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安第斯抗癌草药产品BIRM可导致雄激素受体不稳定,并在前列腺癌中诱导半胱天冬酶-8介导的细胞凋亡。

The andean anticancer herbal product BIRM causes destabilization of androgen receptor and induces caspase-8 mediated-apoptosis in prostate cancer.

作者信息

Shamaladevi Nagarajarao, Araki Shinako, Lyn Dominic A, Ayyathurai Rajnikanth, Gao Jie, Lokeshwar Vinata B, Navarrete Hugo, Lokeshwar Bal L

机构信息

Departments of Urology and Sylvester Cancer Center, Miller School of Medicine, University of Miami, Miami FL, USA.

Okayama University Graduate School of Medicine, Okayama, Japan.

出版信息

Oncotarget. 2016 Dec 20;7(51):84201-84213. doi: 10.18632/oncotarget.12393.

Abstract

BIRM is an anticancer herbal formulation from Ecuador. Previous study established its antitumor and antimetastatic activity against prostate cancer models. The activity of BIRM against human prostate cancer (PCa) cells was investigated to uncover its mechanism of antitumor activity. In androgen receptor (AR)-expressing PCa cells BIRM was 2.5-fold (250%) more cytotoxic in presence of androgen (DHT) compared to cells grown in the absence of DHT. In AR-positive cells (LAPC-4 and LNCaP) BIRM caused a dose and time-dependent down-regulation of AR and increased apoptosis. Exposing cells to BIRM did not affect the synthesis of AR and AR promoter activity but increased degradation of AR via proteasome-pathway. BIRM caused destabilization of HSP90-AR association in LAPC-4 cells. It induced apoptosis in PCa cells by activation of caspase-8 via death receptor and FADD-mediated pathways. A synthetic inhibitor of Caspase-8 cleavage (IETD-CHO) aborted BIRM-induced apoptosis. The effect of BIRM on AKT-mediated survival pathway in both AR+ and AR- negative (PC-3 and DU145) showed decreased levels of p-AKTser 473 in all PCa cell lines. BIRM dosed by oral gavage in mice bearing PC-3ML tumors showed selective efficacy on tumor growth; before tumors are established but limited efficacy when treated on existing tumors. Moreover, BIRM inhibited the LNCaP tumor generated by orthotropic implantation into dorsal prostate of nude mice. Partial purification of BIRM by liquid-liquid extraction and further fractionation by HPLC showed 4-fold increased specific activity on PCa cells. These results demonstrate a mechanistic basis of anti-tumor activity of the herbal extract BIRM.

摘要

BIRM是一种来自厄瓜多尔的抗癌草药配方。先前的研究证实了其对前列腺癌模型的抗肿瘤和抗转移活性。本研究旨在探究BIRM对人前列腺癌细胞(PCa)的活性,以揭示其抗肿瘤活性机制。在表达雄激素受体(AR)的PCa细胞中,与在无双氢睾酮(DHT)条件下培养的细胞相比,BIRM在有雄激素(DHT)存在时的细胞毒性高2.5倍(250%)。在AR阳性细胞(LAPC-4和LNCaP)中,BIRM导致AR剂量和时间依赖性下调并增加细胞凋亡。将细胞暴露于BIRM对AR的合成和AR启动子活性没有影响,但通过蛋白酶体途径增加了AR的降解。BIRM导致LAPC-4细胞中HSP90-AR结合不稳定。它通过死亡受体和FADD介导的途径激活半胱天冬酶-8,从而诱导PCa细胞凋亡。半胱天冬酶-8切割的合成抑制剂(IETD-CHO)可阻止BIRM诱导的细胞凋亡。BIRM对AR阳性和AR阴性(PC-3和DU145)细胞中AKT介导的生存途径的影响显示,所有PCa细胞系中p-AKTser 473水平均降低。通过口服灌胃给予携带PC-3ML肿瘤的小鼠BIRM,对肿瘤生长显示出选择性疗效;在肿瘤形成前给药有效,但对现有肿瘤治疗时疗效有限。此外,BIRM抑制了通过原位植入裸鼠背侧前列腺产生的LNCaP肿瘤。通过液-液萃取对BIRM进行部分纯化,并通过HPLC进一步分级分离,结果显示对PCa细胞的比活性提高了4倍。这些结果证明了草药提取物BIRM抗肿瘤活性的机制基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c61/5356655/22783caadce5/oncotarget-07-84201-g001.jpg

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