RSPO2 abnormal transcripts result from read-through in liver tumours with high ß-catenin activation and CTNNB1 mutations

Q Bayard, JC Nault, J Zucman-Rossi - Gut, 2020 - gut.bmj.com
Q Bayard, JC Nault, J Zucman-Rossi
Gut, 2020gut.bmj.com
Thomas Longerich and collaborators1 recently published an intriguing observation in
hepatocellular adenoma (HCA) showing an activation of the Wnt/ß-catenin signalling
pathway without CTNNB1 or APC mutations. The authors identified a recurrent deletion
leading to a fusion between a short interspersed nuclear element (SINE) sequence and
RSPO2 gene in three HCAs and three hepatocellular carcinomas (HCCs) all activated for ß-
catenin, including one tumour with CTNNB1 mutations and five tumours without APC or …
Thomas Longerich and collaborators1 recently published an intriguing observation in hepatocellular adenoma (HCA) showing an activation of the Wnt/ß-catenin signalling pathway without CTNNB1 or APC mutations. The authors identified a recurrent deletion leading to a fusion between a short interspersed nuclear element (SINE) sequence and RSPO2 gene in three HCAs and three hepatocellular carcinomas (HCCs) all activated for ß-catenin, including one tumour with CTNNB1 mutations and five tumours without APC or CTNNB1 mutations. The authors proposed RSPO2fusion as a recurrent mechanism of ß-catenin activation in liver tumourigenesis.
Following this original observation, we analysed the expression and rearrangement of RSPO2 in a series of 10 HCAs and 163 HCCs analysed with RNAseq. We identified a correlation of RSPO2 mRNA expression with several genes known to be positively regulated by ß-catenin, including GLUL (R2= 0.51, p= 3.39× 10− 28) and TBX3
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