减少BCR信号和代谢转移伴随滤泡性淋巴瘤恶性进展:转录组学的教训

C. Sala, A. Arcangeli
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引用次数: 4

摘要

在题为“离子通道和转运蛋白基因表达谱表明滤泡性淋巴瘤恶性进展期间兴奋性和代谢的转变”的手稿中,我们报告了我们对离子通道和转运蛋白(ICT-GEP)基因表达谱如何有助于识别滤泡性淋巴瘤(FL)的特异性特征的最新理解进展,那些在复发-缓解过程后获得化疗耐药的FL。以及更具侵袭性的弥漫性大细胞淋巴瘤(DLBCL),这可能代表了fl的演变。通过对FL恶性进展过程中ICT-GEP变化的分析,我们发现编码这些通道的基因表达逐渐减少,这些通道负责维持离子稳态和Ca2+进入的驱动力,在细胞激活时,以及从糖酵解到氧化代谢的转变。
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Reduced BCR Signaling and a Metabolic Shift Accompanies Malignant Progression of Follicular Lymphoma: A Lesson from Transcriptomics
In the manuscript entitled “The ion channels and transporters gene expression profile indicates a shift in excitability and metabolisms during malignant progression of Follicular Lymphoma” [1], we reported recent advances in our understanding of how the gene expression profile of ion channels and transporters (ICT-GEP) contributes to identify specific signatures associated with Follicular Lymphoma (FL), with those FL that acquire chemoresistance after a relapsing-remitting course, and with the more aggressive Diffuse Large Cell Lymphoma (DLBCL), which may represent the evolution of FLs. From the analysis of how ICT-GEP changes during FL malignant progression emerged the progressive decrease in the expression of genes encoding those channels which are responsible for the maintenance of the ionic homeostasis and the driving force for Ca2+ entry, upon cell activation, as well as a shift from a glycolytic to an oxidative metabolism.
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