Literature DB >> 6364802

Tumor interaction with hemostasis: the rationale for the use of platelet inhibitors and anticoagulants in the treatment of cancer.

H Al-Mondhiry.   

Abstract

Clinical and experimental observations have firmly established the concept of a two-way interaction between malignancy and the hemostatic system. On the one hand, certain tumors can activate platelets and the coagulation mechanism in vivo, on the other, a convincing case has been made for the involvement of platelets and fibrin in tumor growth and metastasis. A large number of clinical and experimental studies have been conducted in order to test the efficacy of platelet inhibitors and anticoagulants as adjuvants in the treatment of cancer. Antiplatelet drugs gave variable results, depending on the drug and the tumor system tested. Prostaglandin synthetic pathways by both the host and tumor seem to be an important determinant in the response to platelet function inhibitors. Of the various anticoagulants tested, the coumarin derivatives gave somewhat consistent antitumor effect in certain human and experimental cancer. The antitumor effect of oral anticoagulants does not appear to be a primary drug effect and seems related to their role as vitamin K antagonists. It should be emphasized that although the antitumor potential of antithrombotic agents is a subject of keen interest at the present, their use in treating human cancer is still controversial.

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Year:  1984        PMID: 6364802     DOI: 10.1002/ajh.2830160213

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  8 in total

1.  Acoustic driven flow and lattice Boltzmann simulations to study cell adhesion in biofunctionalized mu-fluidic channels with complex geometry.

Authors:  M A Fallah; V M Myles; T Krüger; K Sritharan; A Wixforth; F Varnik; S W Schneider; M F Schneider
Journal:  Biomicrofluidics       Date:  2010-05-19       Impact factor: 2.800

2.  The lack of correlation between experimental metastatic potential and platelet aggregating activity of B16 melanoma clones viewed in relation to tumor cell heterogeneity.

Authors:  A K Kimura; P Mehta; J H Xiang; D Lawson; D Dugger; K J Kao; L Lee-Ambrose
Journal:  Clin Exp Metastasis       Date:  1987 Apr-Jun       Impact factor: 5.150

3.  Investigation of the biological effects of anti-cell adhesive synthetic peptides that inhibit experimental metastasis of B16-F10 murine melanoma cells.

Authors:  M J Humphries; K M Yamada; K Olden
Journal:  J Clin Invest       Date:  1988-03       Impact factor: 14.808

4.  Characterization of platelet aggregation induced by human breast carcinoma and its inhibition by snake venom peptides, trigramin and rhodostomin.

Authors:  H S Chiang; M W Swaim; T F Huang
Journal:  Breast Cancer Res Treat       Date:  1995-03       Impact factor: 4.872

5.  Platelet interaction with a pancreatic ascites tumor.

Authors:  J Hamilton; V Subbarao; K Granack; C Ts'ao
Journal:  Am J Pathol       Date:  1986-01       Impact factor: 4.307

6.  Importance of viability and attachment to an ascites tumor in the release of plasminogen activator.

Authors:  Q Dong; M Zhou; V Subbarao; C Ts'ao
Journal:  Am J Pathol       Date:  1991-05       Impact factor: 4.307

7.  Metastatic brain tumour and fibrinopeptides.

Authors:  K Yumitori; H Handa; T Teraura; J Yamashita; K Yamamura
Journal:  Acta Neurochir (Wien)       Date:  1987       Impact factor: 2.216

8.  The Arg-Gly-Asp-containing peptide, rhodostomin, inhibits in vitro cell adhesion to extracellular matrices and platelet aggregation caused by saos-2 human osteosarcoma cells.

Authors:  H S Chiang; R S Yang; T F Huang
Journal:  Br J Cancer       Date:  1995-02       Impact factor: 7.640

  8 in total

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