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Erschienen in: Targeted Oncology 1/2011

01.03.2011 | Review

Mechanisms of mTOR inhibitor resistance in cancer therapy

verfasst von: Jennifer S. Carew, Kevin R. Kelly, Steffan T. Nawrocki

Erschienen in: Targeted Oncology | Ausgabe 1/2011

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Abstract

Mammalian target of rapamycin (mTOR) is a conserved serine/threonine kinase that regulates cell cycle progression, protein translation, metabolism, and cellular proliferation. The mTOR pathway promotes cell proliferation under energy or nutrient-rich conditions by increasing ribosomal biogenesis and protein synthesis. Since enhanced activity of the mTOR pathway is frequently observed in malignant cells, inhibition of this kinase has become an attractive strategy to treat cancer. Rapamycin and its analogs temsirolimus, everolimus, and ridaforolimus referred to as “rapalogs” have demonstrated promising efficacy against renal cell carcinoma and are under investigation for the treatment of other malignancies. However, the emergence of drug resistance may ultimately limit the utility of rapalog therapy. Here we summarize the known mechanisms of resistance to mTOR-inhibitor therapy and describe potential strategies to overcome these for the current agents that target this pathway.
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Metadaten
Titel
Mechanisms of mTOR inhibitor resistance in cancer therapy
verfasst von
Jennifer S. Carew
Kevin R. Kelly
Steffan T. Nawrocki
Publikationsdatum
01.03.2011
Verlag
Springer-Verlag
Erschienen in
Targeted Oncology / Ausgabe 1/2011
Print ISSN: 1776-2596
Elektronische ISSN: 1776-260X
DOI
https://doi.org/10.1007/s11523-011-0167-8

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