Clinical Significance of Acyl-CoA Dehydrogenase Short Chain and Its Anti-tumor Role in Hepatocellular Carcinoma by Inhibiting Canonical Wnt/β-Catenin Pathway.

IF 2.5 4区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Jiawei Gu, Zhipeng Cao, Gengming Niu, Jianghui Ying, Hui Wang, Hua Jiang, Chongwei Ke
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Abstract

Background: The pathogenesis of hepatocellular carcinoma (HCC) emphasizes metabolic disorders. HCC patients showed abnormally low expression of Acyl-CoA dehydrogenase short chain (ACADS).

Objectives: This study aimed to elucidate the clinical significance and mechanistic role of ACADS in HCC.

Methods: We investigated the expression patterns and significance of ACADS in HCC by analyzing multiple public databases and clinical samples (Chip data). Immunohistochemistry was employed to observe the expression levels of ACADS in HCC tissues. In vitro experiments involved silencing or overexpressing ACADS in HCC cell lines, with protein expression levels determined by Western blotting. Functional validation included CCK-8, Transwell, and scratch wound healing assays. TOPFlash and FOPFlash reporter gene assays, co-immunoprecipitation, and immunofluorescence were used to explore the interaction between ACADS and β-catenin.

Results: ACADS was low expressed in HCC and was clinically associated with vascular invasion, TNM stage, and AFP levels. The low ACADS expression in HCC patients was negatively correlated with their survival. Overexpression of ACADS significantly suppressed the viability, migration, and invasive capacity of HCC cells, whereas silencing ACADS had the opposite effect. Mechanistically, co-immunoprecipitation experiments indicated that there was an interaction between ACADS and β-catenin. Overexpression of ACADS inhibited β-catenin activity and resulted in decreased nuclear β-catenin translocation and increased its cytoplasmic level. Immunofluorescence results also showed a decrease in β-catenin nuclear import following ACADS overexpression, whereas silencing ACADS led to an enhancement of its nuclear translocation.

Conclusion: ACADS emerges as a potentially valuable biomarker for HCC prognosis, exhibiting tumor-suppressive functions in HCC by participating in the regulation of β-catenin activity.

酰基辅酶a脱氢酶短链的临床意义及抑制典型Wnt/β-Catenin通路在肝癌中的抗肿瘤作用
背景:肝细胞癌(HCC)的发病机制强调代谢紊乱。HCC患者的乙酰辅酶脱氢酶短链(ACADS)表达异常低:本研究旨在阐明 ACADS 在 HCC 中的临床意义和机制作用:我们通过分析多个公共数据库和临床样本(芯片数据),研究了 ACADS 在 HCC 中的表达模式和意义。采用免疫组化方法观察 ACADS 在 HCC 组织中的表达水平。体外实验包括在 HCC 细胞系中沉默或过表达 ACADS,并通过 Western 印迹测定蛋白表达水平。功能验证包括 CCK-8、Transwell 和划痕伤口愈合试验。利用TOPFlash和FOPFlash报告基因检测、共免疫沉淀和免疫荧光来探讨ACADS与β-catenin之间的相互作用:结果:ACADS在HCC中低表达,在临床上与血管侵犯、TNM分期和AFP水平相关。ACADS 在 HCC 患者中的低表达与其生存率呈负相关。过表达 ACADS 会显著抑制 HCC 细胞的活力、迁移和侵袭能力,而沉默 ACADS 则会产生相反的效果。共免疫沉淀实验表明,ACADS与β-catenin之间存在相互作用。过量表达 ACADS 可抑制β-catenin 的活性,导致核β-catenin 转位减少,胞质水平升高。免疫荧光结果还显示,过表达 ACADS 后,β-catenin 核导入减少,而沉默 ACADS 则导致其核转位增强:结论:ACADS通过参与调控β-catenin的活性,在HCC中表现出抑制肿瘤的功能,是一种对HCC预后有潜在价值的生物标志物。
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来源期刊
Digestive Diseases and Sciences
Digestive Diseases and Sciences 医学-胃肠肝病学
CiteScore
6.40
自引率
3.20%
发文量
420
审稿时长
1 months
期刊介绍: Digestive Diseases and Sciences publishes high-quality, peer-reviewed, original papers addressing aspects of basic/translational and clinical research in gastroenterology, hepatology, and related fields. This well-illustrated journal features comprehensive coverage of basic pathophysiology, new technological advances, and clinical breakthroughs; insights from prominent academicians and practitioners concerning new scientific developments and practical medical issues; and discussions focusing on the latest changes in local and worldwide social, economic, and governmental policies that affect the delivery of care within the disciplines of gastroenterology and hepatology.
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