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Ras/Raf/MEK/ERK and PI3K/PTEN/Akt/mTOR Inhibitors: Rationale and Importance to Inhibiting These Pathways in Human Health

Oncotarget · 2011 · Vol. 2(3) · pp. 135–164
William H. ChappellLinda S. SteelmanJacquelyn M. LongRuth C. KempfStephen L. AbramsRichard A. FranklinJörg BäseckeFranca StivalaMarco DoniaPaolo FagoneGraziella MalaponteMaría Clorinda MazzarinoFerdinando NicolettiMassimo LibraDanijela Maksimović‐IvanićSanja MijatovićGiuseppe MontaltoMelchiorre CervelloPiotr LaidlerMichèle MilellaAgostino TafuriAntonio BonatiCamilla EvangelistiLucio CoccoAlberto M. MartelliJames A. McCubrey

Abstract

The Ras/Raf/MEK/ERK and PI3K/PTEN/Akt/mTOR cascades are often activated by genetic alterations in upstream signaling molecules such as receptor tyrosine kinases (RTK). Integral components of these pathways, Ras, B-Raf, PI3K, and PTEN are also activated/inactivated by mutations. These pathways have profound effects on proliferative, apoptotic and differentiation pathways. Dysregulation of these pathways can contribute to chemotherapeutic drug resistance, proliferation of cancer initiating cells (CICs) and premature aging. This review will evaluate more recently described potential uses of MEK, PI3K, Akt and mTOR inhibitors in the proliferation of malignant cells, suppression of CICs, cellular senescence and prevention of aging. Ras/Raf/MEK/ERK and Ras/PI3K/PTEN/Akt/mTOR pathways play key roles in the regulation of normal and malignant cell growth. Inhibitors targeting these pathways have many potential uses from suppression of cancer, proliferative diseases as well as aging.

PI3K/AKT/mTOR signaling in cancerMelanoma and MAPK PathwaysSynthesis of Tetrazole DerivativesPTENPI3K/AKT/mTOR pathwayMAPK/ERK pathwayProtein kinase BCancer researchSignal transductionCell growthReceptor tyrosine kinaseRPTORKinase

MeSH terms

Cell Transformation, NeoplasticHumansNeoplasmsras ProteinsPhosphatidylinositol 3-KinasesMitogen-Activated Protein Kinase KinasesMAP Kinase Signaling SystemCell Line, TumorExtracellular Signal-Regulated MAP Kinasesraf KinasesProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseTOR Serine-Threonine Kinases

Funding

  • Fondazione del Monte di Bologna e Ravenna
Citations
575
FWCI
25.95
field-weighted impact
References
279
Percentile
100%
vs. same field & year
Citations per year
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