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

被引:4
|
作者
Yasuda, Naohiro [1 ]
Takenaka, Satoshi [1 ]
Nakai, Sho [1 ]
Nakai, Takaaki [2 ]
Yamada, Shutaro [3 ]
Imura, Yoshinori [4 ]
Outani, Hidetatsu [1 ]
Hamada, Kenichiro [1 ]
Yoshikawa, Hideki [1 ,5 ]
Naka, Norifumi [1 ,4 ]
机构
[1] Osaka Univ, Dept Orthopaed Surg, Grad Sch Med, 2-2 Yamadaoka, Suita, Osaka 5650871, Japan
[2] Kawachi Gen Hosp, Dept Orthopaed Surg, Higashiosaka, Osaka, Japan
[3] Yao Municipal Hosp, Dept Orthopaed Surg, Yao, Japan
[4] Osaka Int Canc Inst, Musculoskeletal Oncol Serv, Osaka, Japan
[5] Toyonaka City Hosp, Dept Orthopaed Surg, Toyonaka, Osaka, Japan
来源
FEBS OPEN BIO | 2020年 / 10卷 / 05期
关键词
LM8; lung metastasis; molecular targeted therapy; osteosarcoma; TAS-115; TYROSINE KINASE INHIBITOR; FACTOR-KAPPA-B; NEOADJUVANT CHEMOTHERAPY; TUMOR PROGRESSION; PHASE-II; MET; ACTIVATION; IMATINIB; SARCOMA;
D O I
10.1002/2211-5463.12827
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:767 / 779
页数:13
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