RET in breast cancer: functional and therapeutic implications

Recent studies demonstrate that the receptor tyrosine kinase RET is overexpressed in a subset of ER-positive breast cancers and that crosstalk between RET and ER is important in responses to endocrine therapy. The development of small molecular inhibitors that target RET allows the opportunity to co...

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Published inTrends in molecular medicine Vol. 17; no. 3; pp. 149 - 157
Main Authors Morandi, Andrea, Plaza-Menacho, Ivan, Isacke, Clare M.
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.03.2011
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ISSN1471-4914
1471-499X
1471-499X
DOI10.1016/j.molmed.2010.12.007

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Summary:Recent studies demonstrate that the receptor tyrosine kinase RET is overexpressed in a subset of ER-positive breast cancers and that crosstalk between RET and ER is important in responses to endocrine therapy. The development of small molecular inhibitors that target RET allows the opportunity to consider combination therapies as a strategy to improve response to treatment and to prevent and combat endocrine resistance. This review discusses: (i) the current knowledge about RET, its co-receptors and ligands in breast cancer; (ii) the breast cancer clinical trials involving agents that target RET; and (iii) the challenges that remain in terms of specificity of available inhibitors and in understanding the complex molecular mechanisms that underlie the resistance to endocrine therapy.
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ISSN:1471-4914
1471-499X
1471-499X
DOI:10.1016/j.molmed.2010.12.007