Papers

International journal
2006

Epigenetic alterations of BRG1 leads to cancer development through its nuclear-cytoplasmic shuttling abnormalities

Medical Hypotheses
  • Esra Gunduz
  • Mehmet Gunduz
  • Hitoshi Nagatsuka
  • Levent Beder
  • Kadir Demircan
  • Ryo Tamamura
  • Omer Faruk Hatipoglu
  • Naila Mahmut
  • Naoki Katase
  • Yoshio Naomoto
  • Noriyuki Nagai
  • Display all

Volume
67
Number
6
First page
1313
Last page
1316
Language
English
Publishing type
Research paper (scientific journal)
DOI
10.1016/j.mehy.2006.05.032

SWI/SNF is a multiprotein chromatin remodeling complex important for gene regulation. BRG1 and its close relative BRM, have ATPase activity necessary for transcriptional regulation by conformational change of nucleosomes. Due to this role on gene expression, several members of SWI/SNF complex including BRG1 and BRM function as a tumor suppressor or negative regulator of cellular proliferation. On the other hand, the shuttling of proteins between nucleus and cytoplasm is strongly involved in the regulation of cell cycle and proliferation. Many of tumor suppressor gene (TSG)s including p53, BRCA1, ING1 play some of their functions through nucleocytoplasmic shuttling. Abnormalities related with this process abrogate the subcellular localization of the TSGs and lead to cancer development. We recently demonstrated BRG1 as a TSG in oral cancer. Our analysis also revealed an interesting finding that one of the splicing forms of BRG1 is selectively lost in cancer tissue as compared to normal counterparts. Our further analysis revealed a putative nuclear retention signal domain for this splicing form. In this article, we speculate the possible mechanism for the inactivation of BRG1 gene in oral cancer through an abnormality in its subcellular localization. © 2006 Elsevier Ltd. All rights reserved.

Link information
DOI
https://doi.org/10.1016/j.mehy.2006.05.032
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/16824695
Scopus
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33748953340&origin=inward
Scopus Citedby
https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=33748953340&origin=inward
ID information
  • DOI : 10.1016/j.mehy.2006.05.032
  • ISSN : 0306-9877
  • Pubmed ID : 16824695
  • SCOPUS ID : 33748953340

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