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Chinese Journal of Neurotraumatic Surgery(Electronic Edition) ›› 2021, Vol. 07 ›› Issue (05): 261-265. doi: 10.3877/cma.j.issn.2095-9141.2021.05.002

• Basic Research • Previous Articles     Next Articles

NHE1 inhibitor improves temozolomide-resistance of human glioblastoma cells

Mingyang Sun1, Yankun Liu2, Si Chen1, Yufeng Li2, Yuhui Li1,()   

  1. 1. Department of Neurosurgery, Tangshan People’s Hospital, Tangshan 063001, China
    2. Cancer Institute, Tangshan People’s Hospital, Tangshan 063001, China
  • Received:2021-06-03 Online:2021-10-15 Published:2021-11-26
  • Contact: Yuhui Li

Abstract:

Objective

To analyze the effect of Na+/H+ exchanger 1 (NHE1) inhibitor Cariporide on improving temozolomide (TMZ)-resistance of human glioblastoma (GBM) cells.

Methods

Each group of cells was treated with TMZ resistant (TR) cell lines U87/TR and U251/TR, Cariporide which established in the early stage of this research group. The NHE1 activity was detected with acetoxymethyl ester of 2’,7’-Bis(2-carboxyethyl)-5(6)-carboxyfluorescein fluorescent probe. The cell viability was analyzed by CCK-8 and the cell survival rate was calculated.

Results

The TMZ-resistances of U87/TR and U251/TR were confirmed by CCK-8 method. The NHE1 activity and cell survival rate of U87/TR and U251/TR were significantly higher than those of parental U87 and U251 cells, respectively (P<0.05). The NHE1 activities of Cariporide-treated U87/TR and U251/TR cells were still significantly higher than their parental cells, they were significantly lower than U87/TR and U251/TR cells without Cariporide, respectively (P<0.05). Under the conditions cultured at 325 μmol/L TMZ, the cell survival rate of Cariporide-treated U87/TR and U251/TR cells remained significantly higher than their parental cells, they were significantly lower than U87/TR and U251/TR cells without Cariporide, respectively (P<0.05).

Conclusion

Inhibition of NHE1 activity with Cariporide could partially improve the TMZ-resistance of GBM cells.

Key words: Glioblastoma, Temozolomide, Drug resistance, NHE1 inhibitor

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