| Literature DB >> 19509234 |
Takemi Tanaka1, Luigi M De Luca.
Abstract
Retinoid X receptor (RXR) is a combinatorial partner for one third of the 48 human nuclear receptor superfamily members and acts as a master coordinator of nuclear receptor signaling pathways involved in the control of cell growth and differentiation. Thus, ligand-dependent simultaneous activation of multiple pathways is an attractive strategy for molecular-targeted therapy of neoplastic disease. However, clinical trials in RXR-targeted molecular therapy with the RXR ligand (rexinoid) have yielded disappointing outcomes. In this review, we discuss a possible mechanism underlying the loss of sensitivity to rexinoid therapy.Entities:
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Year: 2009 PMID: 19509234 DOI: 10.1158/0008-5472.CAN-08-4407
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701