gamma-Glutamyl transpeptidase, a glutathionase: its expression and function in carcinogenesis
- PMID: 9679564
- DOI: 10.1016/s0009-2797(97)00170-1
gamma-Glutamyl transpeptidase, a glutathionase: its expression and function in carcinogenesis
Abstract
gamma-Glutamyl transpeptidase (GGT) is found throughout the plant and animal kingdoms. It is a cell surface glycoprotein that cleaves gamma-glutamyl amide bonds. The most abundant physiologic substrates for the enzyme are glutathione and glutathione-conjugated compounds. GGT initiates the cleavage of extracellular glutathione into its constituent amino acids which can then be transported into the cell. It also catalyzes the initial step in the conversion of glutathione-conjugated compounds to mercapturic acids. GGT is expressed at high levels in many human tumors and in many carcinogen-induced tumors in animals. These observations have lead an increased focus on the role of the enzyme in the development and treatment of tumors. This chapter begins with an overview of the structure and function of GGT in normal tissues. A summary of its expression in neoplastic tissues and the ways in which GGT effects the response of tumors to chemotherapy follows. The chapter concludes with a discussion of strategies for using GGT to activate and target chemotherapy drugs to tumors as a means of improving treatment for common human malignancies.
Similar articles
-
Gamma-glutamyl transpeptidase: redox regulation and drug resistance.Adv Cancer Res. 2014;122:103-41. doi: 10.1016/B978-0-12-420117-0.00003-7. Adv Cancer Res. 2014. PMID: 24974180 Free PMC article. Review.
-
Gamma-glutamyl transpeptidase accelerates tumor growth and increases the resistance of tumors to cisplatin in vivo.Carcinogenesis. 1999 Apr;20(4):553-9. doi: 10.1093/carcin/20.4.553. Carcinogenesis. 1999. PMID: 10223181 Free PMC article.
-
Gamma-glutamyl transpeptidase in glutathione biosynthesis.Methods Enzymol. 2005;401:468-83. doi: 10.1016/S0076-6879(05)01028-1. Methods Enzymol. 2005. PMID: 16399403
-
Extracellular glutathione is a source of cysteine for cells that express gamma-glutamyl transpeptidase.Biochemistry. 1993 Jun 22;32(24):6302-6. doi: 10.1021/bi00075a026. Biochemistry. 1993. PMID: 8099811
-
gamma-Glutamyl transpeptidase. What does the organization and expression of a multipromoter gene tell us about its functions?Am J Pathol. 1995 Nov;147(5):1175-85. Am J Pathol. 1995. PMID: 7485380 Free PMC article. Review.
Cited by
-
Gamma-glutamyl compounds: substrate specificity of gamma-glutamyl transpeptidase enzymes.Anal Biochem. 2011 Jul 15;414(2):208-14. doi: 10.1016/j.ab.2011.03.026. Epub 2011 Mar 27. Anal Biochem. 2011. PMID: 21447318 Free PMC article.
-
Novel Value of Preoperative Gamma-Glutamyltransferase Levels in the Prognosis of AFP-Negative Hepatocellular Carcinoma.Dis Markers. 2020 Jul 10;2020:4269460. doi: 10.1155/2020/4269460. eCollection 2020. Dis Markers. 2020. PMID: 32695241 Free PMC article.
-
Acceleration of anaerobic cysteine transformations to sulfane sulfur consequent to γ-glutamyl transpeptidase inhibition.ScientificWorldJournal. 2012;2012:253724. doi: 10.1100/2012/253724. Epub 2012 Apr 30. ScientificWorldJournal. 2012. PMID: 22629124 Free PMC article.
-
Helicobacter pylori Virulence Factors Exploiting Gastric Colonization and its Pathogenicity.Toxins (Basel). 2019 Nov 19;11(11):677. doi: 10.3390/toxins11110677. Toxins (Basel). 2019. PMID: 31752394 Free PMC article. Review.
-
Deficient glutathione in the pathophysiology of mycotoxin-related illness.Toxins (Basel). 2014 Feb 10;6(2):608-23. doi: 10.3390/toxins6020608. Toxins (Basel). 2014. PMID: 24517907 Free PMC article. Review.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous