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1-羟基-8-甲氧基蒽醌通过抑制癌细胞中的6-磷酸葡萄糖脱氢酶逆转顺铂耐药性。

1-Hydroxy-8-methoxy-anthraquinon Reverses Cisplatin Resistance by Inhibiting 6PGD in Cancer Cells.

作者信息

Zhang Huamin, Zhang Haowei, Wang Sihui, Ni Zhihai, Wang Tiejun

机构信息

Department of Radiotherapy, The Second Hospital of Jilin University, Changchun, 130111, Jilin, China.

The Department of Clinical Laboratory, Xinhua Hospital Affiliated to Dalian University, Dalian 116021, China.

出版信息

Open Life Sci. 2019 Nov 15;14:454-461. doi: 10.1515/biol-2019-0051. eCollection 2019 Jan.

DOI:10.1515/biol-2019-0051
PMID:33817181
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7874785/
Abstract

Targeting 6-phosphogluconate dehydrogenase (6PGD) can inhibit cancer cell proliferation and tumor growth. However, the relationship between 6PGD and cisplatin resistance still needs further study. Cisplatin-sensitive and cisplatin-resistant ovarian cancer OV2008 and C13* lines and lung cancer A549 and A549DDP lines were treated with different concentrations of cisplatin and cell viability was evaluated. We also compared the growth rates and the cell cycle distributions between cisplatin-sensitive and cisplatin-resistant cells. The expression level of 6PGD was detected by immunoblotting. The Chou-Talalay method was used to evaluate the effect of a combination treatment using cisplatin and the small molecule inhibitor 1-Hydroxy-8-methoxy-anthraquinon (S3) that targets 6PGD. The cisplatin-resistant ovarian and lung cancer cell lines grew faster than the cisplatin- sensitive cell lines, with more cells in S and G2 phases in cisplatin-resistant cell lines. The expression level of 6PGD in cisplatin-resistant cell lines was significantly increased compared with cisplatin-sensitive cell lines. Furthermore, treatment of cells with the S3 small molecule inhibitor of 6PGD together with cisplatin could overcome cisplatin resistance. The expression level of 6PGD in cisplatin-resistant cells lines was significantly upregulated, and the resistance to cisplatin of drug-resistant cells lines could be overcome when treated with the small molecule inhibitor S3 that specifically targets 6PGD.

摘要

靶向6-磷酸葡萄糖酸脱氢酶(6PGD)可抑制癌细胞增殖和肿瘤生长。然而,6PGD与顺铂耐药性之间的关系仍需进一步研究。用不同浓度的顺铂处理顺铂敏感和顺铂耐药的卵巢癌OV2008和C13*细胞系以及肺癌A549和A549DDP细胞系,并评估细胞活力。我们还比较了顺铂敏感和顺铂耐药细胞之间的生长速率和细胞周期分布。通过免疫印迹检测6PGD的表达水平。采用Chou-Talalay方法评估顺铂与靶向6PGD的小分子抑制剂1-羟基-8-甲氧基蒽醌(S3)联合治疗的效果。顺铂耐药的卵巢和肺癌细胞系比顺铂敏感细胞系生长更快,顺铂耐药细胞系中处于S期和G2期的细胞更多。与顺铂敏感细胞系相比,顺铂耐药细胞系中6PGD的表达水平显著升高。此外,用6PGD的S3小分子抑制剂与顺铂一起处理细胞可以克服顺铂耐药性。顺铂耐药细胞系中6PGD的表达水平显著上调,当用特异性靶向6PGD的小分子抑制剂S3处理时,耐药细胞系对顺铂的耐药性可以被克服。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f781/7874785/4dddeb0afd4a/biol-14-454-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f781/7874785/5dff712c54c4/biol-14-454-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f781/7874785/3f214fc12b1b/biol-14-454-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f781/7874785/aafe7bf06f47/biol-14-454-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f781/7874785/4dddeb0afd4a/biol-14-454-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f781/7874785/5dff712c54c4/biol-14-454-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f781/7874785/3f214fc12b1b/biol-14-454-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f781/7874785/aafe7bf06f47/biol-14-454-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f781/7874785/4dddeb0afd4a/biol-14-454-g004.jpg

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