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5-氮杂胞苷和曲古抑菌素 A 诱导舌鳞状细胞癌的 DNA 损伤和凋亡反应:体外研究。

5-Azacitidine and Trichostatin A induce DNA damage and apoptotic responses in tongue squamous cell carcinoma: An in vitro study.

机构信息

Dental Research Center, Dentistry Research Institute, Tehran University of Medical Sciences (TUMS), Tehran, Iran.

Department of Genetics, Faculty of Advanced Sciences and Technology, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.

出版信息

Arch Oral Biol. 2022 Jan;133:105296. doi: 10.1016/j.archoralbio.2021.105296. Epub 2021 Oct 25.

Abstract

OBJECTIVE

The present in vitro study aims to investigate the potential use of epigenetic inhibitors as treatment modalities in tongue squamous cell carcinoma.

DESIGN

The human tongue squamous cell carcinoma cell line (CAL-27) was cultured and exposed to varying concentrations of 5-Azacitidine (5-Aza) or Trichostatin A (TSA) in the culture medium. The cell apoptosis was evaluated using Annexin V/PI by flow cytometry. To evaluate DNA damage response, γH2AX foci analysis was performed using immunofluorescence. Single cell gel electrophoresis (SCGE) was applied to measure DNA strand breaks. Gene expression was assessed by quantitative real-time PCR.

RESULTS

The results showed that 5-Aza and TSA had apoptotic effects on the SCC cell line at concentrations of 50-200 µM and 0.5-5 µM, respectively. Immunofluorescence analysis showed increased expression of γH2AX, the marker of DNA damage response after treatment of 5-Aza and TSA that was associated with increased DNA strand breaks. The expressions of urokinase plasminogen activator, its receptor and matrix metalloproteinase-2, were significantly reduced in TSA- and 5-Aza-treated cells.

CONCLUSIONS

Our results showed that 5-Aza and TSA increase apoptotic and DNA damage response in squamous cell carcinoma cell line while reducing the expression of tumor invasion genes that further indicating the potential therapeutic value of two epigenetic modifiers in squamous cell carcinoma.

摘要

目的

本体外研究旨在探讨表观遗传抑制剂作为治疗舌鳞癌细胞癌的潜在用途。

设计

培养人舌鳞癌细胞系(CAL-27)并将其暴露于不同浓度的 5-氮杂胞苷(5-Aza)或曲古抑菌素 A(TSA)的培养基中。通过流式细胞术用 Annexin V/PI 评估细胞凋亡。为了评估 DNA 损伤反应,使用免疫荧光法进行 γH2AX 焦点分析。应用单细胞凝胶电泳(SCGE)测量 DNA 链断裂。通过定量实时 PCR 评估基因表达。

结果

结果表明,5-Aza 和 TSA 在浓度为 50-200 μM 和 0.5-5 μM 时对 SCC 细胞系具有凋亡作用。免疫荧光分析显示,5-Aza 和 TSA 处理后,DNA 损伤反应的标志物 γH2AX 的表达增加,与 DNA 链断裂增加相关。在 TSA 和 5-Aza 处理的细胞中,尿激酶型纤溶酶原激活物、其受体和基质金属蛋白酶-2 的表达显著降低。

结论

我们的结果表明,5-Aza 和 TSA 增加了鳞状细胞癌细胞系的凋亡和 DNA 损伤反应,同时降低了肿瘤侵袭基因的表达,进一步表明两种表观遗传修饰剂在鳞状细胞癌中的潜在治疗价值。

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