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P53 in kidney injury and repair: Mechanism and therapeutic potentials

  • Chengyuan Tang
    ,
  • Zhengwei Ma
    ,
  • Jiefu Zhu
    ,
  • Zhiwen Liu
    ,
  • Yuxue Liu
    ,
  • Yu Liu
*Corresponding author for this work
Scholary Output:
Contribution to journal
Review article
Peer-review

Abstract

Acute kidney injury (AKI) is a major kidney disease with poor clinical outcome. Besides its acute consequence of high mortality, AKI may also contribute significantly to the occurrence and progression of chronic kidney diseases (CKD). Accumulating evidence has demonstrated that maladaptive and incomplete kidney repair after AKI leads to the development of renal fibrosis and, ultimately, CKD. p53, a well-known tumor suppressor, plays a critical role in AKI and subsequent kidney repair through the regulation of various cell biologic processes, including apoptosis, cell cycle arrest, and autophagy. Despite the notable progress in deciphering the involvement of p53 in kidney injury and repair, the underlying mechanisms of p53 in these pathological processes remain largely unknown. Further investigation in this area is essential for the application of p53 as therapeutic target to prevent and treat AKI or impede its progression to CKD. In this review, we summarize the recent advances in understanding p53 regulation of AKI and kidney repair, pinpoint the potential of p53 as a therapeutic target, and present future research interests and directions.

Publication Information

Output type

Scholary Output:
Contribution to journal
Review article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 5-12 (8 pages)

Journal (Volume, Issue Number)

Pharmacology and Therapeutics (Volume 195)

Publication milestones

  • Accepted/In press - 01/01/2018
  • Published - 03/2019

Publication status

Published - 03/2019

ISSN

0163-7258

Publication IDs

  • Scopus: 85055173334
  • PubMed: 30347214

Publication metrics

Metrics

SciVal
FWCI
2.38
SciVal
Author count
8
SciVal
citations
23
SciVal
Paper percentile
97
SciVal
Top percentile
5
Fractional count
1
Fractional count
0.13
Fractional count
7
Fractional count
0.88
Fractional count
1
Fractional count
1
Scopus
citations

PlumX, opens in new tab

Captures
46
Citation count
113

Funding Details

This study was supported partly by the grants from National Natural Science Foundation of China ( 81720108008, 81870474 , 81430017 ), the National Institutes of Health of USA, and Department of Veterans Administration of USA.
FundersFunding numbers
US Department of Veterans Administration
-
NIH
-
NSFC
81720108008, 81870474, 81430017