1 / 25
文档名称:

药学本科毕业论文.doc

格式:doc   大小:2,266KB   页数:25页
下载后只包含 1 个 DOC 格式的文档,没有任何的图纸或源代码,查看文件列表

如果您已付费下载过本站文档,您可以点这里二次下载

分享

预览

药学本科毕业论文.doc

上传人:taotao0c 2021/4/2 文件大小:2.21 MB

下载得到文件列表

药学本科毕业论文.doc

文档介绍

文档介绍:沈 阳 药 科 大 学
本 科 毕 业 论 文
论文题目:化合物A联合 化合物 B对人肝癌HepG2细胞作用机制研究文档来自于网络搜索
起止时间:2014 年10月26日—2015年6月20日个人收集整理 勿做商业用途
姓名学号:
学院专业:
年级班级:
指导教师:XXX 副教授文档来自于网络搜索
实****单位:XXX大学生命科学与生物制药学院药理系文档收集自网络,仅用于个人学****br/>目 录
中文摘要······································································1英文摘要······································································2个人收集整理 勿做商业用途
第1章 绪论··································································3文档收集自网络,仅用于个人学****br/> ·····························································3文档来自于网络搜索
·····························································5资料个人收集整理,勿做商业用途
第2章 实验部分······························································6文档收集自网络,仅用于个人学****br/>·····························································6个人收集整理 勿做商业用途
·····························································7个人收集整理 勿做商业用途
····························································12文档来自于网络搜索
第3章 结论与讨论···························································
17文档收集自网络,仅用于个人学****br/>································································17资料个人收集整理,勿做商业用途
································································18文档收集自网络,仅用于个人学****br/>参考文献·····································································21致谢·········································································23资料个人收集整理,勿做商业用途
摘 要
原发性肝癌是世界常见的恶性肿瘤之一,也是我国的高发恶性肿瘤,由于不易被早期诊断,进展迅速,术后容易复发、转移,因此预后较差。目前肝癌仍以外科手术为公认首选和主要的治疗手段,但由于很多肝癌患者确诊时已是中晚期,失去了手术治疗的机会并于诊断后1年内死亡,手术切除率<30%,术后总体5年生存率仅30%~40%。对于可手术的肝癌患者,术后复发、转移是影响治疗效果及预后的主要因素,对于不能手术的中晚期肝癌患者尚缺乏有效的治疗方法。传统的化疗、放疗对肝癌疗效欠佳,目前仍缺乏行之有效的化学预防和治疗靶位
[1]。因而本课题是对化合物 A联合化合物 B对人肝癌HepG2细胞作用机制研究。文档收集自网络,仅用于个人学****br/>本实验首先用MTT法分别测得不同浓度的A和B单独处理HepG2细胞及不同浓度的A和B联合用药处理HepG2细胞死亡的影响。结果表明不同浓度的A和B单独处理HepG2细胞,增值抑制程度表现为时间剂量依赖效应,并且在A 6μmol/L联合B 100μmol/L协同作用最为显著。流式细胞仪检测细胞凋亡率显示,联合用药组凋亡率升高更为明显。Western Blot法检测蛋白显示,促凋亡相关蛋白Bax、FADD增加,抗凋亡蛋白Bcl-2 表达减少。