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The Melanocyte Lineage Factor miR-211 Promotes BRAFV600E Inhibitor Resistance.
Ostrowski, Stephen M; Fisher, David E.
Affiliation
  • Ostrowski SM; Department of Dermatology, Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts, USA.
  • Fisher DE; Department of Dermatology, Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts, USA. Electronic address: dfisher3@partners.org.
J Invest Dermatol ; 141(2): 250-252, 2021 02.
Article in En | MEDLINE | ID: mdl-33504438
ABSTRACT
Resistance to targeted therapy and immunotherapy remains a major obstacle in improving care for patients with advanced melanoma. MicroRNAs play important roles in regulating gene networks involved in disease progression and resistance to therapy in cancers such as melanoma. MicroRNA miR-211 contributes to melanocyte and melanoma biology and has been implicated in targeted therapy resistance. Lee et al. (2020) report a novel mechanism by which miR-211 promotes resistance to BRAFV600E inhibitor therapy via the upregulation of the extracellular signal-regulated kinase 5 signaling pathway.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: MicroRNAs / Proto-Oncogene Proteins B-raf / Protein Kinase Inhibitors / Melanoma Limits: Humans Language: En Journal: J Invest Dermatol Year: 2021 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: MicroRNAs / Proto-Oncogene Proteins B-raf / Protein Kinase Inhibitors / Melanoma Limits: Humans Language: En Journal: J Invest Dermatol Year: 2021 Document type: Article Affiliation country:
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