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白藜芦醇增强肾细胞癌对替沃扎尼的敏感性:一项体外研究。

Resveratrol enhances sensitivity of renal cell carcinoma to tivozanib: An in-vitro study.

作者信息

Taheri Diana, Ghajar Helia Azodian, Mirzaei Akram, Mashhadi Rahil, Dougaheh Seyedeh Negin Hashemi, Bahri Razman Arabzadeh, Khoshchehreh Mahdi, Tavoosian Ali, Aghamir Seyed Mohammad Kazem

机构信息

Urology Research Center, Tehran University of Medical Sciences, Tehran, Iran; Department of Pathology, Isfahan Kidney Disease Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.

Urology Research Center, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Tissue Cell. 2024 Dec;91:102584. doi: 10.1016/j.tice.2024.102584. Epub 2024 Oct 12.

Abstract

BACKGROUND

Since tivozanib has many side effects in the treatment of kidney cancer, we decided to use resveratrol as a bioactive molecule with anticancer and antioxidant properties to make tivozanib more effective and also reduce its side effects in kidney cancer cell line.

METHOD

In this in vitro study, we evaluated the effect of tivozanib, resveratrol and tivozanib- resveratrol combination therapy in ACHN cell line as representatives of human kidney cancer. The assessment includes Hoechst dye staining, scratch-wound assay, 3D spheroid, 2D colony formation assay, flow cytometric analysis of apoptosis and DNA cell cycle, real-time PCR (BAX/BCL2, E-cadherin, Snail, HIF1α, VEGFC and KLK3 genes).

RESULT

To determine IC50 levels, ACHN cells was exposed to different concentration of tivozanib and resveratrol. Our data indicated that IC50 values for tivozanib (0.5 μM) and resveratrol (30 μM) with MTT in a dose and time-dependent manner. Due to the efficacy of resveratrol in combination with tivozanib, we used 20 μM resveratrol, and 0.25 μM tivozanib instead of 30 μM and 0.25 μM respectively. This data was approved by flow cytometry for ACHN cell line with 38.39, 14.74 and 66.06 percent apoptosis and 8.25, 5.12 and 15.6 percent subG1 for tivozanib, resveratrol and tivozanib-resveratrol combination respectively which was as a consequence of cell cycle arrest at G1/S phase. The treatment also reduced cells' migration, fragmented nuclei, 3D spheroid and colony formation potentials in analyses. Evaluation of gene expression presented that the effect of the tivozanib and resveratrol combination in ACHN cell lines is completely different during the evaluation of apoptosis genes, BAX, P53 genes and E-Cadherin had significantly increased expression compared to single treatment groups (P < 0.01). Meanwhile, a significant decrease was observed in the expression of VEGFC and HIF1α genes in the combination group compared to the monotherapy groups (P < 0.001).

CONCLUSION

Considering that resveratrol can increase the apoptosis of cancer cells alone and in combination with tivozanib and prevent the proliferation of cancer cells and also reduce the side effects of tivozanib, we suggest that resveratrol as a potential bioactive molecule can be used in treatment of kidney cancer should be used in combination with tivozanib.

摘要

背景

由于替沃扎尼在治疗肾癌时有许多副作用,我们决定使用具有抗癌和抗氧化特性的生物活性分子白藜芦醇,以使替沃扎尼在肾癌细胞系中更有效,并减少其副作用。

方法

在这项体外研究中,我们评估了替沃扎尼、白藜芦醇以及替沃扎尼 - 白藜芦醇联合疗法对作为人肾癌代表的ACHN细胞系的影响。评估包括Hoechst染料染色、划痕试验、3D球体、2D集落形成试验、凋亡和DNA细胞周期的流式细胞术分析、实时PCR(BAX/BCL2、E - 钙黏蛋白、Snail、HIF1α、VEGFC和KLK3基因)。

结果

为确定IC50水平,将ACHN细胞暴露于不同浓度的替沃扎尼和白藜芦醇中。我们的数据表明,替沃扎尼(0.5μM)和白藜芦醇(30μM)的IC50值呈剂量和时间依赖性。由于白藜芦醇与替沃扎尼联合的疗效,我们分别使用20μM白藜芦醇和0.25μM替沃扎尼,而非30μM和0.25μM。ACHN细胞系的流式细胞术验证了该数据,替沃扎尼、白藜芦醇和替沃扎尼 - 白藜芦醇联合治疗的凋亡率分别为38.39%、14.74%和66.06%,亚G1期分别为8.25%、5.12%和15.6%,这是细胞周期停滞在G1/S期的结果。该治疗在分析中还降低了细胞的迁移、细胞核碎片化、3D球体和集落形成潜能。基因表达评估表明,在评估凋亡基因时,替沃扎尼和白藜芦醇联合在ACHN细胞系中的作用与单药治疗组完全不同,BAX、P53基因和E - 钙黏蛋白的表达与单药治疗组相比显著增加(P < 0.01)。同时,联合组中VEGFC和HIF1α基因的表达与单药治疗组相比显著降低(P < 0.001)。

结论

鉴于白藜芦醇可单独或与替沃扎尼联合增加癌细胞凋亡,防止癌细胞增殖,并减少替沃扎尼的副作用,我们建议白藜芦醇作为一种潜在的生物活性分子,在治疗肾癌时应与替沃扎尼联合使用。

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