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Preneoplastic somatic mutations including MYD88 L265P in lymphoplasmacytic lymphoma.

Sara RodriguezJon CelayIbai GoicoecheaCristina JiménezCirino BottaMaria-José Garcia-BarchinoJuan-José GarcésMarta LarrayozSusana SantosDiego AlignaniAmaia Vilas-ZornozaCristina PerezSonia GarateSarai SarvideAitziber LopezHans-Christian ReinhardtYolanda R CarrascoIsidro Sanchez-GarciaMaria-Jose LarrayozMaría-José CalasanzCarlos PanizoFelipe ProsperJosé María Lamo-EspinosaMarina MottaAlessandra TucciAntonio SaccoMassimo GentileSara DuarteHelena VitoriaCatarina GeraldesArtur PaivaNoemi PuigMiriam SanteroAldo M RoccaroGema FuerteJesús San F MiguelJose-Angel Martinez-ClimentJuan José Lahuerta
Published in: Science advances (2022)
Normal cell counterparts of solid and myeloid tumors accumulate mutations years before disease onset; whether this occurs in B lymphocytes before lymphoma remains uncertain. We sequenced multiple stages of the B lineage in elderly individuals and patients with lymphoplasmacytic lymphoma, a singular disease for studying lymphomagenesis because of the high prevalence of mutated MYD88 . We observed similar accumulation of random mutations in B lineages from both cohorts and unexpectedly found MYD88 L265P in normal precursor and mature B lymphocytes from patients with lymphoma. We uncovered genetic and transcriptional pathways driving malignant transformation and leveraged these to model lymphoplasmacytic lymphoma in mice, based on mutated MYD88 in B cell precursors and BCL2 overexpression. Thus, MYD88 L265P is a preneoplastic event, which challenges the current understanding of lymphomagenesis and may have implications for early detection of B cell lymphomas.
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