γ分泌酶抑制剂对口腔鳞状细胞癌细胞增殖和侵袭性的影响

Hiroshi Inoue , Yuichi Ohnishi , Yuichi Shoju , Masahiro Nakajima , Kenji Kakudo
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引用次数: 2

摘要

目的探讨γ分泌酶抑制剂对口腔癌细胞增殖介导的细胞周期调节因子和侵袭活性介导的基质金属蛋白酶(MMP) 9表达的影响。材料与方法采用逆转录聚合酶链式反应(RT-PCR)技术,对口腔癌细胞株SAS、HSC-3和HSC-4中γ分泌酶组分和底物的表达进行了研究。使用细胞增殖试验评估γ分泌酶抑制剂处理后HSC-4细胞的增殖,并使用RT-PCR估计细胞周期调节因子的表达。采用基质侵袭法检测γ分泌酶抑制剂对HSC-4细胞的侵袭活性,采用RT-PCR检测MMP9的表达。结果rt - pcr检测口腔癌细胞株SAS和HSC-4中γ分泌酶成分和底物的表达。经γ分泌酶抑制剂处理的HSC-4细胞增殖减少,cyclin D1和cyclin E表达降低,p27 (Kip1)表达升高。此外,在这些细胞中观察到侵袭能力和MMP9表达的降低。结论γ分泌酶的抑制可抑制细胞增殖,介导细胞周期调节因子的表达和介导MMP9表达的侵袭性活性,提示γ分泌酶抑制剂可作为一种潜在的口腔癌治疗药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of a gamma secretase inhibitor on the proliferation and invasiveness of oral squamous cell carcinoma cell lines

Objective

To determine the effects of a gamma secretase inhibitor on the proliferation mediating cell-cycle regulators and invasive activity mediating matrix metalloproteinase (MMP) 9 expression in oral cancer cell lines.

Materials and methods

In the oral cancer cell lines SAS, HSC-3, and HSC-4, we investigated the expression of components and substrates of gamma secretase using the reverse transcription-polymerase chain reaction (RT-PCR). The proliferation of HSC-4 cells after treatment with a gamma secretase inhibitor was evaluated using a cell proliferation assay, and expressions of cell-cycle regulators were estimated using RT-PCR. The invasive activity of HSC-4 cells after treatment with the gamma secretase inhibitor was determined using a matrigel invasion assay, and MMP9 expression was measured employing RT-PCR.

Results

RT-PCR revealed the expression of components and substrates of gamma secretase in oral cancer cell lines SAS and HSC-4. HSC-4 cells treated with the gamma secretase inhibitor showed a reduction in proliferation, as well as a decrease in cyclin D1 and cyclin E expression and an increase of p27 (Kip1) expression. Moreover, a reduction of the invasive capacity and MMP9 expression were observed in these cells.

Conclusion

These results suggest that the inhibition of gamma secretase reduces cell proliferation mediating the expression of cell-cycle regulators and invasive activity mediating MMP9 expression, and that a gamma secretase inhibitor can be applied as a potential therapeutic agent in oral cancer.

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