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作 者:黄瀚 李兵[2] 欧阳林旗[3,2] 李佐军[2] 刘世坤[3,2]
机构地区:[1]湖南省医药学校,湖南长沙410116 [2]中南大学湘雅三医院药剂科,湖南长沙410013 [3]中南大学药学院,湖南长沙410013
出 处:《中国药理学通报》2011年第1期99-103,共5页Chinese Pharmacological Bulletin
基 金:湖南省自然科学基金资助项目(No09JJ6051)
摘 要:目的以人乳腺癌多药耐药细胞系MCF-7/ADR及其敏感亲本系MCF-7为对象,探讨叶酸受体(FOLRα)及其下游基因二氢叶酸还原酶(DHFR)的表达与乳腺癌细胞多药耐药的关系。方法 MTT法测定阿霉素的细胞毒性作用及DHFR抑制剂对MCF-7/ADR细胞多药耐药的逆转作用;RT-PCR检测细胞FOLRα和DHFR mRNA的表达水平;免疫细胞化学检测FOLRα、P-gp的表达水平。结果 MCF-7细胞增殖速度快于MCF-7/ADR细胞,MCF-7细胞FOLRα mRNA转录水平较MCF-7/ADR细胞高,而MCF-7/ADR细胞DHFR mRNA较MCF-7细胞转录水平高;免疫细胞化学显示MCF-7细胞FOLRα的表达高于MCF-7/ADR细胞,而MCF-7/ADR细胞P-gp的表达较MCF-7细胞高;MCF-7/ADR对甲氨蝶啶无耐药性,甲氨蝶啶对MCF-7/ADR细胞多药耐药有逆转作用。结论 MCF-7/ADR细胞FOLRα的表达水平下调可能与细胞增殖水平有关,其下游基因DHFR表达水平与MCF-7/ADR细胞的MDR可能存在相关性。Aim The adriamycin-resistant human breast cancer cell line MCF-7/ADR was used as the experiment subject to investigate the expressions of FOLRα receptor gene and its downstream gene dihydrofolate reductase and their correlation with the breast cancer cell multidrug-resistance.Methods MTT assay was used to investigate the cytotoxicity of ADR and reversal effect of trimethoprim on MCF-7/ADR cells;real time PCR was used to detect transcriptional levels of folate receptor mRNA and dihydrofolate reductase mRNA of MCF-7/S cells and MCF-7/ADR cells,the protein level of P-gp and FOLRα was detected with immunohistochemisty.Results FOLRα receptor mRNA transcriptional levels of MCF-7 cells were higher than those of MCF-7/ADR cells,dihydrofolate reductase mRNA transcriptional levels of MCF-7/ADR cells were increased.It showed that the protein level of P-gp of MCF-7/ADR cells was higher than that of MCF-7/S cells,while the protein level of FOLRα of MCF-7/ADR cells was lower than that of MCF-7/S cells;MCF-7/ADR cells had no drug resistance to MTX,which could in turn reverse their multidrug resistance.Conclusions The down-regulated expression level of FOLRα receptor may be related to the level of MCF-7/ADR cell proliferation.The expression level of DHFR gene may be related to MDR of MCF-7/ADR cells.
关 键 词:叶酸受体 二氢叶酸还原酶 MCF-7 MCF-7/ADR 多药耐药 阿霉素 甲氨蝶啶
分 类 号:R329.24[医药卫生—人体解剖和组织胚胎学] R345.44[医药卫生—基础医学]
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