Access

You are not currently logged in.

Access your personal account or get JSTOR access through your library or other institution:

login

Log in to your personal account or through your institution.

If You Use a Screen Reader

This content is available through Read Online (Free) program, which relies on page scans. Since scans are not currently available to screen readers, please contact JSTOR User Support for access. We'll provide a PDF copy for your screen reader.

Induction of Cyclooxygenase-2 in a Mouse Model of Peutz-Jeghers Polyposis

Derrick J. Rossi, Antti Ylikorkala, Nina Korsisaari, Reijo Salovaara, Keijo Luukko, Virpi Launonen, Mark Henkemeyer, Ari Ristimäki, Lauri A. Aaltonen and Tomi P. Mäkelä
Proceedings of the National Academy of Sciences of the United States of America
Vol. 99, No. 19 (Sep. 17, 2002), pp. 12327-12332
Stable URL: http://www.jstor.org/stable/3073214
Page Count: 6
  • Read Online (Free)
  • Subscribe ($19.50)
  • Cite this Item
Since scans are not currently available to screen readers, please contact JSTOR User Support for access. We'll provide a PDF copy for your screen reader.
Induction of Cyclooxygenase-2 in a Mouse Model of Peutz-Jeghers Polyposis
Preview not available

Abstract

Inactivating germ-line mutations of LKB1 lead to Peutz-Jeghers syndrome (PJS). We have generated mice heterozygous for a targeted inactivating allele of Lkb1 and found that they develop severe gastrointestinal polyposis. In all cases, the polyps arising in the Lkb1+/- mice were found to be hamartomas that were histologically indistinguishable from polyps resected from PJS patients, indicating that Lkb1+/- mice model human PJS polyposis. No evidence for inactivation of the remaining wild-type Lkb1 allele in Lkb1+/--associated polyps was observed. Moreover, polyps and other tissues in heterozygote animals exhibited reduced Lkb1 levels and activity, indicating that Lkb1 was haploinsufficient for tumor suppression. Analysis of the molecular mechanisms characterizing Lkb1+/- polyposis revealed that cyclooxygenase-2 (COX-2) was highly up-regulated in murine polyps concomitantly with activation of the extracellular signal-regulated kinases 1 and 2 (Erk1/2). Subsequent examination of a large series of human PJS polyps revealed that COX-2 was also highly up-regulated in the majority of these polyps. These findings thereby identify COX-2 as a potential target for chemoprevention in PJS patients.

Page Thumbnails

  • Thumbnail: Page 
[12327]
    [12327]
  • Thumbnail: Page 
12328
    12328
  • Thumbnail: Page 
12329
    12329
  • Thumbnail: Page 
12330
    12330
  • Thumbnail: Page 
12331
    12331
  • Thumbnail: Page 
12332
    12332