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中国临床药理学与治疗学 ›› 2017, Vol. 22 ›› Issue (1): 33-36.

• 基础研究 • 上一篇    下一篇

靶向肿瘤新生血管唑来膦酸阳离子隐形脂质体抗肿瘤作用的研究

陈芳君1,王 增1,蔡鑫君2,曹莹莹1,陈 培1,邵 芸1   

  1. 1 浙江省肿瘤医院,2 杭州市红十字会医院药剂科,杭州 310003,浙江
  • 收稿日期:2016-09-06 修回日期:2016-11-01 出版日期:2017-01-26 发布日期:2017-01-23
  • 通讯作者: 王增,硕士,主管药师,研究方向:肿瘤药学研究。 Tel:0571-88122120 E-mail:wangzeng@zjcc.org.cn
  • 作者简介:陈芳君,女,本科,药师,研究方向:肿瘤药学研究。 E-mail:chenfj@zjcc.org.cn
  • 基金资助:

    浙江省医药卫生科技计划(2014KYB039);浙江省中医药科技计划(2015ZA148, 2016ZA038,20172A109);浙江省公益性技术应用研究计划项目(2015C33286);杭州市医药卫生科技计划(201553365),浙江省肿瘤医院“1022”人才项目

Anti-tumor effects of zoledronic acid-loaded stealth cationic liposome by targeting tumor angiogenesis

CHEN Fangjun 1, WANG Zeng 1, CAI Xinjun 2, CAO Yingying 1, CHEN Pei 1, SHAO Yun 1   

  1. 1 Department of Pharmacy, Zhejiang Cancer Hospital, 2 Department of Pharmacy, the Red Cross Hospital of Hangzhou, Hangzhou 310003, Zhejiang, China
  • Received:2016-09-06 Revised:2016-11-01 Online:2017-01-26 Published:2017-01-23

摘要:

目的:研究APRPG(Ala-Pro-Arg-Pro-Gly)修饰的隐形唑来膦酸阳离子脂质体对荷前列腺癌PC-3裸鼠的抗肿瘤作用。方法: 构建荷前列腺癌PC-3裸鼠模型,比较研究唑来膦酸阳离子脂质体、APRPG修饰的隐形唑来膦酸阳离子脂质体对肿瘤体积增长的抑制作用,计算肿瘤抑制率,并通过免疫组化实验分析其对肿瘤相关因子血管内皮生长因子(VEGF)和分化抗原簇44(CD44)表达的影响。结果: 唑来膦酸阳离子脂质体、APRPG修饰的隐形唑来膦酸阳离子脂质体对荷前列腺癌PC-3裸鼠的肿瘤抑制率分别为31.81%、68.18%,后者的肿瘤抑制率明显高于前者(P<0.05),免疫组化结果显示VEGF和CD44蛋白在模型对照组中表达呈强阳性,在唑来膦酸阳离子脂质体组中呈中度阳性表达,而在APRPG修饰的隐形唑来膦酸阳离子脂质体中表达较为微弱。结论:APRPG修饰的隐形唑来膦酸阳离子脂质体对前列腺癌PC-3裸鼠具有更强的肿瘤抑制率。

关键词: 肿瘤新生血管靶向, 唑来膦酸阳离子隐形脂质体, 抗肿瘤

Abstract:

AIM: To investigate the anti-tumor effect of APRPG modified zoledronic acid-loaded stealth cationic liposomes in nude mice bearing PC-3 prostate cancer. METHODS: Prostate cancer cell PC-3 beared nude mice model was constructed, growth inhibition of tumor volume between zoledronic acid cationic liposome and APRPG modificated zoledronic acid-loaded stealth cationic liposomes was compared, and the tumor inhibition rate was calculated. Immunohistochemistry analysis was used to detect the effect on expression of VEGF and CD44. RESULTS: The tumor inhibition rate of zoledronic acid cationic liposome and APRPG modificated zoledronic acid-loaded stealth cationic liposomes were 31.81%,68.18%, respectively, the tumor inhibition rate of the latter was significantly higher than that of the former (P<0.05), immunohistochemical results showed that VEGF and CD44 protein expression was strong positive in the model control group, in zoledronic acid cationic liposome group, it showed a moderate positive expression, and in APRPG modificated zoledronic acid-loaded stealth cationic liposomes group, the expression was very weak. CONCLUSION: The APRPG modified stealth liposome can exert a stronger inhibition effect in PC-3 nude mice.

Key words: targeting tumor angiogenesis, zoledronic acid-loaded stealth cationic liposomes, anti tumor

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