Combined copy number and mutation analysis identifies oncogenic pathways associated with transformation of follicular lymphoma

A. Bouska, W. Zhang, Q. Gong, J. Iqbal, A. Scuto, J. Vose, M. Ludvigsen, K. Fu, D. D. Weisenburger, T. C. Greiner, R. D. Gascoyne, A. Rosenwald, G. Ott, E. Campo, Lisa Rimsza, J. Delabie, E. S. Jaffe, R. M. Braziel, J. M. Connors, C. I. WuL. M. Staudt, F. D‘Amore, T. W. McKeithan, W. C. Chan

Research output: Contribution to journalArticle

39 Scopus citations

Abstract

Follicular lymphoma (FL) is typically an indolent disease, but 30–40% of FL cases transform into an aggressive lymphoma (tFL) with a poor prognosis. To identify the genetic changes that drive this transformation, we sequenced the exomes of 12 cases with paired FL and tFL biopsies and identified 45 recurrently mutated genes in the FL–tFL data set and 39 in the tFL cases. We selected 496 genes of potential importance in transformation and sequenced them in 23 additional tFL cases. Integration of the mutation data with copy-number abnormality (CNA) data provided complementary information. We found recurrent mutations of miR-142, which has not been previously been reported to be mutated in FL/tFL. The genes most frequently mutated in tFL included KMT2D (MLL2), CREBBP, EZH2, BCL2 and MEF2B. Many recurrently mutated genes are involved in epigenetic regulation, the Janus-activated kinase–signal transducer and activator of transcription (STAT) or the nuclear factor-κB pathways, immune surveillance and cell cycle regulation or are TFs involved in B-cell development. Of particular interest are mutations and CNAs affecting S1P-activated pathways through S1PR1 or S1PR2, which likely regulate lymphoma cell migration and survival outside of follicles. Our custom gene enrichment panel provides high depth of coverage for the study of clonal evolution or divergence.Leukemia advance online publication, 8 July 2016; doi:10.1038/leu.2016.175.

Original languageEnglish (US)
JournalLeukemia
DOIs
StateAccepted/In press - Jul 8 2016

ASJC Scopus subject areas

  • Medicine(all)
  • Hematology
  • Cancer Research
  • Anesthesiology and Pain Medicine

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    Bouska, A., Zhang, W., Gong, Q., Iqbal, J., Scuto, A., Vose, J., Ludvigsen, M., Fu, K., Weisenburger, D. D., Greiner, T. C., Gascoyne, R. D., Rosenwald, A., Ott, G., Campo, E., Rimsza, L., Delabie, J., Jaffe, E. S., Braziel, R. M., Connors, J. M., ... Chan, W. C. (Accepted/In press). Combined copy number and mutation analysis identifies oncogenic pathways associated with transformation of follicular lymphoma. Leukemia. https://doi.org/10.1038/leu.2016.175