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Functional studies of the chromosome 3p21.3 candidate tumor suppressor gene BLU/ZMYND10 in nasopharyngeal carcinoma

  1. Author:
    Yau, W. L.
    Lung, H. L.
    Zabarovsky, E. R.
    Lerman, M. I.
    Sham, J. S. T.
    Chua, D. T. T.
    Tsao, S. W.
    Stanbridge, E. J.
    Lung, M. L.
  2. Author Address

    Hong Kong Univ Sci & Technol, Dept Biol, Hong Kong, Hong Kong, Peoples R China. Hong Kong Univ Sci & Technol, Ctr Canc Res, Hong Kong, Hong Kong, Peoples R China. Karolinska Inst, Ctr Microbiol & Tumor Biol, Stockholm, Sweden. Karolinska Inst, Ctr Genom & Bioinformat, Stockholm, Sweden. NCI, Immunobiol Lab, Canc Res Ctr, Frederick, MD 21701 USA. Univ Hong Kong, Dept Clin Oncol, Hong Kong, Hong Kong, Peoples R China. Univ Hong Kong, Dept Anat, Hong Kong, Hong Kong, Peoples R China. Univ Calif Irvine, Dept Microbiol & Mol Genet, Irvine, CA 92717 USA.;Lung, ML, Hong Kong Univ Sci & Technol, Dept Biol, Hong Kong, Hong Kong, Peoples R China.;bomaria@ust.hk
    1. Year: 2006
    2. Date: Dec
  1. Journal: International Journal of Cancer
    1. 119
    2. 12
    3. Pages: 2821-2826
  2. Type of Article: Article
  3. ISSN: 0020-7136
  1. Abstract:

    Chromosome 3p plays an important role in tumorigenesis in many cancers, including nasopharyngeal carcinoma (NPC). We have previously shown chromosome 3p can suppress tumor growth in vivo by using the monochromosome transfer approach, which indicated the chromosome 3p21.3 region was critical for tumor suppression. BLUIZMYND10 is one of the candidate tumor suppressor genes mapping in the 3p21.3 critical region and is a candidate TSG for NPC. By quantitative RT-PCR, it is frequently downregulated in NPC cell lines (83%) and NPC biopsies (80%). However, no functional studies have yet verified the functional role of BLU/ZMYND10 as a tumor suppressor gene. In the current study, a gene inactivation test (GIT) utilizing a tetracycline regulation system was used to study the functional role of BLU/ZMYND10. When BLU/ZMYND10 is expressed in the absence of doxycycline, the stable transfectants were able to induce tumor suppression in nude mice. In contrast, downregulation of BLU/ZMYND10 in these tumor suppressive clones by doxycycline treatment restored the tumor formation ability. This study provides the first significant evidence to demonstrate BLUIZMYNDIO can functionally suppress tumor formation in vivo and is, therefore, likely to be one of the candidate tumor suppressor genes involved in NPC. Published 2006 Wiley-Liss, Inc.

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External Sources

  1. DOI: 10.1002/ijc.22232
  2. WOS: 000242307800013

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