期刊
EXPERT OPINION ON THERAPEUTIC TARGETS
卷 13, 期 11, 页码 1279-1293出版社
TAYLOR & FRANCIS LTD
DOI: 10.1517/14728220903241625
关键词
cancer; mTOR; signalling pathways; translation initiation
资金
- Canadian Institutes of Health Research
- National Cancer Institute of Canada
Mammalian target of rapamycin (mTOR) is a master regulator of translation initiation that controls the recruitment of ribosomes to mRNA templates in response to intracellular and extracellular cues. Evidence suggests that mTOR and its direct downstream targets, S6K and eIF4E/4E-BP, play significant roles in oncogenesis, and that inhibiting this pathway holds promise as an anti-proliferative approach. Recent genome-wide analyses of mutations in human cancers indicate that transformed cells activate a handful of processes and signalling pathways that are major contributors to their phenotype. Here we review the current literature implicating mTOR and translation initiation downstream of many of these various signalling pathways and processes usurped in human cancers. This review highlights the widespread activation of mTOR/eIF4E following acquisition of oncogenic lesions and its implication in promoting the transformation phenotype and indicates that targeting the control of translation initiation makes logical sense as a broad-acting therapeutic approach.
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