Suppr超能文献

sonic 刺猬信号与 CD133high/CD44high 前列腺癌干细胞对唑来膦酸的耐药性有关。

Sonic hedgehog signaling is associated with resistance to zoledronic acid in CD133high/CD44high prostate cancer stem cells.

机构信息

Department of Histology and Embryology, Faculty of Medicine, Van Yuzuncu Yil University, Van, 65080, Turkey.

Department of Medical Genetics, Ege University Medical School, İzmir, 35080, Turkey.

出版信息

Mol Biol Rep. 2021 Apr;48(4):3567-3578. doi: 10.1007/s11033-021-06387-w. Epub 2021 May 4.

Abstract

Cancer stem cells (CSCs) are a unique population that has been linked to drug resistance and metastasis and recurrence of prostate cancer. The sonic hedgehog (SHH) signal regulates stem cells in normal prostate epithelium by affecting cell behavior, survival, proliferation, and maintenance. Aberrant SHH pathway activation leads to an unsuitable expansion of stem cell lineages in the prostate epithelium and the transformation of prostate CSCs (PCSCs). Zoledronic acid (ZOL), one of the third-generation bisphosphonates, effectively prevented bone metastasis and treated advanced prostate cancer despite androgen deprivation therapy. Despite strong evidence for the involvement of the SHH in human PCSCs survival and drug resistance, the roles of SHH in the PCSCs-related resistance to ZOL remain to be fully elucidated. The present study aimed to investigate the role of the SHH pathway in ZOL resistance of PCSCs in 2D and three 3D cell culture conditions. For this purpose, we isolated CD133/ CD44 PCSCs using a flow cytometer. Following ZOL treatment, mRNA and protein expressions of the components of the SHH signaling pathway in PCSCs and non-CSCs were analyzed using qRT-PCR and Immunofluorescence staining, respectively. Our finding suggested that SHH signaling may be activated by different mechanisms that lead to avoidance of the inhibition effect of ZOL. Thereby, SHH pathways may be associated with the resistance to ZOL developed by prostate CSCs. Inhibition of CSCs-related SHH signaling along with ZOL treatment should be considered to achieve improvement in survival or delayed treatment failure and prevention of the CSCs-related drug resistance.

摘要

癌症干细胞(CSCs)是一个独特的群体,与前列腺癌的耐药性、转移和复发有关。 声信号刺猬(SHH)通过影响细胞行为、存活、增殖和维持来调节正常前列腺上皮中的干细胞。异常的 SHH 途径激活导致前列腺上皮中的干细胞谱系不适当扩张和前列腺 CSCs(PCSCs)的转化。唑来膦酸(ZOL)是第三代双膦酸盐之一,尽管进行了雄激素剥夺治疗,但它能有效预防骨转移并治疗晚期前列腺癌。尽管有强有力的证据表明 SHH 参与了人类 PCSCs 的存活和耐药性,但 SHH 在 PCSCs 相关的 ZOL 耐药性中的作用仍有待充分阐明。本研究旨在探讨 SHH 途径在 2D 和三种 3D 细胞培养条件下 PCSCs 对 ZOL 耐药性中的作用。为此,我们使用流式细胞仪分离 CD133/CD44 PCSCs。在 ZOL 处理后,使用 qRT-PCR 和免疫荧光染色分别分析 PCSCs 和非 CSCs 中 SHH 信号通路成分的 mRNA 和蛋白表达。我们的发现表明,SHH 信号可能通过不同的机制被激活,导致 ZOL 的抑制作用被避免。因此,SHH 途径可能与前列腺 CSCs 对 ZOL 的耐药性有关。抑制 CSCs 相关的 SHH 信号以及 ZOL 治疗应被考虑以改善生存或延迟治疗失败并预防 CSCs 相关的耐药性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验