| Literature DB >> 15539922 |
Kunihiro Asanuma1, Hiroki Wakabayashi, Tatsuya Hayashi, Noritaka Okuyama, Masashi Seto, Akihiko Matsumine, Katsuyuki Kusuzaki, Koji Suzuki, Atsumasa Uchida.
Abstract
It is well known that malignant cells show procoagulant activity, which is associated with their metastatic potential. Thrombin, the key enzyme of the blood coagulation system, is generated around tumor cells, promoting the migration and metastasis of tumor cells. In this study, we evaluated the effect of argatroban, a specific thrombin inhibitor, on the migration and metastasis of B16BL6 melanoma cells. In vitro argatroban dose-dependently inhibited cell migration, the maximum inhibition being observed in the presence of 10 microM argatroban (p < 0.0001). In order to investigate the antimetastatic effect of the thrombin inhibitor, we used an animal model that we have reported previously. C57BL6 mice which had received a bone (femur or tibia) transplanted into the dorsal subcutis were injected with B16 melanoma cells into the left heart ventricle. Intraperitoneal injection of argatroban (9 mg/kg/day for 4 weeks) significantly reduced the number of limbs with metastatic lesions as compared to a placebo (p < 0.05). These results suggest that argatroban was associated with reduced melanoma metastases by inhibiting cell migration. Our results showed that argatroban is effective for treatment of bone metastasis. 2004 S. Karger AG, Basel.Entities:
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Year: 2004 PMID: 15539922 DOI: 10.1159/000081004
Source DB: PubMed Journal: Oncology ISSN: 0030-2414 Impact factor: 2.935