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TAS-115抑制血小板衍生生长因子受体α(PDGFRα)/AXL/FLT-3信号传导并抑制骨肉瘤的肺转移。

TAS-115 inhibits PDGFRα/AXL/FLT-3 signaling and suppresses lung metastasis of osteosarcoma.

作者信息

Yasuda Naohiro, Takenaka Satoshi, Nakai Sho, Nakai Takaaki, Yamada Shutaro, Imura Yoshinori, Outani Hidetatsu, Hamada Kenichiro, Yoshikawa Hideki, Naka Norifumi

机构信息

Department of Orthopaedic Surgery, Osaka University Graduate School of Medicine, Suita, Japan.

Department of Orthopaedic Surgery, Kawachi General Hospital, Higashiosaka, Japan.

出版信息

FEBS Open Bio. 2020 May;10(5):767-779. doi: 10.1002/2211-5463.12827. Epub 2020 Mar 30.

Abstract

Osteosarcoma is the most common malignant bone tumor in adolescence and childhood. Metastatic osteosarcoma has a poor prognosis with an overall 5-year survival rate of approximately 20%. TAS-115 is a novel multiple receptor tyrosine kinase inhibitor that is currently undergoing clinical trials. Using the mouse highly lung-metastatic osteosarcoma cell line, LM8, we showed that TAS-115 suppressed the growth of subcutaneous grafted tumor and lung metastasis of osteosarcoma at least partially through the inhibition of platelet-derived growth factor receptor alpha, AXL, and Fms-like tyrosine kinase 3 phosphorylation. We also show that these signaling pathways are activated in various human osteosarcoma cell lines and are involved in proliferation. Our results suggest that TAS-115 may have potential for development into a novel treatment for metastatic osteosarcoma.

摘要

骨肉瘤是青少年和儿童中最常见的恶性骨肿瘤。转移性骨肉瘤预后较差,总体5年生存率约为20%。TAS-115是一种新型多受体酪氨酸激酶抑制剂,目前正在进行临床试验。使用小鼠高肺转移性骨肉瘤细胞系LM8,我们发现TAS-115至少部分通过抑制血小板衍生生长因子受体α、AXL和Fms样酪氨酸激酶3磷酸化来抑制皮下移植瘤的生长和骨肉瘤的肺转移。我们还表明,这些信号通路在各种人类骨肉瘤细胞系中被激活并参与增殖。我们的结果表明,TAS-115可能有潜力开发成为转移性骨肉瘤的一种新型治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad9d/7193166/1d67ba4775dd/FEB4-10-767-g001.jpg

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