Long non-coding RNA ENTPD1-AS1 exerts pro-oncogenic activities in colorectal cancer by acting as a competing endogenous RNA for microRNA-432-5p to increase HDGF expression

H. Deng, Q. Li, ZH. Qi, XK. Bi, QY Huang

Article ID: 4484
Vol 35, Issue 6, 2021
DOI: https://doi.org/10.54517/jbrha4484
Received: 8 January 2022; Accepted: 8 January 2022; Available online: 8 January 2022; Issue release: 8 January 2022

Abstract

ENTPD1 antisense RNA 1 (ENTPD1-AS1), a long non-coding RNA, has been comprehensively studiedin glioblastoma multiforme. This study aimed to measure ENTPD1-AS1 expression in patients withcolorectal cancer (CRC) and identify its function in the behavior of CRC cells. The expression of ENTPD1-AS1 was measured in a panel of tissue specimens obtained from CRC patients via quantitative real-timepolymerase chain reaction. Proliferation, migration, and invasion of CRC cells were evaluated using CellCounting Kit-8, Transwell cell migration, and invasion assays. Moreover, tumor xenografts were establishedto evaluate the growth of CRC cells in vivo, and bioinformatics analysis was performed to identify putativecomplementary miRNAs that interact with ENTPD1-AS1, which was further corroborated in a seriesof mechanistic studies. We found that ENTPD1-AS1 was overexpressed in CRC based on our samplecohort’s Cancer Genome Atlas database. Interference of ENTPD1-AS1 impeded CRC cell proliferation.In addition, in vitro migration and invasion as well as in vivo tumor growth were inhibited after ENTPD1-AS1 knockdown. Mechanistically, ENTPD1-AS1 predominantly functioned as a competing endogenousRNA to sponge microRNA-432-5p (miR-432-5p), resulting in the upregulation of hepatoma-derivedgrowth factor (HDGF) expression in CRC cells. Finally, rescue function tests revealed that miR-432-5pinhibition or HDGF restoration could counteract the inhibitory effects of ENTPD1-AS1 knockdown inCRC cells. Overall, ENTPD1-AS1 may increase HDGF expression in CRC cells by sequestering miR-432-5p, thereby boosting oncogenicity. Thus, the ENTPD1-AS1/miR-432-5p/HDGF regulatory pathway mayprovide a theoretical basis for the identification of novel treatment strategies for CRC


Keywords

ENTPD1 antisense RNA 1;ceRNA;molecular sponge;microRNA-432-5p;hepatoma-derived growth factor


References

Supporting Agencies



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