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姜黄素介导的人胶质瘤CHME细胞凋亡诱导作用

Curcumin-Mediated Induction of Apoptosis in Human Glioma CHME Cells.

作者信息

Zhang Yunqiang, Tu Lijun, Zhou Xiuhong, Li Bin

机构信息

Department of Neurosurgery, Chenzhou No. 1 People's Hospital, Chenzhou, Hunan, China (mainland).

Electrocardiographic Room, Chenzhou No. 1 People's Hospital, Chenzhou, Hunan, China (mainland).

出版信息

Med Sci Monit Basic Res. 2018 Dec 10;24:216-224. doi: 10.12659/MSMBR.912313.

DOI:10.12659/MSMBR.912313
PMID:30531680
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6301257/
Abstract

BACKGROUND Curcumin has clear anti-tumor activity in various carcinomas. It regulates various signaling pathways like Wnt/β-catenin and JAK2/STAT3, which play vital roles in cell proliferation of several carcinomas, but to the best of our knowledge, there are currently no published reports on human glioma CHME cells. Therefore, the aim of this study was to explore the effect of curcumin on human glioma CHME cells. MATERIAL AND METHODS The CHME cell line was purchased from American Type Culture Collection (ATCC). The expressions of caspases 3, caspases 9, PARP, BAX, and BCL2 were detected by Western blot. Annexin V FITC, mitochondrial membrane potential, and reactive oxygen species were detected by flow cytometry. DAPI staining was detected by fluorescence microscopy. Cell viability was assessed by 3-(4,5-Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide (MTT) assay. RESULTS We found that curcumin has cytotoxic activity in human glioma CHME cells, as shown by DAPI staining, annexin V/PI, and nuclear morphology. We found that cell growth decreased with increased concentration of curcumin, as well as sowing effects on expression of caspase-3, caspase-9, and cleavage of PARP, which suggests apoptotic cascade activity. The increase in reactive oxygen species and loss of mitochondrial membrane potential (Δψmt) in concentration-dependent manners suggests biochemical induction of apoptosis in CHME cells. CONCLUSIONS Curcumin has effective anticancer activity in human glioma CHME cells by inducing the apoptotic pathway.

摘要

背景

姜黄素在多种癌症中具有明确的抗肿瘤活性。它可调节多种信号通路,如Wnt/β-连环蛋白和JAK2/STAT3,这些信号通路在多种癌症的细胞增殖中起着至关重要的作用,但据我们所知,目前尚无关于人胶质瘤CHME细胞的已发表报告。因此,本研究的目的是探讨姜黄素对人胶质瘤CHME细胞的影响。

材料与方法

CHME细胞系购自美国典型培养物保藏中心(ATCC)。通过蛋白质免疫印迹法检测半胱天冬酶3、半胱天冬酶9、聚(ADP-核糖)聚合酶(PARP)、Bax和Bcl-2的表达。通过流式细胞术检测膜联蛋白V FITC、线粒体膜电位和活性氧。通过荧光显微镜检测4',6-二脒基-2-苯基吲哚(DAPI)染色。通过3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)法评估细胞活力。

结果

我们发现姜黄素对人胶质瘤CHME细胞具有细胞毒性活性,如DAPI染色、膜联蛋白V/碘化丙啶(PI)和核形态所示。我们发现随着姜黄素浓度的增加,细胞生长减少,同时对半胱天冬酶-3、半胱天冬酶-9的表达及PARP的裂解有影响,这表明存在凋亡级联反应活性。活性氧的增加和线粒体膜电位(Δψmt)以浓度依赖性方式丧失,提示CHME细胞凋亡的生化诱导。

结论

姜黄素通过诱导凋亡途径在人胶质瘤CHME细胞中具有有效的抗癌活性。

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本文引用的文献

1
Molecular Mechanisms and Pathways as Targets for Cancer Prevention and Progression with Dietary Compounds.膳食化合物在癌症预防和进展中的分子机制和途径作为靶点。
Int J Mol Sci. 2017 Sep 25;18(10):2050. doi: 10.3390/ijms18102050.
2
Selenocysteine induces apoptosis in human glioma cells: evidence for TrxR1-targeted inhibition and signaling crosstalk.硒代半胱氨酸诱导人神经胶质瘤细胞凋亡:硫氧还蛋白还原酶 1 靶向抑制和信号串扰的证据。
Sci Rep. 2017 Jul 25;7(1):6465. doi: 10.1038/s41598-017-06979-2.
3
Curcumin AntiCancer Studies in Pancreatic Cancer.
天然化合物作为治疗神经胶质瘤的有前途的辅助剂。
Int J Mol Sci. 2022 Mar 20;23(6):3360. doi: 10.3390/ijms23063360.
4
HSP60 participates in the anti-glioma effects of curcumin.热休克蛋白60参与姜黄素的抗胶质瘤作用。
Exp Ther Med. 2021 Mar;21(3):204. doi: 10.3892/etm.2021.9637. Epub 2021 Jan 11.
5
The Multi-Faceted Effect of Curcumin in Glioblastoma from Rescuing Cell Clearance to Autophagy-Independent Effects.姜黄素在胶质母细胞瘤中的多方面作用:从挽救细胞清除到自噬非依赖性作用。
Molecules. 2020 Oct 20;25(20):4839. doi: 10.3390/molecules25204839.
6
Potential Mechanisms of Action of Curcumin for Cancer Prevention: Focus on Cellular Signaling Pathways and miRNAs.姜黄素预防癌症的作用机制研究进展:聚焦细胞信号通路和 miRNA。
Int J Biol Sci. 2019 May 7;15(6):1200-1214. doi: 10.7150/ijbs.33710. eCollection 2019.
姜黄素在胰腺癌中的抗癌研究。
Nutrients. 2016 Jul 16;8(7):433. doi: 10.3390/nu8070433.
4
Molecular mechanisms of curcumin and its semisynthetic analogues in prostate cancer prevention and treatment.姜黄素及其半合成类似物在前列腺癌预防和治疗中的分子机制
Life Sci. 2016 May 1;152:135-44. doi: 10.1016/j.lfs.2016.03.036. Epub 2016 Mar 24.
5
Curcumin inhibits intracellular fatty acid synthase and induces apoptosis in human breast cancer MDA-MB-231 cells.姜黄素抑制人乳腺癌MDA-MB-231细胞内的脂肪酸合酶并诱导其凋亡。
Oncol Rep. 2016 May;35(5):2651-6. doi: 10.3892/or.2016.4682. Epub 2016 Mar 17.
6
Curcumin inhibits tumor epithelial‑mesenchymal transition by downregulating the Wnt signaling pathway and upregulating NKD2 expression in colon cancer cells.姜黄素通过下调Wnt信号通路和上调结肠癌细胞中NKD2的表达来抑制肿瘤上皮-间质转化。
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7
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8
Curcumin Suppresses Proliferation and Migration of MDA-MB-231 Breast Cancer Cells through Autophagy-Dependent Akt Degradation.姜黄素通过自噬依赖性Akt降解抑制MDA-MB-231乳腺癌细胞的增殖和迁移。
PLoS One. 2016 Jan 11;11(1):e0146553. doi: 10.1371/journal.pone.0146553. eCollection 2016.
9
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Semin Cancer Biol. 2015 Dec;35 Suppl:S151-S184. doi: 10.1016/j.semcancer.2015.03.006. Epub 2015 May 5.
10
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Expert Opin Investig Drugs. 2015 Jun;24(6):781-94. doi: 10.1517/13543784.2015.1026963. Epub 2015 Mar 25.