2015年10月:上海伯豪客户应用案例精选
在胃癌(GC)发生过程中,DAN甲基化转移酶3A的功能作用机制目前还不是很清楚。在该研究中,研究人员发现外源表达的DNMT3A通过打乱G1/S的转换而促进肝癌的细胞增殖。同时该研究找到了DNMT3A的下游靶基因p18INK4C,异位表达DNMT3A在转录层次抑制了p18INK4C的表达水平。在GC细胞中减弱p18INK4C的表达诱导细胞周期过程,在DNMT3A过表达细胞中重表达p18INK4C可减弱G1/S的转换。深入研究发现,DNMT3A通过直接调控p18INK4C启动子区的甲基化程度来影响其表达。临床GC样本检测发现,癌组织中p18INK4C的甲基化水平明显高于配对癌旁组织,DNMT3A的表达水平与p18INK4C的表达呈负相关。这些发现提出了胃致癌过程的新的见解,也为胃癌治疗提供了潜在的靶标。该研究中DNMT3A下游靶基因筛选表达谱芯片Affymetrix HTA2.0由上海伯豪生物技术有限公司提供。详细内容
2015年10月:上海伯豪客户应用案例精选
1 Ai ZY,Shao JJ,Shi XL,Yu MY, Wu YY,Du J,Zhang Y,Guo ZK. Maintenance of Self-Renewal and Pluripotency in J1 Mouse Embryonic Stem Cells through Regulating Transcription Factorand MicroRNA Expression Induced by PD0325901. Stem Cells International.2015.
2 Chen XY, Li R, Geng ZY. Cold stress initiated the Nrf2/UGT1A1/L-FABP signaling pathway in chicken. Poultry Science.2015.3 Cheng P, Wang YF, Li G, Yang SS, Liu C, Hu H, Jin G, Hu XG. Interplay between menin and Dnmt1 reversibly regulates pancreatic cancer cell growth downstream of the hedgehog signaling pathway. CANCER LETT.2015.
4 Miao X, Luo Q, Qin X, Guo Y, Zhao H. Genome-wide mRNA-seq profiling reveals predominant down-regulation of lipid metabolic processes in adipose tissues of Small Tail Han than Dorset sheep. Biochem Biophys Res Commun.2015.
5 Sun M1,Liao B, Tao Y, Chen H, Xiao F, Gu J, Gao S, Jin Y. Calcineurin-NFAT Signaling Controls Somatic Cell Reprogramming in a Stage-Dependent Manner. J Cell Physiol.2015.
6 Tuo YL, Li XM, Luo J. Long noncoding RNA UCA1 modulates breast cancer cell growth and apoptosis through decreasing tumor suppressive miR-143. Eur Rev Med Pharmacol Sci.2015.
7 Wu Y, Chen K, Liu X, Huang L, Zhao D, Li L, Gao M, Pei D, Wang C, Liu X. Srebp-1 Interacts with c-Myc to Enhance Somatic Cell Reprogramming. Stem Cells.2015.
8 Zhang X, Chen X, Jiang J, Yu M, Yin Y, Ma Z. The tubulin cofactor A is involved in hyphal growth, conidiation and cold sensitivity in Fusarium asiaticum. BMC Microbiol.2015.
9 Tang Y, Lin Y, Li C, Hu X, Liu Y, He M, Luo J, Sun G3, Wang T4, Li W, Guo M. MicroRNA-720 promotes in vitro cell migration by targeting Rab35 expression in cervical cancer cells. Cell Biosci.2015.
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