Molecular landscape of distinct follicular lymphoma histologic grades: insights from genomic and transcriptome analyses

IF 12.8 1区 医学 Q1 HEMATOLOGY
Cong Sun, Wei Li, Jingwei Yu, Tingting Zhang, Wenchen Gong, Hengqi Liu, Fenghua Gao, Zheng Song, Lanfang Li, Lihua Qiu, Zhengzi Qian, Shiyong Zhou, Bin Meng, Yanan Gao, Junzhi Li, Xia Liu, Weicheng Ren, Qiang Pan-Hammarström, Xianhuo Wang, Huilai Zhang
{"title":"Molecular landscape of distinct follicular lymphoma histologic grades: insights from genomic and transcriptome analyses","authors":"Cong Sun, Wei Li, Jingwei Yu, Tingting Zhang, Wenchen Gong, Hengqi Liu, Fenghua Gao, Zheng Song, Lanfang Li, Lihua Qiu, Zhengzi Qian, Shiyong Zhou, Bin Meng, Yanan Gao, Junzhi Li, Xia Liu, Weicheng Ren, Qiang Pan-Hammarström, Xianhuo Wang, Huilai Zhang","doi":"10.1038/s41375-025-02603-9","DOIUrl":null,"url":null,"abstract":"<p>The 2022 <i>World Health Organization Classification of Haematolymphoid tumours</i> classifies follicular lymphoma grades 1–2 (FL1-2) and grade 3A (FL3A) as classic follicular lymphoma (cFL) and reclassifies grade 3B (FL3B) as follicular large B-cell lymphoma (FLBL), without addressing cases of patients with concurrent FL and diffuse large B-cell lymphoma (FL/DLBCL). However, genetic information on FL histologic grading remains limited, and the latest classification lacks sufficient evidence to resolve whether these subgroups represent single or multiple distinct biological entities. This study analyzed clinical data from 831 patients, whole-exome sequencing (WES) from 149 patients, and transcriptome sequencing from 63 patients to explore differences among FL1-2, FL3A, FL3B, and FL/DLBCL. Clinical analyses revealed two distinct groups: an indolent group (FL1-2 and FL3A) with favorable prognosis and an aggressive group (FL3B and FL/DLBCL) characterized by poor prognosis. Genomics revealed that FL1-2 and FL3A share a common genetic background, whereas FL3B and FL/DLBCL lack mutations in epigenetic regulators CREBBP and KMT2D but exhibit additional copy number variations (CNVs), such as 1p36.32 losses and 3p21.1 gains, which are linked to poor prognosis. Transcriptomics revealed that with increasing histologic grade, immune-related pathway activity decreases, while the activity of metabolic and cell cycle pathways increases, which may be associated with the upregulation of MYC, IRF4, and BATF expression. Together, these findings define FL3B and FL/DLBCL as biologically and clinically distinct B-cell lymphomas, differing from traditional FL. FL1-2 and FL3A differ in their tumor microenvironments rather than genetic profiles.</p>","PeriodicalId":18109,"journal":{"name":"Leukemia","volume":"247 1","pages":""},"PeriodicalIF":12.8000,"publicationDate":"2025-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Leukemia","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1038/s41375-025-02603-9","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"HEMATOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The 2022 World Health Organization Classification of Haematolymphoid tumours classifies follicular lymphoma grades 1–2 (FL1-2) and grade 3A (FL3A) as classic follicular lymphoma (cFL) and reclassifies grade 3B (FL3B) as follicular large B-cell lymphoma (FLBL), without addressing cases of patients with concurrent FL and diffuse large B-cell lymphoma (FL/DLBCL). However, genetic information on FL histologic grading remains limited, and the latest classification lacks sufficient evidence to resolve whether these subgroups represent single or multiple distinct biological entities. This study analyzed clinical data from 831 patients, whole-exome sequencing (WES) from 149 patients, and transcriptome sequencing from 63 patients to explore differences among FL1-2, FL3A, FL3B, and FL/DLBCL. Clinical analyses revealed two distinct groups: an indolent group (FL1-2 and FL3A) with favorable prognosis and an aggressive group (FL3B and FL/DLBCL) characterized by poor prognosis. Genomics revealed that FL1-2 and FL3A share a common genetic background, whereas FL3B and FL/DLBCL lack mutations in epigenetic regulators CREBBP and KMT2D but exhibit additional copy number variations (CNVs), such as 1p36.32 losses and 3p21.1 gains, which are linked to poor prognosis. Transcriptomics revealed that with increasing histologic grade, immune-related pathway activity decreases, while the activity of metabolic and cell cycle pathways increases, which may be associated with the upregulation of MYC, IRF4, and BATF expression. Together, these findings define FL3B and FL/DLBCL as biologically and clinically distinct B-cell lymphomas, differing from traditional FL. FL1-2 and FL3A differ in their tumor microenvironments rather than genetic profiles.

Abstract Image

不同滤泡淋巴瘤组织学分级的分子图谱:基因组和转录组分析的启示
2022年世界卫生组织血淋巴样肿瘤分类将滤泡性淋巴瘤1-2级(FL1-2)和3A级(FL3A)分类为典型滤泡性淋巴瘤(cFL),并将3B级(FL3B)重新分类为滤泡性大b细胞淋巴瘤(FLBL),未涉及并发滤泡性大b细胞淋巴瘤和弥漫性大b细胞淋巴瘤(FL/DLBCL)的病例。然而,关于FL组织学分级的遗传信息仍然有限,最新的分类缺乏足够的证据来解决这些亚群是代表单一还是多个不同的生物实体。本研究分析了831例患者的临床数据,149例患者的全外显子组测序(WES)和63例患者的转录组测序,以探讨FL1-2、FL3A、FL3B和FL/DLBCL之间的差异。临床分析显示两个不同的组:预后良好的惰性组(FL1-2和FL3A)和预后较差的侵袭组(FL3B和FL/DLBCL)。基因组学显示,FL1-2和FL3A具有共同的遗传背景,而FL3B和FL/DLBCL缺乏表观遗传调控因子CREBBP和KMT2D的突变,但表现出额外的拷贝数变异(cnv),如1p36.32的损失和3p21.1的增加,这与预后不良有关。转录组学结果显示,随着组织学分级的增加,免疫相关通路活性降低,而代谢和细胞周期通路活性增加,这可能与MYC、IRF4和BATF表达上调有关。总之,这些发现将FL3B和FL/DLBCL定义为生物学上和临床上不同的b细胞淋巴瘤,与传统的FL不同。FL1-2和FL3A的不同之处在于它们的肿瘤微环境而不是基因谱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Leukemia
Leukemia 医学-血液学
CiteScore
18.10
自引率
3.50%
发文量
270
审稿时长
3-6 weeks
期刊介绍: Title: Leukemia Journal Overview: Publishes high-quality, peer-reviewed research Covers all aspects of research and treatment of leukemia and allied diseases Includes studies of normal hemopoiesis due to comparative relevance Topics of Interest: Oncogenes Growth factors Stem cells Leukemia genomics Cell cycle Signal transduction Molecular targets for therapy And more Content Types: Original research articles Reviews Letters Correspondence Comments elaborating on significant advances and covering topical issues
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信