Genetic alterations of the transforming growth factor β receptor genes in pancreatic and biliary adenocarcinomas

Michael Goggins, Manu Shekher, Kenan Turnacioglu, Charles J. Yeo, Ralph H. Hruban, Scott E. Kern

Research output: Contribution to journalArticle

Abstract

Transforming growth factor β (TGF-β) is an extracellular ligand that binds to a heterodimeric receptor, initiating signals that regulate growth, differentiation, and apoptosis. Many cancers, including pancreatic cancer, harbor defects in TGF-β signaling and are resistant to TGF-β-mediated growth suppression. Genetic alterations of DPC4, which encodes a DNA binding protein that is a downstream component of the pathway, most frequently occur in pancreatic and biliary carcinomas. We searched for other targets of mutation of the TGF-β pathway in these cancers. We report somatic alterations of the TGF-β type I receptor gene ALK-5. Homozygous deletions of ALK-5 were identified in 1 of 97 pancreatic and 1 of 12 biliary adenocarcinomas. A germ-line variant of ALK-5, presumably a polymorphism, was identified, but no somatic intragenic mutations were identified upon sequencing of all coding regions of ALK-5. Somatic alterations of the TGF-β type II receptor gene (TGFBR2) were identified in 4 of 97 (4.1%) pancreas cancers, including a homozygous deletion in a replication error-negative cancer and three homozygous frameshift mutations of the poly(A) tract of the TGF-β type II receptor in replication error-positive cancers. We also studied other related type I receptors of the TGF-β superfamily. In a panel of pancreas cancers preselected for loss of heterozygosity at the ALK-1 locus, sequencing of all coding exons of the ALK-1 gene revealed no alterations. No homozygous deletions were detected in the ALK-1, ALK-2, ALK- 3, or ALK-6 genes in a panel of 86 pancreatic cancer xenografts and 11 pancreatic cancer and 22 breast cancer cell lines. The rate of genetic inactivation of TGF-β pathway members was determined in 45 pancreatic cancers. Eighty-two % of these pancreatic cancers had genetic inactivation of the DPC4, p15, ALK-5, or TGFBR2 genes. Our results indicate that the TGF-β type I and type II receptor genes are selective targets of genetic inactivation in pancreatic and biliary cancers.

Original languageEnglish (US)
Pages (from-to)5329-5332
Number of pages4
JournalCancer Research
Volume58
Issue number23
StatePublished - Dec 1 1998

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ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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