+HOXA10-AS Promotes Malignant Phenotypes of Gastric Cancer via Upregulating HOXA10
Autor: | Fengyu Cao, Yongbin Zheng, Chao Yang, Suoyang Huang, Xiaobo He, Shilun Tong |
---|---|
Jazyk: | angličtina |
Rok vydání: | 2022 |
Předmět: |
General Immunology and Microbiology
Applied Mathematics Computational Biology Apoptosis General Medicine General Biochemistry Genetics and Molecular Biology Up-Regulation Gene Expression Regulation Neoplastic Homeobox A10 Proteins Phenotype Cell Movement Stomach Neoplasms Cell Line Tumor Gene Knockdown Techniques Modeling and Simulation Humans Neoplasm Invasiveness RNA Antisense RNA Long Noncoding Cell Proliferation |
Zdroj: | Computational and Mathematical Methods in Medicine. |
ISSN: | 1748-670X |
DOI: | 10.1155/2022/1846687 |
Popis: | Objective. To study the role of long noncoding RNA HOXA10-AS in gastric cancer (GC) and its underlying mechanism which is one of the most common and fetal malignancies. Long noncoding RNA HOXA10-AS is highly expressed and acts in an oncogenic role in cancers. However, its roles in GC are still unknown. Methods. The expression of HOXA10-AS and HOXA10 in GC tissues from the TCGA database was analyzed. Western blot and qRT-PCR assays were applied to examine the expression of HOXA10-AS and HOXA10. Cell proliferation was evaluated with CCK-8 and EdU incorporation assays. Cell apoptosis was analyzed by flow cytometry. Migratory and invasive capacities were evaluated with wound healing and transwell assays. Results. HOXA10-AS and HOXA10 were upregulated in GC, and their expressions were positively correlated. Knockdown of HOXA10-AS inhibited HOXA10 expression in GC cells. Furthermore, knockdown of HOXA10-AS restrained GC cell proliferation, migration, and invasion but promoted apoptosis. In addition, overexpression of HOXA10-AS promoted malignant phenotypes of GC cells, but all these effects could be reversed by knockdown of HOXA10. Conclusion. HOXA10-AS promoted GC cell proliferation, migration and invasion and enhanced apoptosis via upregulating HOXA10. Our study implies a novel regulatory mechanism of malignant phenotypes and provides potential therapeutic targets for GC. |
Databáze: | OpenAIRE |
Externí odkaz: | |
Nepřihlášeným uživatelům se plný text nezobrazuje | K zobrazení výsledku je třeba se přihlásit. |