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Initial tumor cell arrest in animals of defined coagulative status
International Journal of Cancer
|June 15, 1978
Summary
This study investigated if blood clotting factors influence tumor cell spread. Anticoagulants did not affect how tumor cells initially arrested in mice with cancer-related clotting issues.
Area of Science:
- Oncology
- Hematology
- Cancer Metastasis Research
Background:
- Cancer patients often develop coagulopathies, similar to disseminated intravascular coagulation.
- Tumor cells spread through the bloodstream (hematogenous metastasis), and thrombogenesis is hypothesized to play a role in their initial arrest.
Purpose of the Study:
- To investigate the role of thrombogenic factors in the early hematogenous arrest of circulating tumor cells.
- To determine if anticoagulation therapy affects tumor cell localization in mice with tumor-induced coagulopathies.
Main Methods:
- Mice with primary tumors were administered anticoagulants (warfarin, aspirin, heparin).
- The early arrest patterns of radiolabeled TA3 carcinoma and Gardner lymphosarcoma cells were examined after intravenous injection.
- Hematologic parameters (thrombocytopenia, elevated fibrinogen) were measured to confirm coagulopathy.
Main Results:
- Mice exhibited coagulopathies similar to human disseminated intravascular coagulation.
- Effective anticoagulation was achieved in the tumor-bearing mice.
- Administration of warfarin, aspirin, or heparin had no effect on the localization patterns of either tumor cell type.
Conclusions:
- The proposed involvement of thrombogenesis in metastasis is unlikely to be mediated by clotting factors targeted by aspirin, warfarin, and heparin.
- These anticoagulants do not appear to influence the early intravascular arrest of circulating tumor cells.