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Induction of Myogenic Differentiation Improves Chemosensitivity of Chemoresistant Cells in Soft-Tissue Sarcoma Cell Lines.
Dawson, Lucy E; D'Agostino, Luca; Hakim, Abraham A; Lackman, Richard D; Brown, Spencer A; Sensenig, Richard B; Antonello, Zeus A; Kuzin, Igor I.
Afiliação
  • Dawson LE; Cooper University Hospital, Camden, NJ, USA.
  • D'Agostino L; Cooper University Hospital, Camden, NJ, USA.
  • Hakim AA; Cooper Medical School of Rowan University, Camden, NJ, USA.
  • Lackman RD; Cooper University Hospital, Camden, NJ, USA.
  • Brown SA; MD Anderson Cancer Center at Cooper, Camden, NJ, USA.
  • Sensenig RB; Cooper University Hospital, Camden, NJ, USA.
  • Antonello ZA; Cooper University Hospital, Camden, NJ, USA.
  • Kuzin II; Cooper University Hospital, Camden, NJ, USA.
Sarcoma ; 2020: 8647981, 2020.
Article em En | MEDLINE | ID: mdl-32300280
Rhabdomyosarcoma (RMS) and rhabdoid tumors (RT) are rare soft-tissue malignancies with the highest incidence in infants, children, and adolescents. Advanced, recurrent, and/or metastatic RMS and RT exhibit poor response to treatment. One of the main mechanisms behind resistance to treatment is believed to be intratumoral heterogeneity. In this study, we investigated the myogenic determination factor 1 (MYOD1) and Noggin (NOG) markers in an embryonal RMS (ERMS) cell line and an RT cell line and the differential response of the MYOD1 and NOG expressing subpopulations to chemotherapy. Importantly, we found that these markers together identify a subpopulation of cells (MYOD1+ NOG+ cells) with primary resistance to Vincristine and Doxorubicin, two commonly used chemotherapies for ERMS and RT. The chemoresistant MYOD1+ NOG+ cells express markers of undifferentiated cells such as myogenin and ID1. Combination of Vincristine with TPA/GSK126, a drug combination shown to induce differentiation of RMS cell lines, is able to partially overcome MYOD1/NOG cells chemoresistance.

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article