Your browser doesn't support javascript.
loading
Arsenic trioxide (As(2)O(3)) induced apoptosis and its mechanisms in a human esophageal squamous carcinoma cell line / 中华医学杂志(英文版)
Chin. med. j ; Chin. med. j;(24): 280-285, 2002.
Article en En | WPRIM | ID: wpr-308101
Biblioteca responsable: WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To study whether As(2)O(3) has an apoptotic effect on human solid tumor cells, and the possible cellular and molecular mechanisms of this treatment using human esophageal squamous carcinoma cells (EC8712) as a model.</p><p><b>METHODS</b>DNA microarray, biochemical and cytological analyses were used.</p><p><b>RESULTS</b>The growth and survival of EC8712 cells were markedly inhibited by As(2)O(3) treatment at a concentration of 1, 2 and 4 micromol/L. EC8712 cells were obviously arrested at G2/M phase with As(2)O(3) treatment and apoptosis induced at micromolar As(2)O(3) concentrations, as shown by morphology, histogram related nuclear DNA contents, and DNA gel electrophoresis. As(2)O(3) activated caspase-3, which might be involved in the process of As(2)O(3), induced apoptosis in EC8712 cells.</p><p><b>CONCLUSIONS</b>As(2)O(3) changes the expression of many genes at transcription level. The regulation of expression of many genes might be involved in the process of As(2)O(3) inducing apoptosis. These results suggest that As(2)O(3) can be clinically useful for solid tumor treatment.</p>
Asunto(s)
Texto completo: 1 Índice: WPRIM Asunto principal: Óxidos / Patología / Farmacología / Arsenicales / Neoplasias Esofágicas / Células Tumorales Cultivadas / Microscopía Electrónica / Carcinoma de Células Escamosas / Regulación Neoplásica de la Expresión Génica / Adhesión Celular Límite: Humans Idioma: En Revista: Chin. med. j Año: 2002 Tipo del documento: Article
Texto completo: 1 Índice: WPRIM Asunto principal: Óxidos / Patología / Farmacología / Arsenicales / Neoplasias Esofágicas / Células Tumorales Cultivadas / Microscopía Electrónica / Carcinoma de Células Escamosas / Regulación Neoplásica de la Expresión Génica / Adhesión Celular Límite: Humans Idioma: En Revista: Chin. med. j Año: 2002 Tipo del documento: Article