Cai Yan-jun, Zheng Da-yong, Luo Rong-cheng, Chen Jin-zhang, Li Ai-ming, Xi Jing-le, Ding Xue-mei
Center of Oncology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China. cyj7728 @163.com
Nan Fang Yi Ke Da Xue Xue Bao. 2007 May;27(5):647-9.
To establish a nude mouse model of malignant ascites with human ovarian carcinoma cell line OVCAR3 which highly expresses VEGF and evaluate the therapeutic of Avastin combined with cisplan.
Forty-eight nude mice with malignant ascites resulting from intraperitoneal transplantation of human ovarian carcinoma cell line OVCAR3 were treated with intraperitoneal injection of Avastin, cisplan, their combination, and PBS, respectively, to observe the effect on ascites development, VEGF content in the ascites, peritoneal permeability, development of new vessels and number of tumor cells in the ascites.
Avastin obviously inhibited ascites accumulation and peritoneal capillary permeability, reduced VEGF protein level and microvascular density in the tumor tissues and the number of red cells and tumor cells in the malignant ascites, and prolonged the survival of the mice. The combination of Avastin and cisplan further enhanced the therapeutic efficacy of Avastin.
The bio-chemotherapeutic strategy with Avastin combined with cisplan can be a promising method for treatment of malignant ascites.
用人卵巢癌细胞系OVCAR3建立高表达血管内皮生长因子(VEGF)的恶性腹水裸鼠模型,并评估阿瓦斯汀联合顺铂的治疗效果。
将48只因腹腔移植人卵巢癌细胞系OVCAR3导致恶性腹水的裸鼠,分别腹腔注射阿瓦斯汀、顺铂、二者联合用药及磷酸盐缓冲液(PBS),观察对腹水生成、腹水中VEGF含量、腹膜通透性、新生血管形成及腹水中肿瘤细胞数量的影响。
阿瓦斯汀明显抑制腹水积聚和腹膜毛细血管通透性,降低肿瘤组织中VEGF蛋白水平和微血管密度,减少恶性腹水中红细胞和肿瘤细胞数量,并延长小鼠生存期。阿瓦斯汀与顺铂联合用药进一步增强了阿瓦斯汀的治疗效果。
阿瓦斯汀联合顺铂的生物化疗策略可能是治疗恶性腹水的一种有前景的方法。