首页 | 本学科首页   官方微博 | 高级检索  
     

人胃癌原代细胞培养化疗药物敏感性评价
引用本文:许洪伟,秦成勇,刘吉勇,王春霞,杨崇美,朱菊人. 人胃癌原代细胞培养化疗药物敏感性评价[J]. 山东大学学报(医学版), 2003, 41(3): 278-281
作者姓名:许洪伟  秦成勇  刘吉勇  王春霞  杨崇美  朱菊人
作者单位:1. 山东省立医院消化内科
2. 山东省立医院中心实验室
摘    要:目的:评价人胃癌原代细胞对7种化疗药物的敏感性。方法:取59例手术切除的新鲜胃癌组织标本,应用人胃癌原代细胞短期培养(混杂非肿瘤细胞)与纯化培养MTT法体外药敏试验,测定每种化疗药物对肿瘤细胞的抑制率。结果:药敏试验测定7种化疗药物抑制率除氨甲蝶呤(MTX)外纯化法均高于短期法,表明纯化法较敏感;两种方法测定药物敏感性顺序一致,由高至低依次为顺铂(DDP)、丝裂霉素(MMC)、阿霉素(ADM)、依托泊甙(VP-16)、5-氟尿嘧啶(5-FU)、羟基喜树碱(HCPT)、MTX。结论:7种化疗药物以DDP、MMC、ADM较敏感,VP-16、5-FU次之,HCPT、MTX最差。

关 键 词:胃肿瘤  肿瘤细胞  培养的  MTT比色法  药物评价
文章编号:1671-7554(2003)03-0278-04
修稿时间:2002-10-26

Evaluation of chemosensitivity of seven antitumor drugs commonly used for human gastric cancer with primary culture cells
XU Hong-wei,QIN Cheng-yong,LIU Ji-yong,et al. Evaluation of chemosensitivity of seven antitumor drugs commonly used for human gastric cancer with primary culture cells[J]. Journal of Shandong University:Health Sciences, 2003, 41(3): 278-281
Authors:XU Hong-wei  QIN Cheng-yong  LIU Ji-yong  et al
Abstract:Objective:To investigate the chemosensitivity of seven antitumor drugs commonly used in the treatment of gastric cancer with primary culture tumor cells.Methods :Fifty-nine fresh samples from patients with gastric cancer were obtained during operation.Chemosensitivity results from MTT assay with short-term culture tumor cells contaminated by nonmalignant cells were compared with those from the same assay with purified primary culture tumor cells.Results:All of the seven antitu-mor drugs but Methotrexate(MTX)using purified cells showed higher inhibition rates than those using short-term method,but the order of drugs in the degree of chemosensitivity was the same.They were(from high to low):Cisplatin(DDP),Mitomycin C(MMC),Adriamycin(ADM),Etoposide(VP-16),5-Fluo-rouracil(5-FU),Hydroxycampothecin (HCPT),MTX.Conclusions :DDP,MMC and ADM are more chemosensitive than VP-16or5-FU,especially than HCPT or MTX for gastric cancer.
Keywords:Stomach neoplasms  Tumor cells  cultured  Colorimetry  Drug evaluation
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号