| Literature DB >> 29610525 |
Qinglian Tang1,2, Jinchang Lu1,2, Changye Zou2, Yang Shao1, Yan Chen1, Swami Narala1, Hui Fang1, Huaiyuan Xu2, Jin Wang2, Jingnan Shen3, Rama Khokha4.
Abstract
The era of cancer genomics now provides an opportunity to discover novel determinants of osteosarcoma (OS), the most common primary bone cancer in children and adolescents known for its poor prognosis due to lung metastasis. Here, we identify CDH4 amplification in 43.6% of human osteosarcoma using array CGH and demonstrate its critical role in osteosarcoma development and progression. Gain or loss-of-function of CDH4, which encodes R-cadherin, causally impacts multiple features of human OS cells including cell migration and invasion, osteogenic differentiation, and stemness. CDH4 overexpression activates c-Jun via the JNK pathway, while CDH4 knockdown suppresses both tumor xenograft growth and lung colonization. In OS patient specimens, high CDH4 expression associates with lung metastases and poor prognosis. Collectively, our bioinformatics, functional, molecular, and clinical analyses uncover an oncogenic function of CDH4 in osteosarcoma and its relationship with patient outcome.Entities:
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Year: 2018 PMID: 29610525 DOI: 10.1038/s41388-018-0231-2
Source DB: PubMed Journal: Oncogene ISSN: 0950-9232 Impact factor: 9.867