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桑亭(5,7-二羟基-3,6,4'-三甲氧基黄酮)增强TRAIL介导的结肠癌细胞凋亡。

Santin (5,7-Dihydroxy-3,6,4'-Trimetoxy-Flavone) Enhances TRAIL-Mediated Apoptosis in Colon Cancer Cells.

作者信息

Kłósek Małgorzata, Jaworska Dagmara, Pietsz Grażyna, Szliszka Ewelina

机构信息

Department of Microbiology and Immunology, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, 40-055 Katowice, Poland.

出版信息

Life (Basel). 2023 Feb 20;13(2):592. doi: 10.3390/life13020592.

Abstract

TRAIL (Tumor necrosis factor-Related Apoptosis-Inducing Ligand) has the ability to selectively kill cancer cells without being toxic to normal cells. This endogenous ligand plays an important role in surveillance and anti-tumor immunity. However, numerous tumor cells are resistant to TRAIL-induced apoptosis. In this study, the apoptotic effect of santin in combination with TRAIL on colon cancer cells was examined. Flow cytometry was used to detect the apoptosis and expression of death receptors (TRAIL-R1/DR4 and TRAIL-R2/DR5). Mitochondrial membrane potential (ΔΨm) was evaluated by DePsipher staining with the use of fluorescence microscopy. We have shown for the first time that flavonoid santin synergizes with TRAIL to induce apoptosis in colon cancer cells. Santin induced TRAIL-mediated apoptosis through increased expression of death receptors TRAIL-R1 and TRAIL-R2 and augmented disruption of the mitochondrial membrane in SW480 and SW620 cancer cells. The obtained data may indicate the potential role of santin in colon cancer chemoprevention through the enhancement of TRAIL-mediated apoptosis.

摘要

肿瘤坏死因子相关凋亡诱导配体(TRAIL)能够选择性地杀死癌细胞,而对正常细胞无毒。这种内源性配体在监测和抗肿瘤免疫中发挥着重要作用。然而,许多肿瘤细胞对TRAIL诱导的凋亡具有抗性。在本研究中,检测了桑亭与TRAIL联合应用对结肠癌细胞的凋亡作用。采用流式细胞术检测凋亡情况及死亡受体(TRAIL-R1/DR4和TRAIL-R2/DR5)的表达。利用荧光显微镜通过DePsipher染色评估线粒体膜电位(ΔΨm)。我们首次表明,黄酮类化合物桑亭与TRAIL协同作用可诱导结肠癌细胞凋亡。桑亭通过增加死亡受体TRAIL-R1和TRAIL-R2的表达以及增强SW480和SW620癌细胞中线粒体膜的破坏,诱导TRAIL介导的凋亡。所获得的数据可能表明桑亭通过增强TRAIL介导的凋亡在结肠癌化学预防中具有潜在作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8561/9962120/ba2e980ab13c/life-13-00592-g001.jpg

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