藤龙补中汤对大肠癌RKO细胞癌药靶基因表达的影响
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  • 英文篇名:Effects of Teng-Long-Bu-Zhong-Tang on expression of cancer drug target genes in colorectal carcinoma RKO cells
  • 作者:胡兵 ; 王双双 ; 黄晓伟 ; 李淼 ; 陈雷
  • 英文作者:HU Bing;WANG Shuang-shuang;HUANG Xiao-wei;LI Miao;CHEN Lei;Longhua Hospital, Shanghai University of Traditional Chinese Medicine;
  • 关键词:大肠癌 ; 中医药 ; 藤龙补中汤 ; 药靶基因 ; 基因表达
  • 英文关键词:Colorectal cancer;;Traditional Chinese Medicine;;Teng-Long-Bu-Zhong-Tang;;Cancer drug targets;;Gene expression
  • 中文刊名:SZGY
  • 英文刊名:Lishizhen Medicine and Materia Medica Research
  • 机构:上海中医药大学附属龙华医院;
  • 出版日期:2019-06-20
  • 出版单位:时珍国医国药
  • 年:2019
  • 期:v.30;No.286
  • 基金:国家自然科学基金(81473625);; 上海市科技支撑项目(16401902500)
  • 语种:中文;
  • 页:SZGY201906012
  • 页数:3
  • CN:06
  • ISSN:42-1436/R
  • 分类号:43-45
摘要
目的 观察藤龙补中汤对人大肠癌RKO细胞癌药靶基因表达影响。方法 藤龙补中汤作用RKO细胞,TRIzol试剂提取RNA,试剂盒纯化RNA,药靶基因PCR芯片(Cancer Drug Targets PCR Array)检测基因表达。结果 藤龙补中汤作用RKO细胞后,PLK3和TP53表达升高,ABCC1、AURKA、BCL2、BIRC5、CDK2、CDK4、FLT4、HDAC1、HIF1A、MDM4、MTOR、NFKB1和PLK1表达降低,涉及细胞增殖、细胞周期、凋亡、细胞衰老、多药耐药、转移、淋巴管生成和表观遗传修饰。结论 藤龙补中汤可调控RKO细胞多个癌药靶基因表达,与藤龙补中汤对大肠癌细胞增殖、细胞周期、凋亡、细胞衰老、转移和表观遗传作用相关;藤龙补中汤还可能对大肠癌多药耐药和淋巴管生成有抑制作用。
        Objective To observe the effects of Teng-Long-Bu-Zhong-Tang(TLBZT) on expression of cancer drug target genes in human colorectal carcinoma RKO cells. Methods RKO cells were treated with TLBZT. RNA was extracted by TRIzol regent and purified with commercial kit. Genes expression were detected by Cancer Drug Targets PCR array. Results After TLBZT treatment, PLK3 and TP53 were up-regulated,ABCC1, AURKA, BCL2, BIRC5, CDK2, CDK4, FLT4, HDAC1, HIF1 A, MDM4, MTOR, NFKB1 and PLK1 were down-regulated in RKO cells. These genes involve cell proliferation, cell cycle, apoptosis, cell senescence, multidrug resistance, metastasis, lymphoangiogenesis and epigenetic modification. Conclusion TLBZT regulates expression of multiple genes of cancer drug targets and are related to the effects of TLBZT on cell proliferation, cell cycle, apoptosis, cell senescence, metastasis and epigenetics in colorectal cancer. TLBZT may also inhibit lymphoangiogenesis and multidrug resistance in colorectal cancer.
引文
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