Rhein 通过 DNMT3B 基因调节细胞周期,从而抑制食管癌的发展。

IF 2.8 4区 医学 Q2 ONCOLOGY Medical Oncology Pub Date : 2024-05-14 DOI:10.1007/s12032-024-02359-9
Cheng Li, Jingjing Yu, Ying Feng, Xiaoxue Sun, Mingming Sun, Weihui Ni, Jun Shao, Baoxin Wang
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引用次数: 0

摘要

尽管 DNMT3B 与多种癌症类型的不良预后有关,但其促进食管癌(ESCA)进展的机制目前尚不清楚。为了研究中药大黄对食管癌(ESCA)的潜在治疗作用,我们采用了一种综合生物信息学方法。首先利用基因组富集分析(Gene Set Enrichment Analysis,GSEA)筛选大黄中的抗食管癌活性成分。然后,我们采用加权基因共表达网络分析(WGCNA)来确定与活性成分和ESCA发病机制相关的关键分子模块和靶标。这种整合多组学数据的系统级策略为揭示大黄等天然产物抗癌活性的分子机制提供了强有力的手段。为了研究模块基因的功能富集,我们进行了基因本体(GO)和京都基因组百科全书(KEGG)通路富集分析。此外,我们还利用 Kaplan-Meier 法评估了 DNMT3B 表达对 ESCA 患者的预测影响。最后,我们进行了细胞增殖和细胞周期实验,以探索 DNMT3B 的生物学作用。在这项研究中,我们发现大黄的主要活性成分大黄酚具有显著的抗 ESCA 活性。大黄苷明显抑制了ESCA细胞的增殖。利用加权基因共表达网络分析(WGCNA)和京都基因组百科全书(KEGG)分析,我们确定蓝色模块与 Rhein 靶基因和细胞周期有关。此外,DNMT3B 也被确定为 Rhein 的靶基因。对癌症基因组图谱(TCGA)数据库的分析表明,较高的 DNMT3B 水平与 ESCA 患者的不良预后有关。此外,Rhein能部分逆转DNMT3B的过表达,从而抑制ESCA细胞的增殖。体外研究表明,抑制 Rhein 和 DNMT3B 会破坏细胞周期的 S 期,并影响细胞周期相关蛋白的生成。在本研究中,我们发现 Rhein 通过靶向 DNMT3B 和调节细胞周期在 ESCA 细胞中发挥抗增殖作用。
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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Rhein suppresses esophageal cancer development by regulating cell cycle through DNMT3B gene.

The mechanism by which DNMT3B facilitates esophageal cancer (ESCA) progression is currently unknown, despite its association with adverse prognoses in several cancer types. To investigate the potential therapeutic effects of the Chinese herbal medicine rhubarb on esophageal cancer (ESCA), we adopted an integrated bioinformatics approach. Gene Set Enrichment Analysis (GSEA) was first utilized to screen active anti-ESCA components in rhubarb. We then employed Weighted Gene Co-expression Network Analysis (WGCNA) to identify key molecular modules and targets related to the active components and ESCA pathogenesis. This system-level strategy integrating multi-omics data provides a powerful means to unravel the molecular mechanisms underlying the anticancer activities of natural products, like rhubarb. To investigate module gene functional enrichment, Gene Ontology (GO), and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses were conducted. In addition, we evaluated the predictive impact of DNMT3B expression on ESCA patients utilizing the Kaplan-Meier method. Finally, we conducted experiments on cell proliferation and the cell cycle to explore the biological roles of DNMT3B. In this study, we identified Rhein as the main active ingredient of rhubarb that exhibited significant anti-ESCA activity. Rhein markedly suppressed ESCA cell proliferation. Utilizing Weighted Gene Co-expression Network Analysis (WGCNA) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis, we determined that the blue module was associated with Rhein target genes and the cell cycle. Additionally, DNMT3B was identified as a Rhein target gene. Analysis of The Cancer Genome Atlas (TCGA) database revealed that higher DNMT3B levels were associated with poor prognosis in ESCA patients. Furthermore, Rhein partially reversed the overexpression of DNMT3B to inhibit ESCA cell proliferation. In vitro studies demonstrated that Rhein and DNMT3B inhibition disrupted the S phase of the cell cycle and affected the production of cell cycle-related proteins. In this study, we found that Rhein exerts its anti-proliferative effects in ESCA cells by targeting DNMT3B and regulating the cell cycle.

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来源期刊
Medical Oncology
Medical Oncology 医学-肿瘤学
CiteScore
4.20
自引率
2.90%
发文量
259
审稿时长
1.4 months
期刊介绍: Medical Oncology (MO) communicates the results of clinical and experimental research in oncology and hematology, particularly experimental therapeutics within the fields of immunotherapy and chemotherapy. It also provides state-of-the-art reviews on clinical and experimental therapies. Topics covered include immunobiology, pathogenesis, and treatment of malignant tumors.
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