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DPC4, a candidate tumor suppressor gene at human chromosome 18q21.1

  • Stephan A. Hahn
  • , Mieke Schutte
  • , A. T.M. Shamsul Hoque
  • , Christopher A. Moskaluk
  • , Luis T. Da Costa
  • , Ester Rozenblum
  • , Craig L. Weinstein
  • , Aryeh Fischer
  • , Charles J. Yeo
  • , Ralph H. Hruban
  • , Scott E. Kern

Research output: Contribution to journalArticlepeer-review

2270 Scopus citations

Abstract

About 90 percent of human pancreatic carcinomas show allelic loss at chromosome 18q. To identify candidate tumor suppressor genes on 18q, a panel of pancreatic carcinomas were analyzed for convergent sites of homozygous deletion. Twenty-five of 84 tumors had homozygous deletions at 18q21.1, a site that excludes DCC (a candidate suppressor gene for colorectal cancer) and includes DPC4, a gene similar in sequence to a Drosophila melanogaster gene (Mad) implicated in a transforming growth factor-β (TGF-β)-like signaling pathway. Potentially inactivating mutations in DPC4 were identified in six of 27 pancreatic carcinomas that did not have homozygous deletions at 18q21.1. These results identify DPC4 as a candidate tumor suppressor gene whose inactivation may play a role in pancreatic and possibly other human cancers.

Original languageEnglish
Pages (from-to)350-353
Number of pages4
JournalScience
Volume271
Issue number5247
DOIs
StatePublished - 19 Jan 1996

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