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Cis-CA1P inhibits tumor cell proliferation and prevents blood vessel formation / 中国应用生理学杂志
Chinese Journal of Applied Physiology ; (6): 15-18, 2012.
Artículo en Chino | WPRIM | ID: wpr-329958
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the effects of cis-combretastatin-A1 phosphate (cis-CA1P) on tumor cell proliferation, and its effects on the blood vessel formations.</p><p><b>METHODS</b>MTT and IC50 values were used to assess the inhibitory effects of cis-CA1P on tumor cell proliferation. Chicken embryo chorioallantoic membrane and thoracic aorta annulations isolated from rats were used to investigate the effects of cis-CAIP on the blood vessel formation.</p><p><b>RESULTS</b>Cis-CA1P concentration-dependently inhibited the proliferations of several cancer cell lines, including human gastric carcinoma cell line MGC-803, human leukemic monocyte lymphoma cell line U937, human melanoma cell line A375, human colon cancer cell line HCT116, human breast carcinoma cell line MDA-MB-231, and human leukemia cell line K562. Cis-CAIP significantly decreased the formation of blood vessels in chicken embryo chorioallantoic membrane and in thoracic aorta annulations.</p><p><b>CONCLUSION</b>Cis-CA1P inhibits cancer cell proliferation and prevents blood vessel formation.</p>
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Aorta / Farmacología / Fosfatos / Estilbenos / Técnicas In Vitro / Química / Línea Celular Tumoral / Membrana Corioalantoides / Proliferación Celular / Neovascularización Patológica Límite: Animales / Humanos Idioma: Chino Revista: Chinese Journal of Applied Physiology Año: 2012 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Aorta / Farmacología / Fosfatos / Estilbenos / Técnicas In Vitro / Química / Línea Celular Tumoral / Membrana Corioalantoides / Proliferación Celular / Neovascularización Patológica Límite: Animales / Humanos Idioma: Chino Revista: Chinese Journal of Applied Physiology Año: 2012 Tipo del documento: Artículo