Page last updated: 2024-10-18

dalteparin and B16 Melanoma

dalteparin has been researched along with B16 Melanoma in 7 studies

Dalteparin: A low-molecular-weight fragment of heparin, prepared by nitrous acid depolymerization of porcine mucosal heparin. The mean molecular weight is 4000-6000 daltons. It is used therapeutically as an antithrombotic agent. (From Merck Index, 11th ed)

Research Excerpts

ExcerptRelevanceReference
"Experimental metastasis of B16F10-VLA-4kd and B16F10 cells and interference by Tinzaparin were analysed in mice."1.40The role of VLA-4 binding for experimental melanoma metastasis and its inhibition by heparin. ( Bendas, G; Borsig, L; Naggi, A; Ortmann, K; Roblek, M; Schlesinger, M; Torri, G, 2014)
"Using the B16 melanoma mouse model of metastasis, subcutaneous (s."1.33Anti-metastatic effect of a non-anticoagulant low-molecular-weight heparin versus the standard low-molecular-weight heparin, enoxaparin. ( Amirkhosravi, A; Francis, JL; Linhardt, R; Mousa, SA, 2006)

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's4 (57.14)29.6817
2010's3 (42.86)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Debergh, I1
Van Damme, N1
Pattyn, P1
Peeters, M1
Ceelen, WP1
Ludwig, RJ1
Alban, S1
Bistrian, R1
Boehncke, WH1
Kaufmann, R1
Henschler, R1
Gille, J1
Mousa, SA2
Linhardt, R1
Francis, JL2
Amirkhosravi, A2
Schlesinger, M1
Roblek, M1
Ortmann, K1
Naggi, A1
Torri, G1
Borsig, L1
Bendas, G1
Goertz, L1
Schneider, SW1
Desch, A1
Mayer, FT1
Koett, J1
Nowak, K1
Karampinis, I1
Bohlmann, MK1
Umansky, V1
Bauer, AT1
Amaya, M1
Kragh, M1
Binderup, L1
Vig Hjarnaa, PJ1
Bramm, E1
Johansen, KB1
Frimundt Petersen, C1

Other Studies

7 other studies available for dalteparin and B16 Melanoma

ArticleYear
The low-molecular-weight heparin, nadroparin, inhibits tumour angiogenesis in a rodent dorsal skinfold chamber model.
    British journal of cancer, 2010, Mar-02, Volume: 102, Issue:5

    Topics: Animals; Anticoagulants; Blood Flow Velocity; Cricetinae; Erythrocytes; Immunoenzyme Techniques; Mel

2010
The ability of different forms of heparins to suppress P-selectin function in vitro correlates to their inhibitory capacity on bloodborne metastasis in vivo.
    Thrombosis and haemostasis, 2006, Volume: 95, Issue:3

    Topics: Animals; Anticoagulants; Antineoplastic Agents; Cell Adhesion; Cell Line, Tumor; Cell Movement; Dose

2006
Anti-metastatic effect of a non-anticoagulant low-molecular-weight heparin versus the standard low-molecular-weight heparin, enoxaparin.
    Thrombosis and haemostasis, 2006, Volume: 96, Issue:6

    Topics: Animals; Anticoagulants; Antineoplastic Agents; Blood Coagulation; Cell Line, Tumor; Dose-Response R

2006
The role of VLA-4 binding for experimental melanoma metastasis and its inhibition by heparin.
    Thrombosis research, 2014, Volume: 133, Issue:5

    Topics: Animals; Anticoagulants; Cell Adhesion; Cell Line, Tumor; Cell Movement; Heparin, Low-Molecular-Weig

2014
Heparins that block VEGF-A-mediated von Willebrand factor fiber generation are potent inhibitors of hematogenous but not lymphatic metastasis.
    Oncotarget, 2016, Oct-18, Volume: 7, Issue:42

    Topics: Animals; Blood Vessels; Cell Line, Tumor; Cells, Cultured; Endothelial Cells; Factor Xa Inhibitors;

2016
Antimetastatic effect of tinzaparin, a low-molecular-weight heparin.
    Journal of thrombosis and haemostasis : JTH, 2003, Volume: 1, Issue:9

    Topics: Animals; Endothelium, Vascular; Fibrinolytic Agents; Heparin, Low-Molecular-Weight; Humans; Lipoprot

2003
Non-anti-coagulant heparin inhibits metastasis but not primary tumor growth.
    Oncology reports, 2005, Volume: 14, Issue:1

    Topics: Animals; Anticoagulants; Carbohydrate Sequence; Cell Line, Tumor; Female; Heparin, Low-Molecular-Wei

2005