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Silencing FAT10 inhibits metastasis of osteosarcoma
Author(s) -
Chengbin Ma,
Zhiyu Zhang,
Yan Cui,
Hongmou Yuan,
Feng Wang
Publication year - 2016
Publication title -
international journal of oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.405
H-Index - 122
ISSN - 1019-6439
DOI - 10.3892/ijo.2016.3549
Subject(s) - osteosarcoma , gene silencing , metastasis , oncogene , cancer research , molecular medicine , matrigel , biology , downregulation and upregulation , cancer , cell cycle , medicine , gene , angiogenesis , genetics
Metastasis is the main challenge of osteosarcoma treatment. Herein, we first reveal the oncogenic role of FAT10 in metastasis of osteosarcoma. FAT10 was upregulated in osteosarcoma, especially in metastatic osteosarcoma. High level of FAT10 was associated with poorer prognosis of osteosarcoma patients. Moreover, Transwell and Matrigel assays revealed that silencing FAT10 significantly inhibited the invasive and migratory abilities of osteosarcoma cells. Metastasis assay in vivo showed that silencing FAT10 decreased the number of mice with distant metastasis. We also found that FAT10 may act its oncogenic functions through regulating HOXB9. Collectively, the results suggested that FAT10 may be a novel therapeutic target for osteosarcoma patients.

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