节点文献

肝脂素对小鼠S37肉瘤与B16黑色素瘤的抗肿瘤作用

The antitumor efficacy of Heplipin on S37 sarcoma and B16 melanoma in mice

  • 推荐 CAJ下载
  • PDF下载
  • 不支持迅雷等下载工具,请取消加速工具后下载。

【作者】 乔艺路建平毛建群沈祖铭林肇辉

【Author】 QIAO Yi,LU Jian Ping,MAO Jian qun,et al (Branch of Shanghai First People’s Hospital,Shanghai 200081,China) [

【机构】 上海市第一人民医院分院耳鼻咽喉科!上海200081复旦大学医学院病理教研室!上海200032中国科学院上海药物研究所!上海200032日本岗山大学医学部病理学教室!日本岗山700

【摘要】 目的 :探讨肝脂素 (Heplipin)对S37和B16两肿瘤细胞株移植瘤的生长抑制作用。方法 :小鼠S37肉瘤和B16黑色素瘤移植瘤在高、中、低剂量 (每天分别为 30 0 0、180 0、110 0mg kg)肝脂素胃饲为治疗组 ,环磷酰胺 (CTX)2 0mg(kg 天 )和生理盐水作为两对照组。比较抑瘤率、癌周边部血管数 ,总肿瘤面积中坏死区所占比例。结果 :肝脂素对S37肉瘤和B16黑色素瘤的抑瘤率分别为大剂量 :75 .1%和 47.0 %、中剂量 :6 9.7%和 32 .1%、小剂量 :6 1.7%和 13.0 % ,显示出明显的剂量效应关系 ,与生理盐水对照组相比有显著性差异。在S37肉瘤荷瘤小鼠的实验中 ,组织学观察发现 ,肝脂素用药组肿瘤周边部单位面积内血管数明显少于阴性对照组和CTX组 ;肝脂素治疗组的肿瘤坏死面积明显大于对照组。结论 :肝脂素可明显抑制小鼠S37肉瘤和B16黑色素瘤的生长 ,其抗肿瘤机制可能与抑制肿瘤新生血管的形成 ,导致肿瘤缺血坏死有关

【Abstract】 Purpose:To investigate inhibitory effect of Heplipin on the growth of S37 and B16 implanted into Kunming and C57 mouse respectively. Methods:Heplipin was administrated through gastric inhabatin with the dose of each day such as 3 000 mg/kg (large dose group) 1800 mg/kg(medial dose group) and 1100 mg/kg different (small dose group). Cycolo phosphaincole(CTX, each day 20 mg/kg) and normal saline wasused as postive and negative control respectively. The rates in tumor inhibition, the number of blood vessels, and the rate of necrosis area was tested.Results:The growth suppression of Heplipin to S37 sarcoma and B16 melanoma was 75.1% (large dose, P <0.0001), 69.7% (intermediate dose, P <0.0001), 61.7% (small dose, P <0.01) in Heplipin treated S37 sarcoma laden mice; and 47.0% (large dose, P <0.01), 32.1% (intermediate dose), 13.0% (small dose) in Heplipin treated B16 melanoma laden mice. Histologic examination showed that the number of blood vessels in S37 sarcoma laden mice of large dose group (1.39/field, P <0.01) and intermediate dose group (2.15/field, P < 0.05) was less than in that of control groups (6.28/field and 4.70/field ). Heplipin treated groups had more extensive tumor necrosis (75.5% and 60.5%) than the negative control group (48.3%). Conclusions:Heplipin can significantly suppress the growth of the S37 sarcoma and B16 melanoma in mice. The anti tumor mechanism of Heplipin may be related to the inhibition of blood vessel formation resulting in ischemic necrosis of the tumor. [

【基金】 上海医科大学与日本国日中永和协会合作课题基金资助(860 2 1199710 6)。
  • 【文献出处】 中国癌症杂志 ,China Oncology , 编辑部邮箱 ,2001年03期
  • 【分类号】R73-36
  • 【被引频次】1
  • 【下载频次】47
节点文献中: 

本文链接的文献网络图示:

本文的引文网络