Xu Jingyu, Wu Xinyu, Yang Luyi, Xu Xiaoxi
Department of Orthodontics, Hospital of Stomatology, Jilin University, Changchun 130021, PR China.
Key Laboratory of Dairy Science, Ministry of Education, College of Food Science, Northeast Agricultural University, Harbin 150030, PR China.
Exp Cell Res. 2025 Feb 1;445(1):114407. doi: 10.1016/j.yexcr.2025.114407. Epub 2025 Jan 8.
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.
结直肠癌(CRC)是全球最常见的恶性肿瘤之一。具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、消除致癌物以及干扰肿瘤细胞增殖和凋亡来阻止CRC的发生和发展。我们选择了六种双歧杆菌来探究其无细胞上清液(CFS)对具核梭杆菌的抑制作用,并筛选出最佳功能菌株长双歧杆菌(B. longum)来探究其对具核梭杆菌感染的CRC细胞的干预效果。在双歧杆菌属中,长双歧杆菌CFS可有效抑制具核梭杆菌的生长和膜形成。长双歧杆菌的代谢产物可抑制具核梭杆菌感染的CRC细胞的增殖、迁移和侵袭。然而,对用长双歧杆菌CFS处理的具核梭杆菌感染的CRC细胞进行的转录组分析表明,长双歧杆菌CFS对特定癌基因(如Myc、IL16、KCNN2、ACSBG1、Pum1、MET、NR5A2)的表达产生抑制作用,同时促进其他癌基因的表达。这种调节可能会增强与CRC细胞相关的增殖、上皮-间质转化(EMT)、干性特性及其他特征。代谢组学还表明,长双歧杆菌CFS改变了具核梭杆菌感染的CRC细胞中的有机酸和脂质代谢,并将能量供应从有氧葡萄糖代谢(三羧酸循环)转变为无氧糖酵解,这增加了CRC细胞的恶性潜能。观察到的结果可能归因于长双歧杆菌衍生代谢产物中同时存在益生菌和有毒物质。因此,本研究得出结论,长双歧杆菌衍生的天然代谢产物的抗结直肠癌(CRC)作用有限。未来的研究应集中于提纯这些天然物质并优化其组成比例,以提取其精华同时去除杂质,从而获得疗效卓越且一致的抗癌生物制品。