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丹皮酚通过降低酰基辅酶A脱氢酶的m6A修饰来抑制A549细胞的糖酵解重编程和增殖。

Paeonol represses A549 cell glycolytic reprogramming and proliferation by decreasing m6A modification of Acyl-CoA dehydrogenase.

作者信息

Zhang Lixin, Wu Lihua, Zhu Xiangrui, Mei Jian, Chen Yingli

机构信息

Central Laboratory of Harbin Medical University, Daqing, China; Department of Immunology, College of Medical Laboratory Science and Technology, Harbin Medical University, Daqing, China.

Department of Geriatrics, Daqing Oilfield General Hospital, Daqing, China.

出版信息

Chin J Physiol. 2023 Jul-Aug;66(4):248-256. doi: 10.4103/cjop.CJOP-D-22-00166.

DOI:10.4103/cjop.CJOP-D-22-00166
PMID:37635484
Abstract

Aberrant glycolytic reprogramming is involved in lung cancer progression by promoting the proliferation of non-small cell lung cancer cells. Paeonol, as a traditional Chinese medicine, plays a critical role in multiple cancer cell proliferation and inflammation. Acyl-CoA dehydrogenase (ACADM) is involved in the development of metabolic diseases. N6-methyladenosine (m6A) modification is important for the regulation of messenger RNA stability, splicing, and translation. Here, we investigated whether paeonol regulates the proliferation and glycolytic reprogramming via ACADM with m6A modification in A549 cells (human non-small cell lung cancer cells). Cell counting kit 8, 5-Bromo-2-deoxyuridine, 5-ethynyl-2'-deoxyuridine (EdU) incorporation, flow cytometry analysis, western blotting and seahorse XFe24 extracellular flux analyzer assays showed that paeonol had a significant inhibitory effect against A549 cell proliferation and glycolysis. Mechanistically, ACADM was a functional target of paeonol. We also showed that the m6A reader YTH domain containing 1 plays an important role in m6A-modified ACADM expression, which is negatively regulated by paeonol, and is involved in A549 cell proliferation and glycolytic reprogramming. These results indicated the central function of paeonol in regulating A549 cell glycolytic reprogramming and proliferation via m6A modification of ACADM.

摘要

异常的糖酵解重编程通过促进非小细胞肺癌细胞的增殖参与肺癌进展。丹皮酚作为一种中药,在多种癌细胞增殖和炎症中发挥关键作用。酰基辅酶A脱氢酶(ACADM)参与代谢性疾病的发展。N6-甲基腺苷(m6A)修饰对于调节信使核糖核酸的稳定性、剪接和翻译很重要。在此,我们研究了丹皮酚是否通过对A549细胞(人非小细胞肺癌细胞)中的ACADM进行m6A修饰来调节增殖和糖酵解重编程。细胞计数试剂盒8、5-溴-2'-脱氧尿苷、5-乙炔基-2'-脱氧尿苷(EdU)掺入、流式细胞术分析、蛋白质印迹和海马XFe24细胞外通量分析仪检测表明,丹皮酚对A549细胞增殖和糖酵解具有显著抑制作用。机制上,ACADM是丹皮酚的功能靶点。我们还表明,m6A阅读蛋白含YTH结构域1在m6A修饰的ACADM表达中起重要作用,其受丹皮酚负调控,并参与A549细胞增殖和糖酵解重编程。这些结果表明了丹皮酚通过对ACADM进行m6A修饰在调节A549细胞糖酵解重编程和增殖中的核心作用。

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