| Literature DB >> 32435407 |
Baris Kucukkaraduman1, Can Turk2, Anna L Fallacara3, Murat Isbilen4, Kerem M Senses5, Zeynep O Ayyildiz6, Muhammad W Akbar1, Michal Lotem7, Maurizio Botta3, Ali O Gure1.
Abstract
Melanoma is a highly aggressive cancer with poor prognosis. Although more than 80% of melanomas harbor an activating mutation in genes within the MAPK pathway, which are mutually exclusive, usefulness of therapies targeting MAPK pathway are impeded by innate and/or acquired resistance in most patients. In this study, using melanoma cells, we report the efficacy of a recently developed pyrazolo[3,4-d]pyrimidine derived c-Src inhibitor 10a and identify a molecular signature which is predictive of 10a chemosensitivity. We show that the expression of TMED7, PLOD2, XRCC5, and NSUN5 are candidate biomarkers for 10a sensitivity. Although an undifferentiated/mesenchymal/invasive status of melanoma cells is associated with resistance to 10a, we show here for the first time that melanoma cells can be sensitized to 10a via treatment with valproic acid, a histone deacetylase inhibitor.Entities:
Year: 2020 PMID: 32435407 PMCID: PMC7236227 DOI: 10.1021/acsmedchemlett.9b00679
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345