长芽孢杆菌代谢物对Fnevs致癌能力的干预:一把潜在的双刃剑。

IF 3.3 3区 生物学 Q3 CELL BIOLOGY Experimental cell research Pub Date : 2025-02-01 DOI:10.1016/j.yexcr.2025.114407
Jingyu Xu , Xinyu Wu , Luyi Yang , Xiaoxi Xu
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引用次数: 0

摘要

结直肠癌(CRC)是全球最常见的恶性肿瘤之一。核梭杆菌及其代谢产物是促进结肠癌的有效生物学靶点。双歧杆菌等益生菌可通过调节宿主肠道黏膜免疫,消除致癌物,干扰肿瘤细胞增殖和凋亡,阻断结直肠癌的发生发展。我们选取6种双歧杆菌,探讨其无细胞上清液(CFS)对核梭杆菌的抑制作用,并筛选功能最佳的长双歧杆菌(B. longum)菌株,探讨其对Fnevs感染结直肠癌细胞的干预作用。在双歧杆菌属中,B. longum-CFS能有效抑制核梭杆菌的生长和成膜。长芽孢杆菌的代谢物可抑制fnev感染的结直肠癌细胞的增殖、迁移和侵袭。然而,用Bl-CFS处理fnev感染的CRC细胞的转录组学分析显示,Bl-CFS对特定癌基因(如Myc、IL16、KCNN2、ACSBG1、Pum1、MET、NR5A2)的表达有抑制作用,同时促进其他癌基因的表达。这种调节可能会增强CRC细胞的增殖、上皮-间质转化(EMT)、干细胞特性和其他与CRC细胞相关的特征。代谢组学还显示,Bl-CFS改变了fnev感染的结直肠癌细胞的有机酸和脂质代谢,并将能量供应从有氧糖代谢(TCA循环)转变为厌氧糖酵解,从而增加了结直肠癌细胞的恶性潜能。观察到的结果可能归因于长双歧杆菌代谢产物中益生菌和有毒物质的存在。因此,本研究得出结论,长双歧杆菌天然代谢物的抗结直肠癌(CRC)作用有限。未来的研究应着眼于对这些天然物质进行提炼,优化其组成比例,提取其精华,同时去除杂质,从而获得具有卓越和稳定疗效的抗癌生物制剂。
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The intervention of B. longum metabolites in Fnevs' carcinogenic capacity: A potential double-edged sword
Colorectal cancer (CRC) ranks among the most prevalent malignant tumors globally. Fusobacterium nucleatum and its metabolites are effective biological targets for colon cancer promotion. Probiotics such as Bifidobacterium can block the occurrence and development of CRC by regulating the host intestinal mucosal immunity, eliminating carcinogens, and interfering with tumor cell proliferation and apoptosis. We selected six Bifidobacterium species to explore the inhibitory effect of their cell-free supernatant (CFS) on Fusobacterium nucleatum, and screened the best functional strain Bifidobacterium longum (B. longum) to explore its intervention effect on Fnevs infection of CRC cells. In the genus Bifidobacterium, B. longum-CFS can effectively inhibit the growth and membrane formation of Fusobacterium nucleatum. The metabolites of B. longum can inhibit the proliferation, migration and invasion of Fnevs-infected CRC cells. However, the transcriptomic analysis of Fnevs-infected CRC cells treated with Bl-CFS revealed that Bl-CFS exerted inhibitory effects on the expression of specific oncogenes (e.g., Myc, IL16, KCNN2, ACSBG1, Pum1, MET, NR5A2), while simultaneously promoting the expression of other oncogenes. This modulation potentially enhances the proliferation, epithelial-mesenchymal transition (EMT), stemness properties and other characteristics associated with CRC cells. Metabolomics also showed that Bl-CFS altered organic acid and lipid metabolism in Fnevs-infected CRC cells, and switched energy supply from aerobic glucose metabolism (TCA cycle) to anaerobic glycolysis, which increased the malignancy potential of CRC cells. The observed outcome may be attributed to the presence of both probiotics and toxic substances in the metabolites derived from Bifidobacterium longum. Therefore, this study concludes that the anti-colorectal cancer (CRC) effect of natural metabolites derived from Bifidobacterium longum is limited. Future investigations should focus on refining these natural substances and optimizing their composition ratios to extract their essence while eliminating impurities, thereby obtaining anticancer biologics with exceptional and consistent efficacy.
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来源期刊
Experimental cell research
Experimental cell research 医学-细胞生物学
CiteScore
7.20
自引率
0.00%
发文量
295
审稿时长
30 days
期刊介绍: Our scope includes but is not limited to areas such as: Chromosome biology; Chromatin and epigenetics; DNA repair; Gene regulation; Nuclear import-export; RNA processing; Non-coding RNAs; Organelle biology; The cytoskeleton; Intracellular trafficking; Cell-cell and cell-matrix interactions; Cell motility and migration; Cell proliferation; Cellular differentiation; Signal transduction; Programmed cell death.
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