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肝脂素对小鼠S37肉瘤与B16黑色素瘤的抗肿瘤作用
引用本文:乔艺,路建平,毛建群,沈祖铭,林肇辉.肝脂素对小鼠S37肉瘤与B16黑色素瘤的抗肿瘤作用[J].中国癌症杂志,2001,11(3):223-225.
作者姓名:乔艺  路建平  毛建群  沈祖铭  林肇辉
作者单位:1. 上海市第一人民医院分院耳鼻咽喉科,
2. 复旦大学医学院病理教研室,
3. 中国科学院上海药物研究所,
4. 日本岗山大学医学部病理学教室,
基金项目:上海医科大学与日本国日中永和协会合作课题基金资助(860211997106).
摘    要:目的:探讨肝脂素(Heplipin)对S37和B16两种肿瘤细胞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3000、1800、1100mg/kg)肝脂素胃饲为治疗组,环磷酰胺(CTX)20mg(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黑色素瘤的抑瘤分别为大剂量:75.1%和47.0%、中剂量:69.7%和32.1%、小剂量:61.7%和13.0%,显示出明显的剂量效关系,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痊面积血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生长血管的生成,导肿瘤缺血坏死有关。

关 键 词:抗癌药  肝脂素  小鼠  移植性肿瘤  S37肉瘤  B16黑色素瘤
文章编号:1007-3639(2001)03-0223-03
修稿时间:2000年11月24

The antitumor efficacy of Heplipin on S37 sarcoma and B16 melanoma in mice
QIAO Yi,LU Jian Ping,MAO Jian qun,et al.The antitumor efficacy of Heplipin on S37 sarcoma and B16 melanoma in mice[J].China Oncology,2001,11(3):223-225.
Authors:QIAO Yi  LU Jian Ping  MAO Jian qun  
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.
Keywords:anti  cancer remedy  heplipin  mice transplanted tumor
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