代谢组学
弥漫性大B细胞淋巴瘤
代谢途径
淋巴瘤
生发中心
生物
代谢物
癌症研究
病理
新陈代谢
医学
生物化学
B细胞
免疫学
生物信息学
抗体
作者
Carla Isabelly Rodrigues‐Fernandes,Roberta Rayra Martins‐Chaves,Jéssica Gardone Vitório,Filipe Fideles Duarte‐Andrade,Thaís dos Santos Fontes Pereira,Ciro Dantas Soares,Victor Rezende Moreira,Yuri Abner Rocha Lebron,Lucilaine Valéria de Souza Santos,Liséte Celina Lange,Gisele André Baptista Canuto,Carolina Cavaliéri Gomes,Adriana Nori de Macedo,Hélder Antônio Rebelo Pontes,Rommel Mário Rodríguez Burbano,Manoela Domingues Martins,Fábio Ramôa Pires,Ricardo Alves Mesquita,Ricardo Santiago Gomez,Alan Roger Santos‐Silva,Márcio Ajudarte Lopes,Pablo Agustín Vargas,Felipe Paiva Fonseca
标识
DOI:10.1080/10428194.2023.2234523
摘要
Altered metabolic fingerprints of Diffuse large B-cell lymphoma, not otherwise specified (DLBCL NOS) may offer novel opportunities to identify new biomarkers and improve the understanding of its pathogenesis. This study aimed to investigate the modified metabolic pathways in extranodal, germinal center B-cell (GCB) and non-GCB DLBCL NOS from the head and neck. Formalin-fixed paraffin-embedded (FFPE) tissues from eleven DLBCL NOS classified according to Hans' algorithm using immunohistochemistry, and five normal lymphoid tissues (LT) were analyzed by high-performance liquid chromatography-mass spectrometry-based untargeted metabolomics. Partial Least Squares Discriminant Analysis showed that GCB and non-GCB DLBCL NOS have a distinct metabolomics profile, being the former more similar to normal lymphoid tissues. Metabolite pathway enrichment analysis indicated the following altered pathways: arachidonic acid, tyrosine, xenobiotics, vitamin E metabolism, and vitamin A. Our findings support that GCB and non-GCB DLBCL NOS has a distinct metabolomic profile, in which GCB possibly shares more metabolic similarities with LT than non-GCB DLBCL NOS.
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