| First Author | Lechpammer M | Year | 2005 |
| Journal | Oncogene | Volume | 24 |
| Issue | 10 | Pages | 1683-8 |
| PubMed ID | 15674336 | Mgi Jnum | J:97212 |
| Mgi Id | MGI:3574739 | Doi | 10.1038/sj.onc.1208375 |
| Citation | Lechpammer M, et al. (2005) Flavopiridol reduces malignant transformation of the esophageal mucosa in p27 knockout mice. Oncogene 24(10):1683-8 |
| abstractText | The cyclin-dependent kinase (cdk) inhibitor p27 preferentially inactivates cdk complexes required for progression through the G1/S transition. Loss of p27 is associated with aggressive behavior in a variety of tumors, including Barrett's associated adenocarcinoma (BAA). We have previously shown that gastroduodenal-esophageal reflux (GDER) together with N-methyl-N-benzylnitrosamine (MBN) induces Barrett's esophagus (BE) and malignant transformation of the esophageal mucosa in mice. This process is enhanced in a p27 null background. Here, we show that chronic flavopiridol administration sharply reduced the prevalence of BE in GDER/MBN-treated p27 knockout mice when compared to animals treated with diluent only (7 vs 26%, P=0.0079). Similarly, flavopiridol reduced the prevalence of BAA (11 vs 32%, P=0.0098) and overall cancer prevalence (15 vs 60%, P<0.0001). In addition, appropriate molecular targeting by flavopiridol in tumor cells was confirmed by downregulation of cyclin D1, a known target of this pan-cdk inhibitor. The results of this study represent the experimental basis for chemoprevention with cdk inhibitors in human BE and BAA. |
