The major subtypes of human B-cell lymphomas lack mutations in BCL-2 family member BAD

Int J Cancer. 2006 Oct 1;119(7):1738-40. doi: 10.1002/ijc.22010.

Abstract

Members of the BCL-2 gene family are well known for their role in the pathogenesis of B-cell lymphomas in humans and in mouse models. A recent report that knockout mice deficient for the proapoptotic BCL-2 family member gene BAD frequently develop B-cell lymphomas prompted us to analyze a large collection of human B-cell lymphomas for inactivating mutations in the BAD gene. All 3 exons of the BAD gene were amplified and directly sequenced. The 81 lymphomas analyzed included 16 cases of B-cell chronic lymphocytic leukemia, 11 mantle-cell lymphomas, 10 follicular lymphomas, 7 MALT lymphomas, 8 Burkitt's lymphoma cell lines, 3 cell lines of multiple myeloma, 15 cases and 4 cell lines of diffuse large B-cell lymphoma and 7 Hodgkin's lymphoma lines. No mutations were found in any of the cases. We conclude that mutations in the BAD gene do not play a role in the pathogenesis of the major subtypes of human B-cell lymphomas.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Humans
  • Lymphoma, B-Cell / classification*
  • Lymphoma, B-Cell / genetics*
  • Lymphoma, B-Cell / pathology
  • Mutation / genetics
  • bcl-Associated Death Protein / genetics*

Substances

  • bcl-Associated Death Protein