Leukemia Research
Volume 30, Issue 4 , Pages 449-457, April 2006

Four human t(11;14)(q13;q32)-containing cell lines having classic and variant features of Mantle Cell Lymphoma

  • Catherine A. Tucker

      Affiliations

    • The Department of Advanced Therapeutics, BC Cancer Research Center, 675 West 10th Avenue, 5th Floor, Vancouver, BC, Canada
    • The Department of Pathology and Laboratory Medicine at the University of British Columbia, Vancouver, BC, Canada
    • Corresponding Author InformationCorresponding author. Tel.: +1 604 675 8000/7025; fax: +1 604 675 8183.
  • ,
  • Gwyn Bebb

      Affiliations

    • The Department of Advanced Therapeutics, BC Cancer Research Center, 675 West 10th Avenue, 5th Floor, Vancouver, BC, Canada
    • Divisions of Medical Oncology and Pathology, British Columbia Cancer Agency, Vancouver, BC, Canada
  • ,
  • Richard J. Klasa

      Affiliations

    • Divisions of Medical Oncology and Pathology, British Columbia Cancer Agency, Vancouver, BC, Canada
  • ,
  • Mukesh Chhanabhai

      Affiliations

    • Divisions of Medical Oncology and Pathology, British Columbia Cancer Agency, Vancouver, BC, Canada
  • ,
  • Valia Lestou

      Affiliations

    • Divisions of Medical Oncology and Pathology, British Columbia Cancer Agency, Vancouver, BC, Canada
  • ,
  • Douglas E. Horsman

      Affiliations

    • Divisions of Medical Oncology and Pathology, British Columbia Cancer Agency, Vancouver, BC, Canada
  • ,
  • Randy D. Gascoyne

      Affiliations

    • Divisions of Medical Oncology and Pathology, British Columbia Cancer Agency, Vancouver, BC, Canada
  • ,
  • Adrian Wiestner

      Affiliations

    • Metabolism Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD, USA
  • ,
  • Dana Masin

      Affiliations

    • The Department of Advanced Therapeutics, BC Cancer Research Center, 675 West 10th Avenue, 5th Floor, Vancouver, BC, Canada
  • ,
  • Marcel Bally

      Affiliations

    • The Department of Advanced Therapeutics, BC Cancer Research Center, 675 West 10th Avenue, 5th Floor, Vancouver, BC, Canada
    • The Department of Pathology and Laboratory Medicine at the University of British Columbia, Vancouver, BC, Canada
  • ,
  • Michael E. Williams

      Affiliations

    • Hematology/Oncology Division and Hematologic Malignancy Program, University of Virginia Cancer Center and School of Medicine, Charlottesville, VA, USA

Received 21 April 2005; received in revised form 11 August 2005; accepted 12 August 2005. published online 07 March 2011.

Abstract 

The objectives of this study were foremost to further characterize pre-existing cell lines containing the t(11;14)(q13;q32) translocation. This translocation along with cyclin D1 overexpression is characteristic of Mantle Cell Lymphoma (MCL), an aggressive B cell neoplasm. Considerable variation in the abundance of cyclin D1 expression was observed. mRNA levels were examined by RT-PCR as differences in cyclin D1 mRNA abundance have been shown to synergize with INK4A/Arf deletions to dictate proliferation rate and survival in MCL patient samples. In this study, the cell lines, Z-138 and HBL-2, which exhibited the fastest growth rates and the shortest survival times in Rag2-M mice, had high expression of either one or both cyclin D1 mRNA isoforms and had negligible expression of p16. On the other hand, NCEB-1 and JVM-2 had low expression of both mRNA isoforms, retained p16 expression, and had slower growth rates and exhibited longer survival times in Rag2-M mice. Furthermore, JVM-2, which was found to have the lowest expression of cyclin D1, was the only cell line that expressed cyclin D2. The results of the characterization of Z-138, HBL-2, NCEB-1 and JVM-2 reveal that this group of cell lines represents both classic and variant features of MCL.

Keywords: MCL, Cell line, Cyclin D1, p16, mRNA isoforms

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PII: S0145-2126(05)00323-1

doi:10.1016/j.leukres.2005.08.016

Leukemia Research
Volume 30, Issue 4 , Pages 449-457, April 2006