作者
Sı́lvia Beà,Rafael Valdés‐Mas,Alba Navarro,Itziar Salaverría,David Martin‐García,Pedro Jares,Eva Giné,Magda Pinyol,Cristina Royo,Ferran Nadeu,Laura Conde,Manel Juan,Guillem Clot,Pedro Vizán,Luciano Di Croce,Diana Puente,Mònica López‐Guerra,Alexandra Moros,Gaël Roué,Marta Aymerich,Neus Villamor,Luís Colomo,Antonio Martı́nez,Alexandra Valera,José I. Martín‐Subero,Virginia Amador,Luís Hernández,Marı́a Rozman,Anna Enjuanes,Pilar Forcada,Ana Muntañola,Elena Hartmann,Marı́a José Calasanz,Andreas Rosenwald,German Ott,Jesús María Hernández‐Rivas,Wolfram Klapper,Reiner Siebert,Adrian Wiestner,Wyndham H. Wilson,Dolors Colomer,Armando López‐Guillermo,Carlos López‐Otín,Xosé S. Puente,Elı́as Campo
摘要
Significance This is a comprehensive whole-genome/whole-exome analysis of mantle cell lymphoma (MCL). We sequenced 29 MCL cases and validated the findings by target sequencing of 172 additional tumors. We identified recurrent mutations in genes regulating chromatin modification and genes such as NOTCH2 that have a major impact on clinical outcome. Additionally, we demonstrated the subclonal heterogeneity of the tumors already at diagnosis and the modulation of the mutational architecture in the progression of the disease. The identification of new molecular mechanisms may open perspectives for the management of MCL patients.