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凋亡 CK2 抑制剂 CX4945 对人前列腺癌细胞 LNCap 中雄激素受体的拮抗作用。

Anti-androgen receptor activity of apoptotic CK2 inhibitor CX4945 in human prostate cancer LNCap cells.

机构信息

Laboratory of Translational Therapeutics, Pharmacology Research Center, Yuseong-gu, Daejeon 305-600, Republic of Korea.

出版信息

Bioorg Med Chem Lett. 2012 Sep 1;22(17):5470-4. doi: 10.1016/j.bmcl.2012.07.031. Epub 2012 Jul 14.

Abstract

Androgen receptor (AR) is crucial for transcriptional signaling in prostate cancers. The anti-cancer activity of protein kinase CK2 (formerly called casein kinase 2)-specific small molecule inhibitors have been reported in several cancers including prostate cancers. The orally available CX4945, a potent and selective small molecule inhibitor of CK2, has advanced into human clinical trials and has exhibited strong anti-tumor activity. The inhibition of CK2 leads to a down-regulation of the AR-dependent transcription, but the functional relevance of CX4945 to AR-dependent transcription in AR-positive LNCap cells has not been studied yet. Our observation of inhibitory effects of CX4945 on the expression or phosphorylation levels of CK2α, Akt and anti-apoptotic molecules including IAP family members agreed with a previous study showing the effect of CK2 inhibition in cancer cells. This study also provides novel information on the impact of CX4945 in the inhibition of AR-dependent transcriptional activation in LNCap cells via its down-regulation. Pharmacologic inhibition experiment revealed that CX4945 could exhibit its anti-cancer activity in LNCap cells via the independent inhibitions of AR and Akt-survivin signalings.

摘要

雄激素受体 (AR) 在前列腺癌的转录信号中起着至关重要的作用。蛋白激酶 CK2(以前称为酪蛋白激酶 2)的抗癌活性已在包括前列腺癌在内的几种癌症中得到报道。口服有效的 CX4945 是一种 CK2 的强效和选择性小分子抑制剂,已进入人体临床试验,并表现出很强的抗肿瘤活性。CK2 的抑制导致 AR 依赖性转录的下调,但 CX4945 对 AR 阳性 LNCap 细胞中 AR 依赖性转录的功能相关性尚未得到研究。我们观察到 CX4945 对 CK2α、Akt 和抗凋亡分子(包括 IAP 家族成员)的表达或磷酸化水平的抑制作用与先前的研究一致,该研究表明 CK2 抑制在癌细胞中的作用。这项研究还提供了关于 CX4945 通过下调抑制 LNCap 细胞中 AR 依赖性转录激活的影响的新信息。药理抑制实验表明,CX4945 可以通过独立抑制 AR 和 Akt-survivin 信号通路在 LNCap 细胞中发挥其抗癌活性。

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