Publication: LncRNA CERS6-AS1, sponging miR-6838-5p, promotes proliferation and invasion in cervical carcinoma cells by upregulating FOXP2
| dc.contributor.author | Yan, Kun | |
| dc.contributor.author | Hu, Chunyan | |
| dc.contributor.author | Liu, Chen | |
| dc.contributor.author | Chu, Guanghua | |
| dc.contributor.author | Wang, Xinru | |
| dc.contributor.author | Ma, Shuyun | |
| dc.contributor.author | Li, Long | |
| dc.date.accessioned | 2023-09-07T10:45:55Z | |
| dc.date.available | 2023-09-07T10:45:55Z | |
| dc.date.issued | 2023 | |
| dc.description.abstract | Cervical cancer (CC) is a common disease in women characterized by high recurrence rate. LncRNA ceramide synthase 6 antisense RNA 1 (CERS6-AS1) has been found to play a crucial role in the progression of breast cancer and pancreatic cancer. Nevertheless, the regulatory role of CERS6-AS1 in CC remains largely unclear. Here, we found that the expression of CERS6- AS1 was upregulated in CC tissues and cell lines compared with adjacent tissues and normal human cervical epithelial cells. CERS6-AS1 overexpression promoted proliferation and invasion, and inhibited apoptosis in CC cells, while silencing of CERS6-AS1 led to the opposite results. CERS6-AS1 was verified as a sponge of miR-6838-5p by RNA pull-down and luciferase reporter gene assays. Functional investigations revealed that CERS6-AS1 knockdown inhibited proliferation and invasion, and promoted apoptosis in CC cells, which was reversed by miR-6838-5p inhibitor. Furthermore, forkhead box P2 (FOXP2) was identified as a target for miR-6838-5p, and overexpression of miR6838-5p decreased the expression level of FOXP2. Besides, CERS6-AS1 was able to sponge miR-6838-5p to accelerate CC cell proliferation and invasion and inhibited cell apoptosis through upregulating FOXP2 expression. In general, CERS6-AS1 was able to regulate CC cell proliferation, invasion and apoptosis by the miR-6838-5p/FOXP2 axis, which suggested that CERS6-AS1 may be a potential target for the treatment of CC. | es |
| dc.format | application/pdf | es |
| dc.format.extent | 13 | es |
| dc.identifier.citation | Histology and Histopathology, Vol.38, nÂş7, (2023) | |
| dc.identifier.doi | https://doi.org/10.14670/HH-18-555 | |
| dc.identifier.issn | 0213-3911 | |
| dc.identifier.issn | 1699-5848 | |
| dc.identifier.uri | http://hdl.handle.net/10201/133731 | |
| dc.language | eng | es |
| dc.publisher | Universidad de Murcia. Departamento de BiologĂa Celular e HistologĂa | es |
| dc.relation | Sin financiaciĂłn externa a la Universidad | es |
| dc.rights | info:eu-repo/semantics/openAccess | es |
| dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 Internacional | * |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
| dc.subject | Cervical cancer | es |
| dc.subject | lncRNA CERS6-AS1 | es |
| dc.subject | miR-6838-5p | es |
| dc.subject | FOXP2 | es |
| dc.subject.other | CDU::6 - Ciencias aplicadas::61 - Medicina::616 - PatologĂa. Medicina clĂnica. OncologĂa | es |
| dc.title | LncRNA CERS6-AS1, sponging miR-6838-5p, promotes proliferation and invasion in cervical carcinoma cells by upregulating FOXP2 | es |
| dc.type | info:eu-repo/semantics/article | es |
| dspace.entity.type | Publication | es |
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