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Targeting the PI3K/Akt/mTOR Pathway - Beyond Rapalogs

Oncotarget · 2010 · Vol. 1(7) · pp. 530–543
Ben MarkmanRodrigo DienstmannJosep Tabernero

Abstract

It is well established that the PI3K pathway plays a central role in various cellular processes that can contribute to the malignant phenotype. Accordingly, pharmacological inhibition of key nodes in this signaling cascade has been a focus in developmental therapeutics. To date, agents targeting upstream receptor tyrosine kinases are best studied and have achieved greatest clinical success. Further downstream, despite efficacy in certain tumor types, the rapalogs have been somewhat disappointing in the clinic. Novel inhibitors of PI3K, Akt, and mTORC1 and 2 are now passing through early phase clinical trials. It is hoped that these agents will circumvent some of the shortcomings of the rapalogs and lead to meaningful benefits for cancer patients.

PI3K/AKT/mTOR signaling in cancerCancer Mechanisms and TherapyAdvanced Breast Cancer TherapiesPI3K/AKT/mTOR pathwaymTORC1MedicineReceptor tyrosine kinaseProtein kinase BCancer researchSignal transductionBioinformaticsBiologyReceptor

MeSH terms

Phosphoinositide-3 Kinase InhibitorsAnimalsHumansModels, BiologicalNeoplasmsSignal TransductionPhosphatidylinositol 3-KinasesProtein Kinase InhibitorsProto-Oncogene Proteins c-aktTOR Serine-Threonine KinasesMolecular Targeted Therapy
Citations
342
FWCI
12.44
field-weighted impact
References
88
Percentile
99%
vs. same field & year
Citations per year
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