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来自索诺拉南瓜的葫芦素 IIb 通过抑制 STAT3 诱导细胞凋亡和细胞周期停滞。

Cucurbitacin IIb from Ibervillea sonorae Induces Apoptosis and Cell Cycle Arrest via STAT3 Inhibition.

机构信息

Departamento de Ciencias Quimico Biologicas, Universidad de Sonora, Blvd. Luis Encinas y Rosales, Hermosillo, Sonora 83000, Mexico.

Dipartimento di Scienze Farmaceutiche, Universita degli Studi di Perugia - Via del Liceo, 1, 06123 Perugia, Italy.

出版信息

Anticancer Agents Med Chem. 2020;20(10):1188-1196. doi: 10.2174/1871520620666200415101701.

Abstract

BACKGROUND

Cucurbitacin IIb (CIIb) from Ibervillea sonorae has a high capacity to suppress cancer cell proliferation and induce apoptosis. This study investigated the molecular mechanisms related to the antiproliferative and apoptosis induction capacity of CIIb in HeLa cells.

MATERIALS AND METHODS

The cell viability and anti-proliferative effect of CIIb were evaluated by using the trypan blue exclusion assay. The effect of CIIb on the mitochondrial membrane potential was determined by flow cytometry using JC-1. The activity of caspase-3 and caspase-9 was evaluated by flow cytometry using commercial kits. The effect of CIIb on the cell cycle was investigated using Fluorescence-Activated Cell Sorting (FACS) analysis. Western blot analysis was used to evaluate both the inhibitory effect of CIIb on the STAT3 signaling pathway and cyclin -B1, and DNA damage by the comet assay.

RESULTS

CIIb triggers disruption of the mitochondrial membrane potential (Δψm) and consequently activated the caspases -3 and -9, as a result of the activation of the intrinsic pathway of the apoptosis. Likewise, the CIIbinduced cell cycle was arrested in S and G2/M after 24h of treatment. CIIb also reduced the expression of STAT3 and cyclin -B1. Finally, CIIb produced an antiproliferative effect at 48 and 72 h, inducing DNA damage.

CONCLUSION

These results demonstrate CIIb-induced apoptosis and cell cycle arrest in HeLa through the inhibition of STAT3.

摘要

背景

来自 Ibervillea sonorae 的葫芦素 IIb(CIIb)具有很强的抑制癌细胞增殖和诱导细胞凋亡的能力。本研究探讨了 CIIb 在 HeLa 细胞中抑制增殖和诱导凋亡的分子机制。

材料和方法

通过台盼蓝排斥试验评估 CIIb 的细胞活力和抗增殖作用。通过使用 JC-1 通过流式细胞术测定 CIIb 对线粒体膜电位的影响。通过使用商业试剂盒通过流式细胞术评估 caspase-3 和 caspase-9 的活性。通过荧光激活细胞分选(FACS)分析研究 CIIb 对细胞周期的影响。使用 Western blot 分析评估 CIIb 对 STAT3 信号通路和细胞周期蛋白 -B1 的抑制作用,以及彗星试验的 DNA 损伤。

结果

CIIb 触发线粒体膜电位(Δψm)的破坏,从而激活了 caspase-3 和 caspase-9,这是凋亡的内在途径激活的结果。同样,CIIb 处理 24 小时后,细胞周期被阻滞在 S 和 G2/M 期。CIIb 还降低了 STAT3 和细胞周期蛋白 -B1 的表达。最后,CIIb 在 48 和 72 小时产生了抗增殖作用,诱导了 DNA 损伤。

结论

这些结果表明 CIIb 通过抑制 STAT3 诱导 HeLa 细胞凋亡和细胞周期阻滞。

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