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作 者:王振月[1] 唐先明[1,2] 赵海鹏[1,3] 王宗权[1,4] 陈智岩[1]
机构地区:[1]黑龙江中医药大学药学院,黑龙江哈尔滨150040 [2]哈尔滨市食品药品检验检测中心,黑龙江哈尔滨150525 [3]鲁南制药集团股份有限公司,山东临沂276005 [4]以领医药集团医药研究院,河北石家庄050035
出 处:《第四军医大学学报》2008年第23期2141-2143,共3页Journal of the Fourth Military Medical University
基 金:黑龙江省自然科学基金重点项目(ZJY005006-02);黑龙江省研究生创新科研基金项目
摘 要:目的:探讨毛脉酸模提取物二苯乙烯类成分与肝癌发生、发展的关系及其作用机制.方法:用二苯乙烯类成分处理人肝癌细胞株HepG248h后,提取药物处理组和对照组细胞的总RNA,将两组RNA纯化为mRNA,逆转录成cDNA,用Cy3和Cy5两种不同的荧光染料进行线性扩增标记,然后与人肿瘤相关基因表达谱芯片杂交,扫描后对获得的数据用LuxScan3.0软件分析.结果:经二苯乙烯类成分诱导后HepG2细胞的2474个肿瘤相关基因中,有GADD153,HPRG等5个基因表达明显上调,PRL-1,PAI-1等9个基因明显下调.结论:二苯乙烯类成分能改变细胞周期进程、细胞增殖、细胞凋亡、血管生成等相关基因的表达,此可能是其抗肿瘤作用的机制.AIM :To investigate the effects of chrysophenine fi'om Rumex gmelini Turez on the cancer-related gene expressions of HepG2 cells by gene expresion profile chip and to study its relationship with the development of hepatic cancer and the relative mechanisms. METHODS: The total RNAs were extracted from chrysophenine untreated or treated HepG2 cells to synthesize doub- le-stranded cDNAs by reverse transcription. Then cDNA labeled with the incorporation of Cy3 and CyS-dUT were amplified linearly. Probes were hybridized with oligonucleotide microarray. The chips were scanned and then analyzed by LuxScan 3. 0 software. RESULTS:After chrysophenine induction, expressions of 9 out of 2474 cancer related genes, including PRL-1, PAI-1, ere, were dowrl-regulated notably. Meanwhile, expressions of 5 out of 2474- cancer genes, including GADD153,HPRG, etc, were up-regulated markedly. CONCLUSION: The alterations in specific genes involved in modulating the cell cycle progress, cell proliferation, cell apoptosis,and antiangiogenesis may be responsible for anticancer molecular mechanism of chrysophenine.
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