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[抑制GRP78表达可逆转人卵巢癌顺铂耐药性]

[Inhibition of GRP78 expression reverses cisplatin resistance in human ovarian cancer].

作者信息

Fan Li-mei, Su Jing, Dong Hui, Wei Min, Cui Man-hua

机构信息

Department of Obstetrics & Gynecology, Second Hospital of Jilin University, Changchun 130041, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2013 May 7;93(17):1341-4.

PMID:24029486
Abstract

OBJECTIVE

To explore the effects of GRP78 suppression on the sensitivity to cisplatin and elucidate the role and mechanism of GRP78 in ovarian cancer cisplatin resistance.

METHODS

The GRP78 siRNA expression plasmid was constructed to suppress GRP78 expression. Cell viability was detected by methyl thiazolyl tetrazolium (MTT) assay. Endoplasmic reticulum stress-related apoptosis related protein expressions were detected by reverse transcription-polymerase chain reaction (RT-PCR) and Western blot. And cell apoptosis was detected by flow cytometry.

RESULTS

The expressions of GRP78, CHOP and cleaved-caspase 4 were induced significantly by cisplatin (6 mg/L) in SKOV3 cells. And the expression of GRP78 was induced significantly by cisplatin in SKOV3/DDP cells. But the expressions of CHOP and cleaved-caspase 4 showed no significant difference. Inhibition of GRP78 expression and cisplatin combined treatment significantly increased the expressions of cleaved-caspase 4 and cleaved-caspase 3 in SKOV3/DDP cells. Inhibition of GRP78 expression reduced the cisplatin-induced up-regulations of p-Akt and p-mTOR and induced XBP1 mRNA shear expression and CHOP mRNA expression.

CONCLUSION

Inhibition of GRP78 expression reverses cisplatin resistance in SKOV3/DDP cells. The mechanism may be through the activity of Akt/mTOR signaling pathway, CHOP expression levels and caspase activity.

摘要

目的

探讨抑制葡萄糖调节蛋白78(GRP78)表达对顺铂敏感性的影响,阐明GRP78在卵巢癌顺铂耐药中的作用及机制。

方法

构建GRP78小干扰RNA(siRNA)表达质粒以抑制GRP78表达。采用甲基噻唑基四氮唑(MTT)法检测细胞活力。通过逆转录-聚合酶链反应(RT-PCR)和蛋白质免疫印迹法检测内质网应激相关凋亡蛋白的表达。采用流式细胞术检测细胞凋亡。

结果

顺铂(6 mg/L)可显著诱导SKOV3细胞中GRP78、C/EBP同源蛋白(CHOP)和裂解型半胱天冬酶4的表达。顺铂可显著诱导SKOV3/DDP细胞中GRP78的表达。但CHOP和裂解型半胱天冬酶4的表达无显著差异。抑制GRP78表达并联合顺铂处理可显著增加SKOV3/DDP细胞中裂解型半胱天冬酶4和裂解型半胱天冬酶3的表达。抑制GRP78表达可降低顺铂诱导的蛋白激酶B(Akt)和哺乳动物雷帕霉素靶蛋白(mTOR)磷酸化上调,并诱导X盒结合蛋白1(XBP1)mRNA剪切表达和CHOP mRNA表达。

结论

抑制GRP78表达可逆转SKOV3/DDP细胞的顺铂耐药。其机制可能与Akt/mTOR信号通路活性、CHOP表达水平及半胱天冬酶活性有关。

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