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滤泡性淋巴瘤的多组学全景进展。

Advances in the multi-omics landscape of follicular lymphoma.

机构信息

Shanghai Institute of Hematology, State Key Laboratory of Medical Genomics, National Research Center for Translational Medicine at Shanghai, Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China.

出版信息

Int J Biol Sci. 2023 Mar 27;19(6):1955-1967. doi: 10.7150/ijbs.80401. eCollection 2023.

DOI:10.7150/ijbs.80401
PMID:37063433
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10092758/
Abstract

Follicular lymphoma (FL) is the most common indolent lymphoma originating from germinal center B cells. FL represents a clinically and biologically heterogeneous disease. Most patients have favorable outcomes, but a subset of patients experiences early progression or transformation and has a poor prognosis. Abnormalities in FL cells and tumor microenvironment have been revealed using multi-omics techniques, including genomic, epigenomic, transcriptomic and proteomic analysis. Recurrent somatic gene aberrations mainly involve epigenetic modifiers, transcription factors, oncogenic pathways and microenvironment modulators. Single-cell transcriptomic analysis show marked inter- and intra-patient FL subclone heterogeneity. In addition, a comprehensive profile of microenvironmental components is provided, unveiling the crosstalk between tumor and microenvironment that induce FL progression and facilitate immune escape. Together, these studies provide insights into the mechanisms and biomarkers of high-risk FL populations, as well as the potential targeted and immunotherapy options. Future research should focus on integrating multi-omics aberrations to optimize therapeutic strategies in FL.

摘要

滤泡性淋巴瘤(FL)是最常见的起源于生发中心 B 细胞的惰性淋巴瘤。FL 是一种临床表现和生物学特征均具有异质性的疾病。大多数患者预后良好,但有一部分患者早期进展或转化,预后不良。应用包括基因组、表观基因组、转录组和蛋白质组分析在内的多组学技术,揭示了 FL 细胞和肿瘤微环境的异常。复发性体细胞基因异常主要涉及表观遗传修饰物、转录因子、致癌途径和微环境调节剂。单细胞转录组分析显示出明显的患者间和患者内 FL 亚克隆异质性。此外,还提供了微环境成分的综合图谱,揭示了肿瘤与微环境之间的相互作用,这些相互作用导致 FL 的进展并促进免疫逃逸。综上所述,这些研究为高危 FL 人群的发病机制和生物标志物,以及潜在的靶向和免疫治疗选择提供了深入的见解。未来的研究应集中于整合多组学异常,以优化 FL 的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/307d/10092758/4adabe955aa2/ijbsv19p1955g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/307d/10092758/4adabe955aa2/ijbsv19p1955g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/307d/10092758/4adabe955aa2/ijbsv19p1955g001.jpg

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A single-cell atlas of non-haematopoietic cells in human lymph nodes and lymphoma reveals a landscape of stromal remodelling.人类淋巴结和淋巴瘤中非造血细胞的单细胞图谱揭示了基质重塑的全景。
Nat Cell Biol. 2022 Apr;24(4):565-578. doi: 10.1038/s41556-022-00866-3. Epub 2022 Mar 24.
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Follicular lymphoma-associated mutations in the V-ATPase chaperone VMA21 activate autophagy creating a targetable dependency.
滤泡性淋巴瘤相关枢纽基因的鉴定与功能研究
Biochem Genet. 2024 May 27. doi: 10.1007/s10528-024-10831-4.
滤泡性淋巴瘤相关的 V-ATPase 伴侣 VMA21 突变激活自噬,产生可靶向的依赖性。
Autophagy. 2022 Aug;18(8):1982-2000. doi: 10.1080/15548627.2022.2050663. Epub 2022 Mar 24.
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Mechanistic convergence of the TIGIT and PD-1 inhibitory pathways necessitates co-blockade to optimize anti-tumor CD8 T cell responses.TIGIT 和 PD-1 抑制途径的机制趋同需要联合阻断以优化抗肿瘤 CD8 T 细胞反应。
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