Data from KDM5B Promotes Drug Resistance by Regulating Melanoma-Propagating Cell Subpopulations Article Swipe
YOU?
·
· 2023
· Open Access
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· DOI: https://doi.org/10.1158/1535-7163.c.6538539.v1
Tumor heterogeneity is a major challenge for cancer treatment, especially due to the presence of various subpopulations with stem cell or progenitor cell properties. In mouse melanomas, both CD34+p75− (CD34+) and CD34−p75− (CD34−) tumor subpopulations were characterized as melanoma-propagating cells (MPC) that exhibit some of those key features. However, these two subpopulations differ from each other in tumorigenic potential, ability to recapitulate heterogeneity, and chemoresistance. In this study, we demonstrate that CD34+ and CD34− subpopulations carrying the BRAFV600E mutation confer differential sensitivity to targeted BRAF inhibition. Through elevated KDM5B expression, melanoma cells shift toward a more drug-tolerant, CD34− state upon exposure to BRAF inhibitor or combined BRAF inhibitor and MEK inhibitor treatment. KDM5B loss or inhibition shifts melanoma cells to the more BRAF inhibitor–sensitive CD34+ state. These results support that KDM5B is a critical epigenetic regulator that governs the transition of key MPC subpopulations with distinct drug sensitivity. This study also emphasizes the importance of continuing to advance our understanding of intratumor heterogeneity and ultimately develop novel therapeutics by altering the heterogeneous characteristics of melanoma.
Related Topics
- Type
- preprint
- Language
- en
- Landing Page
- https://doi.org/10.1158/1535-7163.c.6538539.v1
- OA Status
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- OpenAlex ID
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Raw OpenAlex JSON
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https://openalex.org/W4362493139Canonical identifier for this work in OpenAlex
- DOI
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https://doi.org/10.1158/1535-7163.c.6538539.v1Digital Object Identifier
- Title
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Data from KDM5B Promotes Drug Resistance by Regulating Melanoma-Propagating Cell SubpopulationsWork title
- Type
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preprintOpenAlex work type
- Language
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enPrimary language
- Publication year
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2023Year of publication
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2023-04-03Full publication date if available
- Authors
-
Xiaoni Liu, Shang‐Min Zhang, Meaghan K. McGeary, Irina Krykbaeva, Ling‐Ping Lai, Daniel J. Jansen, Stephen C. Kales, Anton Simeonov, Matthew D. Hall, Daniel P. Kelly, Marcus Bosenberg, Qin YanList of authors in order
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https://doi.org/10.1158/1535-7163.c.6538539.v1Publisher landing page
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YesWhether a free full text is available
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goldOpen access status per OpenAlex
- OA URL
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https://doi.org/10.1158/1535-7163.c.6538539.v1Direct OA link when available
- Concepts
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Melanoma, Molecular biology, Cancer research, Chemistry, BiologyTop concepts (fields/topics) attached by OpenAlex
- Cited by
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0Total citation count in OpenAlex
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10Other works algorithmically related by OpenAlex
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