LINC00641 contributes to nasopharyngeal carcinoma cell malignancy through FOXD1 upregulation at the post-transcriptional level
| Autor: | Weiming Xiong, Yongli Wang, Dan Ren, He Jiang, Jinlong Lu, Xing Han, Yun-Zhong Wei |
|---|---|
| Rok vydání: | 2021 |
| Předmět: |
medicine.diagnostic_test
Competing endogenous RNA Cell growth Cell RNA Cell Biology Biology medicine.disease Biochemistry Flow cytometry stomatognathic diseases medicine.anatomical_structure Downregulation and upregulation Nasopharyngeal carcinoma Apoptosis otorhinolaryngologic diseases medicine Cancer research Molecular Biology |
| Zdroj: | Biochemistry and Cell Biology. 99:750-758 |
| ISSN: | 1208-6002 0829-8211 |
| DOI: | 10.1139/bcb-2020-0295 |
| Popis: | Nasopharyngeal carcinoma (NPC) is a common tumor in the head and neck and is prevalent in China, especially in the southern regions. Molecular mechanisms have attracted much attention in NPC research. FOXD1 has been reported to be a tumor promoter in various cancers. The present study was designed to explore the function of FOXD1 in NPC cells. Functional analyses, including the trypan blue staining assay, EdU and JC-1 assay, and flow cytometry analysis, revealed that FOXD1 facilitated NPC cell proliferation and inhibited NPC cell apoptosis. Next, by means of “starBase” database and mechanism analyses, such as RIP assay, RNA pull-down assay and luciferase reporter assay, miR-378a-3p was found to target FOXD1 and negatively regulate FOXD1 expression in NPC cells. Moreover, miR-378a-3p plays a suppressive role in NPC cells. LINC00641 was identified as a sponge of miR-378a-3p and positively modulated FOXD1 expression in NPC cells. Finally, a series of rescue assays indicated that LINC00641 accelerated NPC cell proliferation and hindered NPC cell apoptosis through FOXD1 upregulation. In conclusion, the present study demonstrated an innovative ceRNA mechanism of LINC00641/miR-378a-3p/FOXD1 in NPC cells, which might provide new insights into NPC treatment. |
| Databáze: | OpenAIRE |
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