• Title of article

    Inhibition of cancer cell growth by cyclin dependent kinase 4 inhibitors synthesized based on the structure of fascaplysin

  • Author/Authors

    Mahale، نويسنده , , Sachin and Aubry، نويسنده , , Carine and Jenkins، نويسنده , , Paul R. and Maréchal، نويسنده , , Jean-Didier and Sutcliffe، نويسنده , , Michael J. and Chaudhuri، نويسنده , , Bhabatosh، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2006
  • Pages
    11
  • From page
    287
  • To page
    297
  • Abstract
    Tryptamine derivatives, a new structural class of cyclin dependent kinase 4 inhibitors, have been identified during extensive biological screening of synthetic molecules. The molecules were synthesized based on the structure of fascaplysin, which is not only a specific inhibitor of the Cdk4-cyclin D1 enzyme but also a relatively toxic molecule, probably because it binds and intercalates DNA. Interestingly, the new structural analogues of fascaplysin do not interact or intercalate with double-stranded DNA, although they inhibit Cdk4-cyclin D1 specifically. We found that compound CA199 was the most potent molecule, showing at least 25-fold specificity towards Cdk4-cyclin D1 (IC50 for Cdk4-cyclin D1 = 20 μM, Cdk2 > 500 μM). CA199 inhibits the growth of different cancer cell lines at concentrations ranging from 10–40 μM. It blocks growth of asynchronous cells at G0/G1 in a retinoblastoma protein (pRb) dependent manner. Moreover, CA199 blocks growth only at early G1 in synchronised cells released from a mimosine-induced G1/S block. These observations are reminiscent of a true Cdk4 inhibitor.
  • Keywords
    G0/G1 arrest , pRb phosphorylation , cell cycle , Cell Proliferation , Cancer chemotherapeutics , cyclin dependent kinases
  • Journal title
    Bioorganic Chemistry: an International Journal
  • Serial Year
    2006
  • Journal title
    Bioorganic Chemistry: an International Journal
  • Record number

    1385865