MEK inhibition leads to PI3K/AKT activation by relieving a negative feedback on ERBB receptors.
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Molecular Subtypes and Personalized Therapy in Metastatic Colorectal CancerMEK and PI3K inhibition in solid tumors: rationale and evidence to dateDual Inhibition of MEK and PI3K Pathway in KRAS and BRAF Mutated Colorectal CancersAdaptive resistance to targeted therapies in cancerGene expression markers of efficacy and resistance to cetuximab treatment in metastatic colorectal cancer: results from CALGB 80203 (Alliance)Negative feedback regulation of the ERK1/2 MAPK pathwayGrb2 depletion under non-stimulated conditions inhibits PTEN, promotes Akt-induced tumor formation and contributes to poor prognosis in ovarian cancerDiscovery of novel AKT inhibitors with enhanced anti-tumor effects in combination with the MEK inhibitorHER2+ Cancer Cell Dependence on PI3K vs. MAPK Signaling Axes Is Determined by Expression of EGFR, ERBB3 and CDKN1BCell type-dependent Erk-Akt pathway crosstalk regulates the proliferation of fetal neural progenitor cellsSuppression of KRas-mutant cancer through the combined inhibition of KRAS with PLK1 and ROCKTranslating genomic profiling to gastrointestinal cancer treatment.Development of a RSK Inhibitor as a Novel Therapy for Triple-Negative Breast Cancer.p70S6 kinase is a critical node that integrates HER-family and PI3 kinase signaling networks.ERBB receptors: from oncogene discovery to basic science to mechanism-based cancer therapeutics.Ras Dimer Formation as a New Signaling Mechanism and Potential Cancer Therapeutic Target.Epidermal Growth Factor Receptor Cell Proliferation Signaling PathwaysObatoclax overcomes resistance to cell death in aggressive thyroid carcinomas by countering Bcl2a1 and Mcl1 overexpression.A comprehensive evaluation of biomarkers predictive of response to PI3K inhibitors and of resistance mechanisms in head and neck squamous cell carcinoma.Suppression of feedback loops mediated by PI3K/mTOR induces multiple overactivation of compensatory pathways: an unintended consequence leading to drug resistance.FGFR4 profile as a prognostic marker in squamous cell carcinoma of the mouth and oropharynx.Comparative profile of cutaneous adverse events: BRAF/MEK inhibitor combination therapy versus BRAF monotherapy in melanomaOvercoming endocrine resistance due to reduced PTEN levels in estrogen receptor-positive breast cancer by co-targeting mammalian target of rapamycin, protein kinase B, or mitogen-activated protein kinase kinase.Genetic events that limit the efficacy of MEK and RTK inhibitor therapies in a mouse model of KRAS-driven pancreatic cancerEnhancing therapeutic efficacy of the MEK inhibitor, MEK162, by blocking autophagy or inhibiting PI3K/Akt signaling in human lung cancer cells.Evaluation of efficacy of a new MEK inhibitor, RO4987655, in human tumor xenografts by [(18)F] FDG-PET imaging combined with proteomic approaches.A phase I trial of vertical inhibition of IGF signalling using cixutumumab, an anti-IGF-1R antibody, and selumetinib, an MEK 1/2 inhibitor, in advanced solid tumours.Molecular markers predictive of chemotherapy response in colorectal cancerTitration of signalling output: insights into clinical combinations of MEK and AKT inhibitors.A combination of trastuzumab and BAG-1 inhibition synergistically targets HER2 positive breast cancer cellsA Probabilistic Boolean Network Approach for the Analysis of Cancer-Specific Signalling: A Case Study of Deregulated PDGF Signalling in GIST.Selumetinib with and without erlotinib in KRAS mutant and KRAS wild-type advanced nonsmall-cell lung cancer.RHOA-FAK is a required signaling axis for the maintenance of KRAS-driven lung adenocarcinomasCombined EGFR/MEK Inhibition Prevents the Emergence of Resistance in EGFR-Mutant Lung Cancer.IL15 Agonists Overcome the Immunosuppressive Effects of MEK Inhibitors.Combined PI3K/mTOR and MEK inhibition provides broad antitumor activity in faithful murine cancer modelsCombining radiotherapy with MEK1/2, STAT5 or STAT6 inhibition reduces survival of head and neck cancer lines.Overcoming IGF1R/IR resistance through inhibition of MEK signaling in colorectal cancer models.Reduced Proteolytic Shedding of Receptor Tyrosine Kinases Is a Post-Translational Mechanism of Kinase Inhibitor ResistanceBypass mechanisms of resistance to receptor tyrosine kinase inhibition in lung cancer.
P2860
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P2860
MEK inhibition leads to PI3K/AKT activation by relieving a negative feedback on ERBB receptors.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
MEK inhibition leads to PI3K/A ...... ve feedback on ERBB receptors.
@en
MEK inhibition leads to PI3K/A ...... ve feedback on ERBB receptors.
@nl
type
label
MEK inhibition leads to PI3K/A ...... ve feedback on ERBB receptors.
@en
MEK inhibition leads to PI3K/A ...... ve feedback on ERBB receptors.
@nl
prefLabel
MEK inhibition leads to PI3K/A ...... ve feedback on ERBB receptors.
@en
MEK inhibition leads to PI3K/A ...... ve feedback on ERBB receptors.
@nl
P2093
P2860
P1433
P1476
MEK inhibition leads to PI3K/A ...... ve feedback on ERBB receptors.
@en
P2093
Alexa B Turke
Carlos L Arteaga
Carlotta Costa
Jeffrey A Engelman
John M Asara
Rebecca Cook
Youngchul Song
P2860
P304
P356
10.1158/0008-5472.CAN-11-3747
P407
P577
2012-05-02T00:00:00Z