Blood · 2016
The genetics of nodal marginal zone lymphoma.
СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
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Spina Valeria, Khiabanian Hossein, Messina Monica, Monti Sara, Cascione Luciano, Bruscaggin Alessio, Spaccarotella Elisa, Holmes Antony B, Arcaini Luca, Lucioni Marco, Tabbò Fabrizio, Zairis Sakellarios, Diop Fary, Cerri Michaela, Chiaretti Sabina, Marasca Roberto, Ponzoni Maurilio, Deaglio Silvia, Ramponi Antonio, Tiacci Enrico, Pasqualucci Laura, Paulli Marco, Falini Brunangelo, Inghirami Giorgio, Bertoni Francesco, Foà Robin, Rabadan Raul, Gaidano Gianluca, Rossi Davide
Аннотация
Nodal marginal zone lymphoma (NMZL) is a rare, indolent B-cell tumor that is distinguished from splenic marginal zone lymphoma (SMZL) by the different pattern of dissemination. NMZL still lacks distinct markers and remains orphan of specific cancer gene lesions. By combining whole-exome sequencing, targeted sequencing of tumor-related genes, whole-transcriptome sequencing, and high-resolution single nucleotide polymorphism array analysis, we aimed at disclosing the pathways that are molecularly deregulated in NMZL and we compare the molecular profile of NMZL with that of SMZL. These analyses identified a distinctive pattern of nonsilent somatic lesions in NMZL. In 35 NMZL patients, 41 genes were found recurrently affected in ≥3 (9%) cases, including highly prevalent molecular lesions of MLL2 (also known as KMT2D; 34%), PTPRD (20%), NOTCH2 (20%), and KLF2 (17%). Mutations of PTPRD, a receptor-type protein tyrosine phosphatase regulating cell growth, were enriched in NMZL across mature B-cell tumors, functionally caused the loss of the phosphatase activity of PTPRD, and were associated with cell-cycle transcriptional program deregulation and increased proliferation index in NMZL. Although NMZL shared with SMZL a common mutation profile, NMZL harbored PTPRD lesions that were otherwise absent in SMZL. Collectively, these findings provide new insights into the genetics of NMZL, identify PTPRD lesions as a novel marker for this lymphoma across mature B-cell tumors, and support the distinction of NMZL as an independent clinicopathologic entity within the current lymphoma classification.