HDAC inhibitors in kidney development and disease

被引:47
作者
Brilli, Lauren L. [1 ]
Swanhart, Lisa M. [1 ]
de Caestecker, Mark P. [2 ]
Hukriede, Neil A. [1 ]
机构
[1] Univ Pittsburgh, Dept Dev Biol, Pittsburgh, PA 15213 USA
[2] Vanderbilt Univ, Med Ctr, Dept Med, Div Nephrol, Nashville, TN USA
基金
美国国家卫生研究院;
关键词
Histone deacetylase; HDACi; Kidney development; Kidney regeneration; Renal injury; Renal disease; HISTONE DEACETYLASE INHIBITOR; RENAL-CELL-CARCINOMA; TO-MESENCHYMAL TRANSITION; RETINOIC ACID; VALPROIC ACID; PHASE-II; INTERSTITIAL FIBROSIS; GENE-EXPRESSION; TGF-BETA; GROWTH;
D O I
10.1007/s00467-012-2320-8
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
The discovery that histone deacetylase inhibitors (HDACis) can attenuate acute kidney injury (AKI)-mediated damage and reduce fibrosis in kidney disease models has opened the possibility of utilizing HDACis as therapeutics for renal injury. Studies to date have made it abundantly clear that HDACi treatment results in a plethora of molecular changes, which are not always linked to histone acetylation, and that there is an essential need to understand the specific target(s) of any HDACi of interest. New lines of investigation are beginning to delve more deeply into target identification of specific HDACis and to address the relative toxicity of different HDACi classes. This review will focus on the utilization of HDACis during kidney organogenesis, injury, and disease, as well as on the development of these compounds as therapeutics.
引用
收藏
页码:1909 / 1921
页数:13
相关论文
共 115 条
  • [1] Long-Term Administration of the Histone Deacetylase Inhibitor Vorinostat Attenuates Renal Injury in Experimental Diabetes through an Endothelial Nitric Oxide Synthase-Dependent Mechanism
    Advani, Andrew
    Huang, Qingling
    Thai, Kerri
    Advani, Suzanne L.
    White, Kathryn E.
    Kelly, Darren J.
    Yuen, Darren A.
    Connelly, Kim A.
    Marsden, Philip A.
    Gilbert, Richard E.
    [J]. AMERICAN JOURNAL OF PATHOLOGY, 2011, 178 (05) : 2205 - 2214
  • [2] The promise of retinoids to fight against cancer
    Altucci, L
    Gronemeyer, H
    [J]. NATURE REVIEWS CANCER, 2001, 1 (03) : 181 - 193
  • [3] Restoration of CREB function ameliorates cisplatin cytotoxicity in renal tubular cells
    Arany, Istvan
    Herbert, Johann
    Herbert, Zsolt
    Safirstein, Robert L.
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2008, 294 (03) : F577 - F581
  • [4] Arany I, 2011, ANTICANCER RES, V31, P3267
  • [5] A Phase II study of 13-cis-retinoic acid in patients with advanced renal cell carcinoma
    Berg, WJ
    Schwartz, LH
    Amsterdam, A
    Mazumdar, M
    Vlamis, V
    Law, TM
    Nanus, DM
    Motzer, RJ
    [J]. INVESTIGATIONAL NEW DRUGS, 1997, 15 (04) : 353 - 355
  • [6] Deletion of histone deacetylase 3 reveals critical roles in S phase progression and DNA damage control
    Bhaskara, Srividya
    Chyla, Brenda J.
    Amann, Joseph M.
    Knutson, Sarah K.
    Cortez, David
    Sun, Zu-Wen
    Hiebert, Scott W.
    [J]. MOLECULAR CELL, 2008, 30 (01) : 61 - 72
  • [7] Isoform-selective histone deacetylase inhibitors
    Bieliauskas, Anton V.
    Pflum, Mary Kay H.
    [J]. CHEMICAL SOCIETY REVIEWS, 2008, 37 (07) : 1402 - 1413
  • [8] Anticancer activities of histone deacetylase inhibitors
    Bolden, Jessica E.
    Peart, Melissa J.
    Johnstone, Ricky W.
    [J]. NATURE REVIEWS DRUG DISCOVERY, 2006, 5 (09) : 769 - 784
  • [9] Chemical phylogenetics of histone deacetylases
    Bradner, James E.
    West, Nathan
    Grachan, Melissa L.
    Greenberg, Edward F.
    Haggarty, Stephen J.
    Warnow, Tandy
    Mazitschek, Ralph
    [J]. NATURE CHEMICAL BIOLOGY, 2010, 6 (03) : 238 - 243
  • [10] Protein Acetylation in the Cardiorenal Axis The Promise of Histone Deacetylase Inhibitors
    Bush, Erik W.
    McKinsey, Timothy A.
    [J]. CIRCULATION RESEARCH, 2010, 106 (02) : 272 - 284