Literature DB >> 16340240

Therapeutics in renal disease: the road ahead for antiproliferative targets.

Peter J Nelson1, Stuart J Shankland.   

Abstract

Discovery into the molecular basis of renal disease is occurring at an unprecedented rate. With the advent of the NIH Roadmap, there is a greater expectation of translating this knowledge into new treatments. Here, we review the therapeutic strategy to preserve renal function in proliferative renal diseases by directly inhibiting the mitogenic pathways within renal parenchymal cells that promote G0 to G1/S cell-cycle phase progression. Reductionist methodologies have identified several antiproliferative molecular targets, and promising preclinical testing of leading small-molecule drugs to modulate these targets has now led to landmark clinical trials. Yet, this advancement into targeted therapy highlights important differences between the therapeutic goals of molecular nephrology versus molecular oncology and, by extension, the poorly understood role of alternative target activity in drug efficacy. Systems research to clarify these issues should accelerate the development of this promising therapeutic strategy. 2006 S. Karger AG, Basel.

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Year:  2005        PMID: 16340240      PMCID: PMC1440889          DOI: 10.1159/000090138

Source DB:  PubMed          Journal:  Nephron Exp Nephrol        ISSN: 1660-2129


  83 in total

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Authors:  Elias Zerhouni
Journal:  Science       Date:  2003-10-03       Impact factor: 47.728

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Authors:  David B Searls
Journal:  Nat Rev Drug Discov       Date:  2003-08       Impact factor: 84.694

3.  Rapamycin markedly slows disease progression in a rat model of polycystic kidney disease.

Authors:  Yunxia Tao; Jun Kim; Robert W Schrier; Charles L Edelstein
Journal:  J Am Soc Nephrol       Date:  2004-11-24       Impact factor: 10.121

4.  Limitation of podocyte proliferation improves renal function in experimental crescentic glomerulonephritis.

Authors:  Siân V Griffin; Ronald D Krofft; Jeffrey W Pippin; Stuart J Shankland
Journal:  Kidney Int       Date:  2005-03       Impact factor: 10.612

Review 5.  Clinical biomarkers in drug discovery and development.

Authors:  Richard Frank; Richard Hargreaves
Journal:  Nat Rev Drug Discov       Date:  2003-07       Impact factor: 84.694

6.  Inhibition of renal cystic disease development and progression by a vasopressin V2 receptor antagonist.

Authors:  Vincent H Gattone; Xiaofang Wang; Peter C Harris; Vicente E Torres
Journal:  Nat Med       Date:  2003-09-21       Impact factor: 53.440

7.  Pentoxifylline inhibits platelet-derived growth factor-stimulated cyclin D1 expression in mesangial cells by blocking Akt membrane translocation.

Authors:  Shuei-Liong Lin; Ruey-Hwa Chen; Yung-Ming Chen; Wen-Chih Chiang; Tun-Jun Tsai; Bor-Shen Hsieh
Journal:  Mol Pharmacol       Date:  2003-10       Impact factor: 4.436

8.  PPARgamma ligand attenuates PDGF-induced mesangial cell proliferation: role of MAP kinase.

Authors:  Siddhartha S Ghosh; Todd W B Gehr; Shobha Ghosh; Itaf Fakhry; Domenic A Sica; Vijay Lyall; Anton C Schoolwerth
Journal:  Kidney Int       Date:  2003-07       Impact factor: 10.612

9.  Chemical proteomic analysis reveals alternative modes of action for pyrido[2,3-d]pyrimidine kinase inhibitors.

Authors:  Josef Wissing; Klaus Godl; Dirk Brehmer; Stephanie Blencke; Martina Weber; Peter Habenberger; Matthias Stein-Gerlach; Andrea Missio; Matt Cotten; Stefan Müller; Henrik Daub
Journal:  Mol Cell Proteomics       Date:  2004-10-08       Impact factor: 5.911

10.  Combination treatment of PKD utilizing dual inhibition of EGF-receptor activity and ligand bioavailability.

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  2 in total

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Authors:  Derek P DiRocco; John Bisi; Patrick Roberts; Jay Strum; Kwok-Kin Wong; Norman Sharpless; Benjamin D Humphreys
Journal:  Am J Physiol Renal Physiol       Date:  2013-12-11

Review 2.  The cell cycle and acute kidney injury.

Authors:  Peter M Price; Robert L Safirstein; Judit Megyesi
Journal:  Kidney Int       Date:  2009-06-17       Impact factor: 10.612

  2 in total

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