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将岩藻糖基转移酶FUT8作为弥漫性大B细胞淋巴瘤(DLBCL)的一种潜在治疗方法。

Targeting fucosyltransferase FUT8 as a prospective therapeutic approach for DLBCL.

作者信息

Xu Hao, Li Qi, Zhang Yuchen, He Chuan, Zhang Xinyun, Wang Zhiming, Zhao Meifang, Chai Yali, Zhuang Wenzhuo, Li Bingzong

机构信息

Department of Hematology, The Second Affiliated Hospital of Soochow University, Suzhou, China.

Department of Cell Biology, School of Biology & Basic Medical Sciences, Suzhou Medical College of Soochow University, Suzhou, China.

出版信息

Oncogenesis. 2025 Jan 29;14(1):1. doi: 10.1038/s41389-025-00544-7.

DOI:10.1038/s41389-025-00544-7
PMID:39881135
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11779920/
Abstract

Diffuse large B-cell lymphoma (DLBCL) is characterized by its aggressive nature and resistance to standard chemotherapy, necessitating the development of new therapeutic approaches. The emergence of natural products and their derivatives has notably influenced cancer treatment, making morusinol, a medicine-derived monomer, a promising candidate. Here, we showed that morusinol exerted antitumor effects on DLBCL in vitro by inducing apoptosis and cell cycle arrest. Impressively, morusinol treatment exhibited potent tumor growth inhibition in vivo, proving both well-tolerated and safe in mouse models. Moreover, our investigation identified FUT8, a fucosyltransferase, as a potential target for morusinol. FUT8's role as an oncogene in DLBCL and its correlation with poor survival further underscored its significance. Furthermore, our screening efforts involving clinical and preclinical drugs unveiled a compelling synergistic effect between chidamide and morusinol. Additionally, morusinol's ability to hinder M2-like polarization of tumor-associated macrophages suggested its potential in immune response modulation within DLBCL. Collectively, morusinol showcased substantial promise as an anti-tumor agent for potential clinical application in DLBCL management, potentially augmenting established therapeutic strategies. Moreover, our findings offered promising prospects for natural products to effectively leverage its therapeutic advantages. Working model: The role of Morusinol in treating DLBCL.

摘要

弥漫性大B细胞淋巴瘤(DLBCL)具有侵袭性且对标准化疗耐药,因此需要开发新的治疗方法。天然产物及其衍生物的出现显著影响了癌症治疗,使药物来源的单体桑辛醇成为一个有前景的候选物。在此,我们表明桑辛醇通过诱导细胞凋亡和细胞周期阻滞在体外对DLBCL发挥抗肿瘤作用。令人印象深刻的是,桑辛醇治疗在体内表现出强大的肿瘤生长抑制作用,在小鼠模型中证明耐受性良好且安全。此外,我们的研究确定岩藻糖基转移酶FUT8是桑辛醇的一个潜在靶点。FUT8作为DLBCL中的一个癌基因的作用及其与不良生存的相关性进一步凸显了其重要性。此外,我们对临床和临床前药物的筛选工作揭示了西达本胺和桑辛醇之间令人信服的协同作用。此外,桑辛醇阻碍肿瘤相关巨噬细胞向M2样极化的能力表明其在DLBCL免疫反应调节中的潜力。总体而言,桑辛醇作为一种抗肿瘤药物在DLBCL治疗中的潜在临床应用显示出巨大前景,可能增强既定的治疗策略。此外,我们的研究结果为天然产物有效利用其治疗优势提供了有希望的前景。工作模型:桑辛醇在治疗DLBCL中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8de1/11779920/9f94bf84d394/41389_2025_544_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8de1/11779920/ae861bef4503/41389_2025_544_Figa_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8de1/11779920/ee0d7dc232c8/41389_2025_544_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8de1/11779920/09811e1f2172/41389_2025_544_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8de1/11779920/aa76da82592c/41389_2025_544_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8de1/11779920/d116668e8699/41389_2025_544_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8de1/11779920/9f94bf84d394/41389_2025_544_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8de1/11779920/ae861bef4503/41389_2025_544_Figa_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8de1/11779920/ee0d7dc232c8/41389_2025_544_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8de1/11779920/09811e1f2172/41389_2025_544_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8de1/11779920/aa76da82592c/41389_2025_544_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8de1/11779920/d116668e8699/41389_2025_544_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8de1/11779920/9f94bf84d394/41389_2025_544_Fig5_HTML.jpg

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本文引用的文献

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High-Throughput Mass Spectrometry Analysis of -Glycans and Protein Markers after Knockdown in the Syngeneic SW480/SW620 Colorectal Cancer Cell Model.在同基因 SW480/SW620 结直肠癌细胞模型中敲低后的 -聚糖和蛋白质标志物的高通量质谱分析。
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Morusinol Extracted from Inhibits Cell Proliferation and Induces Autophagy via FOXO3a Nuclear Accumulation-Mediated Cholesterol Biosynthesis Obstruction in Colorectal Cancer.
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Morusinol extracted from Morus alba induces cell cycle arrest and apoptosis via inhibition of DNA damage response in melanoma by CHK1 degradation through the ubiquitin-proteasome pathway.从桑白皮中提取的桑色呋喃通过 CHK1 降解通过泛素-蛋白酶体途径抑制黑色素瘤中的 DNA 损伤反应诱导细胞周期停滞和凋亡。
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