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人类肝癌中的谷胱甘肽S-转移酶

Glutathione S-transferases in human liver cancer.

作者信息

Hayes P C, May L, Hayes J D, Harrison D J

机构信息

Department of Medicine, University of Edinburgh.

出版信息

Gut. 1991 Dec;32(12):1546-9. doi: 10.1136/gut.32.12.1546.

DOI:10.1136/gut.32.12.1546
PMID:1663474
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1379260/
Abstract

An immunohistochemical study of glutathione S-transferase (GST) expression in hepatocellular carcinoma and cholangiocarcinoma is described. Unlike most animal models of hepatic malignancy pi class GST was not consistently overexpressed in hepatocellular carcinoma. This tumour type either predominantly expressed alpha class GST or failed to express GST. By contrast, cholangiocarcinoma always expressed pi class GST, presumably reflecting the tissue of origin, since in human biliary epithelium pi class GST is the predominant GST. The variable expression of pi class GST which was observed in hepatocellular carcinoma may reflect transformation of hepatocytes damaged by toxins, since this GST can be induced after a chemical insult such as alcohol. As well as indicating the biochemical heterogeneity of hepatocellular carcinoma with respect to GST, this study indicates the need for further study of the nature of inherent drug resistance in these tumour types.

摘要

本文描述了一项关于谷胱甘肽S-转移酶(GST)在肝细胞癌和胆管癌中表达的免疫组织化学研究。与大多数肝恶性肿瘤动物模型不同,π类GST在肝细胞癌中并非始终过度表达。这种肿瘤类型要么主要表达α类GST,要么不表达GST。相比之下,胆管癌总是表达π类GST,这可能反映了其起源组织,因为在人胆管上皮中,π类GST是主要的GST。在肝细胞癌中观察到的π类GST的可变表达可能反映了受毒素损伤的肝细胞的转化,因为这种GST可在化学损伤(如酒精)后被诱导。这项研究不仅表明了肝细胞癌在GST方面的生化异质性,还表明有必要进一步研究这些肿瘤类型中固有耐药性的本质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/943e/1379260/25d0c7b1a5f7/gut00593-0130-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/943e/1379260/a6bd2ece6280/gut00593-0129-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/943e/1379260/d341f0340e38/gut00593-0129-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/943e/1379260/f4e393df23bd/gut00593-0129-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/943e/1379260/3f9cfbbb6b47/gut00593-0129-d.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/943e/1379260/25d0c7b1a5f7/gut00593-0130-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/943e/1379260/a6bd2ece6280/gut00593-0129-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/943e/1379260/d341f0340e38/gut00593-0129-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/943e/1379260/f4e393df23bd/gut00593-0129-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/943e/1379260/3f9cfbbb6b47/gut00593-0129-d.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/943e/1379260/25d0c7b1a5f7/gut00593-0130-a.jpg

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本文引用的文献

1
Microsomal glutathione S-transferase. Purification, initial characterization and demonstration that it is not identical to the cytosolic glutathione S-transferases A, B and C.微粒体谷胱甘肽S-转移酶。纯化、初步特性鉴定及证明其与胞质谷胱甘肽S-转移酶A、B和C不同。
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Purification of human hepatic glutathione S-transferases and the development of a radioimmunoassay for their measurement in plasma.人肝谷胱甘肽S-转移酶的纯化及其血浆中含量测定的放射免疫分析方法的建立。
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Glutathione S-transferase in human hepatocellular carcinoma.
谷胱甘肽 S-转移酶 P 缺乏通过 JNK 依赖性增强肝糖异生诱导葡萄糖不耐受。
Am J Physiol Endocrinol Metab. 2018 Nov 1;315(5):E1005-E1018. doi: 10.1152/ajpendo.00345.2017. Epub 2018 Aug 28.
4
Identification of Candidate Serum Biomarkers for Schistosoma mansoni Infected Mice Using Multiple Proteomic Platforms.使用多种蛋白质组学平台鉴定曼氏血吸虫感染小鼠的候选血清生物标志物
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5
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Infect Immun. 2010 Feb;78(2):618-28. doi: 10.1128/IAI.00647-09. Epub 2009 Nov 23.
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Multifactorial nature of hepatocellular carcinoma drug resistance: could plant polyphenols be helpful?肝细胞癌耐药性的多因素本质:植物多酚会有所帮助吗?
World J Gastroenterol. 2007 Apr 14;13(14):2037-43. doi: 10.3748/wjg.v13.i14.2037.
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Increased resistance to acetaminophen hepatotoxicity in mice lacking glutathione S-transferase Pi.缺乏谷胱甘肽S-转移酶Pi的小鼠对乙酰氨基酚肝毒性的抵抗力增强。
Proc Natl Acad Sci U S A. 2000 Nov 7;97(23):12741-5. doi: 10.1073/pnas.220176997.
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J Cancer Res Clin Oncol. 1996;122(10):619-24. doi: 10.1007/BF01221194.
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Gut. 1993 Apr;34(4):549-53. doi: 10.1136/gut.34.4.549.
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Expression of glutathione S-transferases in normal and malignant pancreas: an immunohistochemical study.
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