[PDF][PDF] Mesenchymal tumors can derive from Ng2/Cspg4-expressing pericytes with β-catenin modulating the neoplastic phenotype

S Sato, YJ Tang, Q Wei, M Hirata, A Weng, I Han… - Cell reports, 2016 - cell.com
S Sato, YJ Tang, Q Wei, M Hirata, A Weng, I Han, A Okawa, S Takeda, H Whetstone…
Cell reports, 2016cell.com
The cell of origin for most mesenchymal tumors is unclear. One cell type that contributes to
this lineages is the pericyte, a cell expressing Ng2/Cspg4. Using lineage tracing, we
demonstrated that bone and soft tissue sarcomas driven by the deletion of the Trp53 tumor
suppressor, or desmoid tumors driven by a mutation in Apc, can derive from cells expressing
Ng2/Cspg4. Deletion of the Trp53 tumor suppressor gene in these cells resulted in the bone
and soft tissue sarcomas that closely resemble human sarcomas, while stabilizing β-catenin …
Summary
The cell of origin for most mesenchymal tumors is unclear. One cell type that contributes to this lineages is the pericyte, a cell expressing Ng2/Cspg4. Using lineage tracing, we demonstrated that bone and soft tissue sarcomas driven by the deletion of the Trp53 tumor suppressor, or desmoid tumors driven by a mutation in Apc, can derive from cells expressing Ng2/Cspg4. Deletion of the Trp53 tumor suppressor gene in these cells resulted in the bone and soft tissue sarcomas that closely resemble human sarcomas, while stabilizing β-catenin in this same cell type caused desmoid tumors. Comparing expression between Ng2/Cspg4-expressing pericytes lacking Trp53 and sarcomas that arose from deletion of Trp53 showed inhibition of β-catenin signaling in the sarcomas. Activation of β-catenin inhibited the formation and growth of sarcomas. Thus, pericytes can be a cell of origin for mesenchymal tumors, and β-catenin dysregulation plays an important role in the neoplastic phenotype.
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