• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

靶向淋巴瘤肿瘤微环境:新兴的生物学见解和治疗策略。

Targeting The Tumor Microenvironment in Lymphomas: Emerging Biological Insights and Therapeutic Strategies.

机构信息

Division of Hematology and Oncology, Lombardi Comprehensive Cancer Center, Georgetown University Hospital, Washington, DC, USA.

出版信息

Curr Oncol Rep. 2022 Sep;24(9):1121-1131. doi: 10.1007/s11912-022-01250-y. Epub 2022 Apr 11.

DOI:10.1007/s11912-022-01250-y
PMID:35403972
Abstract

PURPOSE OF REVIEW

This review aims to discuss recent advances in elucidating the tumor microenvironment (TME) in B lymphomas and resultant novel therapeutic development.

RECENT FINDINGS

While tumor morphology, immunophenotype, and molecular profile are established factors that predict outcome and guide therapy, the prognostic impact of infiltrating, non-tumor cells is now emerging. This is simultaneously facilitating the development of new therapies that target non-tumor cells. The tumor microenvironment (TME) is a complex ecosystem composed of infiltrating cells and byproducts, extracellular matrix, and other non-cellular tissues. In lymphomas, our current understanding of the role of the TME is principally informed by studies in B-cell lineage diseases. As we improve our understanding of lymphoma biology, the importance of the impact of the non-tumor cell microenvironment is becoming more apparent. This lays the foundation for the investigation and development of novel therapies and combination strategies that target non-tumor cells and tumor cell/non-tumor cell interactions.

摘要

目的综述

本文旨在讨论阐明 B 细胞淋巴瘤肿瘤微环境(TME)的最新进展及其带来的新的治疗策略。

最近的发现

虽然肿瘤形态、免疫表型和分子特征是预测预后和指导治疗的既定因素,但浸润性非肿瘤细胞的预后影响现在正在显现。这同时促进了针对非肿瘤细胞的新疗法的发展。肿瘤微环境(TME)是一个由浸润细胞和代谢产物、细胞外基质和其他非细胞组织组成的复杂生态系统。在淋巴瘤中,我们对 TME 作用的理解主要来自于 B 细胞谱系疾病的研究。随着我们对淋巴瘤生物学认识的提高,非肿瘤细胞微环境的影响变得越来越明显。这为研究和开发针对非肿瘤细胞以及肿瘤细胞/非肿瘤细胞相互作用的新型治疗方法和联合策略奠定了基础。

相似文献

1
Targeting The Tumor Microenvironment in Lymphomas: Emerging Biological Insights and Therapeutic Strategies.靶向淋巴瘤肿瘤微环境:新兴的生物学见解和治疗策略。
Curr Oncol Rep. 2022 Sep;24(9):1121-1131. doi: 10.1007/s11912-022-01250-y. Epub 2022 Apr 11.
2
Characterisation of tumour microenvironment and immune checkpoints in primary central nervous system diffuse large B cell lymphomas.原发性中枢神经系统弥漫性大 B 细胞淋巴瘤的肿瘤微环境和免疫检查点特征。
Virchows Arch. 2020 Jun;476(6):891-902. doi: 10.1007/s00428-019-02695-6. Epub 2019 Dec 6.
3
The tumor microenvironment of lymphomas: Insights into the potential role and modes of actions of checkpoint inhibitors.淋巴瘤的肿瘤微环境:检查点抑制剂的潜在作用和作用方式的深入了解。
Hematol Oncol. 2021 Feb;39(1):3-10. doi: 10.1002/hon.2821. Epub 2020 Nov 6.
4
Updates in the role of the tumor microenvironment cellular crosstalk and genetic signatures in diffuse large B-cell lymphoma: a narrative review.肿瘤微环境细胞串扰和弥漫性大 B 细胞淋巴瘤遗传特征的作用更新:叙述性综述。
Chin Clin Oncol. 2024 Jun;13(3):38. doi: 10.21037/cco-23-124. Epub 2024 May 11.
5
Targeting the Immune Microenvironment in Lymphomas of B-Cell Origin: From Biology to Clinical Application.靶向B细胞起源淋巴瘤的免疫微环境:从生物学到临床应用
Cancers (Basel). 2019 Jun 29;11(7):915. doi: 10.3390/cancers11070915.
6
The circuitry of the tumor microenvironment in adult and pediatric Hodgkin lymphoma: cellular composition, cytokine profile, EBV, and exosomes.成人和儿童霍奇金淋巴瘤肿瘤微环境的电路:细胞组成、细胞因子谱、EBV 和外泌体。
Cancer Rep (Hoboken). 2021 Apr;4(2):e1311. doi: 10.1002/cnr2.1311. Epub 2020 Oct 26.
7
Targeting the tumor microenvironment in B-cell lymphoma: challenges and opportunities.靶向 B 细胞淋巴瘤的肿瘤微环境:挑战与机遇。
J Hematol Oncol. 2021 Aug 17;14(1):125. doi: 10.1186/s13045-021-01134-x.
8
The Effect of the Tumor Microenvironment on Lymphoid Neoplasms Derived from B Cells.肿瘤微环境对源自B细胞的淋巴样肿瘤的影响。
Diagnostics (Basel). 2022 Feb 23;12(3):573. doi: 10.3390/diagnostics12030573.
9
Single-Cell Transcriptome Analysis Reveals Disease-Defining T-cell Subsets in the Tumor Microenvironment of Classic Hodgkin Lymphoma.单细胞转录组分析揭示经典霍奇金淋巴瘤肿瘤微环境中的疾病定义性 T 细胞亚群。
Cancer Discov. 2020 Mar;10(3):406-421. doi: 10.1158/2159-8290.CD-19-0680. Epub 2019 Dec 19.
10
[Characterization of the tumor microenvironment by highly multiplexed microscopy].[通过高度多重显微镜对肿瘤微环境进行表征]
Pathologie (Heidelb). 2022 Aug;43(Suppl 1):21-24. doi: 10.1007/s00292-022-01129-6. Epub 2022 Oct 12.

引用本文的文献

1
Efficient 3D imaging and pathological analysis of the human lymphoma tumor microenvironment using light-sheet immunofluorescence microscopy.利用光片免疫荧光显微镜对人淋巴瘤肿瘤微环境进行高效 3D 成像和病理分析。
Theranostics. 2024 Jan 1;14(1):406-419. doi: 10.7150/thno.86221. eCollection 2024.
2
[Bacteriological analysis of nasal secretions in patients with nasal lymphoma].[鼻淋巴瘤患者鼻分泌物的细菌学分析]
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2023 Apr;37(4):247-251. doi: 10.13201/j.issn.2096-7993.2023.04.002.
3
Cuproptosis key gene FDX1 is a prognostic biomarker and associated with immune infiltration in glioma.

本文引用的文献

1
ROBUST: A Phase III Study of Lenalidomide Plus R-CHOP Versus Placebo Plus R-CHOP in Previously Untreated Patients With ABC-Type Diffuse Large B-Cell Lymphoma.ROBUST:来那度胺联合 R-CHOP 与安慰剂联合 R-CHOP 治疗初治 ABC 型弥漫性大 B 细胞淋巴瘤的 III 期研究。
J Clin Oncol. 2021 Apr 20;39(12):1317-1328. doi: 10.1200/JCO.20.01366. Epub 2021 Feb 23.
2
Addition of Lenalidomide to R-CHOP Improves Outcomes in Newly Diagnosed Diffuse Large B-Cell Lymphoma in a Randomized Phase II US Intergroup Study ECOG-ACRIN E1412.在美国一项随机II期组间研究ECOG-ACRIN E1412中,来那度胺添加至R-CHOP方案可改善新诊断弥漫性大B细胞淋巴瘤的预后。
J Clin Oncol. 2021 Apr 20;39(12):1329-1338. doi: 10.1200/JCO.20.01375. Epub 2021 Feb 8.
3
铜死亡关键基因FDX1是一种预后生物标志物,与胶质瘤中的免疫浸润相关。
Front Med (Lausanne). 2022 Nov 29;9:939776. doi: 10.3389/fmed.2022.939776. eCollection 2022.
Tumor interferon signaling and suppressive myeloid cells are associated with CAR T-cell failure in large B-cell lymphoma.
肿瘤干扰素信号和抑制性髓系细胞与大 B 细胞淋巴瘤中嵌合抗原受体 T 细胞治疗失败相关。
Blood. 2021 May 13;137(19):2621-2633. doi: 10.1182/blood.2020007445.
4
Primary Central Nervous System Lymphoma: Evolving Biologic Insights and Recent Therapeutic Advances.原发性中枢神经系统淋巴瘤:不断发展的生物学认识和近期治疗进展。
Clin Lymphoma Myeloma Leuk. 2021 Feb;21(2):73-79. doi: 10.1016/j.clml.2020.10.015. Epub 2020 Oct 30.
5
Tumor and microenvironment response but no cytotoxic T-cell activation in classic Hodgkin lymphoma treated with anti-PD1.经典型霍奇金淋巴瘤接受抗 PD-1 治疗后出现肿瘤和微环境反应,但无细胞毒性 T 细胞激活。
Blood. 2020 Dec 17;136(25):2851-2863. doi: 10.1182/blood.2020008553.
6
PI3Kδ inhibition reshapes follicular lymphoma-immune microenvironment cross talk and unleashes the activity of venetoclax.PI3Kδ 抑制重塑滤泡性淋巴瘤-免疫微环境相互作用并释放 venetoclax 的活性。
Blood Adv. 2020 Sep 8;4(17):4217-4231. doi: 10.1182/bloodadvances.2020001584.
7
Spatial signatures identify immune escape via PD-1 as a defining feature of T-cell/histiocyte-rich large B-cell lymphoma.空间特征将 PD-1 免疫逃逸鉴定为 T 细胞/组织细胞丰富型大 B 细胞淋巴瘤的一个决定性特征。
Blood. 2021 Mar 11;137(10):1353-1364. doi: 10.1182/blood.2020006464.
8
Treatment of Patients with Relapsed or Refractory Mantle-Cell Lymphoma with Zanubrutinib, a Selective Inhibitor of Bruton's Tyrosine Kinase.泽布替尼治疗复发/难治性套细胞淋巴瘤患者的疗效:一种选择性布鲁顿酪氨酸激酶抑制剂。
Clin Cancer Res. 2020 Aug 15;26(16):4216-4224. doi: 10.1158/1078-0432.CCR-19-3703. Epub 2020 May 27.
9
Efficacy of Nivolumab and AVD in Early-Stage Unfavorable Classic Hodgkin Lymphoma: The Randomized Phase 2 German Hodgkin Study Group NIVAHL Trial.纳武利尤单抗联合 AVd 方案治疗早期不良预后经典型霍奇金淋巴瘤的疗效:德国霍奇金研究组 NIVAHL 随机 2 期试验。
JAMA Oncol. 2020 Jun 1;6(6):872-880. doi: 10.1001/jamaoncol.2020.0750.
10
Cathepsin S Alterations Induce a Tumor-Promoting Immune Microenvironment in Follicular Lymphoma.组织蛋白酶 S 的改变诱导滤泡性淋巴瘤中促进肿瘤的免疫微环境。
Cell Rep. 2020 May 5;31(5):107522. doi: 10.1016/j.celrep.2020.107522. Epub 2020 Apr 23.