Journal
CANCER RESEARCH COMMUNICATIONS
Volume 1, Issue 1, Pages 17-29Publisher
AMER ASSOC CANCER RESEARCH
DOI: 10.1158/2767-9764.CRC-21-0033
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Funding
- NIH [NCIP01CA114046, NCI R01CA139319, NCI R01CA241490, NCI P01CA114046, NCI T32CA009171, NCIK99/R00CA241367]
- NIHNCI [CA010815]
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This study showed that astrocytes enhance the sensitivity of melanoma tumors to MEK inhibitors, while ID3 acts as a mediator of adaptive resistance. By combining HSP70 inhibitors with MEK inhibitors, the survival rate of mice with NRAS-mutant melanoma was significantly improved.
NRAS-mutant melanoma is currently a challenge to treat. This is due to an absence of inhibitors directed against mutant NRAS, along with adaptive and acquired resistance of this tumor type to inhibitors in the MAPK pathway. Inhibitors to MEK have shown some promise for NRAS-mutant melanoma. In this work, we explored the use of MEK inhibitors for NRASmutant melanoma. At the same time, we investigated the impact of the brain microenvironment, specifically astrocytes, on the response of a melanoma brain metastatic cell line to MEK inhibition. These parallel avenues 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 transcriptional regulator ID3, which confers resistance. This upregulation of ID3 is blocked by conditioned media from astrocytes. We show that silencing ID3 enhances the sensitivity of melanoma to MEKi, 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 MEKi 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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