Overexpression of Glutathione S-Transferases in Human Diseases: Drug Targets and Therapeutic Implications

被引:14
作者
Lv, Ning [1 ]
Huang, Chunyan [1 ]
Huang, Haoyan [1 ]
Dong, Zhiqiang [2 ]
Chen, Xijing [1 ]
Lu, Chengcan [2 ,3 ]
Zhang, Yongjie [1 ]
机构
[1] China Pharmaceut Univ, Sch Basic Med & Clin Pharm, Clin Pharmacol Res Ctr, Nanjing 211198, Peoples R China
[2] Nanjing Med Univ, Dept Pharm, Affiliated Jiangning Hosp, Nanjing 211100, Peoples R China
[3] Jiangsu Univ, Jiangning Clin Med Coll, Nanjing 211100, Peoples R China
关键词
glutathione S-transferases; overexpression; chemoresistance; neurodegenerative disease; pulmonary fibrosis; GST inhibitors; MULTIDRUG-RESISTANCE PROTEIN-1; ALTERED REDOX REGULATION; CARBONYL N-ANALOGS; GST-PI; CELL-PROLIFERATION; ANTITUMOR-ACTIVITY; SELECTIVE INHIBITORS; MEDIATED RESISTANCE; PARKINSONS-DISEASE; ALZHEIMER-DISEASE;
D O I
10.3390/antiox12111970
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 S-transferases (GSTs) are a major class of phase II metabolic enzymes. Besides their essential role in detoxification, GSTs also exert diverse biological activities in the occurrence and development of various diseases. In the past few decades, much research interest has been paid to exploring the mechanisms of GST overexpression in tumor drug resistance. Correspondingly, many GST inhibitors have been developed and applied, solely or in combination with chemotherapeutic drugs, for the treatment of multi-drug resistant tumors. Moreover, novel roles of GSTs in other diseases, such as pulmonary fibrosis and neurodegenerative diseases, have been recognized in recent years, although the exact regulatory mechanisms remain to be elucidated. This review, firstly summarizes the roles of GSTs and their overexpression in the above-mentioned diseases with emphasis on the modulation of cell signaling pathways and protein functions. Secondly, specific GST inhibitors currently in pre-clinical development and in clinical stages are inventoried. Lastly, applications of GST inhibitors in targeting cell signaling pathways and intracellular biological processes are discussed, and the potential for disease treatment is prospected. Taken together, this review is expected to provide new insights into the interconnection between GST overexpression and human diseases, which may assist future drug discovery targeting GSTs.
引用
收藏
页数:29
相关论文
共 214 条
  • [1] The gold complex auranofin: new perspectives for cancer therapy
    Abdalbari, Farah H.
    Telleria, Carlos M.
    [J]. DISCOVER ONCOLOGY, 2021, 12 (01)
  • [2] Role of redox potential and reactive oxygen species in stress signaling
    Adler, V
    Yin, ZM
    Tew, KD
    Ronai, Z
    [J]. ONCOGENE, 1999, 18 (45) : 6104 - 6111
  • [3] Regulation of JNK signaling by GSTp
    Adler, V
    Yin, ZM
    Fuchs, SY
    Benezra, M
    Rosario, L
    Tew, KD
    Pincus, MR
    Sardana, M
    Henderson, CJ
    Wolf, CR
    Davis, RJ
    Ronai, Z
    [J]. EMBO JOURNAL, 1999, 18 (05) : 1321 - 1334
  • [4] Arsenic-induced apoptosis in malignant cells in vitro
    Akao, Y
    Yamada, H
    Nakagawa, Y
    [J]. LEUKEMIA & LYMPHOMA, 2000, 37 (1-2) : 53 - +
  • [5] Ali-Osman F, 1997, CLIN CANCER RES, V3, P2253
  • [6] Functional analysis of the evolutionarily conserved proline 53 residue in Proteus mirabilis glutathione transferase B1-1
    Allocati, N
    Casalone, E
    Masulli, M
    Ceccarelli, I
    Carletti, E
    Parker, MW
    Di Ilio, C
    [J]. FEBS LETTERS, 1999, 445 (2-3) : 347 - 350
  • [7] Myricetin as a Potential Adjuvant in Chemotherapy: Studies on the Inhibition of Human Glutathione Transferase A1-1
    Alqarni, Mohammed Hamed
    Foudah, Ahmed Ibrahim
    Muharram, Magdy Mohamed
    Alam, Aftab
    Labrou, Nikolaos E.
    [J]. BIOMOLECULES, 2022, 12 (10)
  • [8] The Interaction of the Flavonoid Fisetin with Human Glutathione Transferase A1-1
    Alqarni, Mohammed Hamed
    Foudah, Ahmed Ibrahim
    Muharram, Magdy Mohamed
    Labrou, Nikolaos E.
    [J]. METABOLITES, 2021, 11 (03)
  • [9] Rational design of platinum(IV) compounds to overcome glutathione-S-transferase mediated drug resistance
    Ang, WH
    Khalaila, I
    Allardyce, CS
    Juillerat-Jeanneret, L
    Dyson, PJ
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (05) : 1382 - 1383
  • [10] ARMSTRONG RN, 1993, ADV ENZYMOL RAMB, V69, P1