• DocumentCode
    825145
  • Title

    Investigating the Interaction Between Oncogene and Tumor Suppressor Protein

  • Author

    Pirogova, E. ; Akay, M. ; Cosic, I.

  • Author_Institution
    Sch. of Electr. & Comput. Eng., Univ. Melbourne, Melbourne, VIC
  • Volume
    13
  • Issue
    1
  • fYear
    2009
  • Firstpage
    10
  • Lastpage
    15
  • Abstract
    It is known that cancer develops when cells in a part of the body begin to grow out of control. Because cancer cells continue to grow and divide with no order, they never differentiate into the specific tissue, and thus, they are functionally different from normal cells. However, there are some genes that help to prevent cells´ malignant behavior, and therefore, are referred to as tumor suppressor genes. Here, we have investigated the structural and functional relationships of p53, oncogene and interleukin 2 (IL2) proteins using the resonant recognition model (RRM), a physico-mathematical approach based on digital signal processing methods. In addition, using the RRM concepts, we have designed the peptide analoges that would exhibit tumor-suppression-like activity and be used in anticancer vaccine development.
  • Keywords
    cancer; genetics; medical signal processing; molecular biophysics; proteins; tumours; anticancer vaccine development; cancer cells; cell malignancy; digital signal processing method; interleukin 2 proteins; oncogene; p53; peptide analoges; resonant recognition model; tumor suppressor genes; tumor suppressor protein; tumor-suppression-like activity; Characteristic frequency; oncogenic proteins; protein function; signal processing; tumor; Algorithms; Amino Acid Sequence; Amino Acids; Fourier Analysis; Humans; Interleukin-2; Molecular Sequence Data; Oncogene Proteins; Oncogenes; Peptides; Protein Conformation; Protein Interaction Domains and Motifs; Signal Processing, Computer-Assisted; Tumor Suppressor Protein p53;
  • fLanguage
    English
  • Journal_Title
    Information Technology in Biomedicine, IEEE Transactions on
  • Publisher
    ieee
  • ISSN
    1089-7771
  • Type

    jour

  • DOI
    10.1109/TITB.2008.2003338
  • Filename
    4588346