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在基因分类时代,MYC/BCL2双表达在弥漫性大B细胞淋巴瘤中的预后意义。

The prognostic significance of MYC/BCL2 double expression in DLBCL in the genetic classification era.

作者信息

Wu Yi-Fan, Yuan Qun-Hui, Shen Hao-Rui, Du Kai-Xin, Shang Chun-Yu, Li Yue, Zhang Xin-Yu, Wu Jia-Zhu, Gao Rui, Wang Li, Li Jian-Yong, Yin Hua, Liang Jin-Hua, Xu Wei

机构信息

Department of Hematology, The First Affiliated Hospital of Nanjing Medical University, Jiangsu Province Hospital, Nanjing, China.

Department of Endocrinology, The First Affiliated Hospital of Nanjing Medical University, Jiangsu Province Hospital, Nanjing, China.

出版信息

Cancer Sci. 2025 Jan;116(1):257-270. doi: 10.1111/cas.16377. Epub 2024 Nov 4.

DOI:10.1111/cas.16377
PMID:39492801
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11711038/
Abstract

Double expression (DE) is a World Health Organization-recognized adverse prognostic factor in diffuse large B-cell lymphoma (DLBCL). However, the prognostic value of DE in the genetic subtyping era and potential mechanisms remain to be explored. We enrolled 246 DLBCL patients diagnosed between December 2021 and September 2023 in a Jiangsu Province Hospital cohort and included 930 DLBCL patients from three published studies in an external cohort. Double-expression DLBCL (DEL) in the external cohort was mainly distributed in the OTHER subtype (42.0%), EZB subtype (28.3%), and MCD subtype (15.0%), whereas the MCD subtype exhibited the highest ratio of DEL. DEL was significantly related to unfavorable overall survival (OS) and progression-free survival (PFS) in DLBCL, but only in EZB and OTHER subtypes that DEL retained remarkably adverse impacts on survivals compared to non-DEL. We explored the prognostic value of clinical and genetic parameters in DEL patients and found only ST2 showed better OS than A53 in DEL patients, whereas the other subtypes showed no significant difference. DEL showed similarities with the MCD subtype in mutation profiles. Furthermore, RNA-sequencing analyses exhibited upregulation in tumor proliferation-related pathways in DEL patients, but downregulation in extracellular matrix organization, T-cell activation and proliferation, type II interferon production, and pathways associated with cell death might contribute to the poor outcomes of DEL patients.

摘要

双表达(DE)是世界卫生组织认可的弥漫性大B细胞淋巴瘤(DLBCL)的不良预后因素。然而,在基因亚型分类时代DE的预后价值及潜在机制仍有待探索。我们纳入了江苏省某医院队列中2021年12月至2023年9月期间诊断的246例DLBCL患者,并将来自三项已发表研究的930例DLBCL患者纳入外部队列。外部队列中的双表达DLBCL(DEL)主要分布在OTHER亚型(42.0%)、EZB亚型(28.3%)和MCD亚型(15.0%),而MCD亚型中DEL的比例最高。DEL与DLBCL患者不良的总生存期(OS)和无进展生存期(PFS)显著相关,但仅在EZB和OTHER亚型中,与非DEL相比,DEL对生存期仍有显著不利影响。我们探讨了DEL患者临床和基因参数的预后价值,发现仅在DEL患者中,ST2的OS优于A53,而其他亚型无显著差异。DEL在突变谱方面与MCD亚型相似。此外,RNA测序分析显示DEL患者肿瘤增殖相关通路上调,但细胞外基质组织、T细胞活化和增殖、II型干扰素产生以及与细胞死亡相关的通路下调,这可能是DEL患者预后不良的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ce3/11711038/f36ce8aa1197/CAS-116-257-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ce3/11711038/f32b74623bbc/CAS-116-257-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ce3/11711038/25fdb392aef2/CAS-116-257-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ce3/11711038/5876842dd2c1/CAS-116-257-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ce3/11711038/4940d8f860cf/CAS-116-257-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ce3/11711038/f36ce8aa1197/CAS-116-257-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ce3/11711038/f32b74623bbc/CAS-116-257-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ce3/11711038/25fdb392aef2/CAS-116-257-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ce3/11711038/5876842dd2c1/CAS-116-257-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ce3/11711038/4940d8f860cf/CAS-116-257-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ce3/11711038/f36ce8aa1197/CAS-116-257-g003.jpg

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