大麻二酚增强依托泊苷对前列腺癌细胞的抗癌活性

IF 3.1 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Yalcin Erzurumlu, Deniz Catakli
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引用次数: 0

摘要

简介大麻提取物自古以来就被用作草药。它是研究最多的提取物之一,尤其是在抗癌辅助疗法中。前列腺癌是全球男性最常确诊的癌症类型之一,预计 2023 年将新增 288,300 例病例。如今,许多先进的治疗方法已用于前列腺癌,如免疫疗法和化疗,但获得性耐药性、长期用药和癌细胞分化大多限制了疗法的效率。因此,利用天然产物来克服这些局限性并提高现有疗法的有效性可能是一种很有前景的方法。本研究主要探讨大麻的有效成分之一大麻二酚(CBD)对化疗药物依托泊苷在前列腺癌细胞中可能的增强作用。方法:在此,我们通过检测依托泊苷的细胞毒性作用、形态学改变、凋亡效应、自噬、未折叠蛋白反应(UPR)信号传导、内质网相关降解机制(ERAD)、血管生成因子和雄激素因子以及上皮-间质转化(EMT),测试了大麻二酚对依托泊苷在前列腺癌细胞中的增效作用。此外,我们还研究了 CBD 和依托泊苷联合治疗对菌落生长、迁移、侵袭能力、三维肿瘤形成和细胞衰老的影响。结果我们的研究结果表明,依托泊苷与 CBD 联合处理可显著抑制 LNCaP 细胞的自噬通量,并诱导 ERAD 和 UPR 信号转导。此外,CBD 还能增强依托泊苷介导的雄激素信号、血管生成因子 VEGF-A、原癌基因 c-Myc、EMT 的抑制作用,并通过激活 caspase-3 和 PARP-1 诱导细胞凋亡。此外,联合用药还能显著降低肿瘤的致病性,如增殖能力、菌落生长、迁移和三维肿瘤形成,并诱导衰老。总之,我们的数据表明,CBD 对依托泊苷相关的抗癌活性具有有效的增强作用。结论本研究表明,在现有的化疗方法中使用 CBD 作为辅助疗法可能是一种很有前景的选择,但这种有效性还需要进行大规模的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cannabidiol Enhances the Anticancer Activity of Etoposide on Prostate Cancer Cells.

Introduction: Cannabis sativa extract has been used as an herbal medicine since ancient times. It is one of the most researched extracts, especially among supportive treatments against cancer. Prostate cancer is one of the most frequently diagnosed cancer types in men worldwide and an estimated 288,300 new cases were diagnosed in 2023. Today, many advanced therapeutic approaches are used for prostate cancer, such as immunotherapy and chemotherapy, but acquired drug resistance, long-term drug usage and differentiation of cancer cells mostly restricted the efficiency of therapies. Therefore, it is thought that the use of natural products to overcome these limitations and improve the effectiveness of existing therapies may offer promising approaches. The present study focused on the investigation of the possible enhancer role of cannabidiol (CBD), which is a potent ingredient compound of Cannabis, on the chemotherapeutic agent etoposide in prostate cancer cells. Methods: Herein, we tested the potentiator role of CBD on etoposide in prostate cancer cells by testing the cytotoxic effect, morphological alterations, apoptotic effects, autophagy, unfolded protein response (UPR) signaling, endoplasmic reticulum-associated degradation mechanism (ERAD), angiogenic and androgenic factors, and epithelial-mesenchymal transition (EMT). In addition, we examined the combined treatment of CBD and etoposide on colonial growth, migrative, invasive capability, 3D tumor formation, and cellular senescence. Results: Our findings demonstrated that cotreatment of etoposide with CBD importantly suppressed autophagic flux and induced ERAD and UPR signaling in LNCaP cells. Also, CBD strongly enhanced the etoposide-mediated suppression of androgenic signaling, angiogenic factor VEGF-A, protooncogene c-Myc, EMT, and also induced apoptosis through activation caspase-3 and PARP-1. Moreover, coadministration markedly decreased tumorigenic properties, such as proliferative capacity, colonial growth, migration, and 3D tumor formation and also induced senescence. Altogether, our data revealed that CBD has a potent enhancer effect on etoposide-associated anticancer activities. Conclusion: The present study suggests that the use of CBD as a supportive therapy in existing chemotherapeutic approaches may be a promising option, but this effectiveness needs to be investigated on a large scale.

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来源期刊
Cannabis and Cannabinoid Research
Cannabis and Cannabinoid Research PHARMACOLOGY & PHARMACY-
CiteScore
6.80
自引率
7.90%
发文量
164
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