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A Novel Substrate Mimetic Inhibitor of PKB/Akt Inhibits Prostate Cancer Tumor Growth in Mice by Blocking the PKB Pathway

机译:通过阻断PKB途径,PKB / AKT的新型衬底模拟物抑制剂抑制了小鼠中的前列腺癌肿瘤生长

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摘要

We describe a novel, potent peptide substrate mimetic inhibitor of protein kinase B (PKB/ Akt). The compound selectively kills prostate cancer cells, in which PKB is highly activated, but not normal cells, or cancer cells in which PKB is not activated. The inhibitor induces apoptosis and inhibits the phosphorylation of PKB substrates in prostate cancer cell lines and significantly increases the efficacy of chemotherapy agents to induce prostate cancer cell death, when given in combination. In vivo, the inhibitor exhibits a strong antitumor effect in two prostate cancer mouse models. Moreover, treated animals develop significantly less lung metastases compared to untreated ones, and the effect is accompanied by a significant decrease in blood PSA [prostate-specific antigen] levels in treated animals. This compound and its potential analogues may be developed into novel, potent, and safe anticancer agents, both as standalone treatment and in combination with other chemotherapy agents.
机译:我们描述了一种新颖的有效的肽底物模拟蛋白激酶B(PKB / AKT)的抑制剂。 该化合物选择性地杀死前列腺癌细胞,其中PKB是高度活化的,但不是正常的细胞,或未激活PKB的癌细胞。 抑制剂诱导细胞凋亡并抑制前列腺癌细胞中PKB底物的磷酸化,并在组合给出时显着提高化疗试剂诱导前列腺癌细胞死亡的疗效。 在体内,抑制剂在两种前列腺癌小鼠模型中表现出强烈的抗肿瘤作用。 此外,与未处理的动物相比,处理的动物显着减少肺转移,并且效果伴随着处理动物中血液PSA [前列腺特异性抗原]水平的显着降低。 该化合物及其潜在的类似物可开发成新的,有效和安全的抗癌剂,无论是独立治疗还是与其他化疗剂组合。

著录项

  • 来源
    《Biochemistry》 |2007年第16期|共9页
  • 作者单位

    DeveloGen Israel Ltd. Kiryat Weizmann Building 16 Rehovot Israel 76326 Unit of Pathology Meir Medical Center Kfar Saba Israel and Wolf son Centre of Applied Structural Biology and Unit of Cellular Signaling Department of Biological Chemistry;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;
  • 关键词

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