ceRNA to combine with miR-338-3P and miR-362-3P to up-regulate the expression ofE2F1, and ultimately play a role in promoting cancer. It may be used as a therapeutic target and a biomarker for prognosis.Entities:
Year: 2021 PMID: 33436941 PMCID: PMC7804443 DOI: 10.1038/s41598-020-80817-w
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379