Transcription Factor FXR Activates DHRS9 to Inhibit the Cell Oxidative Phosphorylation and Suppress Colon Cancer Progression.

IF 2.6 4区 医学 Q3 CELL BIOLOGY Analytical Cellular Pathology Pub Date : 2022-10-26 eCollection Date: 2022-01-01 DOI:10.1155/2022/8275574
Jinlai Zhao, Yigang Wang, Yang Wang, Jianchao Gao, Haichao Yang, Xiaotang Wu, Hua Li
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引用次数: 2

Abstract

Background: Colon cancer is a common gastrointestinal malignancy. It has been discovered that Farnesoid X receptor (FXR) plays an imperative regulatory role in multitype cancers in recent years. However, its regulatory mechanism in colon cancer has not been clearly explored. This study intended to explore the molecular regulatory mechanism of FXR and its downstream genes on the malignant progression of colon cancer.

Methods: The mRNA and protein expression of FXR in colon cancer cells were measured by quantitative real-time polymerase chain reaction and Western blot. The effects of FXR on the biological function of colon cancer cells were measured by Cell Counting Kit-8, colony formation, and transwell assays. The downstream target gene of FXR was predicted by bioinformatics analysis and found to be associated with cellular oxidative phosphorylation. The binding relationship between FXR and its downstream gene dehydrogenase/reductase member 9 (DHRS9) was verified through luciferase reporter assay and chromatin immunoprecipitation assay. The changes of oxidative phosphorylation were detected by Western blot and oxygen consumption rate determination. The effect of FXR/DHRS9 axis on the malignant progression of colon cancer cells was further confirmed by rescue experiments.

Results: FXR was underexpressed in colon cancer tissues and cells, and overexpressing FXR could repress the malignant behaviors of colon cancer cells. Besides, DHRS9 was a downstream gene of FXR, and FXR/DHRS9 inhibited the deterioration of colon cancer through inhibiting oxidative phosphorylation. Moreover, promoting FXR expression in colon cancer cells could partially reverse the biological function changes caused by silencing DHRS9 expression.

Conclusion: FXR inhibited the oxidative phosphorylation and inhibited the malignant progression of colon cancer cells via targeting DHRS9.

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转录因子FXR激活DHRS9抑制细胞氧化磷酸化抑制结肠癌进展
背景:结肠癌是一种常见的胃肠道恶性肿瘤。近年来,法内索酮X受体(Farnesoid X receptor, FXR)在多类型癌症中起着重要的调控作用。然而,其在结肠癌中的调控机制尚不清楚。本研究旨在探讨FXR及其下游基因在结肠癌恶性进展中的分子调控机制。方法:采用实时定量聚合酶链反应和Western blot检测结肠癌细胞中FXR mRNA和蛋白的表达。通过细胞计数试剂盒-8、集落形成和transwell实验检测FXR对结肠癌细胞生物学功能的影响。通过生物信息学分析预测了FXR的下游靶基因,发现其与细胞氧化磷酸化有关。通过荧光素酶报告基因实验和染色质免疫沉淀实验验证FXR与其下游基因脱氢酶/还原酶成员9 (DHRS9)的结合关系。采用Western blot和耗氧量测定法检测氧化磷酸化水平的变化。拯救实验进一步证实了FXR/DHRS9轴对结肠癌细胞恶性进展的影响。结果:FXR在结肠癌组织和细胞中低表达,过表达FXR可抑制结肠癌细胞的恶性行为。此外,DHRS9是FXR的下游基因,FXR/DHRS9通过抑制氧化磷酸化抑制结肠癌恶化。此外,促进结肠癌细胞中FXR的表达可以部分逆转沉默DHRS9表达引起的生物学功能变化。结论:FXR通过靶向DHRS9抑制结肠癌细胞的氧化磷酸化并抑制其恶性进展。
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来源期刊
Analytical Cellular Pathology
Analytical Cellular Pathology ONCOLOGY-CELL BIOLOGY
CiteScore
4.90
自引率
3.10%
发文量
70
审稿时长
16 weeks
期刊介绍: Analytical Cellular Pathology is a peer-reviewed, Open Access journal that provides a forum for scientists, medical practitioners and pathologists working in the area of cellular pathology. The journal publishes original research articles, review articles, and clinical studies related to cytology, carcinogenesis, cell receptors, biomarkers, diagnostic pathology, immunopathology, and hematology.
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