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Polycystic kidney disease in 2011

Connecting the dots toward a polycystic kidney disease therapy

Understanding the complex interactions between the various pathways disrupted in polycystic kidney and liver disease is essential to identify and optimize therapies for these disorders. Studies published in the past year have demonstrated a functional interaction between the main proteins implicated in these diseases and identified novel therapeutic approaches.

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References

  1. Fedeles, S. V. et al. A genetic interaction network of five genes for human polycystic kidney and liver diseases defines polycystin-1 as the central determinant of cyst formation. Nat. Genet. 43, 639–647 (2011).

    Article  CAS  Google Scholar 

  2. Reif, G. A. et al. Tolvaptan inhibits ERK-dependent cell proliferation, Cl secretion, and in vitro cyst growth of human ADPKD cells stimulated by vasopressin. Am. J. Physiol. Renal Physiol. 301, F1005–F1013 (2011).

    Article  CAS  Google Scholar 

  3. Higashihara, E. et al. for the TEMPOFormula and 156-05-002 Study Investigators. Tolvaptan in autosomal dominant polycystic kidney disease: three years' experience. Clin. J. Am. Soc. Nephrol. 6, 2499–2507 (2011).

    Article  CAS  Google Scholar 

  4. Takiar, V. et al. Activating AMP-activated protein kinase (AMPK) slows renal cystogenesis. Proc. Natl Acad. Sci. USA 108, 2462–2467 (2011).

    Article  CAS  Google Scholar 

  5. Yoshihara, D. et al. PPAR-γ agonist ameliorates kidney and liver disease in an orthologous rat model of human autosomal recessive polycystic kidney disease. Am. J. Physiol. Renal Physiol. 300, F465–F474 (2011).

    Article  CAS  Google Scholar 

  6. Blazer-Yost, B. L. et al. Pioglitazone attenuates cystic burden in the PCK rodent model of polycystic kidney disease. PPAR Res. 2010, 274376 (2010).

    PubMed  PubMed Central  Google Scholar 

  7. Karihaloo, A. et al. Macrophages promote cyst growth in polycystic kidney disease. J. Am. Soc. Nephrol. 22, 1809–1814 (2011).

    Article  CAS  Google Scholar 

  8. Talbot, J. J. et al. Polycystin-1 regulates STAT activity by a dual mechanism. Proc. Natl Acad. Sci. USA 108, 7985–7990 (2011).

    Article  CAS  Google Scholar 

  9. Takakura, A. et al. Pyrimethamine inhibits adult polycystic kidney disease by modulating STAT signaling pathways. Hum. Mol. Genet. 20, 4143–4154 (2011).

    Article  CAS  Google Scholar 

  10. Leonhard, W. N. et al. Curcumin inhibits cystogenesis by simultaneous interference of multiple signaling pathways: in vivo evidence from a Pkd1-deletion model. Am. J. Physiol. Renal Physiol. 300, F1193–F1202 (2011).

    Article  CAS  Google Scholar 

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Acknowledgements

V. E. Torres and P. C. Harris are supported by the NIH grant DK090728.

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Correspondence to Vicente E. Torres.

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V. E. Torres has received a grant from Otsuka Pharmaceuticals. P. C. Harris declares no competing interests.

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Torres, V., Harris, P. Connecting the dots toward a polycystic kidney disease therapy. Nat Rev Nephrol 8, 66–68 (2012). https://doi.org/10.1038/nrneph.2011.196

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