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槲皮素通过线粒体和内质网介导的信号通路诱导人口腔癌SAS细胞凋亡。

Quercetin induced apoptosis of human oral cancer SAS cells through mitochondria and endoplasmic reticulum mediated signaling pathways.

作者信息

Ma Yi-Shih, Yao Chien-Ning, Liu Hsin-Chung, Yu Fu-Shun, Lin Jen-Jyh, Lu Kung-Wen, Liao Ching-Lung, Chueh Fu-Shin, Chung Jing-Gung

机构信息

School of Chinese Medicine for Post-Baccalaureate, I-Shou University, Kaohsiung 84001, Taiwan, R.O.C.

Department of Chinese Medicine, E-Da Hospital, Kaohsiung 82445, Taiwan, R.O.C.

出版信息

Oncol Lett. 2018 Jun;15(6):9663-9672. doi: 10.3892/ol.2018.8584. Epub 2018 Apr 26.

Abstract

Oral cancer is a cause of cancer-associated mortality worldwide and the treatment of oral cancer includes radiation, surgery and chemotherapy. Quercetin is a component from natural plant products and it has been demonstrated that quercetin is able to induce cytotoxic effects through induction of cell apoptosis in a number of human cancer cell lines. However, there is no available information to demonstrate that quercetin is able to induce apoptosis in human oral cancer cells. In the present study, the effect of quercetin on the cell death via the induction of apoptosis in human oral cancer SAS cells was investigated using flow cytometry, Annexin V/propidium iodide (PI) double staining, western blotting and confocal laser microscopy examination, to test for cytotoxic effects at 6-48 h after treatment with quercetin. The rate of cell death increased with the duration of quercetin treatment based on the results of a cell viability assay, increased Annexin V/PI staining, increased reactive oxygen species and Ca production, decreased the levels of mitochondrial membrane potential (ΔΨ), increased proportion of apoptotic cells and altered levels of apoptosis-associated protein expression in SAS cells. The results from western blotting revealed that quercetin increased Fas, Fas-Ligand, fas-associated protein with death domain and caspase-8, all of which associated with cell surface death receptor. Furthermore, quercetin increased the levels of activating transcription factor (ATF)-6α, ATF-6β and gastrin-releasing peptide-78 which indicated an increase in endoplasm reticulum stress, increased levels of the pro-apoptotic protein BH3 interacting-domain death antagonist, and decreased levels of anti-apoptotic proteins B-cell lymphoma (Bcl) 2 and Bcl-extra large which may have led to the decreases of ΔΨ. Additionally, confocal microscopy suggested that quercetin was able to increase the expression levels of cytochrome , apoptosis-inducing factor and endonuclease G, which are associated with apoptotic pathways. Therefore, it is hypothesized that quercetin may potentially be used as a novel anti-cancer agent for the treatment of oral cancer in future.

摘要

口腔癌是全球癌症相关死亡的一个原因,口腔癌的治疗包括放疗、手术和化疗。槲皮素是天然植物产品中的一种成分,已证明槲皮素能够通过诱导多种人类癌细胞系的细胞凋亡来产生细胞毒性作用。然而,尚无可用信息表明槲皮素能够诱导人类口腔癌细胞凋亡。在本研究中,使用流式细胞术、膜联蛋白V/碘化丙啶(PI)双染色、蛋白质印迹法和共聚焦激光显微镜检查,研究了槲皮素通过诱导人类口腔癌SAS细胞凋亡对细胞死亡的影响,以检测槲皮素处理6 - 48小时后的细胞毒性作用。基于细胞活力测定的结果,细胞死亡速率随槲皮素处理时间的延长而增加,膜联蛋白V/PI染色增加、活性氧和钙离子产生增加、线粒体膜电位(ΔΨ)水平降低、SAS细胞中凋亡细胞比例增加以及凋亡相关蛋白表达水平改变。蛋白质印迹法的结果显示,槲皮素增加了Fas、Fas配体、死亡结构域相关蛋白和半胱天冬酶 - 8的水平,所有这些都与细胞表面死亡受体相关。此外,槲皮素增加了活化转录因子(ATF)-6α、ATF - 6β和胃泌素释放肽 - 78的水平,这表明内质网应激增加,促凋亡蛋白BH3相互作用结构域死亡拮抗剂水平增加,抗凋亡蛋白B细胞淋巴瘤(Bcl)2和Bcl - 超大蛋白水平降低,这可能导致了ΔΨ的降低。此外,共聚焦显微镜检查表明,槲皮素能够增加与凋亡途径相关的细胞色素、凋亡诱导因子和核酸内切酶G的表达水平。因此,推测槲皮素未来可能有潜力用作治疗口腔癌的新型抗癌药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac39/6004715/fb3ef4c22450/ol-15-06-9663-g00.jpg

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