gneSeqCOO: a novel method for classifying diffuse large B-cell lymphoma cell of origin based on bulk tumor RNA sequencing profiles.

IF 2.2 4区 医学 Q3 HEMATOLOGY
Will Harris, Yi Cao, Franck Morschhauser, Gilles Salles, Yanwen Jiang, Alessia Bottos, Georg Lenz, Christopher R Bolen
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引用次数: 0

Abstract

The cell of origin (COO) classification is an expression-based tumor algorithm identifying molecular subtypes of diffuse large B-cell lymphoma (DLBCL) with distinct prognostic characteristics. Traditional immunohistochemical methods for classifying COO subtypes have poor concordance and limited prognostic value in frontline DLBCL. In contrast, RNA-based metrics like the NanoString Lymphoma Subtyping Test (LST) define more robust subtypes with validated prognostic associations. This study introduces gneSeqCOO, an algorithm using bulk RNA Sequencing (RNASeq) profiles of individual tumor biopsies for COO classification based on a fixed reference. This method produced consistent per-sample results and was robust to variation in RNA quality and sequencing bias. Validation in >1000 DLBCL samples showed high concordance with the NanoString LST assay, even in cohorts containing only one COO subtype. gneSeqCOO presents a robust and versatile alternative to existing assays, potentially reducing the need for additional samples where RNASeq was already generated. The package is available at https://github.com/Genentech/gneSeqCOO.

gneSeqCOO:一种基于肿瘤整体RNA测序谱的弥漫性大b细胞淋巴瘤细胞起源分类的新方法。
起源细胞(COO)分类是一种基于表达的肿瘤算法,可识别具有不同预后特征的弥漫性大b细胞淋巴瘤(DLBCL)的分子亚型。传统的免疫组织化学方法对一线DLBCL的COO亚型分类一致性差,预后价值有限。相比之下,基于rna的指标,如纳米串淋巴瘤亚型测试(LST)定义了更可靠的亚型,并证实了与预后的关联。本研究介绍了gneSeqCOO,这是一种基于固定参考的基于单个肿瘤活检的大量RNA测序(RNASeq)谱进行COO分类的算法。该方法产生了一致的单样本结果,并且对RNA质量和测序偏差的变化具有鲁棒性。在bbbb1000个DLBCL样本中的验证显示,即使在仅包含一种COO亚型的队列中,也与NanoString LST检测结果高度一致。gneSeqCOO提供了一种强大而通用的替代现有检测方法,潜在地减少了对已经生成RNASeq的额外样品的需求。该软件包可在https://github.com/Genentech/gneSeqCOO上获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Leukemia & Lymphoma
Leukemia & Lymphoma 医学-血液学
CiteScore
4.10
自引率
3.80%
发文量
384
审稿时长
1.8 months
期刊介绍: Leukemia & Lymphoma in its fourth decade continues to provide an international forum for publication of high quality clinical, translational, and basic science research, and original observations relating to all aspects of hematological malignancies. The scope ranges from clinical and clinico-pathological investigations to fundamental research in disease biology, mechanisms of action of novel agents, development of combination chemotherapy, pharmacology and pharmacogenomics as well as ethics and epidemiology. Submissions of unique clinical observations or confirmatory studies are considered and published as Letters to the Editor
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