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癌细胞干性抑制剂那帕博西尼抑制前列腺癌进展

Suppression of prostate cancer progression by cancer cell stemness inhibitor napabucasin.

作者信息

Zhang Yiming, Jin Zhong, Zhou Huimin, Ou Xueting, Xu Yawen, Li Hulin, Liu Chunxiao, Li Bingkun

机构信息

Department of Urology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.

Department of Gastroenterology, The First Affiliated Hospital of Clinical Medicine of Guangdong Pharmaceutical University, Guangdong Pharmaceutical University, Guangzhou, China.

出版信息

Cancer Med. 2016 Jun;5(6):1251-8. doi: 10.1002/cam4.675. Epub 2016 Feb 21.

Abstract

A small population of cells with stem cell-like properties in prostate cancer (PCa), called prostate cancer stem cells (PrCSCs) or prostate stemness-high cancer cells, displays highly tumorigenic and metastatic features and may be responsible for the therapy resistance. A small molecule, napabucasin (BBI608), recently have been identified with suppression of stemness-high cancer cells in a variety of cancers. However, the effects of napabucasin on PCa cells as well as PrCSCs isolated from PCa cells have not yet been defined. The effect of napabucasin on PCa cells in cell proliferation, colony formation, and cell migration in vitro were measured by MTS, colony formation assay, and Transwell, respectively. Flow cytometry was employed to evaluate cell cycle and cell apoptosis, and the effect on tumorigenesis in vivo was examined by tumor growth assays. Furthermore, the role of napabucasin on self-renewal and survival of PrCSCs was evaluated by their ability to grow spheres and cell viability assay, respectively. Western Blot and qRT-PCR were used to determine the effect of napabucasin on the expressions of stemness markers. Decrease in cell viability, colony formation, migration, and survival with cell cycle arrest, higher sensitivity to docetaxel in vitro, and repressed tumorigenesis in vivo was observed upon napabucasin treatment. More importantly, napabucasin can obviously inhibit spherogenesis and even kill PrCSCs in vitro. Downregulation of stemness markers was observed after PrCSCs were treated with napabucasin. This study demonstrates that napabucasin may be a novel approach in the treatment of advanced PCa, specifically for castration-resistant prostate cancer (CRPC).

摘要

前列腺癌(PCa)中一小部分具有干细胞样特性的细胞,称为前列腺癌干细胞(PrCSCs)或前列腺干性高癌细胞,表现出高度致瘤和转移特征,可能是治疗耐药的原因。一种小分子化合物纳巴卡辛(BBI608),最近已被证实可抑制多种癌症中干性高癌细胞。然而,纳巴卡辛对PCa细胞以及从PCa细胞中分离出的PrCSCs的作用尚未明确。分别通过MTS法、集落形成试验和Transwell法测定纳巴卡辛对PCa细胞体外增殖、集落形成和细胞迁移的影响。采用流式细胞术评估细胞周期和细胞凋亡,并通过肿瘤生长试验检测其对体内肿瘤发生的影响。此外,分别通过PrCSCs形成球体的能力和细胞活力测定评估纳巴卡辛对PrCSCs自我更新和存活的作用。使用蛋白质免疫印迹法(Western Blot)和定量逆转录聚合酶链反应(qRT-PCR)确定纳巴卡辛对干性标志物表达的影响。纳巴卡辛处理后,观察到细胞活力、集落形成、迁移和存活降低,细胞周期停滞,对多西他赛体外敏感性更高,体内肿瘤发生受到抑制。更重要的是,纳巴卡辛在体外可明显抑制球体形成,甚至杀死PrCSCs。用纳巴卡辛处理PrCSCs后,观察到干性标志物下调。本研究表明,纳巴卡辛可能是治疗晚期PCa,特别是去势抵抗性前列腺癌(CRPC)的一种新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18f0/4924383/2a851507c72e/CAM4-5-1251-g001.jpg

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