机构地区:[1]Department of Gynecology,Aviation General Hospital,Beijing 200022,Chine [2]Department of Gynecology and Obstetrics,First Affiliated Hospital of Nanchang University,Nanchang 330006,China
出 处:《Chinese Journal of Cancer Research》2012年第3期245-248,共4页中国癌症研究(英文版)
基 金:supported by the National Natural Science Foundation of China (No.30860301)
摘 要:Objective: To investigate the dys-psychological stress effect on the growth of subcutaneous xenotransplanted tumor in nude mice bearing human epithelium ovarian carcinoma, and the influence on P53 and NFκBp65 expressions. Methods: The subcutaneous tumor xenografts were established by implanting human epithelium ovarian carcinoma tissues into nude mice and the dys-psychological stress model was established with restraint. The mice were randomized into the following four treatment groups with each group six mice respectively: tumor group (group A), normal saline intraperitoneal injection; tumor with stress group (group B), normal saline intraperitoneal injection; tumor therapy group (group C), cisplatin intraperitoneal injection; and tumor therapy with stress group (group D), cisplatin intraperitoneal injection. The expressions of P53 and NFκBp65 in tumor tissues were determined by Western blotting. Results: The expressions of P53 and NFκBp65 in each restraint group were enhanced compared with the control groups (P0.05). Conclusion: The dys-psychological stress may induce the high expressions of P53 and NFκBp65 proteins and further promote tumor growth.Objective: To investigate the dys-psychological stress effect on the growth of subcutaneous xenotransplanted tumor in nude mice bearing human epithelium ovarian carcinoma, and the influence on P53 and NFκBp65 expressions. Methods: The subcutaneous tumor xenografts were established by implanting human epithelium ovarian carcinoma tissues into nude mice and the dys-psychological stress model was established with restraint. The mice were randomized into the following four treatment groups with each group six mice respectively: tumor group (group A), normal saline intraperitoneal injection; tumor with stress group (group B), normal saline intraperitoneal injection; tumor therapy group (group C), cisplatin intraperitoneal injection; and tumor therapy with stress group (group D), cisplatin intraperitoneal injection. The expressions of P53 and NFκBp65 in tumor tissues were determined by Western blotting. Results: The expressions of P53 and NFκBp65 in each restraint group were enhanced compared with the control groups (P0.05). Conclusion: The dys-psychological stress may induce the high expressions of P53 and NFκBp65 proteins and further promote tumor growth.
关 键 词:Constraint stress ONCOPROTEIN Ovarian cancer animal model
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