Mutations and elevated transcriptional activity of conductin (AXIN2) in hepatoblastomas

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Item Type:	Article
Title:	Mutations and elevated transcriptional activity of conductin (AXIN2) in hepatoblastomas
Creators Name:	Koch, A., Weber, N., Waha, A., Hartmann, W., Denkhaus, D., Behrens, J., Birchmeier, W., von Schweinitz, D. and Pietsch, T.
Abstract:	Hepatoblastoma (HB) is the most frequent malignant liver tumour of childhood. Most HBs develop sporadically but their incidence is highly elevated in patients with familial adenomatous polyposis coli (FAP). These patients carry germline mutations in the adenomatous polyposis coli (APC) tumour suppressor gene. APC forms a multi-protein complex involved in the WNT signalling pathway that controls the stability of β -catenin, the central effector in this cascade. Whereas APC mutations are rare in sporadic HBs, a high frequency of β-catenin mutations leading to overactivation of WNT signalling was previously found in these tumours. This pathway is negatively controlled by conductin (axin2), representing a further partner in this signalling complex. To investigate whether alterations in conductin may also be involved in the pathogenesis of sporadic HBs, 37 HBs and five HB cell lines were screened for mutations using single-strand conformation polymorphism (SSCP) analysis, reverse transcription-polymerase chain reaction (RT-PCR), and direct sequencing. In two cases, larger deletions (52 and 1624 bp) leading to frameshifts were found. In addition, one HB carried a somatic point mutation. Expression analysis by competitive RT-PCR in HBs revealed up-regulation of conductin mRNA compared with adjacent liver samples. This mRNA overexpression resulted in increased conductin protein levels demonstrated by western blot analysis. Tumours with activating β-catenin mutations revealed higher levels of conductin mRNA transcripts. This finding indicates that conductin is a direct target gene of WNT signalling in HBs, as has been demonstrated in other tissues. In summary, conductin mutations may represent an alternative mechanism leading to activation of WNT signalling in HBs. The overexpression of conductin mRNA in HBs reflects activation of the WNT pathway because conductin represents a target gene of WNT signalling in liver tissue.
Keywords:	Childhood Liver Tumours, Competitive RT-PCR, Conductin, Hepatoblastoma, Mutations, Western Blotting
Source:	Journal of Pathology
ISSN:	0022-3417
Publisher:	John Wiley & Sons
Volume:	204
Number:	5
Page Range:	546-554
Date:	1 January 2004
Official Publication:	https://doi.org/10.1002/path.1662
PubMed:	View item in PubMed

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