SNRPB is a mediator for cellular response to cisplatin in non-small-cell lung cancer.
Nianli LiuAoxing ChenNing FengXiaochen LiuLongzhen ZhangPublished in: Medical oncology (Northwood, London, England) (2021)
The small nuclear ribonucleoprotein polypeptides B And B' (SNRPB) is a core component of spliceosome and plays a key role in pre-mRNA splicing. Emerging evidence suggests that it involves in the development of several types of cancer. Our previous study has demonstrated SNRPB is highly expressed in non-small-cell lung cancer (NSCLC) and functions as an oncogene. However, whether SNRPB contributes to cisplatin resistance in NSCLC is still unknown. In this study, we found that SNRPB negatively regulates cisplatin resistance in NSCLC cells. Knocking out of SNRPB could significantly decrease cisplatin-induced cell growth inhibition, cell cycle arrest and apoptosis in H1299 cells. However, enforced expression of SNRPB in H460 cells can markedly promote cisplatin-induced cell growth inhibition, cell cycle arrest and apoptosis. Our results also indicate that overexpression of SNRPB enhances the inhibitory effects of cisplatin on H460 cell-mediated xenograft tumors. Our results suggest that SNRPB may be a prediction marker for NSCLC patients in response to cisplatin-based chemotherapy.
Keyphrases
- cell cycle arrest
- cell death
- pi k akt
- small cell lung cancer
- advanced non small cell lung cancer
- signaling pathway
- cell proliferation
- stem cells
- ejection fraction
- induced apoptosis
- end stage renal disease
- oxidative stress
- poor prognosis
- brain metastases
- transcription factor
- mesenchymal stem cells
- cell therapy
- rectal cancer