Expression of cyclin D1 in mouse B cell lymphomas of different histologic types and differentiation stages

Leuk Res. 1998 May;22(5):395-404. doi: 10.1016/s0145-2126(97)00189-6.

Abstract

The G1 cyclin, cyclin D1, has been implicated in the development of human and mouse tumors. Here we describe immunohistochemical analyses of cyclin D1 for a large panel of mouse B cell tumors. In addition, we characterize cyclin D1 expression in a series of cultured cell lines that represent transformed B cells at different stages of development. Immunohistochemical analysis showed that for low-grade lymphomas, cyclin D1 was expressed by 83% of centroblastic centrocytic (CBCC) and 14% of small lymphocytic lymphomas (SLL). For high-grade tumors, 28% of B lymphoblastic and 23% of centroblastic tumors expressed cyclin D1, while all immunoblastic lymphomas were negative. Studies of RNA and protein prepared from cultured B lineage tumors showed that cyclin D1 was expressed by all pre-B and most B cell tumors but not by cell lines representative of late B cell differentiation or by plasma cells. Expression of cyclin D1 in the lymphomas was not associated with alterations in the genomic structure of the Fis-1 (Bcl-1) common proviral integration site or cyclin D1 itself or with cell growth activity as assessed by expression of proliferating cell nuclear antigen (PCNA).

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Carrier Proteins / genetics
  • Cell Differentiation
  • Cyclin D1 / genetics*
  • DNA / analysis
  • Factor For Inversion Stimulation Protein
  • Gene Expression
  • Genes, myc / genetics
  • Immunohistochemistry
  • Integration Host Factors
  • Lymphoma, B-Cell / chemistry
  • Lymphoma, B-Cell / genetics*
  • Lymphoma, B-Cell / pathology
  • Lymphoma, T-Cell / genetics
  • Mice
  • Nucleic Acid Hybridization
  • Proliferating Cell Nuclear Antigen / biosynthesis
  • RNA, Messenger / analysis
  • Tumor Cells, Cultured

Substances

  • Carrier Proteins
  • Factor For Inversion Stimulation Protein
  • Integration Host Factors
  • Proliferating Cell Nuclear Antigen
  • RNA, Messenger
  • Cyclin D1
  • DNA