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

表观遗传学 生物 滤泡性淋巴瘤 DNA甲基化 肿瘤微环境 癌症研究 淋巴瘤 染色质 表观基因组 免疫学 免疫系统 遗传学 基因 基因表达
作者
Ferran Araujo‐Ayala,Wendy Béguelin
出处
期刊:Blood [Elsevier BV]
卷期号:146 (15): 1759-1769 被引量:10
标识
DOI:10.1182/blood.2024026020
摘要

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.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
大模型的应助被书墨间采纳,获得10
刚刚
Jindyla发布了新的文献求助10
刚刚
FashionBoy的应助被书墨间采纳,获得10
刚刚
aaaa的应助被书墨间采纳,获得20
刚刚
慕青的应助被书墨间采纳,获得10
刚刚
刚刚
上官若男的应助被书墨间采纳,获得10
刚刚
刚刚
华仔的应助被西南采纳,获得30
2秒前
期待发布了新的文献求助10
2秒前
科研通AI6.2的应助被美好乐松采纳,获得10
2秒前
李健的应助被stupider采纳,获得10
3秒前
等广东下雪w完成签到,获得积分10
3秒前
3秒前
3秒前
4秒前
小徐发布了新的文献求助10
4秒前
XiaoTong发布了新的文献求助10
4秒前
li发布了新的文献求助10
5秒前
细腻的书雁完成签到,获得积分10
6秒前
6秒前
小小田完成签到,获得积分10
6秒前
moo发布了新的文献求助10
7秒前
科研通AI6.4的应助被xx采纳,获得30
7秒前
zgliu78发布了新的文献求助10
7秒前
1q完成签到,获得积分20
8秒前
sonia0720完成签到,获得积分10
8秒前
8秒前
8秒前
aix发布了新的文献求助10
9秒前
9秒前
科研通AI6.4的应助被hulahula采纳,获得10
10秒前
牛马完成签到,获得积分10
10秒前
小小田发布了新的文献求助10
10秒前
可爱的函函的应助被zzz采纳,获得10
10秒前
紫杉罗罗完成签到,获得积分10
11秒前
12秒前
QiQi发布了新的文献求助10
12秒前
pkn发布了新的文献求助10
12秒前
院士候选人的应助被软嘴唇采纳,获得10
13秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Aspects of Post-SPE Phonology 2000
Performance standards for antimicrobial disk and dilution susceptibility tests for bacteria isolated from animals 888
Rosenblum, Global Change Biology 800
Holistic Discourse Analysis, Second Edition by Robert E. Longacre (2012-09-10) 666
Final Report for the 2-D Test of Model 901 Rotor and Wing Airfoils (BSWT 592) 528
Berberine regulates the TLR4 signaling pathway to suppress hypoxia-induced proliferation and migration of pulmonary arterial smooth muscle cells 520
热门求助领域 (近24小时)
化学 材料科学 医学 生物 计算机科学 工程类 纳米技术 物理 有机化学 化学工程 内科学 生物化学 复合材料 催化作用 心理学 细胞生物学 无机化学 电极 光电子学 人工智能
热门帖子
关注 科研通微信公众号,转发送积分 7889195
求助须知:如何正确求助?哪些是违规求助? 9400814
关于积分的说明 20842270
捐赠科研通 7491976
什么是DOI,文献DOI怎么找? 3357420
关于科研通互助平台的介绍 2496064
邀请新用户注册赠送积分活动 2385731