AI Article Synopsis

  • Non-small cell lung cancer (NSCLC) is common globally, and while lncRNA SLC9A3-AS1 has known cancer-promoting roles in other cancers, its impact on NSCLC is not fully understood.
  • Research showed that SLC9A3-AS1 is elevated in NSCLC tissues and cell lines, indicating its potential as a diagnostic marker, where higher levels correlate with worse patient outcomes.
  • Functional studies revealed that reducing SLC9A3-AS1 decreased NSCLC cell growth, migration, and invasion, and it was found to influence cancer progression by mimicking a regulatory role on miR-760, pointing to its potential as a new biomarker and treatment target for NSCLC.

Article Abstract

Background: Non-small cell lung cancer (NSCLC) is a prevalent type of lung cancer worldwide. Long noncoding RNA (lncRNA) SLC9A3-AS1 is reported to play a carcinogenic role in nasopharyngeal carcinoma, but its full-scale role in NSCLC remains elusive.

Methods: SLC9A3-AS1 expression was detected in serum and tissue of NSLCC patients and NSCLC cell lines. The effects of SLC9A3-AS1 on NSCLC proliferation, migration and invasion were evaluated using CCK-8 and transwell assays. In addition, the potential downstream molecules of SLC9A3-AS1 were searched and explored by bioinformatics analysis, RT-qPCR, dual-luciferase reporter, and rescue experiments.

Results: SLC9A3-AS1 was upregulated in NSCLC tissues and cell lines. SLC9A3-AS1 possessed a favorable ability in diagnosing NSCLC. A high level of SLC9A3-AS1 was associated with poor prognosis in NSCLC patients. Functionally, SLC9A3-AS1 knockdown inhibited cell proliferation, migration, and invasion of NSCLC cells. Mechanistically, SLC9A3-AS1 acted as competing endogenous RNA for miR-760 to regulate NSCLC progression. In addition, rescue assay showed that downregulation of miR-760 could reverse the modulatory activity of SLC9A3-AS1 knockdown on NSCLC cells.

Conclusion: SLC9A3-AS1 was upregulated in NSCLC, and SLC9A3-AS1 knockdown hindered NSCLC progression through targeting miR-760, suggesting that it may prove to be a novel biomarker and therapeutic target for NSCLC.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8921674PMC
http://dx.doi.org/10.2147/CMAR.S352308DOI Listing

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