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

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RONCAGLIA Eleonora GAFFO Enrico CALABRETTO Giulia FUERSTENAU Moritz ROGERS Kerry A BALIAKAS Panagiotis CUI Chenghua MILLER Cecelia HAFERLACH Claudia PLEVOVÁ Karla OSCIER David DAVIS Zadie NGUYEN-KHAC Florence RIGOLIN Gian Matteo ATHANASIADOU Anastasia BARAN-MARSZAK Fanny VALIENTE Alberto TEROL Maria Jose ABRISQUETA Pau ESPINET Blanca PUIGGROS Anna MARTINES Annalisa BONALDI Laura MAURO Francesca Romana SCARFO Lydia CHATZIKONSTANTINOU Thomas TAUSCH Eugen KREUZER Karl-Anton KATER Arnon BOSCH Francesc DOUBEK Michael PANAGIOTIDIS Panagiotis KALASHNIKOVA Olga FREZZATO Federica RUOCCO Valeria ORSI Silvia SALEK Kimia MERLO Roberto CAREGARI Alberto GLOGOVITIS Ilias CELLINI Alessandro ANGOTZI Francesco SERAFIN Andrea YI Shuhua EICHHORST Barbara WOYACH Jennifer A CUNEO Antonio GHIA Paolo STAMATOPOULOS Kostas TRENTIN Livio VISENTIN Andrea BORTOLUZZI Stefania

Rok publikování 2025
Druh Článek v odborném periodiku
Časopis / Zdroj JOURNAL OF HEMATOLOGY & ONCOLOGY
Fakulta / Pracoviště MU

Lékařská fakulta

Citace
www https://jhoonline.biomedcentral.com/articles/10.1186/s13045-025-01725-y
Doi https://doi.org/10.1186/s13045-025-01725-y
Klíčová slova CLL; T(14;19); Circular RNA; BCL3
Popis In Chronic Lymphocytic Leukemia (CLL), t(14;19)(q32;q13), leading to the overexpression of BCL3, is found in similar to 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).

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