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Blocking the hedgehog pathway inhibits hepatoblastoma growth
Author(s) -
Eichenmüller Melanie,
Gruner Ivonne,
Hagl Beate,
Häberle Beate,
MüllerHöcker Josef,
von Schweinitz Dietrich,
Kappler Roland
Publication year - 2009
Publication title -
hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.488
H-Index - 361
eISSN - 1527-3350
pISSN - 0270-9139
DOI - 10.1002/hep.22649
Subject(s) - hepatoblastoma , hedgehog , blocking (statistics) , hedgehog signaling pathway , medicine , cancer research , microbiology and biotechnology , biology , computer science , signal transduction , computer network
Recent evidence has indicated that Hedgehog (Hh) signaling significantly contributes to liver development and regeneration and that activation of the pathway may contribute to growth of hepatocellular carcinoma (HCC) in adults. However, the role of Hh signaling in pediatric liver tumors remains to be elucidated. In this study, we show that Hh signaling is activated in hepatoblastoma (HB), the most common liver tumor in childhood, with most occurrences before the age of 3 years. The Hh target genes glioma‐associated oncogene homolog 1 ( GLI1 ) and Patched ( PTCH1 ) showed increased transcript levels in 65% and 30% of HB samples, respectively, compared with normal liver tissues. Most interestingly, the gene encoding the hedgehog interacting protein ( HHIP ) is transcriptionally silenced by cytosine‐phospho‐guanosine (CpG) island promoter hypermethylation in 26% of HB cases and treatment with the DNA‐demethylating agent 5‐aza‐2′‐deoxycytidine partially restored HHIP expression. Blocking Hh signaling with the antagonist cyclopamine had a strong inhibitory effect on cell proliferation of HB cell lines with an activated pathway. We further demonstrate that this decrease in cell viability is caused by a massive induction of apoptosis, as shown by morphological changes and phosphatidylserine membrane asymmetry. In cyclopamine‐exposed HB cells, caspase 3 and poly(adenosine diphosphate‐ribose) polymerase proteins were specifically activated by their proteolytic cleavage. Conclusion: This study demonstrates, for the first time, the frequent occurrence of GLI1 and PTCH1 overexpression and HHIP promoter methylation in early childhood HB, thus indicating a key role for Hh signaling activation in the malignant transformation of embryonal liver cells. (H EPATOLOGY 2009;49:482–490.)