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Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

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The effect of MEK inhibition on transcription in melanoma [Batch 1]

ABSTRACT: In order to reveal the downstream targets of MAPK in melanoma, we measured the expression of 12 melanoma cell lines pre and post MEK inhibition Samples were treated with 50nM of the MEK inhibitor PD901 and collected 8 hours after treatment

ORGANISM(S): Homo sapiens

SUBMITTER: Dana Pe'er

PROVIDER: E-GEOD-51051 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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The effect of MEK inhibition on transcription in melanoma [Batch 2]

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Project description:In order to reveal the downstream targets of MAPK in melanoma, we measured the expression of 12 melanoma cell lines pre and post MEK inhibition

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2009-02-21 | E-GEOD-10088 | biostudies-arrayexpress

Transcription profiling of human cell lines in culture (n=12) and murine xenografts (n=2) were treated with the MEK inhibitor PD0325901 or vehicle alone as controlPaired MEK inhibited and control

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2009-02-21 | E-GEOD-10087 | biostudies-arrayexpress

HSP70 inhibition synergizes with MEK inhibition for the treatment of NRAS mutant melanoma

Project description:NRAS-mutant melanoma is currently a challenge to treat. This is due to an absence of inhibitors directed against NRAS, along with acquired and adaptive resistance of this tumor type to inhibitors in the MAPK pathway. Inhibitors to MEK (mitogen-activated protein kinase kinase) have shown some promise for this tumor type. In this work we explored the use of MEK inhibitors for NRAS-mutant melanoma, and at the same time investigated the impact of the brain micro-environment, specifically astrocytes, on the response of a melanoma brain metastatic cell line to MEK inhibition. This led to the surprising finding that astrocytes enhance the sensitivity of melanoma tumors to MEK inhibitors (MEKi). We show that MEKi cause an upregulation of the transcription factor ID3, but this is blocked by conditioned media from astrocytes. We show that silencing ID3 enhances the sensitivity of melanoma to MEK inhibitors, thus mimicking the effect of the brain microenvironment. Moreover, we report that ID3 is a client protein of the chaperone HSP70, and that HSP70 inhibition causes ID3 to misfold and accumulate in a detergent-insoluble fraction in cells. We show that HSP70 inhibitors synergize with MEK inhibitors against NRAS-mutant melanoma, and that this combination significantly enhances the survival of mice in two different models of NRAS-mutant melanoma. These studies highlight ID3 as a mediator of adaptive resistance, and support the combined use of MEK and HSP70 inhibitors for the therapy of NRAS-mutant melanoma.

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