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Effect of bFGF on the MCF-7 Cell Cycle with CD44+/CD24-: Promoting the G0/G1-->G2/S Transition / 한국유방암학회지
Journal of Breast Cancer ; : 388-392, 2012.
Artigo em Inglês | WPRIM | ID: wpr-56441
ABSTRACT

PURPOSE:

Few cells with stem cell characteristics possess capabilities of self-renewal and differentiation, which leads to high tumorigenesis and resistance to standard chemotherapeutic agents. These cells are mostly quiescent, and arrest occurs at the mitotic G0/G1 phase in mitosis. We explored the effects of basic fibroblast growth factor (bFGF) on the MCF-7 cell cycle with CD44+/CD24-.

METHODS:

Cancer-initiating cells were propagated as mammospheres. The CD44+/CD24- subpopulation was sorted by a fluorescence activating cell sorter-Vantage flow cytometer. A cell cycle analysis was performed with different bFGF concentrations.

RESULTS:

Differences in the CD44+/CD24- cell proliferation under different bFGF concentrations were observed (p=0.001). When the bFGF concentration was increased, the proportion of CD44+/CD24- at G0/G1 decreased (p=0.023).

CONCLUSION:

We conclude that bFGF may sustain CD44+/CD24- cell proliferation and could promote cell progression through the G0/G1-->G2/S phase transition.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Células-Tronco / Neoplasias da Mama / Ciclo Celular / Transformação Celular Neoplásica / Fator 2 de Crescimento de Fibroblastos / Transição de Fase / Proliferação de Células / Fatores de Crescimento de Fibroblastos / Células MCF-7 / Fluorescência Idioma: Inglês Revista: Journal of Breast Cancer Ano de publicação: 2012 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Células-Tronco / Neoplasias da Mama / Ciclo Celular / Transformação Celular Neoplásica / Fator 2 de Crescimento de Fibroblastos / Transição de Fase / Proliferação de Células / Fatores de Crescimento de Fibroblastos / Células MCF-7 / Fluorescência Idioma: Inglês Revista: Journal of Breast Cancer Ano de publicação: 2012 Tipo de documento: Artigo