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

      Science (New York, N.Y.)
      Alleles, Amino Acid Sequence, Animals, Base Sequence, Cell Division, Chromosome Mapping, Chromosomes, Human, Pair 18, DNA-Binding Proteins, Gene Deletion, Gene Expression, Genes, Tumor Suppressor, Genetic Markers, Humans, Mice, Molecular Sequence Data, Mutation, Neoplasm Transplantation, Pancreatic Neoplasms, genetics, pathology, Proteins, chemistry, physiology, Signal Transduction, Smad4 Protein, Trans-Activators, Transforming Growth Factor beta, Transplantation, Heterologous, Tumor Cells, Cultured

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          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-beta (TGF-beta)-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.

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