Overcoming MCL-1-driven adaptive resistance to targeted therapies
- PMID: 31988312
- PMCID: PMC6985132
- DOI: 10.1038/s41467-020-14392-z
Overcoming MCL-1-driven adaptive resistance to targeted therapies
Abstract
Two complementary studies in Nature Communications define a critical role for the anti-apoptotic protein MCL-1 as a driver of adaptive survival in tumor cells treated with oncogene targeted therapies, providing a rationale for combining these agents with newly developed MCL-1 inhibitors in the clinic.
Conflict of interest statement
The author declares no competing interests.
Comment on
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Targeting melanoma's MCL1 bias unleashes the apoptotic potential of BRAF and ERK1/2 pathway inhibitors.Nat Commun. 2019 Nov 14;10(1):5167. doi: 10.1038/s41467-019-12409-w. Nat Commun. 2019. PMID: 31727888 Free PMC article.
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Destabilization of NOXA mRNA as a common resistance mechanism to targeted therapies.Nat Commun. 2019 Nov 14;10(1):5157. doi: 10.1038/s41467-019-12477-y. Nat Commun. 2019. PMID: 31727958 Free PMC article.
References
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- Hata AN, Engelman JA, Faber AC. The BCL2 family: key mediators of the apoptotic response to targeted anticancer therapeutics. Cancer Discov. 2015;5:475–487. doi: 10.1158/2159-8290.CD-15-0011. - DOI - PMC - PubMed
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