Expression of pro-apoptotic Bfk isoforms reduces during malignant transformation in the human gastrointestinal tract

FEBS Lett. 2005 Jul 4;579(17):3646-50. doi: 10.1016/j.febslet.2005.05.050.

Abstract

Reduced expression of pro-apoptotic Bcl-2 family proteins has been described in many gastrointestinal cancers, and may play a role in tumourigenesis. The human homologue of the pro-apoptotic Bcl-2 protein, Bfk, is predominantly expressed in tissues of the gastrointestinal tract. In colon, four alternatively spliced isoforms were identified; of which two are pro-apoptotic when overexpressed. In the transition from normal tissue to tumour, pro-apoptotic Bfk isoform expression is substantially reduced in up to 80% of tumours isolated from the human gastrointestinal tract (8/10 colonic tumours and 26/37 of all gastrointestinal tumours) compared to 3/117 tumours from outside the gastrointestinal tract. These data suggest that pro-apoptotic isoforms of Bfk may help to protect against the development of human gastrointestinal malignancy.

MeSH terms

  • Alternative Splicing
  • Amino Acid Sequence
  • Apoptosis
  • Cell Transformation, Neoplastic / genetics
  • Cell Transformation, Neoplastic / metabolism*
  • Cytoplasm / chemistry
  • Down-Regulation*
  • Gastrointestinal Neoplasms / genetics
  • Gastrointestinal Neoplasms / metabolism*
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Molecular Sequence Data
  • Protein Isoforms / analysis
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • Proto-Oncogene Proteins c-bcl-2 / analysis
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Proto-Oncogene Proteins c-bcl-2 / metabolism*
  • RNA, Messenger / analysis
  • RNA, Messenger / metabolism

Substances

  • BCL2L15 protein, human
  • Protein Isoforms
  • Proto-Oncogene Proteins c-bcl-2
  • RNA, Messenger