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祁州漏芦转化根提取物抑制人胶质瘤细胞活力,诱导双链DNA损伤、H2A.X磷酸化和PARP1裂解。

Rhaponticum carthamoides transformed root extract inhibits human glioma cells viability, induces double strand DNA damage, H2A.X phosphorylation, and PARP1 cleavage.

作者信息

Skała Ewa, Toma Monika, Kowalczyk Tomasz, Śliwiński Tomasz, Sitarek Przemysław

机构信息

Department of Biology and Pharmaceutical Botany, Medical University of Łódź, Muszyńskiego 1, 90-151, Łódź, Poland.

Laboratory of Medical Genetics, Faculty of Biology and Environmental Protection, University of Łódź, Pomorska 141/143, 90-236, Łódź, Poland.

出版信息

Cytotechnology. 2018 Dec;70(6):1585-1594. doi: 10.1007/s10616-018-0251-3. Epub 2018 Aug 31.

DOI:10.1007/s10616-018-0251-3
PMID:30171426
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6269353/
Abstract

Rhaponticum carthamoides transformed root extract induces double strand DNA damage by increasing the number of phosphorylated H2A.X- and cleaved PARP1-positive U87MG cells and patient-derived IV grade glioma cells. Furthermore, treatment of these cells with root extract causes down-regulation of UHRF1 and DNMT1. Transformed root extract is rich in caffeoylquinic acid derivatives, especially tricaffeoylquinic acid derivatives. Our findings demonstrate that the R. carthamoides transformed root extract may trigger apoptosis in glioma cells by induction of DNA damage, PARP cleavage and epigenetic modification.

摘要

刺续断转化根提取物通过增加磷酸化H2A.X和裂解PARP1阳性的U87MG细胞以及患者来源的IV级神经胶质瘤细胞的数量来诱导双链DNA损伤。此外,用根提取物处理这些细胞会导致UHRF1和DNMT1的下调。转化根提取物富含咖啡酰奎宁酸衍生物,尤其是三咖啡酰奎宁酸衍生物。我们的研究结果表明,刺续断转化根提取物可能通过诱导DNA损伤、PARP裂解和表观遗传修饰来触发神经胶质瘤细胞的凋亡。

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本文引用的文献

1
Plant Secondary Metabolites as Anticancer Agents: Successes in Clinical Trials and Therapeutic Application.植物次生代谢产物作为抗癌剂:临床试验和治疗应用的成功。
Int J Mol Sci. 2018 Jan 16;19(1):263. doi: 10.3390/ijms19010263.
2
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Mol Cell Biochem. 2018 Aug;445(1-2):89-97. doi: 10.1007/s11010-017-3254-z. Epub 2017 Dec 14.
3
Anti-cancer potential of flavonoids: recent trends and future perspectives.
草药的表观遗传学效应。
Clin Epigenetics. 2023 May 13;15(1):85. doi: 10.1186/s13148-023-01481-1.
4
Chlorogenic acid: Potential source of natural drugs for the therapeutics of fibrosis and cancer.绿原酸:用于纤维化和癌症治疗的天然药物潜在来源。
Transl Oncol. 2022 Jan;15(1):101294. doi: 10.1016/j.tranon.2021.101294. Epub 2021 Nov 30.
5
Transformed Root Extract Has Potent Anticancer Activity in Human Leukemia and Lung Adenocarcinoma Cell Lines.转化根提取物在人白血病和肺腺癌细胞系中具有很强的抗癌活性。
Oxid Med Cell Longev. 2018 Dec 9;2018:8198652. doi: 10.1155/2018/8198652. eCollection 2018.
类黄酮的抗癌潜力:最新趋势与未来展望
3 Biotech. 2013 Dec;3(6):439-459. doi: 10.1007/s13205-013-0117-5. Epub 2013 Feb 12.
4
UHRF1: The key regulator of epigenetics and molecular target for cancer therapeutics.UHRF1:表观遗传学的关键调节因子及癌症治疗的分子靶点。
Tumour Biol. 2017 Feb;39(2):1010428317692205. doi: 10.1177/1010428317692205.
5
Hazelnut (Corylus avellana L.) Shells Extract: Phenolic Composition, Antioxidant Effect and Cytotoxic Activity on Human Cancer Cell Lines.榛子(欧洲榛)壳提取物:酚类成分、抗氧化作用及对人癌细胞系的细胞毒性活性
Int J Mol Sci. 2017 Feb 13;18(2):392. doi: 10.3390/ijms18020392.
6
A systematic review on ethnomedicines of anti-cancer plants.关于抗癌植物民族药物的系统评价。
Phytother Res. 2017 Feb;31(2):202-264. doi: 10.1002/ptr.5751. Epub 2017 Jan 17.
7
An overview on the role of dietary phenolics for the treatment of cancers.膳食酚类物质在癌症治疗中的作用综述。
Nutr J. 2016 Dec 1;15(1):99. doi: 10.1186/s12937-016-0217-2.
8
PARP1 inhibitor olaparib (Lynparza) exerts synthetic lethal effect against ligase 4-deficient melanomas.聚(ADP-核糖)聚合酶1(PARP1)抑制剂奥拉帕利(Lynparza)对连接酶4缺陷型黑色素瘤具有合成致死效应。
Oncotarget. 2016 Nov 15;7(46):75551-75560. doi: 10.18632/oncotarget.12270.
9
Inhibition of human glioma cell proliferation by altered Bax/Bcl-2-p53 expression and apoptosis induction by Rhaponticum carthamoides extracts from transformed and normal roots.通过改变Bax/Bcl-2-p53表达抑制人胶质瘤细胞增殖以及刺续断转化根和正常根提取物诱导细胞凋亡
J Pharm Pharmacol. 2016 Nov;68(11):1454-1464. doi: 10.1111/jphp.12619. Epub 2016 Oct 2.
10
Polyphenols: Extraction Methods, Antioxidative Action, Bioavailability and Anticarcinogenic Effects.多酚:提取方法、抗氧化作用、生物利用度及抗癌作用
Molecules. 2016 Jul 11;21(7):901. doi: 10.3390/molecules21070901.