Modulatory Effect of Vitamin C on Hypoxia Induced Breast Cancer Stem Cells.

IF 3.1 Q2 PHARMACOLOGY & PHARMACY Advanced pharmaceutical bulletin Pub Date : 2023-11-01 Epub Date: 2023-02-21 DOI:10.34172/apb.2023.073
Masoumeh Kazemi, Soheila Montazersaheb, Mina Noroozpour, Safar Farajnia, Hojjatollah Nozad Charoudeh
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Abstract

Purpose: Eliminating cancer stem cells (CSCs) is a challenge because of their enhanced resistance to anti-cancer drugs. Vitamin C, which is insufficient in patients with higher stages of cancer, has been gaining attention as a potential treatment for human malignancies. Hence this study aimed to analyze the effect of high-dose vitamin C treatment on the gene expression level of HIF-1α, NF-κB1, BAX, and DNMT1 in the MCF7 cells undergoing hypoxia, as an inducer of CSCs characteristics. As a result, vitamin C could be possibly used as a promising therapeutic adjuvant.

Methods: Here we first analyzed the breast CSC population alteration in MCF7 cells following hypoxia induction. Then, we evaluated the impact of vitamin C treatment on the gene expression level of four stemness-related genes in hypoxic MCF7 cells.

Results: Our results indicate that vitamin C could reduce proliferation and stemness states in CSCs possibly by induction of apoptotic markers such as BAX, along with attenuating stemness markers, including NF-κB1, and DNMT1 gene expressions.

Conclusion: According to our findings, vitamin C administration would become a new approach to avoiding the stimulation of CSCs during cancer therapies.

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维生素C对缺氧诱导乳腺癌干细胞的调节作用
目的:消除癌症干细胞(CSCs)是一个挑战,因为它们对抗癌药物的抵抗力增强。晚期癌症患者缺乏维生素C,但作为人类恶性肿瘤的潜在治疗手段,它一直备受关注。因此,本研究旨在分析高剂量维生素C处理对缺氧MCF7细胞中HIF-1α、NF-κB1、BAX和DNMT1基因表达水平的影响,作为CSCs特征的诱导剂。因此,维生素C有可能作为一种有前景的治疗辅助剂。方法:我们首先分析了缺氧诱导后乳腺癌干细胞MCF7细胞群的变化。然后,我们评估了维生素C处理对缺氧MCF7细胞中四个干细胞相关基因表达水平的影响。结果:我们的研究结果表明,维生素C可能通过诱导BAX等凋亡标记物,以及NF-κB1和DNMT1等干性标记物的表达,降低CSCs的增殖和干性状态。结论:根据我们的研究结果,维生素C政府将成为癌症治疗中避免CSCs刺激的新途径。
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来源期刊
Advanced pharmaceutical bulletin
Advanced pharmaceutical bulletin PHARMACOLOGY & PHARMACY-
CiteScore
6.80
自引率
2.80%
发文量
51
审稿时长
12 weeks
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