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发现可减少癌细胞中MICA分泌的蛋白质二硫键异构酶P5抑制剂。

Discovery of protein disulfide isomerase P5 inhibitors that reduce the secretion of MICA from cancer cells.

作者信息

Horibe Tomohisa, Torisawa Aya, Okuno Yukiko, Kawakami Koji

机构信息

Department of Pharmacoepidemiology, Graduate School of Medicine and Public Health, Kyoto University, Kyoto, 606-8501 (Japan).

出版信息

Chembiochem. 2014 Jul 21;15(11):1599-606. doi: 10.1002/cbic.201400050. Epub 2014 Jun 11.

Abstract

In order to regulate the activity of P5, which is a member of the protein disulfide isomerase family, we screened a chemical compound library for P5-specific inhibitors, and identified two candidate compounds (anacardic acid and NSC74859). Interestingly, anacardic acid inhibited the reductase activity of P5, but did not inhibit the activity of protein disulfide isomerase (PDI), thiol-disulfide oxidoreductase ERp57, or thioredoxin. NSC74859 inhibited all these enzymes. When we examined the effects of these compounds on the secretion of soluble major histocompatibility complex class-I-related gene A (MICA) from cancer cells, anacardic acid was found to decrease secretion. In addition, anacardic acid was found to reduce the concentration of glutathione up-regulated by the anticancer drug 17-demethoxygeldanamycin in cancer cells. These results suggest that anacardic acid can both inhibit P5 reductase activity and decrease the secretion of soluble MICA from cancer cells. It might be a novel and potent anticancer treatment by targeting P5 on the surface of cancer cells.

摘要

为了调控属于蛋白质二硫键异构酶家族成员的P5的活性,我们针对P5特异性抑制剂筛选了一个化合物文库,并鉴定出两种候选化合物(漆树酸和NSC74859)。有趣的是,漆树酸抑制了P5的还原酶活性,但未抑制蛋白质二硫键异构酶(PDI)、硫醇-二硫键氧化还原酶ERp57或硫氧还蛋白的活性。NSC74859抑制了所有这些酶。当我们检测这些化合物对癌细胞中可溶性主要组织相容性复合体I类相关基因A(MICA)分泌的影响时,发现漆树酸可减少其分泌。此外,还发现漆树酸可降低癌细胞中由抗癌药物17-去甲氧基格尔德霉素上调的谷胱甘肽浓度。这些结果表明,漆树酸既能抑制P5还原酶活性,又能减少癌细胞中可溶性MICA的分泌。它可能是一种通过靶向癌细胞表面的P5的新型强效抗癌治疗方法。

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