南方医科大学学报 ›› 2004, Vol. 24 ›› Issue (07): 821-823.

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醋酸甲羟孕酮对卵巢癌裸鼠移植瘤的抗血管生成作用

谢守珍1, 王晶1, 李德忠2, 王艳1   

  1. 1. 广州军区武汉总医院妇产科, 湖北, 武汉, 430070;
    2. 广州军区武汉总医院中心实验室, 湖北, 武汉, 430070
  • 出版日期:2004-07-20 发布日期:2004-07-20
  • 基金资助:
    收稿日期:2004-1-13。
    作者简介:谢守珍(1953- ),女,硕士,主任医师,电话:027-87308279,E-mail:xieshouzhen@163.com

Medroxyprogesterone acetate therapy against antiangiogenesis of transpIanted ovarian cancer in nude mice

XIE Shou-zhen1, WANG Jing1, LI De-zhong2, WANG yan1   

  1. 1. 广州军区武汉总医院妇产科, 湖北, 武汉, 430070;
    2. 广州军区武汉总医院中心实验室, 湖北, 武汉, 430070
  • Online:2004-07-20 Published:2004-07-20

摘要: 目的 观察醋酸甲羟孕酮(MPA)对人卵巢癌裸鼠移植瘤内血管生成及肿瘤细胞的抑制作用。方法 建立30只裸鼠人卵巢癌移植模型,并随机均分成对照组和2个MPA治疗组。2个治疗组分别每次皮下注射MPA60和120 mg/kg·b.w,2次/周,共4周。对照组注射相同体积生理盐水。测定三组抑瘤率,用Ⅷ因子多克隆抗原抗体测定肿瘤内微血管密度(MVD)并进行形态学观察。结果 MPA(60 mg/kg·b.w.)组的抑瘤率为23.76%,MPA(120 mg/kg·b.w.)组抑瘤率为43.80%(P<0.05)。MPA高、低剂量组的MVD则分别为2.11±0.12、3.64±0.02,与对照组(5.14±0.74)比较,差异有显著性(P<0.01、P<0.05)。而2个MPA组间差异也极显著(P<0.01)。MPA组形态学观察可见大量的凋亡细胞和凋亡小体及变性坏死,而对照组少见。结论 MPA对人卵巢癌COCI细胞裸鼠移植瘤内的肿瘤细胞及新生微血管具有明显抑制作用,并呈现剂量一效应关系;其对肿瘤细胞的作用机制,可能是抑制并破坏肿瘤区新生血管的生长,阻断血供所产生的结果,而并非直接对肿瘤细胞的作用。

Abstract: Objective To investigate the effects of medroxyprogesterone acetate (MPA) on angiogenesis and growth of transplanted human ovarian cancer cells in nude mice. Methods Ovarian cancer cell line COC Ⅰ derived from human ovarian serous adenocarcinoma was transplanted into 30 nude mice, which were then randomized equally into 3 groups consisting of two treatment groups (in which MPA was administered at 60 and 120 mg/kg, respectively, twice a week for 4 weeks) and a control group. Six weeks later, the body mass of the nude mice was recorded and the morphology of tumor cells observed by electron microscope. The microvascular density (MVD) was examined by immunohistochemical staining with anti-human factor Ⅷ antibody. Results Compared with the control group, the growth inhibitory rate in the two treatment groups were 23.76% and 43.80%, respectively, corresponding to the doses of 60 and 120 mg/kg. MVD of 60 mg/kg MPA group (3.64±0.02) and 120 mg/kg MPA group (2.11±0.12) was lower than that of the control group (5.14±0.74) (P<0.05 and P<0.01, respectively), and there was also significant difference between the two treatment groups (P<0.01). The morphological changes including compaction and margination of the nuclear chromatin, apoptotic bodies, and cell necrosis were significantly increased in the two treatment groups. Conclusions MPA can inhibit the angiogenesis and growth of transplanted human ovarian cancer cells in nude mice in a dose-dependent manner, and its anticancer effect may involve induction of cell apoptosis as the result of its effect against angiogenesis.

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