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替莫唑胺与百里醌对人多形性胶质母细胞瘤细胞系(U87MG)的协同作用。

Synergistic effect of temozolomide and thymoquinone on human glioblastoma multiforme cell line (U87MG).

作者信息

Pazhouhi Mona, Sariri Reyhaneh, Khazaei Mohammad Rasoul, Moradi Mohammad Taher, Khazaei Mozafar

机构信息

Department of Biology, Faculty of Sciences, University of Guilan, Rasht, Iran.

Fertility and Infertility Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran.

出版信息

J Cancer Res Ther. 2018 Jul-Sep;14(5):1023-1028. doi: 10.4103/0973-1482.187241.

Abstract

AIMS

Temozolomide (TMZ) is an alkylating agent used for glioblastoma multiforme (GBM) treatment. Nevertheless, resistance to TMZ is a major obstacle to successful treatment of this cancer. The aim of the present study was to investigate the effects of TMZ and thymoquinone (TQ) on U87MG cell line.

MATERIALS AND METHODS

The effect of TMZ and/or TQ on viability and invasion potential of U87MG cells was evaluated using various techniques including 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide, lactate dehydrogenase activity, cell invasion, migration, and adhesion assays. Enzyme-linked immunosorbent assay and polymerase chain reaction were used to study the expression and secretion of matrix metalloproteinases (MMPs).

RESULTS

Combination of TMZ and TQ had a synergistic cytotoxic effect on U87MG cells. TMZ and/or TQ significantly reduced the potential of U87MG cells invasion. In addition, after treating with TMZ and/or TQ, there was a decrease in the levels of matrix matrix metalloproteinase 2 nad 9 (MMP 2 and 9) expression and secretion in U87MG cells.

CONCLUSIONS

The combination of TMZ and TQ may emerge as a promising strategy for the successful treatment of GBM.

摘要

目的

替莫唑胺(TMZ)是一种用于治疗多形性胶质母细胞瘤(GBM)的烷化剂。然而,对TMZ的耐药性是成功治疗这种癌症的主要障碍。本研究的目的是探讨TMZ和百里醌(TQ)对U87MG细胞系的影响。

材料与方法

采用多种技术,包括3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐、乳酸脱氢酶活性、细胞侵袭、迁移和黏附试验,评估TMZ和/或TQ对U87MG细胞活力和侵袭潜能的影响。采用酶联免疫吸附测定和聚合酶链反应研究基质金属蛋白酶(MMPs)的表达和分泌。

结果

TMZ和TQ联合使用对U87MG细胞具有协同细胞毒性作用。TMZ和/或TQ显著降低了U87MG细胞的侵袭潜能。此外,用TMZ和/或TQ处理后,U87MG细胞中基质金属蛋白酶2和9(MMP 2和9)的表达和分泌水平降低。

结论

TMZ和TQ联合使用可能成为成功治疗GBM的一种有前景的策略。

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