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Biochem Pharmacol:PAK1抑制剂IPA-3能够减轻转移前列腺癌诱导的骨重建

2020-04-14 AlexYang MedSci原创

转移前列腺癌(PCa)具有高度的致死性和低的5年生存率,主要是由于缺乏有效的治疗措施。骨是人类PCa转移的主要位点,对骨转移PCa可靠治疗选择开发将对减少这些患者的死亡率产生重大影响。

转移前列腺癌(PCa)具有高度的致死性和低的5年生存率,主要是由于缺乏有效的治疗措施。骨是人类PCa转移的主要位点,对骨转移PCa可靠治疗选择开发将对减少这些患者的死亡率产生重大影响。

尽管P21激酶激活(PAKs)在癌症中的作用已经有所研究,而靶向PAKs来治疗肺和骨转移PCa还没有进行过测试。最近,有研究人员报道了使用IPA-3(一种PAK1激酶活性的变构抑制剂)能够显著的抑制体外小鼠转移PCa(RM1)的细胞增殖和迁移,以及体内肺部的转移。更重要的是,通过3维计算机断层扫描分析,研究人员首次阐释了IPA-3治疗能够延缓体内转移PCa诱导的骨重建。

最后,研究人员指出,IPA-3是治疗骨转移PCa的一种可能的药物。

原始出处:

Verma A, Artham S, Alwhaibi A et al. PAK1 inhibitor IPA-3 mitigates metastatic prostate cancer-induced bone remodeling. Biochem Pharmacol. 30 Mar 2020

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    2020-04-20 yb6560
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    2020-10-25 jj000001
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    2020-12-08 jklm09
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    2020-05-18 sunylz
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    2020-04-14 misszhang

    前列腺癌相关研究,学习了,谢谢梅斯

    0

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前列腺癌(PCa)神经支配能够导致PCa的恶化。然而,神经支配对PCa细胞的精细影响仍旧了解很少。

Radiother Oncol:中风险和高风险前列腺癌多中心II期hypo-FLAME试验的主要终点分析

前列腺癌(PCa)放疗后的局部复发常发生在肉眼可见的肿瘤部位。由于PCa细胞对高剂量敏感,低分割全腺体立体定向体放射治疗(SBRT)同时结合前列腺内宏观肿瘤(s)消融微烧蚀可能是降低局部失败风险的一种

Cancers (Basel):KLF5对雄激素-AR信号反式激活基因和促进细胞增殖至关重要

雄激素/雄激素受体(AR)信号能够促使正常前列腺发育和前列腺癌的形成,并且晚期前列腺癌患者往往发展出对雄激素阻断治疗的抗性。转录因子Krüppel-like factor5(KLF5)能够对

Biochem Pharmacol:前列腺癌中代谢稳定的二苯胺衍生物能够抑制雄激素受体和BET蛋白

雄激素受体(AR)是前列腺癌(PC)的一种关键的驱使因子。目前,AR相关的抗性仍旧是去势抵抗性前列腺癌(CRPC)治疗的重大挑战。溴域和末端外结构域(BET)家族是AR的关键共调控因子。

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