Glutathione dysregulation and the etiology and progression of human diseases

被引:846
作者
Ballatori, Nazzareno [1 ]
Krance, Suzanne M. [1 ]
Notenboom, Sylvia [1 ]
Shi, Shujie [1 ]
Tieu, Kim [1 ]
Hammond, Christine L. [1 ]
机构
[1] Univ Rochester, Sch Med, Dept Environm Med, Rochester, NY 14642 USA
关键词
aging; cancer; cardiovascular diseases; glutathione; metabolic diseases; neurodegenerative diseases; GAMMA-GLUTAMYLCYSTEINE SYNTHETASE; MULTIDRUG-RESISTANCE PROTEIN-1; TUMOR-NECROSIS-FACTOR; CONDUCTANCE REGULATOR PROTEIN; ANTIGEN-PRESENTING CELLS; SUBUNIT GENE-EXPRESSION; PANCREATIC BETA-CELLS; B16; MELANOMA-CELLS; N-ACETYL-CYSTEINE; OXIDATIVE STRESS;
D O I
10.1515/BC.2009.033
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Glutathione (GSH) plays an important role in a multitude of cellular processes, including cell differentiation, proliferation, and apoptosis, and as a result, disturbances in GSH homeostasis are implicated in the etiology and/or progression of a number of human diseases, including cancer, diseases of aging, cystic fibrosis, and cardiovascular, inflammatory, immune, metabolic, and neurodegenerative diseases. Owing to the pleiotropic effects of GSH on cell functions, it has been quite difficult to define the role of GSH in the onset and/or the expression of human diseases, although significant progress is being made. GSH levels, turnover rates, and/or oxidation state can be compromised by inherited or acquired defects in the enzymes, transporters, signaling molecules, or transcription factors that are involved in its homeostasis, or from exposure to reactive chemicals or metabolic intermediates. GSH deficiency or a decrease in the GSH/glutathione disulfide ratio manifests itself largely through an increased susceptibility to oxidative stress, and the resulting damage is thought to be involved in diseases, such as cancer, Parkinson's disease, and Alzheimer's disease. In addition, imbalances in GSH levels affect immune system function, and are thought to play a role in the aging process. Just as low intracellular GSH levels decrease cellular antioxidant capacity, elevated GSH levels generally increase antioxidant capacity and resistance to oxidative stress, and this is observed in many cancer cells. The higher GSH levels in some tumor cells are also typically associated with higher levels of GSH-related enzymes and transporters. Although neither the mechanism nor the implications of these changes are well defined, the high GSH content makes cancer cells chemoresistant, which is a major factor that limits drug treatment. The present report highlights and integrates the growing connections between imbalances in GSH homeostasis and a multitude of human diseases.
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收藏
页码:191 / 214
页数:24
相关论文
共 309 条
[71]   INHIBITION OF THE DIFFERENTIATION OF HUMAN MYELOID CELL-LINES BY REDOX CHANGES INDUCED THROUGH GLUTATHIONE DEPLETION [J].
ESPOSITO, F ;
AGOSTI, V ;
MORRONE, G ;
MORRA, F ;
CUOMO, C ;
RUSSO, T ;
VENUTA, S ;
CIMINO, F .
BIOCHEMICAL JOURNAL, 1994, 301 :649-653
[72]   Glutathione in cancer biology and therapy [J].
Estrela, JM ;
Ortega, A ;
Obrador, E .
CRITICAL REVIEWS IN CLINICAL LABORATORY SCIENCES, 2006, 43 (02) :143-181
[73]   Apoptosis in human disease: A new skin for the old ceremony? [J].
Fadeel, B ;
Orrenius, S ;
Zhivotovsky, B .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 266 (03) :699-717
[74]  
Franco R., 2007, Archives of Physiology and Biochemistry, V113, P234, DOI 10.1080/13813450701661198
[75]   Abnormal glutathione transport in cystic fibrosis airway epithelia [J].
Gao, L ;
Kim, KJ ;
Yankaskas, JR ;
Forman, HJ .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1999, 277 (01) :L113-L118
[76]   Synthetic chloride channel restores glutathione secretion in cystic fibrosis airway epithelia [J].
Gao, L ;
Broughman, JR ;
Iwamoto, T ;
Tomich, JM ;
Venglarik, CJ ;
Forman, HJ .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2001, 281 (01) :L24-L30
[77]   Redox regulation of hepatocyte apoptosis [J].
Garcia-Ruiz, Carmen ;
Fernandez-Checa, Jose C. .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2007, 22 :S38-S42
[78]   Differential effect of nitric oxide on glutathione metabolism and mitochondrial function in astrocytes and neurones: implications for neuroprotection/neurodegeneration? [J].
Gegg, ME ;
Beltran, B ;
Salas-Pino, S ;
Bolanos, JP ;
Clark, JB ;
Moncada, S ;
Heales, SJR .
JOURNAL OF NEUROCHEMISTRY, 2003, 86 (01) :228-237
[79]   Glutathionylation pathways in drug response [J].
Ghezzi, Pietro ;
Di Sirnplicio, Paolo .
CURRENT OPINION IN PHARMACOLOGY, 2007, 7 (04) :398-403
[80]   Rescue of cells from apoptosis by inhibition of active GSH extrusion [J].
Ghibelli, L ;
Fanelli, C ;
Rotilio, G ;
Lafavia, E ;
Coppola, S ;
Colussi, C ;
Civitareale, P ;
Ciriolo, MR .
FASEB JOURNAL, 1998, 12 (06) :479-486