Oxidative Stress in Cancer Therapy: Friend or Enemy?

被引:84
作者
Azmanova, Maria [2 ]
Pitto-Barry, Anais [1 ,2 ]
机构
[1] Univ Paris Saclay, CNRS, Inst Galien Paris Saclay, 5 Rue JB Clement, F-92296 Chatenay Malabry, France
[2] Univ Bradford, Sch Chem & Biosci, Bradford BD7 1DP, W Yorkshire, England
关键词
antitumour agents; bioinorganic chemistry; metal complexes; reactive oxygen species; redox chemistry; ENDOPLASMIC-RETICULUM STRESS; TUMOR-NECROSIS-FACTOR; HYDROGEN-PEROXIDE; THIOREDOXIN REDUCTASE; CELL-DEATH; PROSTATE-CANCER; LUNG-CANCER; VITAMIN-E; MATRIX METALLOPROTEINASES; POLYPYRIDYL COMPLEXES;
D O I
10.1002/cbic.202100641
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
Excessive cellular oxidative stress is widely perceived as a key factor in pathophysiological conditions and cancer development. Healthy cells use several mechanisms to maintain intracellular levels of reactive oxygen species (ROS) and overall redox homeostasis to avoid damage to DNA, proteins, and lipids. Cancer cells, in contrast, exhibit elevated ROS levels and upregulated protective antioxidant pathways. Counterintuitively, such elevated oxidative stress and enhanced antioxidant defence mechanisms in cancer cells provide a therapeutic opportunity for the development of drugs with different anticancer mechanisms of action (MoA). In this review, oxidative stress and the role of ROS in cells are described. The tumour-suppressive and tumour-promotive functions of ROS are discussed, and these two different therapeutic strategies (increasing or decreasing ROS to fight cancer) are compared. Clinically approved drugs with demonstrated oxidative stress anticancer MoAs are highlighted followed by description of examples of metal-based anticancer drug candidates causing oxidative stress in cancer cells via novel MoAs.
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页数:16
相关论文
共 195 条
[61]   Redox compartmentalization in eukaryotic cells [J].
Go, Young-Mi ;
Jones, Dean P. .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2008, 1780 (11) :1271-1290
[62]  
Gogos CA, 1998, CANCER, V82, P395, DOI 10.1002/(SICI)1097-0142(19980115)82:2<403::AID-CNCR21>3.0.CO
[63]  
2-1
[64]   Mitochondrial targeted catalase suppresses invasive breast cancer in mice [J].
Goh, Jorming ;
Enns, Linda ;
Fatemie, Soroosh ;
Hopkins, Heather ;
Morton, John ;
Pettan-Brewer, Christina ;
Ladiges, Warren .
BMC CANCER, 2011, 11
[65]   Beclin 1 and autophagy are required for the tumorigenicity of breast cancer stem-like/progenitor cells [J].
Gong, C. ;
Bauvy, C. ;
Tonelli, G. ;
Yue, W. ;
Delomenie, C. ;
Nicolas, V. ;
Zhu, Y. ;
Domergue, V. ;
Marin-Esteban, V. ;
Tharinger, H. ;
Delbos, L. ;
Gary-Gouy, H. ;
Morel, A-P ;
Ghavami, S. ;
Song, E. ;
Codogno, P. ;
Mehrpour, M. .
ONCOGENE, 2013, 32 (18) :2261-2272
[66]   The beta-carotene and retinol efficacy trial:: Incidence of lung cancer and cardiovascular disease mortality during 6-year follow-up after stopping β-carotene and retinol supplements [J].
Goodman, GE ;
Thornquist, MD ;
Balmes, J ;
Cullen, MR ;
Meyskens, FL ;
Omenn, GS ;
Valanis, B ;
Williams, JH .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2004, 96 (23) :1743-1750
[67]   DIRECT EVIDENCE FOR TUMOR NECROSIS FACTOR-INDUCED MITOCHONDRIAL REACTIVE OXYGEN INTERMEDIATES AND THEIR INVOLVEMENT IN CYTOTOXICITY [J].
GOOSSENS, V ;
GROOTEN, J ;
DEVOS, K ;
FIERS, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (18) :8115-8119
[68]   Modulation of oxidative stress as an anticancer strategy [J].
Gorrini, Chiara ;
Harris, Isaac S. ;
Mak, Tak W. .
NATURE REVIEWS DRUG DISCOVERY, 2013, 12 (12) :931-947
[69]   Use of antioxidant supplements during breast cancer treatment: a comprehensive review [J].
Greenlee, Heather ;
Hershman, Dawn L. ;
Jacobson, Judith S. .
BREAST CANCER RESEARCH AND TREATMENT, 2009, 115 (03) :437-452
[70]   Cellular and cell-free studies of catalytic DNA cleavage by ruthenium polypyridyl complexes containing redox-active intercalating ligands [J].
Griffith, Cynthia ;
Dayoub, Adam S. ;
Jaranatne, Thamara ;
Alatrash, Nagham ;
Mohamedi, Ali ;
Abayan, Kenneth ;
Breitbach, Zachary S. ;
Armstrong, Daniel W. ;
MacDonnell, Frederick M. .
CHEMICAL SCIENCE, 2017, 8 (05) :3726-3740