Chronic Exposure of Cisplatin Induces GRP78 Expression in Ovarian Cancer

Tai‐An Chen, Shan Xu
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引用次数: 6

Abstract

Glucose regulated protein 78 (GRP78) is a type of molecular chaperone. Previous research indicates that it may possibly be induced by exposure of cisplatin in ovarian cancer and related to survival rate. Methods: The expression of GRP78 in HOSE cells and ovarian cancer cells are tested by Western Blotting. Kaplan Meier Analysis is utilized to show the relationship between GRP78 expression and survival rate of patients who receives cisplatin treatment. Both acute cisplatin treatment and chronic exposure to cisplatin are carried out on ovarian cancer cell lines, followed by the subsequent Western Blotting. Results: GRP78 is expressed in both HOSE cells and Ovarian Cancer Cells, but the HOSE cell line shows evidently less expression of GRP78 than the tested ovarian cancer cell lines. Kaplan Meier Analysis shows that higher GRP78 expression level correlates to lower 5-year progression free survival rate. Chronic exposure to cisplatin induces GRP78 expression. Conclusions: GRP78 is expressed in both HOSE cells and ovarian cancer cells. The hypothesis is that efficient metabolism of cancer cells, which relates to accumulation of unfolded polypeptides in the ER, may be responsible for the over-expression of GRP78 of some ovarian cancer cell lines. Kaplan Meier Analysis suggests an important role of GRP78 in cancer progression and the potential of GRP78 as an ovarian cancer diagnosis marker. Chronic exposure to cisplatin induces GRP78 may increase the chemoresistance that GRP78 generates. Why acute cisplatin treatment cannot induce GRP78 needs further researches.
顺铂慢性暴露诱导卵巢癌GRP78表达
葡萄糖调节蛋白78 (GRP78)是一种分子伴侣。既往研究表明,这可能与卵巢癌患者暴露于顺铂所致,并与生存率有关。方法:采用Western Blotting检测卵巢癌细胞和卵巢癌细胞中GRP78的表达。Kaplan Meier分析法显示GRP78表达与顺铂治疗患者生存率的关系。对卵巢癌细胞系进行急性顺铂治疗和慢性暴露于顺铂,随后进行Western Blotting。结果:GRP78在HOSE细胞和卵巢癌细胞中均有表达,但HOSE细胞系表达GRP78明显低于卵巢癌细胞系。Kaplan Meier分析显示,GRP78表达水平越高,5年无进展生存率越低。慢性顺铂暴露诱导GRP78表达。结论:GRP78在卵巢癌细胞和HOSE细胞中均有表达。假设癌细胞的高效代谢与内质网中未折叠多肽的积累有关,这可能是一些卵巢癌细胞系GRP78过度表达的原因。Kaplan Meier分析提示GRP78在癌症进展中的重要作用以及GRP78作为卵巢癌诊断标志物的潜力。慢性暴露于顺铂诱导GRP78可能增加GRP78产生的化疗耐药。急性顺铂治疗不能诱导GRP78的原因有待进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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