Daidzein and puerarin synergistically suppress gastric cancer proliferation via STAT3/FAK pathway Inhibition.

IF 2.5 3区 生物学
Jun Ge, Binguo Liu, Ling Ma, Jianyong Su, Ying Ding
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引用次数: 0

Abstract

Background: Gastric cancer (GC) is the world's health is seriously threatened by a prevalent form of aggressive tumor with a dismal prognosis. The occurrence of gastric cancer poses a concern for public health since it is a malignant tumor with an enhanced incidence and fatality level.

Objective: The purpose of this study was to determine if the natural drug Daidzein (DZN) and Puerarin (PRN) together effectively suppress the proliferation of GC cells by blocking the STAT3/FAK intervention signalling pathways in BGC-823 cells.

Materials and methods: Following a 24-hour treatment with the combination of DZN and PRN, the cells were examined for a number of assays. The MTT test was used to investigate the cytotoxicity of the DZN + PNR combination. Acridine orange/ethidium bromide (AO/EtBr) dual staining experiments were utilized to investigate apoptotic alterations, and Western blotting and flow cytometry were used to assess the protein expressions of the cell survival, cell cycle, proliferation, and apoptosis proteins.

Results: Our findings showed that, DZN and PRN possessed anticancer properties by blocking the STAT3/FAK signaling cascade. Moreover, we discovered that the DZN and PRN combo reduced the protein levels of STAT3-FAK-dependent targeted genes, such as cyclin-D1, Bcl-2, Bax, MMP-2, prevented the phosphorylation and activation of STAT3, FAK.

Conclusion: The current study's findings suggest that the simultaneous administration of DZN and PNR can stop gastric cancer cells from proliferating, trigger apoptosis, and disrupt their cell cycle.

大豆苷元与葛根素通过STAT3/FAK通路协同抑制胃癌增殖。
背景:胃癌(GC)是一种普遍存在的严重威胁世界健康的侵袭性肿瘤,预后差。胃癌是一种发病率高、病死率高的恶性肿瘤,其发生引起了公众健康的关注。目的:研究天然药物Daidzein (DZN)和葛根素(PRN)是否通过阻断BGC-823细胞STAT3/FAK干预信号通路,有效抑制GC细胞的增殖。材料和方法:DZN和PRN联合作用24小时后,对细胞进行多项检测。采用MTT法观察DZN + PNR联合用药的细胞毒性。采用吖啶橙/溴化乙啶(AO/EtBr)双染色实验观察细胞凋亡变化,采用Western blotting和流式细胞术检测细胞存活、细胞周期、增殖和凋亡蛋白的表达。结果:我们的研究结果表明,DZN和PRN通过阻断STAT3/FAK信号级联具有抗癌特性。此外,我们发现DZN和PRN组合降低STAT3-FAK依赖性靶基因(如cyclin-D1, Bcl-2, Bax, MMP-2)的蛋白水平,阻止STAT3, FAK的磷酸化和激活。结论:本研究结果提示,DZN和PNR同时给药可抑制胃癌细胞增殖,引发细胞凋亡,破坏细胞周期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Hereditas
Hereditas Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.80
自引率
3.70%
发文量
0
期刊介绍: For almost a century, Hereditas has published original cutting-edge research and reviews. As the Official journal of the Mendelian Society of Lund, the journal welcomes research from across all areas of genetics and genomics. Topics of interest include human and medical genetics, animal and plant genetics, microbial genetics, agriculture and bioinformatics.
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