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首页> 外文期刊>Anti-cancer agents in medicinal chemistry >Targeted regulation of Pi3K/Akt/mTOR/NF-κB signaling by indole compounds and their derivatives: Mechanistic details and biological implications for cancer therapy
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Targeted regulation of Pi3K/Akt/mTOR/NF-κB signaling by indole compounds and their derivatives: Mechanistic details and biological implications for cancer therapy

机译:吲哚化合物及其衍生物对Pi3K / Akt / mTOR /NF-κB信号的靶向调节:机理细节和对癌症治疗的生物学意义

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摘要

Indole compounds, found in cruciferous vegetables, are potent anti-cancer agents. Studies with indole-3-carbinol (I3C) and its dimeric product, 3,3'-diindolylmethane (DIM) suggest that these compounds have the ability to deregulate multiple cellular signaling pathways, including PI3K/Akt/mTOR signaling pathway. These natural compounds are also effective modulators of downstream transcription factor NF-κB signaling which might help explain their ability to inhibit invasion and angiogenesis, and the reversal of epithelial-to-mesenchymal transition (EMT) phenotype and drug resistance. Signaling through PI3K/Akt/mTOR and NF-κB pathway is increasingly being realized to play important role in EMT through the regulation of novel miRNAs which further validates the importance of this signaling network and its regulations by indole compounds. Here we will review the available literature on the modulation of PI3K/Akt/mTOR/NF-κB signaling by both parental I3C and DIM, as well as their analogs/derivatives, in an attempt to catalog their anticancer activity.
机译:在十字花科蔬菜中发现的吲哚化合物是有效的抗癌剂。对吲哚-3-甲醇(I3C)及其二聚体产物3,3'-diindolylmethane(DIM)的研究表明,这些化合物具有解除多种细胞信号通路(包括PI3K / Akt / mTOR信号通路)的能力。这些天然化合物还是下游转录因子NF-κB信号传导的有效调节剂,可能有助于解释其抑制侵袭和血管生成的能力以及上皮-间质转化(EMT)表型和药物耐药性的逆转。通过PI3K / Akt / mTOR和NF-κB途径的信号转导正通过新型miRNA的调控在EMT中发挥重要作用,这进一步验证了该信号网络的重要性及其吲哚化合物对其的调控。在这里,我们将回顾有关父母I3C和DIM以及它们的类似物/衍生物对PI3K / Akt / mTOR /NF-κB信号传导的调节的现有文献,以试图对其抗癌活性进行分类。

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