Abstract | BACKGROUND: METHODS: MDA-231 breast cancer cells were treated with thrombin in presence or absence of argatroban, and TF activity was measured in the form of activated factor X. Enzyme-linked immunosorbent assay (ELISA) was used to measure VEGF concentrations in the medium. MDA-231 cells were injected into the left heart ventricle of mice, and then argatroban or saline was administered intraperitoneally for 28 days. After 28 days, incidence of bone metastasis was evaluated in the limbs by radiography. RESULTS: TF activity and VEGF secretion were upregulated by thrombin. Argatroban inhibited the enhancement of TF activity and VEGF secretion induced by thrombin. In vivo analysis revealed that the number of metastasized limbs in the argatroban group was significantly lower compared with the saline group (P < 0.05). CONCLUSIONS:
Thrombin not only enhances VEGF secretion but also has a positive feedback mechanism to reexpress TF. These results indicate that inhibition of thrombin is of great value in suppression of tumor metastasis. Argatroban is a noteworthy and useful thrombin inhibitor because it has already been used in the clinical setting and has antimetastatic effects in vivo.
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Authors | Kunihiro Asanuma, Hiroki Wakabayashi, Takayuki Okamoto, Yumiko Asanuma, Nobuyuki Akita, Tomoaki Yoshikawa, Tatsuya Hayashi, Akihiko Matsumine, Atsumasa Uchida, Akihiro Sudo |
Journal | Breast cancer (Tokyo, Japan)
(Breast Cancer)
Vol. 20
Issue 3
Pg. 241-6
(Jul 2013)
ISSN: 1880-4233 [Electronic] Japan |
PMID | 22359194
(Publication Type: Journal Article)
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Chemical References |
- Antithrombins
- Pipecolic Acids
- Sulfonamides
- Vascular Endothelial Growth Factor A
- vascular endothelial growth factor A, mouse
- Thromboplastin
- Arginine
- Thrombin
- argatroban
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Topics |
- Animals
- Antithrombins
(pharmacology)
- Arginine
(analogs & derivatives)
- Body Weight
(drug effects)
- Bone Neoplasms
(prevention & control, secondary)
- Breast Neoplasms
(pathology, prevention & control)
- Enzyme-Linked Immunosorbent Assay
- Female
- Humans
- Mice
- Pipecolic Acids
(pharmacology)
- Sulfonamides
- Thrombin
(antagonists & inhibitors)
- Thromboplastin
(metabolism)
- Tumor Cells, Cultured
- Vascular Endothelial Growth Factor A
(metabolism)
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