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Downregulation of miR-1826 Indicates a Poor Prognosis for Osteosarcoma Patients and Regulates Tumor Cell Proliferation, Migration, and Invasion
| Content Provider | Semantic Scholar |
|---|---|
| Author | Li, Peng Zhu, Wenshuai |
| Copyright Year | 2020 |
| Abstract | Background Osteosarcoma (OS) is the most frequent bone tumor with high metastasis. This study is aimed at assessing the expression and prognostic significance of microRNA-1826 (miR-1826) in OS patients, as well as its biological function in tumor progression. Methods Quantitative Real-Time PCR was employed to measure the expression of miR-1826 in OS tissues and cell lines. Kaplan-Meier survival analysis and Cox regression model were used to evaluate the prognostic value of miR-1826. CCK-8 and Transwell assay were conducted to investigate the effect of miR-1826 on OS cell proliferation, migration, and invasion. Results miR-1826 expression was downregulated in OS tissues and cell lines and associated with OS patients' clinical stage and distant metastasis. Low levels of miR-1826 were related with shorter survival time and determined as an independent prognostic indicator for the overall survival of OS patients. The overexpression of miR-1826 in OS cells led to inhibited cell proliferation, migration, and invasion. Conclusion The decreased expression of miR-1826 predicts a poor prognosis in OS patients, and its overexpression inhibits OS cell proliferation, migration, and invasion. This newly identified miR-1826 provides a novel sight into the pathogenesis of OS and offers a candidate prognostic biomarker and therapeutic target for OS treatment. |
| File Format | PDF HTM / HTML |
| DOI | 10.1155/2020/7968407 |
| PubMed reference number | 32104674 |
| Journal | Medline |
| Volume Number | 2020 |
| Alternate Webpage(s) | http://downloads.hindawi.com/journals/ijg/2020/7968407.pdf |
| Alternate Webpage(s) | https://doi.org/10.1155/2020%2F7968407 |
| Journal | International journal of genomics |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |