BCL2 mutations are associated with increased risk of transformation and shortened survival in follicular lymphoma

Author:

Correia Cristina1,Schneider Paula A.1,Dai Haiming1,Dogan Ahmet2,Maurer Matthew J.3,Church Amy K.4,Novak Anne J.4,Feldman Andrew L.2,Wu Xiaosheng5,Ding Husheng1,Meng X. Wei1,Cerhan James R.6,Slager Susan L.3,Macon William R.2,Habermann Thomas M.4,Karp Judith E.7,Gore Steven D.7,Kay Neil E.4,Jelinek Diane F.45,Witzig Thomas E.4,Nowakowski Grzegorz S.4,Kaufmann Scott H.14

Affiliation:

1. Division of Oncology Research, Department of Oncology,

2. Division of Hematopathology, Department of Laboratory Medicine and Pathology,

3. Division of Biomedical Statistics and Bioinformatics, Department of Health Sciences Research,

4. Division of Hematology, Department of Medicine,

5. Department of Immunology, and

6. Division of Epidemiology, Department of Health Sciences Research, Mayo Clinic, Rochester, MN; and

7. Division of Hematological Malignancies, Sidney Kimmel Cancer Center at Johns Hopkins, Baltimore, MD

Abstract

Key Points BCL2 mutations in FL correlate with activation-induced cytidine deaminase expression and frequently alter the amino acid sequence of the protein. Mutations in the BCL2 coding sequence at diagnosis are associated with shortened time to transformation and earlier death due to lymphoma.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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