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DOI 10.1038/s41591-022-01927-8

Медицинская библиотека · Nature medicine · 2022

Detection of early seeding of Richter transformation in chronic lymphocytic leukemia.

Nadeu Ferran, Royo Romina, Massoni-Badosa Ramon, Playa-Albinyana Heribert, Garcia-Torre Beatriz, Duran-Ferrer Martí, Dawson Kevin J, Kulis Marta, Diaz-Navarro Ander, Villamor Neus, Melero Juan L, Chapaprieta Vicente, Dueso-Barroso Ana, Delgado Julio, Moia Riccardo, Ruiz-Gil Sara, Marchese Domenica, Giró Ariadna, Verdaguer-Dot Núria, Romo Mónica, Clot Guillem, Rozman Maria, Frigola Gerard, Rivas-Delgado Alfredo, Baumann Tycho, Alcoceba Miguel, González Marcos, Climent Fina, Abrisqueta Pau, Castellví Josep, Bosch Francesc, Aymerich Marta, Enjuanes Anna, Ruiz-Gaspà Sílvia, López-Guillermo Armando, Jares Pedro, Beà Sílvia, Capella-Gutierrez Salvador, Gelpí Josep Ll, López-Bigas Núria, Torrents David, Campbell Peter J, Gut Ivo, Rossi Davide, Gaidano Gianluca, Puente Xose S, Garcia-Roves Pablo M, Colomer Dolors, Heyn Holger, Maura Francesco, Martín-Subero José I, Campo Elías

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Аннотация

Richter transformation (RT) is a paradigmatic evolution of chronic lymphocytic leukemia (CLL) into a very aggressive large B cell lymphoma conferring a dismal prognosis. The mechanisms driving RT remain largely unknown. We characterized the whole genome, epigenome and transcriptome, combined with single-cell DNA/RNA-sequencing analyses and functional experiments, of 19 cases of CLL developing RT. Studying 54 longitudinal samples covering up to 19 years of disease course, we uncovered minute subclones carrying genomic, immunogenetic and transcriptomic features of RT cells already at CLL diagnosis, which were dormant for up to 19 years before transformation. We also identified new driver alterations, discovered a new mutational signature (SBS-RT), recognized an oxidative phosphorylation (OXPHOS)high-B cell receptor (BCR)low-signaling transcriptional axis in RT and showed that OXPHOS inhibition reduces the proliferation of RT cells. These findings demonstrate the early seeding of subclones driving advanced stages of cancer evolution and uncover potential therapeutic targets for RT.

Для цитирования: Nadeu Ferran, Royo Romina, Massoni-Badosa Ramon, Playa-Albinyana Heribert, Garcia-Torre Beatriz, Duran-Ferrer Martí, Dawson Kevin J, Kulis Marta, Diaz-Navarro Ander, Villamor Neus, Melero Juan L, Chapaprieta Vicente, Dueso-Barroso Ana, Delgado Julio, Moia Riccardo, Ruiz-Gil Sara, Marchese Domenica, Giró Ariadna, Verdaguer-Dot Núria, Romo Mónica, Clot Guillem, Rozman Maria, Frigola Gerard, Rivas-Delgado Alfredo, Baumann Tycho, Alcoceba Miguel, González Marcos, Climent Fina, Abrisqueta Pau, Castellví Josep, Bosch Francesc, Aymerich Marta, Enjuanes Anna, Ruiz-Gaspà Sílvia, López-Guillermo Armando, Jares Pedro, Beà Sílvia, Capella-Gutierrez Salvador, Gelpí Josep Ll, López-Bigas Núria, Torrents David, Campbell Peter J, Gut Ivo, Rossi Davide, Gaidano Gianluca, Puente Xose S, Garcia-Roves Pablo M, Colomer Dolors, Heyn Holger, Maura Francesco, Martín-Subero José I, Campo Elías. Detection of early seeding of Richter transformation in chronic lymphocytic leukemia.. Nature medicine. 2022. DOI: 10.1038/s41591-022-01927-8.

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