[No authors listed]
Osteosarcoma (OS) is the most common type of primary bone malignancy with high recurrence and metastasis. Peptidylarginine deiminase 4 as an important protein post-translational modification enzyme, has been identified as a potential regulator in the invasion and migration in several types of tumors. The role of in osteosarcoma metastasis remains unknown. In this study, we revealed significant positive correlation between duanyu1563I4 and pulmonary metastasis of osteosarcoma. Wound-healing and transwell assay indicated that duanyu1563I4 induced invasion and migration of osteosarcoma cell in vitro while duanyu1563I4 inhibitor has repressive effect. duanyu1563I4 mutation with no deimination activity exhibited no significant effect on invasion and migration of osteosarcoma cells. Moreover, we evaluated the effect of duanyu1563I4 on expression of the markers of epithelial-mesenchymal transition and results showed that duanyu1563I4 promoted EMT while duanyu1563I4 inhibitor suppressed EMT in osteosarcoma cells. We also detected the expression of duanyu1563I4 and E-Cadherin in the tissues of osteosarcoma patients with or without pulmonary metastasis. Results showed positive relationship between the expression of duanyu1563I4 and osteosarcoma metastasis. In contrast, the expression of E-Cadherin exhibited negative correlation with duanyu1563I4 and osteosarcoma metastasis. Our research offered a novel link between duanyu1563I4 and osteosarcoma metastasis and demonstrated duanyu1563I4 as a promising target for treatment of osteosarcoma metastasis.
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