A monoclonal antibody against the Wnt signaling inhibitor dickkopf-1 inhibits osteosarcoma metastasis in a preclinical model

被引:62
作者
Goldstein, Seth D. [1 ]
Trucco, Matteo [2 ]
Guzman, Wendy Bautista [1 ]
Hayashi, Masanori [1 ]
Loeb, David M. [1 ]
机构
[1] Johns Hopkins Univ, Sidney Kimmel Comprehens Canc Ctr, Div Pediat Oncol, Baltimore, MD USA
[2] Baylor Coll Med, Dept Pediat, Hematol Oncol Sect, Houston, TX 77030 USA
关键词
sarcoma; metastasis; Wnt signaling; DKK-1; mouse model; PROGNOSTIC-FACTORS; DRUG DEVELOPMENT; SURVIVAL; EPIDEMIOLOGY; SURVEILLANCE; DISEASE; FAMILY; CELLS;
D O I
10.18632/oncotarget.8522
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The outcome of patients with metastatic osteosarcoma has not improved since the introduction of chemotherapy in the 1970s. Development of therapies targeting the metastatic cascade is a tremendous unmet medical need. The Wnt signaling pathway has been the focus of intense investigation in osteosarcoma because of its role in normal bone development. Although the role of Wnt signaling in the pathogenesis of osteosarcoma is controversial, there are several reports of dickkopf-1 (DKK-1), a Wnt signaling antagonist, possibly playing a pro-tumorigenic role. In this work we investigated the effect of anti-DKK-1 antibodies on the growth and metastasis of patient-derived osteosarcoma xenografts. We were able to detect human DKK-1 in the blood of tumor-bearing mice and found a correlation between DKK-1 level and tumor proliferation. Treatment with the anti-DKK-1 antibody, BHQ880, slowed the growth of orthotopically implanted patient-derived osteosarcoma xenografts and inhibited metastasis. This effect was correlated with increased nuclear beta-catenin staining and increased expression of the bone differentiation marker osteopontin. These findings suggest that Wnt signaling is anti-tumorigenic in osteosarcoma, and support the targeting of DKK-1 as an anti-metastatic strategy for patients with osteosarcoma.
引用
收藏
页码:21114 / 21123
页数:10
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