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谷胱甘肽转移酶:克服实体瘤化疗耐药性的潜在靶点。

Glutathione Transferases: Potential Targets to Overcome Chemoresistance in Solid Tumors.

机构信息

Institute of Medical and Clinical Biochemistry, Faculty of Medicine, University of Belgrade, 11 000 Belgrade, Serbia.

Faculty of Medicine, University of Belgrade, 11 000 Belgrade, Serbia.

出版信息

Int J Mol Sci. 2018 Nov 28;19(12):3785. doi: 10.3390/ijms19123785.

Abstract

Multifunctional enzymes glutathione transferases (GSTs) are involved in the development of chemoresistance, thus representing a promising target for a novel approach in cancer treatment. This superfamily of polymorphic enzymes exhibits extraordinary substrate promiscuity responsible for detoxification of numerous conventional chemotherapeutics, at the same time regulating signaling pathways involved in cell proliferation and apoptosis. In addition to upregulated GST expression, different cancer cell types have a unique GST signature, enabling targeted selectivity for isoenzyme specific inhibitors and pro-drugs. As a result of extensive research, certain GST inhibitors are already tested in clinical trials. Catalytic properties of GST isoenzymes are also exploited in bio-activation of specific pro-drugs, enabling their targeted accumulation in cancer cells with upregulated expression of the appropriate GST isoenzyme. Moreover, the latest approach to increase specificity in treatment of solid tumors is development of GST pro-drugs that are derivatives of conventional anti-cancer drugs. A future perspective is based on the design of new drugs, which would selectively target GST overexpressing cancers more prone to developing chemoresistance, while decreasing side effects in off-target cells.

摘要

多功能酶谷胱甘肽转移酶 (GSTs) 参与化疗耐药的发展,因此代表了癌症治疗新方法的有前途的靶点。这种多态性酶的超家族表现出非凡的底物混杂性,负责解毒许多常规化疗药物,同时调节参与细胞增殖和凋亡的信号通路。除了 GST 表达上调外,不同的癌细胞类型还有独特的 GST 特征,能够针对同工酶特异性抑制剂和前药进行靶向选择性。由于广泛的研究,某些 GST 抑制剂已经在临床试验中进行了测试。GST 同工酶的催化特性也被用于特定前药的生物激活,使它们能够在 GST 同工酶表达上调的癌细胞中靶向积累。此外,增加实体瘤治疗特异性的最新方法是开发 GST 前药,这些前药是传统抗癌药物的衍生物。未来的前景是基于设计新的药物,这些药物将选择性地针对 GST 过表达的癌症,这些癌症更容易产生化疗耐药性,同时减少对非靶细胞的副作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4264/6321424/06c41ed0a4c2/ijms-19-03785-g001.jpg

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