Circular RNA signature of aggressive CLL with t(14;19)(q32;q13). An ERIC study

IF 40.4 1区 医学 Q1 HEMATOLOGY
Eleonora Roncaglia, Enrico Gaffo, Giulia Calabretto, Moritz Fürstenau, Kerry A. Rogers, Panagiotis Baliakas, Chenghua Cui, Cecelia Miller, Claudia Haferlach, Karla Plevova, David Oscier, Zadie Davis, Florence Nguyen-Khac, Gian Matteo Rigolin, Anastasia Athanasiadou, Fanny Baran-Marszak, Alberto Valiente, Maria José Terol, Pau Abrisqueta, Blanca Espinet, Anna Puiggros, Annalisa Martines, Laura Bonaldi, Francesca Romana Mauro, Lydia Scarfò, Thomas Chatzikonstantinou, Eugen Tausch, Karl-Anton Kreuzer, Arnon Kater, Francesc Bosch, Michael Doubek, Panagiotis Panagiotidis, Olga Kalashnikova, Federica Frezzato, Valeria Ruocco, Silvia Orsi, Kimia Salek, Roberto Merlo, Alberto Caregari, Ilias Glogovitis, Alessandro Cellini, Francesco Angotzi, Andrea Serafin, Shuhua Yi, Barbara Eichhorst, Jennifer A. Woyach, Antonio Cuneo, Paolo Ghia, Kostas Stamatopoulos, Livio Trentin, Andrea Visentin, Stefania Bortoluzzi
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引用次数: 0

Abstract

In Chronic Lymphocytic Leukemia (CLL), t(14;19)(q32;q13), leading to the overexpression of BCL3, is found in ∼1% of cases and is associated with an aggressive disease. In this study, leveraging a large CLL patient cohort collected thanks to an international collaboration, we investigate for the first time the circular transcriptome (circRNAome) associated with the rare t(14;19), in comparison with CLL without t(14;19) and B cells of age-matched healthy donors. We described the circRNAs commonly dysregulated in CLL, including circCSNK1G3 and circEXOC6B(3–5), which were depleted, and circZNF609 and circLPAR3, which were overexpressed in malignant cells. Of importance, we disclosed the circRNA signature of CLL with t(14;19), formed by circRNAs with expression significantly altered specifically in link with this lesion, ectopically expressed like circCDK14(3–4), circCORO1C, circCLEC2D, and circEMB, or downregulated like circCEP70(3–6). Several of these molecules were previously shown to be dysregulated or play a role in cancer, whereas most of the signature circRNAs deserve further investigation. CLL patients with high circCORO1C and circCLEC2D expression had significantly worse clinical outcomes, with shorter time to first treatment and overall survival. This study disclosed new molecular features of the aggressive CLL subtype with t(14;19).
t侵袭性CLL的环状RNA特征(14;19)(q32;q13)。ERIC研究
在慢性淋巴细胞白血病(CLL)中,t(14;19)(q32;q13)导致BCL3过表达,在约1%的病例中发现,并与侵袭性疾病相关。在这项研究中,利用国际合作收集的大量CLL患者队列,我们首次研究了与罕见t(14;19)相关的环状转录组(circRNAome),与无t的CLL(14;19)和年龄匹配的健康供者的B细胞进行比较。我们描述了在CLL中通常失调的circRNAs,包括circCSNK1G3和circEXOC6B(3-5),它们被耗尽,以及circZNF609和circLPAR3,它们在恶性细胞中过表达。重要的是,我们揭示了CLL的circRNA特征(14;19),由与该病变相关的表达显著改变的circRNA形成,如circCDK14(3-4), circccoro1c, circcec2d和circEMB,或下调如circCEP70(3-6)。这些分子中的一些先前被证明是失调的或在癌症中发挥作用,而大多数特征环状rna值得进一步研究。circCORO1C和circec2d高表达的CLL患者临床预后明显差,首次治疗时间短,总生存期短。这项研究揭示了带有t的侵袭性CLL亚型新的分子特征(14;19)。
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来源期刊
CiteScore
48.10
自引率
2.10%
发文量
169
审稿时长
6-12 weeks
期刊介绍: The Journal of Hematology & Oncology, an open-access journal, publishes high-quality research covering all aspects of hematology and oncology, including reviews and research highlights on "hot topics" by leading experts. Given the close relationship and rapid evolution of hematology and oncology, the journal aims to meet the demand for a dedicated platform for publishing discoveries from both fields. It serves as an international platform for sharing laboratory and clinical findings among laboratory scientists, physician scientists, hematologists, and oncologists in an open-access format. With a rapid turnaround time from submission to publication, the journal facilitates real-time sharing of knowledge and new successes.
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