mTORC1 activation blocks BrafV600E-induced growth arrest but is insufficient for melanoma formation.
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Targeting LKB1 in cancer - exposing and exploiting vulnerabilitiesGenetics of melanocytic neviMembrane-binding and activation of LKB1 by phosphatidic acid is essential for development and tumour suppression.Expression of oncogenic BRAFV600E in melanocytes induces Schwannian differentiation in vivo.CDKN2B Loss Promotes Progression from Benign Melanocytic Nevus to Melanoma.PERK Is a Haploinsufficient Tumor Suppressor: Gene Dose Determines Tumor-Suppressive Versus Tumor Promoting Properties of PERK in Melanoma.AKT1 Activation Promotes Development of Melanoma Metastases.Suppression of Type I Interferon Signaling Overcomes Oncogene-Induced Senescence and Mediates Melanoma Development and ProgressionOncogenic BRAF-Mediated Melanoma Cell Invasion.Melanoma metastases caught in the AKTImmunogenic, cellular, and angiogenic drivers of tumor dormancy--a melanoma view.Melanocytic nevi and melanoma: unraveling a complex relationship.DNMT3b Modulates Melanoma Growth by Controlling Levels of mTORC2 Component RICTOR.Evaluation of tubulin β-3 as a novel senescence-associated gene in melanocytic malignant transformation.Genetically engineered mouse models of melanoma.Intratumoral delivery of mTORC2-deficient dendritic cells inhibits B16 melanoma growth by promoting CD8(+) effector T cell responses.The YUMM lines: a series of congenic mouse melanoma cell lines with defined genetic alterationsmTORC2 Signaling Drives the Development and Progression of Pancreatic Cancer.Induction of Therapeutic Senescence in Vemurafenib-Resistant Melanoma by Extended Inhibition of CDK4/6The mTOR-S6K pathway links growth signalling to DNA damage response by targeting RNF168.LKB1 loss cooperating with BRAF V600E promotes melanoma cell invasion and migration by up-regulation MMP-2 via PI3K/Akt/mTOR pathway.Attenuation of genome-wide 5-methylcytosine level is an epigenetic feature of cutaneous malignant melanomas.Multiparameter analysis of naevi and primary melanomas identifies a subset of naevi with elevated markers of transformation.mTOR signaling-related MicroRNAs and Cancer involvement.CDK4/6 Inhibitors: The Mechanism of Action May Not Be as Simple as Once ThoughtAcquired resistance to BRAFi reverses senescence-like phenotype in mutant BRAF melanoma
P2860
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P2860
mTORC1 activation blocks BrafV600E-induced growth arrest but is insufficient for melanoma formation.
description
2015 nî lūn-bûn
@nan
2015 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2015年の論文
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2015年学术文章
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2015年学术文章
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2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
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2015年學術文章
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name
mTORC1 activation blocks BrafV ...... icient for melanoma formation.
@ast
mTORC1 activation blocks BrafV ...... icient for melanoma formation.
@en
mTORC1 activation blocks BrafV ...... icient for melanoma formation.
@nl
type
label
mTORC1 activation blocks BrafV ...... icient for melanoma formation.
@ast
mTORC1 activation blocks BrafV ...... icient for melanoma formation.
@en
mTORC1 activation blocks BrafV ...... icient for melanoma formation.
@nl
prefLabel
mTORC1 activation blocks BrafV ...... icient for melanoma formation.
@ast
mTORC1 activation blocks BrafV ...... icient for melanoma formation.
@en
mTORC1 activation blocks BrafV ...... icient for melanoma formation.
@nl
P2093
P2860
P50
P1433
P1476
mTORC1 activation blocks BrafV ...... icient for melanoma formation.
@en
P2093
David P Curley
Glenn Merlino
Ildiko Erdelyi
James T Platt
Katrina Meeth
Laura Huang
Manjula Santhanakrishnan
Marcus Bosenberg
Martin McMahon
Michael A Davies
P2860
P356
10.1016/J.CCELL.2014.11.014
P577
2015-01-01T00:00:00Z