Literature DB >> 18682572

Regulation and pathological role of p53 in cisplatin nephrotoxicity.

Man Jiang1, Zheng Dong.   

Abstract

Cisplatin is one of the most potent chemotherapy drugs widely used for cancer treatment. However, its use is limited by side effects in normal tissues, particularly the kidneys. Recent studies, using both in vitro and in vivo experimental models, have suggested a critical role for p53 in cisplatin nephrotoxicity. The signaling pathways upstream and downstream of p53 are being investigated and related to renal cell injury and death. Along with the mechanistic studies, renoprotective approaches targeting p53 have been suggested. Further research may integrate p53 signaling with other nephrotoxic signaling pathways, providing a comprehensive understanding of cisplatin nephrotoxicity and leading to the development of effective renoprotective strategies during cancer therapy.

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Year:  2008        PMID: 18682572     DOI: 10.1124/jpet.108.139162

Source DB:  PubMed          Journal:  J Pharmacol Exp Ther        ISSN: 0022-3565            Impact factor:   4.030


  58 in total

1.  Inhibition of PKCδ reduces cisplatin-induced nephrotoxicity without blocking chemotherapeutic efficacy in mouse models of cancer.

Authors:  Navjotsingh Pabla; Guie Dong; Man Jiang; Shuang Huang; M Vijay Kumar; Robert O Messing; Zheng Dong
Journal:  J Clin Invest       Date:  2011-07       Impact factor: 14.808

2.  Renal-targeting triptolide-glucosamine conjugate exhibits lower toxicity and superior efficacy in attenuation of ischemia/reperfusion renal injury in rats.

Authors:  Yu Fu; Qing Lin; Tao Gong; Xun Sun; Zhi-Rong Zhang
Journal:  Acta Pharmacol Sin       Date:  2016-07-11       Impact factor: 6.150

3.  Nephroprotective effect of bee honey and royal jelly against subchronic cisplatin toxicity in rats.

Authors:  Abdelazim Ibrahim; Mabrouk A Abd Eldaim; Mohamed M Abdel-Daim
Journal:  Cytotechnology       Date:  2015-02-27       Impact factor: 2.058

Review 4.  Cellular and Molecular Mechanisms of AKI.

Authors:  Anupam Agarwal; Zheng Dong; Raymond Harris; Patrick Murray; Samir M Parikh; Mitchell H Rosner; John A Kellum; Claudio Ronco
Journal:  J Am Soc Nephrol       Date:  2016-02-09       Impact factor: 10.121

5.  hMSH2 recruits ATR to DNA damage sites for activation during DNA damage-induced apoptosis.

Authors:  Navjotsingh Pabla; Zhengwei Ma; Michael A McIlhatton; Richard Fishel; Zheng Dong
Journal:  J Biol Chem       Date:  2011-02-01       Impact factor: 5.157

Review 6.  Autophagy: molecular machinery, regulation, and implications for renal pathophysiology.

Authors:  Sudharsan Periyasamy-Thandavan; Man Jiang; Patricia Schoenlein; Zheng Dong
Journal:  Am J Physiol Renal Physiol       Date:  2009-03-11

Review 7.  Mitochondrial dysregulation and protection in cisplatin nephrotoxicity.

Authors:  Yuan Yang; Hong Liu; Fuyou Liu; Zheng Dong
Journal:  Arch Toxicol       Date:  2014-05-24       Impact factor: 5.153

8.  FGF21 is induced in cisplatin nephrotoxicity to protect against kidney tubular cell injury.

Authors:  Fanghua Li; Zhiwen Liu; Chengyuan Tang; Juan Cai; Zheng Dong
Journal:  FASEB J       Date:  2018-01-22       Impact factor: 5.191

9.  Inhibitors of histone deacetylases suppress cisplatin-induced p53 activation and apoptosis in renal tubular cells.

Authors:  Guie Dong; Jia Luo; Vijay Kumar; Zheng Dong
Journal:  Am J Physiol Renal Physiol       Date:  2009-11-04

10.  Bromate-induced Changes in p21 DNA Methylation and Histone Acetylation in Renal Cells.

Authors:  Ramya T Kolli; Travis C Glenn; Bradley T Brown; Sukhneeraj P Kaur; Lillie M Barnett; Lawrence H Lash; Brian S Cummings
Journal:  Toxicol Sci       Date:  2019-04-01       Impact factor: 4.849

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