期刊文献+

丙酮酸乙酯联合顺铂作用裸鼠肝移植瘤的研究

下载PDF
导出
摘要 目的:研究丙酮酸乙酯(EP)与顺铂(CDDP)联合处理裸鼠对裸鼠肝癌HepG2移植瘤的作用效果,及对个体的副作用;方法:为裸鼠接种p-Gluc荧光标记的HepG2细胞,分为PBS处理组、CDDP(9.6mM)与EP(60μg)单独注射组、CDDP与EP联合注射组;对各组裸鼠的个体体重、移植瘤体积进行观察测量;结果:药物联合组的肿瘤体积显著小于对照组(*P=0.0146),而CDDP处理组无显著变化。药物联合组与CDDP组中肿瘤抑制率分别为36.8%和62.9%;药物联合组体重平均为21g,CDDP组为19g,EP组与对照组约为25g;结论:EP是CDDP增效剂,药物联合处理有望为肝癌治疗方案提出新的思路,并可能缓解化疗药物单独使用带来的副作用。 Objective:To study the effect of ethyl pyruvate(EP)combined with cisplatin(CDDP)on HepG2 transplanted tumor in nude mice and the side effects on individuals;Method:Inoculating p-Gluc fluorescently labeled HepG2 cells into nude mice,then divided into PBS-treated group,CDDP(9.6 mM)and EP(60μg)Separate injection group,and CDDP-EP combined injection group;O bserving and measuring individual body weight and transplanted tumor volume of each group;Results:The tumor volume of CDDP-EP therapy group was significantly smaller than that of the control group(*P=0.0146),while there was no significant change in the CDDP therapy group.The tumor inhibition rates in CDDP-EP therapy group and the CDDP group were 36.8%and 62.9%,respectively;the average body weight of CDDP-EP therapy group was 21g,the CDDP group was 19g,while the EP group and the control group were nearly 25g;Conclusion:EP is a CDDP synergist,the drug combination therapy is expected to provide new ideas for the treatment of liver cancer,and may alleviate the side effects caused by the separate use of chemotherapy drugs.
机构地区 杭州医学院
出处 《科学技术创新》 2019年第27期18-21,共4页 Scientific and Technological Innovation
基金 浙江省省教育厅科研一般项目(Y201636957) 杭州医学院校级博士启动金(2016B04) 浙江省大学生科技创新活动计划(新苗人才计划)(2019R425004)
关键词 顺铂 丙酮酸乙酯 裸鼠 肝癌移植瘤 Cisplatin Ethyl Pyruvate Nude mice Hepatocellular Carcinoma
  • 相关文献

参考文献8

二级参考文献43

  • 1田杰,李慧萍,任配友,刘春禹,李锐.姜黄素通过激活AMPK抑制人肝癌细胞HL-7702的增殖[J].中国老年学杂志,2014,34(7):1897-1898. 被引量:3
  • 2刘波,白庆咸,陈协群,高广勋,顾宏涛.姜黄素对人多发性骨髓瘤细胞表达Survivin、Bcl-2、Bax的影响[J].中国实验血液学杂志,2007,15(4):762-766. 被引量:13
  • 3Lefebvre JL, Chevalier D, Luboinski B, et al. Larynx preservation in pyriform sinus cancer: preliminary results of a European Organization for research and treatment of Cancer phaseⅢ trail: EORTC Head and Neck Cancer Cooperative Group[J]. J Natl Cancer Inst, 1996,88:890. 被引量:1
  • 4Cheng CC, Yang SM, Huang CY, et al. Molecular mechanisms of ginsenoside Rh2-mediated G1 growth arrest and apoptosis in human lung adenocarcinoma A549 cells [ J ]. Cancer Chemother Pharmacol, 2005, 55(6) :531. 被引量:1
  • 5Brown JM, Attardi LD. The role of apoptosis in cancer development and treatment response[J]. Nat Rev Cancer, 2005,5(3):231. 被引量:1
  • 6Damia G, Broggini M. Improving the selectivity of cancer treatments by interferingwith cell response pathways[J]. Eur J Cancer, 2004,40(17) :2550. 被引量:1
  • 7Radulovic S, Tesic Z, Manic S. Trans-platinum complexes as anticancer drugs: recent developments and future prospects[J]. Curr Med Chem,2002,9(17):1611. 被引量:1
  • 8张梅春,赵子文,曾军,何卫国,黄侃.姜黄素对耐顺铂人肺腺癌细胞Survivin表达及其化疗敏感性的影响[J].中华肿瘤防治杂志,2007,14(19):1454-1457. 被引量:13
  • 9Cheung ST, Cheung PF, Cheng CK, et al. Granulin-epithelin pre- cursor and ATP-dependent binding cassette(ABC)B5 regulate liv- er Cancer cell chemoresistance [J]. Gastroenterology, 2011, 140 (1) :344-355. 被引量:1
  • 10Williamson JM,Thairu N,Katsoulas N,et al. Impact of portal vein embolization on expression of Cancer stem cell markers in regen- erated liver and colorectal liver metastases[J]. Scand J Gastroen- terol, 2010,45 (12) : 1472-1479. 被引量:1

共引文献16

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部