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PELP1: A Novel Therapeutic Target for Hormonal Cancers

Journal

IUBMB LIFE
Volume 62, Issue 3, Pages 163-169

Publisher

WILEY
DOI: 10.1002/iub.287

Keywords

estrogen receptor; coregulators; PELP1; hormonal signaling; therapy resistance

Funding

  1. Susan G. Komen Foundation [KG091267, KG090477]
  2. NIH [CA75018, CA095681]
  3. DOD BCRP [BC074432]
  4. NATIONAL CANCER INSTITUTE [R01CA095681, R01CA075018] Funding Source: NIH RePORTER

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Recent studies implicate that the estrogen receptor (ER) coregulator proline-, glutamic acid-, and leucine-rich protein (PELP) 1 as playing critical roles in ER-genomic, ER-nongenomic, and ER-signaling cross talk with growth factor signaling pathways. PELP1 expression is deregulated in hormonal cancers and recent studies further elucidated the molecular mechanisms by which PELP1 regulates hormone therapy response. Although PELP1 is important for normal functions of the ER, the possibility to target ER-PELP1 axis appears to be an effective strategy for preventing hormonal carcinogenesis and therapy resistance. Thus, PELP1 may be useful as prognostic marker for hormonal cancers and PELP1 signaling may be useful to generate targeted therapeutics to overcome hormonal therapy resistance. (C) 2009 IUBMB IUBMB Life, 62(3): 163-169, 2010

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