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Identification of Cancer Stem Cell Subpopulations in Head and Neck Metastatic Malignant Melanoma.
Yoganandarajah, Vithushiya; Patel, Josie; van Schaijik, Bede; Bockett, Nicholas; Brasch, Helen D; Paterson, Erin; Sim, Dalice; Davis, Paul F; Roth, Imogen M; Itinteang, Tinte; Tan, Swee T.
Afiliación
  • Yoganandarajah V; Gillies McIndoe Research Institute, Newtown, Wellington 6021, New Zealand.
  • Patel J; Gillies McIndoe Research Institute, Newtown, Wellington 6021, New Zealand.
  • van Schaijik B; Gillies McIndoe Research Institute, Newtown, Wellington 6021, New Zealand.
  • Bockett N; Gillies McIndoe Research Institute, Newtown, Wellington 6021, New Zealand.
  • Brasch HD; Gillies McIndoe Research Institute, Newtown, Wellington 6021, New Zealand.
  • Paterson E; Gillies McIndoe Research Institute, Newtown, Wellington 6021, New Zealand.
  • Sim D; Biostatistical Group/Dean's Department, University of Otago, Wellington 6242, New Zealand.
  • Davis PF; Gillies McIndoe Research Institute, Newtown, Wellington 6021, New Zealand.
  • Roth IM; Gillies McIndoe Research Institute, Newtown, Wellington 6021, New Zealand.
  • Itinteang T; Gillies McIndoe Research Institute, Newtown, Wellington 6021, New Zealand.
  • Tan ST; Gillies McIndoe Research Institute, Newtown, Wellington 6021, New Zealand.
Cells ; 9(2)2020 01 30.
Article en En | MEDLINE | ID: mdl-32019273
ABSTRACT
Cancer stem cells (CSCs) have been identified in many cancer types. This study identified and characterized CSCs in head and neck metastatic malignant melanoma (HNmMM) to regional lymph nodes using induced pluripotent stem cell (iPSC) markers. Immunohistochemical (IHC) staining performed on 20 HNmMM tissue samples demonstrated expression of iPSC markers OCT4, SOX2, KLF4, and c-MYC in all samples, while NANOG was expressed at low levels in two samples. Immunofluorescence (IF) staining demonstrated an OCT4+/SOX2+/KLF4+/c-MYC+ CSC subpopulation within the tumor nests (TNs) and another within the peritumoral stroma (PTS) of HNmMM tissues. IF also showed expression of NANOG by some OCT4+/SOX2+/KLF4+/c-MYC+ cells within the TNs in an HNmMM tissue sample that expressed NANOG on IHC staining. In situ hybridization (n = 6) and reverse-transcription quantitative polymerase chain reaction (n = 5) on the HNmMM samples confirmed expression of all five iPSC markers. Western blotting of primary cell lines derived from four of the 20 HNmMM tissue samples showed expression of SOX2, KLF4, and c-MYC but not OCT4 and NANOG, and three of these cell lines formed tumorspheres in vitro. We demonstrate the presence of two putative CSC subpopulations within HNmMM, which may be a novel therapeutic target in the treatment of this aggressive cancer.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Células Madre Neoplásicas / Neoplasias de Cabeza y Cuello / Melanoma Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Cells Año: 2020 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Células Madre Neoplásicas / Neoplasias de Cabeza y Cuello / Melanoma Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Cells Año: 2020 Tipo del documento: Article