Cisplatin-induced nephrotoxicity and targets of nephroprotection: an update

被引:376
作者
Guinaim dos Santos, Neife Aparecida [1 ]
Carvalho Rodrigues, Maria Augusta [1 ]
Martins, Nadia Maria [1 ]
dos Santos, Antonio Cardozo [1 ]
机构
[1] Univ Sao Paulo, Dept Clin Toxicol Anal & Food Sci, Sch Pharmaceut Sci Ribeirao Preto, BR-14049 Ribeirao Preto, SP, Brazil
关键词
Cisplatin; Nephrotoxicity; Nephroprotection; Oxidative stress; Apoptosis; Molecular mechanisms; Mitochondria; GAMMA-GLUTAMYL-TRANSPEPTIDASE; PLATELET-ACTIVATING-FACTOR; ACUTE-RENAL-FAILURE; COPPER TRANSPORTER CTR1; INDUCED CELL-DEATH; ENDOPLASMIC-RETICULUM STRESS; INDUCED LIPID-PEROXIDATION; NECROSIS-FACTOR-ALPHA; CONJUGATE BETA-LYASE; INDUCED APOPTOSIS;
D O I
10.1007/s00204-012-0821-7
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 [卫生毒理学];
摘要
Cisplatin is a highly effective antitumor agent whose clinical application is limited by the inherent nephrotoxicity. The current measures of nephroprotection used in patients receiving cisplatin are not satisfactory, and studies have focused on the investigation of new possible protective strategies. Many pathways involved in cisplatin nephrotoxicity have been delineated and proposed as targets for nephroprotection, and many new potentially protective agents have been reported. The multiple pathways which lead to renal damage and renal cell death have points of convergence and share some common modulators. The most frequent event among all the described pathways is the oxidative stress that acts as both a trigger and a result. The most exploited pathways, the proposed protective strategies, the achievements obtained so far as well as conflicting data are summarized and discussed in this review, providing a general view of the knowledge accumulated with past and recent research on this subject.
引用
收藏
页码:1233 / 1250
页数:18
相关论文
共 207 条
[1]
Life-or-death decisions by the Bcl-2 protein family [J].
Adams, JM ;
Cory, S .
TRENDS IN BIOCHEMICAL SCIENCES, 2001, 26 (01) :61-66
[2]
Co-supplementation of single and multi doses of vitamins C and E ameliorates cisplatin-induced acute renal failure in mice [J].
Ajith, T. A. ;
Abhishek, G. ;
Roshny, D. ;
Sudheesh, N. P. .
EXPERIMENTAL AND TOXICOLOGIC PATHOLOGY, 2009, 61 (06) :565-571
[3]
Agents ameliorating or augmenting the nephrotoxicity of cisplatin and other platinum compounds: A review of some recent research [J].
Ali, Badreldin H. ;
Al Moundhri, Mansour S. .
FOOD AND CHEMICAL TOXICOLOGY, 2006, 44 (08) :1173-1183
[4]
Antunes LMG, 2000, PHARMACOL RES, V41, P405, DOI 10.1006/phrs.1999.0600
[5]
Cisplatin nephrotoxicity [J].
Arany, I ;
Safirstein, RL .
SEMINARS IN NEPHROLOGY, 2003, 23 (05) :460-464
[6]
Effects of lycopene against cisplatin-induced nephrotoxicity and oxidative stress in rats [J].
Atessahin, A ;
Yilmaz, S ;
Karahan, I ;
Ceribasi, AO ;
Karaoglu, A .
TOXICOLOGY, 2005, 212 (2-3) :116-123
[7]
Naringenin attenuates cisplatin nephrotoxicity in rats [J].
Badary, OA ;
Abdel-Maksoud, S ;
Ahmed, WA ;
Owieda, GH .
LIFE SCIENCES, 2005, 76 (18) :2125-2135
[8]
α-Lipoic acid prevents cisplatin-induced acute kidney injury in rats [J].
Bae, Eun Hui ;
Lee, JongUn ;
Ma, Seong Kwon ;
Kim, In Jin ;
Frokiaer, Jorgen ;
Nielsen, Soren ;
Kim, Sun Young ;
Kim, Soo Wan .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2009, 24 (09) :2692-2700
[9]
Differential roles of hydrogen peroxide and hydroxyl radical in cisplatin-induced cell death in renal proximal tubular epithelial cells [J].
Baek, SM ;
Kwon, CH ;
Kim, JH ;
Woo, JS ;
Jung, JS ;
Kim, YK .
JOURNAL OF LABORATORY AND CLINICAL MEDICINE, 2003, 142 (03) :178-186
[10]
BAJORIN DF, 1986, CANCER RES, V46, P5969