The genomic landscape of mantle cell lymphoma is related to the epigenetically determined chromatin state of normal B cells

Author:

Zhang Jenny12,Jima Dereje1,Moffitt Andrea B.1,Liu Qingquan1,Czader Magdalena3,Hsi Eric D.4,Fedoriw Yuri5,Dunphy Cherie H.5,Richards Kristy L.5,Gill Javed I.6,Sun Zhen1,Love Cassandra1,Scotland Paula1,Lock Eric7,Levy Shawn8,Hsu David S.12,Dunson David7,Dave Sandeep S.129

Affiliation:

1. Duke Institute for Genome Sciences and Policy, Duke University, Durham, NC;

2. Duke Cancer Institute, Duke University Medical Center, Durham NC;

3. Indiana University, Indianapolis IN;

4. Cleveland Clinic, Cleveland OH;

5. University of North Carolina, Chapel Hill, NC;

6. Baylor University Medical Center, Dallas, TX;

7. Department of Statistical Science, Duke University, Durham, NC;

8. Hudson Alpha Institute for Biotechnology, Huntsville, AL; and

9. Department of Medicine, Duke University, Durham, NC

Abstract

Key Points We identified novel recurrently mutated genes, including WHSC1, RB1, POT1, and SMARCA4, through exome sequencing of 56 cases of MCL. Genetic mutations defining MCL and Burkitt lymphoma were associated with the epigenetically defined chromatin state of their respective B cells of origin.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference48 articles.

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