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Regulation of Differentiation of HC11 Mouse Breast Epithelial Cells by the Signal Transducer and Activator of Transcription-3.
Niit, Maximillian; Geletu, Mulu; Taha, Zaid; Arulanandam, Rozanne; Cass, Jamaica; Hoskin, Victoria; Elliott, Bruce; Gunning, Patrick; Raptis, Leda.
Afiliação
  • Niit M; Department of Biomedical and Molecular Sciences and Department of Pathology and Molecular Medicine, Queen's University, Kingston, ON, Canada.
  • Geletu M; Department of Chemical and Physical Sciences, University of Toronto, Mississauga, ON, Canada mulu.geletu@utoronto.ca.
  • Taha Z; Department of Biomedical and Molecular Sciences and Department of Pathology and Molecular Medicine, Queen's University, Kingston, ON, Canada.
  • Arulanandam R; Center for Innovative Cancer Research, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
  • Cass J; Center for Innovative Cancer Research, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
  • Hoskin V; Department of Biomedical and Molecular Sciences and Department of Pathology and Molecular Medicine, Queen's University, Kingston, ON, Canada.
  • Elliott B; Department of Biomedical and Molecular Sciences and Department of Pathology and Molecular Medicine, Queen's University, Kingston, ON, Canada.
  • Gunning P; Department of Biomedical and Molecular Sciences and Department of Pathology and Molecular Medicine, Queen's University, Kingston, ON, Canada.
  • Raptis L; Center for Innovative Cancer Research, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
Anticancer Res ; 39(6): 2749-2756, 2019 Jun.
Article em En | MEDLINE | ID: mdl-31177110
ABSTRACT
BACKGROUND/

AIM:

The differentiation of the mouse breast epithelial cell line HC11 is known to require confluence as well as the addition of hydrocortisone, insulin and prolactin. MATERIALS AND

METHODS:

Since confluence, which triggers the engagement of the cell-to-cell adhesion molecule E-cadherin, induces a dramatic increase in the activity of signal transducer and activator of transcription-3 (Stat3), we examined the role of Stat3 in HC11 cell differentiation.

RESULTS:

Stat3 inhibition abolished differentiation, indicating that Stat3 activity is critically required. However, expression of the mutationally activated form of Stat3 (Stat3C), rather than promoting, it was found to block cell differentiation, even when expressed in low levels, and in the absence of full neoplastic conversion.

CONCLUSION:

The strength of the E-cadherin/Stat3 signal is key for the outcome of the differentiation process.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células Epiteliais / Fator de Transcrição STAT3 / Glândulas Mamárias Animais Limite: Animals Idioma: En Revista: Anticancer Res Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células Epiteliais / Fator de Transcrição STAT3 / Glândulas Mamárias Animais Limite: Animals Idioma: En Revista: Anticancer Res Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Canadá