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Diversity of the intracellular mechanisms underlying the anti-tumor properties of indirubins

机译:内胆管抗肿瘤性质的细胞内机制的多样性

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Indirubin is a bis-indole isomer of indigo which can be obtained from indigo-producing plants, several species of marine molhisks, several recombinant bacteria and mammalian urine, hidirubin is the active ingredient of a traditional Chinese medicine recipe, Danggui Longhui Wan, reported as a treatment for chronic myelocytic leukemia. Following the discovery of indirubin's interaction with cyclin-dependent kinases, numerous derivatives have been chemically synthesized aiming at the optimization of indirubins' selectivity, solubility and efficacy against tumor growth. Recent studies show that the mechanism of action of indirubins is complex. Additional targets include glycogen synthase kinase-3, c-Src and activation of the Stat3 transcription factor, aryl hydrocarbon receptor, glycogen phosphorylase, and other targets. Interaction with these multiple targets may contribute to the antiproliferative and cell death inducing effects of indirubins, and avoid the appearance of indirubiri-resistant cells. ? 2007 Published by Hsevier B.V.
机译:Indirubin是靛蓝的双吲哚异构体,可从靛蓝生产植物获得,几种海洋莫霍克斯,几种重组细菌和哺乳动物尿液,Hidirubin是中药食谱,据报道的中药食谱的活性成分慢性髓细胞白血病的治疗方法。在发现与细胞周期蛋白依赖性激酶的相互作用之后,许多衍生物已经在化学合成的旨在优化内核选择性,溶解度和抗肿瘤生长的效果。最近的研究表明,吲哚素的作用机制是复杂的。另外的靶标包括糖原合酶激酶-3,C-SRC和STAT3转录因子,芳基烃受体,糖原磷酸化酶和其他靶标的活化。与这些多种靶点的相互作用可能有助于抗抗增殖和细胞死亡诱导诱导吲哚醌的影响,并避免抗胆管细胞的外观。还是2007年由Hsevier B.V发布。

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