| Literature DB >> 26527604 |
Naoki Shimozono1, Masatoshi Jinnin2, Mamiko Masuzawa3, Mikio Masuzawa4, Zhongzhi Wang1, Ayaka Hirano1, Yukiko Tomizawa1, Tomomi Etoh-Kira1, Ikko Kajihara1, Miho Harada1, Satoshi Fukushima1, Hironobu Ihn1.
Abstract
Angiosarcoma is a malignant vascular tumor originating from endothelial cells of blood vessels or lymphatic vessels. The specific driver mutations in angiosarcoma remain unknown. In this study, we investigated this issue by transcriptome sequencing of patient-derived angiosarcoma cells (ISO-HAS), identifying a novel fusion gene NUP160-SLC43A3 found to be expressed in 9 of 25 human angiosarcoma specimens that were examined. In tumors harboring the fusion gene, the duration between the onset of symptoms and the first hospital visit was significantly shorter, suggesting more rapid tumor progression. Stable expression of the fusion gene in nontransformed human dermal microvascular endothelial cells elicited a gene-expression pattern mimicking ISO-HAS cells and increased cell proliferation, an effect traced in part to NUP160 truncation. Conversely, RNAi-mediated attenuation of NUP160 in ISO-HAS cells decreased cell number. Confirming the oncogenic effects of the fusion protein, subcutaneous implantation of NUP160-SLC43A3-expressing fibroblasts induced tumors resembling human angiosarcoma. Collectively, our findings advance knowledge concerning the genetic causes of angiosarcoma, with potential implications for new diagnostic and therapeutic approaches. ©2015 American Association for Cancer Research.Entities:
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Year: 2015 PMID: 26527604 DOI: 10.1158/0008-5472.CAN-15-0418
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701