p16INK4a promoter mutations are frequent in primary sclerosing cholangitis (PSC) and PSC-associated cholangiocarcinoma

Makiko Taniai, Hajime Higuchi, Lawrence J. Burgart, Gregory J. Gores

Research output: Contribution to journalArticlepeer-review

87 Scopus citations


Background and Aims: Primary sclerosing cholangitis (PSC) predisposes individuals to cholangiocarcinoma; however, the molecular mechanisms involved in the carcinogenesis process remain unclear. Because p16INK4a inactivation has been implicated in cholangiocarcinoma, our aims were to examine PSC cholangiocytes for p16INK4a gene mutations. Methods: We studied 4 patient groups: PSC patients without cholangiocarcinoma (n = 10), patients with PSC-associated cholangiocarcinoma (n = 10), non-PSC controls (n = 10), and disease controls with primary biliary cirrhosis (n = 10). Cholangiocytes and hepatocytes were isolated from tissue sections using laser capture microdissection. Genomic DNA was extracted, and the promoter region and the 3 exons for p16INK4a were amplified by PCR and directly sequenced. Results: In the promoter region, 8-point mutations in 5 PSC cases and 14 mutations in 8 cholangiocarcinoma cases were observed. In exon 1, 1 PSC patient and 3 cholangiocarcinoma patients had point mutations. In contrast, no case had a mutation in exon 2 or 3. Mutations were not detected in cholangiocytes from control patients or primary biliary cirrhosis patients nor in hepatocytes from any of the groups; these data indicate that the observed base changes were disease specific and not genetic polymorphisms. Several of the promoter mutations (4 of 8) dramatically decreased promoter activity (<50% reduction in luciferase activity) in a reporter gene assay. Conclusions: The results show that functional point mutations in the p16INK4a promoter region likely contribute to the initiation/progression of cholangiocarcinoma in PSC. Promoter mutations in CpG islands may function as a methylation equivalent phenomenon resulting in gene inactivation.

Original languageEnglish (US)
Pages (from-to)1090-1098
Number of pages9
Issue number4
StatePublished - Oct 1 2002

ASJC Scopus subject areas

  • Hepatology
  • Gastroenterology


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