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壳聚糖水凝胶载姜黄素对胶质母细胞瘤细胞系中 DNMT1、DNMT3A、DNMT3B、MEG3、HOTAIR 基因表达的影响评价。

The evaluation of chitosan hydrogel based curcumin effect on DNMT1, DNMT3A, DNMT3B, MEG3, HOTAIR gene expression in glioblastoma cell line.

机构信息

Department of Biology, Faculty of Sciences, Payame Noor University, Shahre Rey, Iran.

Department of Biology, Faculty of Sciences, Payame Noor University, Tehran, Iran.

出版信息

Mol Biol Rep. 2023 Jul;50(7):5977-5989. doi: 10.1007/s11033-023-08531-0. Epub 2023 Jun 3.


DOI:10.1007/s11033-023-08531-0
PMID:37268862
Abstract

BACKGROUND: Cancer is one of the most important causes of death worldwide. Some types of cancer, including glioblastoma, with a high potential for growth, invasion, and resistance to general treatments, chemotherapy, and radiotherapy, have a high potential for recurrence. Many chemical drugs have been used to treat it, but herbal drugs are more effective with fewer side effects; Therefore, this research aims to investigate the effect of curcumin-chitosan nano-complex on the expression of MEG3, HOTAIR, DNMT1, DNMT3A, DNMT3B genes in the glioblastoma cell line. METHODS: In this research, glioblastoma cell line, PCR and spectrophotometry techniques, MTT test and transmission, field emission transmission, and fluorescent electron microscopes were used. RESULTS: The morphological examination of the curcumin-chitosan nano-complex was without clumping, and the fluorescent microscope examination showed the nano-complex enters the cell and affects the genes expression. In its bioavailability studies, it was found that it significantly increases the death of cancer cells in a dose- and time-dependent manner. Gene expression tests showed that this nano-complex increased MEG3 gene expression compared to the control group, which is statistically significant (p < 0.05). It also decreased HOTAIR gene expression compared to the control group, which was not statistically significant (p > 0.05). It decreased the expression of DNMT1, DNMT3A, and DNMT3B genes compared to the control group, which is statistically significant (p < 0.05). CONCLUSION: By using active plant substances such as curcumin, the active demethylation of brain cells can be directed to the path of inhibiting the growth of brain cancer cells and eliminating them.

摘要

背景:癌症是全球最重要的死亡原因之一。某些类型的癌症,包括具有高度生长、侵袭和对一般治疗、化疗和放疗的耐药性的胶质母细胞瘤,具有很高的复发潜力。许多化学药物已被用于治疗它,但草药药物更有效,副作用更少;因此,这项研究旨在研究姜黄素-壳聚糖纳米复合物对胶质母细胞瘤细胞系中 MEG3、HOTAIR、DNMT1、DNMT3A、DNMT3B 基因表达的影响。

方法:在这项研究中,使用了胶质母细胞瘤细胞系、PCR 和分光光度技术、MTT 试验和传输、场发射传输和荧光电子显微镜。

结果:姜黄素-壳聚糖纳米复合物的形态检查无结块,荧光显微镜检查显示纳米复合物进入细胞并影响基因表达。在其生物利用度研究中,发现它以剂量和时间依赖的方式显著增加癌细胞的死亡。基因表达试验表明,与对照组相比,该纳米复合物显著增加了 MEG3 基因的表达(p<0.05)。与对照组相比,它还降低了 HOTAIR 基因的表达,但无统计学意义(p>0.05)。与对照组相比,它降低了 DNMT1、DNMT3A 和 DNMT3B 基因的表达,具有统计学意义(p<0.05)。

结论:通过使用姜黄素等活性植物物质,可以将脑细胞的活性去甲基化引导到抑制脑癌细胞生长和消除它们的途径上。

相似文献

[1]
The evaluation of chitosan hydrogel based curcumin effect on DNMT1, DNMT3A, DNMT3B, MEG3, HOTAIR gene expression in glioblastoma cell line.

Mol Biol Rep. 2023-7

[2]
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[3]
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Int J Nanomedicine. 2021

[4]
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Curr Drug Deliv. 2022

[5]
Combination treatment of berberine and solid lipid curcumin particles increased cell death and inhibited PI3K/Akt/mTOR pathway of human cultured glioblastoma cells more effectively than did individual treatments.

PLoS One. 2019-12-16

[6]
Antiglioma activity of curcumin-loaded lipid nanoparticles and its enhanced bioavailability in brain tissue for effective glioblastoma therapy.

Acta Biomater. 2012-4-4

[7]
Epigenetic reactivation of RANK in glioblastoma cells by curcumin: involvement of STAT3 inhibition.

DNA Cell Biol. 2013-4-27

[8]
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[9]
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[10]
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Int J Nanomedicine. 2014-1-13

引用本文的文献

[1]
Novel Biological Strategies for Melanoma Therapy: A Focus on lncRNAs and Their Targeting.

Cancers (Basel). 2025-4-9

[2]
In Vitro and In Vivo Preventive Effects of Thymoquinone against Breast Cancer: Role of DNMT1.

Molecules. 2024-1-16

本文引用的文献

[1]
Curcumin: An epigenetic regulator and its application in cancer.

Biomed Pharmacother. 2022-12

[2]
Emerging role of different DNA methyltransferases in the pathogenesis of cancer.

Front Pharmacol. 2022-8-25

[3]
Curcumin suppresses tumorigenesis by ferroptosis in breast cancer.

PLoS One. 2022

[4]
Multifunctional and Self-Healable Intelligent Hydrogels for Cancer Drug Delivery and Promoting Tissue Regeneration In Vivo.

Polymers (Basel). 2021-8-11

[5]
Antidiabetic Properties of Curcumin: Insights on New Mechanisms.

Adv Exp Med Biol. 2021

[6]
Curcumin: Modulator of Key Molecular Signaling Pathways in Hormone-Independent Breast Cancer.

Cancers (Basel). 2021-7-8

[7]
Curcumin attenuates Adriamycin-resistance of acute myeloid leukemia by inhibiting the lncRNA HOTAIR/miR-20a-5p/WT1 axis.

Lab Invest. 2021-10

[8]
Anticancer Mechanism of Curcumin on Human Glioblastoma.

Nutrients. 2021-3-16

[9]
Curcumin suppresses tumor growth of gemcitabine-resistant non-small cell lung cancer by regulating lncRNA-MEG3 and PTEN signaling.

Clin Transl Oncol. 2021-7

[10]
Antitumor Activity of Curcumin in Glioblastoma.

Int J Mol Sci. 2020-12-11

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