Home    中文  
 
  • Search
  • lucene Search
  • Citation
  • Fig/Tab
  • Adv Search
Just Accepted  |  Current Issue  |  Archive  |  Featured Articles  |  Most Read  |  Most Download  |  Most Cited

Chinese Journal of Lung Diseases(Electronic Edition) ›› 2020, Vol. 13 ›› Issue (06): 724-730. doi: 10.3877/cma.j.issn.1674-6902.2020.06.002

• Original Article • Previous Articles     Next Articles

Overexpression of LNCRNA 00593 regulates cisplatin resistance in non-small cell lung cancer through the p53 pathway

Zheng Li1, Meng Zhao1, Peng Ge1, Aimin Zhang1, Li Ren1,()   

  1. 1. Department of Clinical Laboratory, Tumor Hospital, Tianjin Medical University, Tianjin 300060, China
  • Received:2020-05-16 Online:2020-12-25 Published:2021-07-27
  • Contact: Li Ren

Abstract:

Objective

To investigate the mechanism of LNCRNA 00593 regulating cisplatin resistance in non-small cell lung cancer.

Methods

Quantitative real-time PCR (RT-qPCR) was used to detect the expression of LNCRNA 00593 in normal paracancer tissues (Normal), lung adenocarcinoma (LUAD) and lung squamous cell carcinoma (LUSC), HEB cell, A549 cell, H1299 cell, PC9 cell, H460 cell and calu3 cell. H1299 cells were treated with different concentrations of CDPP (0 μM, 5 μM, 10 μM), the expression of LNCRNA 00593 in cisplatin-treated cells was detected by RT-qPCR. After treating H1299 cells with CDPP for 0 h, 12 h, 24 h, 36 h, 48 h, the expression of LNCRNA 00593 in the H1299 cells was detected by RT-qPCR. The effects of overexpression and down-regulation of LNCRNA 00593 on cisplatin resistance of H1299 cells were analyzed by CCK-8 and flow cytometry. The expression of p53 in H1299 cells was detected by RT-qPCR and Western blot after overexpression and down-regulation of LNCRNA 00593, and the binding of LNCRNA 00593 and p53 was verified by RNA-pull down. The effects of LNCRNA 00593 on the viability and apoptosis of H1299 cells induced by cisplatin were detected after PFT-α treatment.

Results

The expression level of LNCRNA 00593 in non-small cell lung cancer tissues was significantly lower than that in adjacent normal tissues (P<0.05). The expression levels of LNCRNA 00593 in A549, H1299, PC9, H460 and calu3 cells were significantly lower than that of HEB cells (P<0.01). After treating H1299 cells with 0 μM, 5 μM, and 10 μM CDPP respectively, the expression of LNCRNA 00593 increased in a concentration-dependent manner (P<0.01). After treating H1299 cells with 10 μM CDPP for 12 h, 24 h, 36 h, 48 h, the expression of LNCRNA 00593 increased in a time-dependent manner (P<0.01). After CDPP treatment, down-regulation of LNCRNA 00593 significantly increased H1299 cell activity and decreased apoptosis rate, while overexpression of LNCRNA 00593 significantly decreased H1299 cell activity and increased apoptosis rate. Overexpression of LNCRNA 00593 activated the p53 pathway, and LNCRNA 00593 can bind to p53. The regulation of cisplatin resistance of H1299 cells by LNCRNA 00593 was down-regulated in PFT-α-treated cells.

Conclusion

Overexpression of LNCRNA 00593 regulates cisplatin resistance in non-small cell lung cancer cells through the p53 pathway.

Key words: LNCRNA 00593, p53 pathway, Non-small cell lung cancer, Cisplatin resistance

京ICP 备07035254号-28
Copyright © Chinese Journal of Lung Diseases(Electronic Edition), All Rights Reserved.
Tel: 023-65425691 E-mail: xqcjld@163.com
Powered by Beijing Magtech Co. Ltd