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替莫唑胺与高压氧对胶质瘤U251细胞系的协同治疗作用伴随着血管内皮生长因子和多药耐药相关蛋白-1水平的改变。

The synergistic therapeutic effect of temozolomide and hyperbaric oxygen on glioma U251 cell lines is accompanied by alterations in vascular endothelial growth factor and multidrug resistance-associated protein-1 levels.

作者信息

Lu X-Y, Cao K, Li Q-Y, Yuan Z-C, Lu P-S

机构信息

Department of Neurosurgery, People's Hospital Affiliated to Jiangsu University, Zhenjiang, Jiangsu Province, China.

出版信息

J Int Med Res. 2012;40(3):995-1004. doi: 10.1177/147323001204000318.

Abstract

OBJECTIVE

Temozolomide (TMZ) is an oral alkylating agent widely used in the treatment of refractory glioma. Its efficacy is limited, however, by poor cancer cell penetration and drug resistance. The present study, therefore, aimed to investigate whether hyperbaric oxygen (HBO) may facilitate drug delivery and enhance the anticancer effect of TMZ.

METHODS

Cultured glioma U251 cells were treated with HBO, TMZ, or TMZ + HBO, or were untreated (controls). Rates of growth inhibition, cell death and apoptosis were investigated using the 3-(4,5-dimethyl thiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay, propidium iodide staining and flow cytometry, respectively. Protein levels of vascular endothelial growth factor (VEGF) and multidrug resistance-associated protein-1 (MRP-1) were evaluated by enzyme-linked immunosorbent assay.

RESULTS

Compared with TMZ or HBO alone, combined treatment with both therapies synergistically inhibited growth and induced apoptosis and death of cultured glioma U251 cells, which was accompanied by a significant decrease in levels of VEGF and MRP-1.

CONCLUSIONS

TMZ and HBO synergistically induced the apoptosis of glioma cells, possibly through reduced vascularization and inhibition of drug resistance. The combination of TMZ and HBO may be a powerful treatment for malignant glioma.

摘要

目的

替莫唑胺(TMZ)是一种口服烷化剂,广泛用于治疗难治性胶质瘤。然而,其疗效受到癌细胞穿透性差和耐药性的限制。因此,本研究旨在探讨高压氧(HBO)是否可促进药物递送并增强TMZ的抗癌效果。

方法

用HBO、TMZ、TMZ + HBO处理培养的胶质瘤U251细胞,或不进行处理(作为对照)。分别使用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基-2H-四氮唑溴盐(MTT)法、碘化丙啶染色和流式细胞术研究生长抑制率、细胞死亡和凋亡情况。通过酶联免疫吸附测定评估血管内皮生长因子(VEGF)和多药耐药相关蛋白-1(MRP-1)的蛋白质水平。

结果

与单独使用TMZ或HBO相比,两种疗法联合治疗可协同抑制培养的胶质瘤U251细胞的生长并诱导其凋亡和死亡,同时VEGF和MRP-1水平显著降低。

结论

TMZ和HBO协同诱导胶质瘤细胞凋亡,可能是通过减少血管生成和抑制耐药性实现的。TMZ和HBO联合应用可能是治疗恶性胶质瘤的有效方法。

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