Biology as vulnerability in follicular lymphoma: genetics, epigenetics, and immunogenetics.

IF 23.1 1区 医学 Q1 HEMATOLOGY
Blood Pub Date : 2025-10-09 DOI:10.1182/blood.2024026020
Ferran Araujo-Ayala, Wendy Béguelin
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引用次数: 0

Abstract

Abstract: Follicular lymphoma (FL) represents a heterogeneous group of B-cell neoplasms with distinct genetic, epigenetic, microenvironmental, and clinical features. It is the most prevalent indolent non-Hodgkin lymphoma, characterized by a relapsing course and risk of transformation to aggressive diffuse large B-cell lymphoma. Recent advances in high-throughput sequencing, spatial transcriptomics, and imaging technologies uncovered genetic, epigenetic, and immunogenetic features underpinning FL, offering insights into its biology and potential therapeutic vulnerabilities. Although FL is primarily driven by the hallmark t(14;18) translocation involving BCL2, its pathogenesis requires additional oncogenic mutations, particularly in genes regulating chromatin and histone modifications. These early genetic and epigenetic alterations promote the persistence and evolution of cancer precursor cells, setting the stage for lymphomagenesis. The tumor microenvironment is also crucial in FL progression and patient prognosis, with T cells, stromal cells, and macrophages playing pivotal roles in facilitating tumor immune escape. Targeted therapies, including B-cell lymphoma 2 (BCL2) inhibitors, epigenetic modulators, and immunotherapies, have emerged from this deeper understanding of FL biology. Achieving a cure for FL will require targeted therapies that selectively eliminate cancer precursor cells with minimal impact on normal cells, thus preventing relapse and avoiding harmful side effects. Eradicating minimal residual disease should be a primary objective rather than waiting for clinical relapse. Future research must prioritize the development of accurate experimental models, the elucidation of FL precursors, and a deeper understanding of its heterogeneity, dependencies, progression, and mechanisms driving transformation. Implementing targeted therapies at FL early stages, instead of the current "watch and wait" approach, will be essential to improve patient outcomes.

生物学作为滤泡性淋巴瘤的易感性:遗传学、表观遗传学和免疫遗传学。
滤泡性淋巴瘤(FL)是一种异质性的b细胞肿瘤,具有独特的遗传、表观遗传、微环境和临床特征。它是最常见的惰性非霍奇金淋巴瘤,其特点是复发过程和转化为侵袭性弥漫性大b细胞淋巴瘤的风险。高通量测序、空间转录组学和成像技术的最新进展揭示了FL的遗传、表观遗传学和免疫遗传学特征,为其生物学和潜在的治疗脆弱性提供了见解。虽然FL主要由涉及BCL2的标志t(14;18)易位驱动,但其发病机制需要额外的致癌突变,特别是在调节染色质和组蛋白修饰的基因中。这些早期的遗传和表观遗传改变促进了癌症前体细胞的持续和进化,为淋巴瘤的发生奠定了基础。肿瘤微环境对FL的进展和患者预后也至关重要,其中t细胞、基质细胞和巨噬细胞在促进肿瘤免疫逃逸中起关键作用。靶向治疗,包括BCL2抑制剂、表观遗传调节剂和免疫疗法,已经从对FL生物学的深入了解中出现。要想治愈FL,就需要靶向治疗,在对正常细胞影响最小的情况下,选择性地消除癌症前体细胞,从而防止复发并避免有害的副作用。根除微小残留疾病应该是首要目标,而不是等待临床复发。未来的研究必须优先发展准确的实验模型,阐明FL前体,并更深入地了解其异质性、依赖性、进展性和驱动转化的机制。在FL早期阶段实施靶向治疗,而不是目前的“观察和等待”方法,将对改善患者的预后至关重要。
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来源期刊
Blood
Blood 医学-血液学
CiteScore
23.60
自引率
3.90%
发文量
955
审稿时长
1 months
期刊介绍: Blood, the official journal of the American Society of Hematology, published online and in print, provides an international forum for the publication of original articles describing basic laboratory, translational, and clinical investigations in hematology. Primary research articles will be published under the following scientific categories: Clinical Trials and Observations; Gene Therapy; Hematopoiesis and Stem Cells; Immunobiology and Immunotherapy scope; Myeloid Neoplasia; Lymphoid Neoplasia; Phagocytes, Granulocytes and Myelopoiesis; Platelets and Thrombopoiesis; Red Cells, Iron and Erythropoiesis; Thrombosis and Hemostasis; Transfusion Medicine; Transplantation; and Vascular Biology. Papers can be listed under more than one category as appropriate.
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