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L-canavanine as a radiosensitization agent for human pancreatic cancer cells

Producción científica: Review articlerevisión exhaustiva

22 Citas (Scopus)

Resumen

This study evaluated the in vitro effect of L-canavanine on cell cycle progression in the two human pancreatic cancer cells lines PANC-1 and MIA PaCa-2. After 72 h of exposure to L-canavanine, the percentage of cells in the radiosensitive G2/M phase of the cell cycle increased 6-fold in PANC-1 cells and 4-fold in MIA PaCa-2 cells, when compared to untreated cells. The capacity of L-canavanine to redistribute cells into the G2/M phase of the cell cycle was both concentration- and time-dependent. Since many drugs that cause cells to accumulate in the G2/M phase of the cell cycle are effective radiosensitization agents, the potential of L-canavanine to synergistically enhance the effects of ionizing radiation also was evaluated. The interaction between these treatment modalities was quantified using the median-effect equation and combination index analysis. L-Canavanine was found to be synergistic with radiation when either PANC-1 or MIA PaCa-2 cells were exposed to L-canavanine for 72 h prior to irradiation. These results suggest that L-canavanine in combination with radiation may have clinical potential in the treatment of pancreatic cancer.

Idioma originalEnglish
Páginas (desde-hasta)37-43
Número de páginas7
PublicaciónMolecular and Cellular Biochemistry
Volumen244
N.º1-2
DOI
EstadoPublished - feb 2003

Nota bibliográfica

Funding Information:
The authors gratefully acknowledge the American Foundation for Pharmaceutical Education Fellowships for fellowship support of AKB.

Financiación

The authors gratefully acknowledge the American Foundation for Pharmaceutical Education Fellowships for fellowship support of AKB.

Financiadores
American Foundation for Pharmaceutical Education

    ODS de las Naciones Unidas

    Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

    1. Good health and well being
      Good health and well being

    ASJC Scopus subject areas

    • Molecular Biology
    • Clinical Biochemistry
    • Cell Biology

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