Literature DB >> 3742892

Promotion of lung tumor colonization in mice by the synthetic thrombin inhibitor (no. 805) and its reversal by leech salivary gland extracts.

A Iwakawa, T B Gasic, E D Viner, G J Gasic.   

Abstract

The role of anticoagulation per se in the reduction of experimental or spontaneous metastasis still remains to be determined, as shown by the conflicting results reported by the literature using different conventional anticoagulants. A new compound has been synthesized (compound no. 805) which prolongs or suppresses coagulation via specific inhibition of thrombin and its possible use in a model of experimental metastasis to clarify the role of anticoagulants in tumor spread was investigated. Contrary to our expectations, this compound increased rather than decreased the number of lung colonies induced by intravenous injections of a variety of murine neoplasias. Studies of the mechanism of this effect indicated that the compound increases retention of tumor cells by the lung without apparent impairment of the natural cell immune system, suggesting that the synthetic thrombin inhibitor may enhance vascular attachment of tumor cells. The promoting effect of compound no. 805 on metastasis was totally reversed by the administration of leech salivary gland extracts, which appear to protect capillaries from damage produced by cyclophosphamide, as revealed by other studies.

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Year:  1986        PMID: 3742892     DOI: 10.1007/bf00117933

Source DB:  PubMed          Journal:  Clin Exp Metastasis        ISSN: 0262-0898            Impact factor:   5.150


  29 in total

1.  Mechanism of lung tumour colony reduction caused by coumarin anticoagulation.

Authors:  P Hilgard; B Maat
Journal:  Eur J Cancer       Date:  1979-02       Impact factor: 9.162

2.  Tumour growth and spontaneous metastasis spread in two syngeneic systems.

Authors:  B Hagmar
Journal:  Acta Pathol Microbiol Scand A       Date:  1970

3.  Effects of chemotherapeutic drugs on platelet and metastatic tumor cell-endothelial cell interactions as a model for assessing vascular endothelial integrity.

Authors:  G L Nicolson; S E Custead
Journal:  Cancer Res       Date:  1985-01       Impact factor: 12.701

4.  Tumor cell-platelet aggregation: induced by cathepsin B-like proteinase and inhibited by prostacyclin.

Authors:  K V Honn; P Cavanaugh; C Evens; J D Taylor; B F Sloane
Journal:  Science       Date:  1982-08-06       Impact factor: 47.728

5.  Potent inhibition of thrombin by the newly synthesized arginine derivative No. 805. The importance of stereo-structure of its hydrophobic carboxamide portion.

Authors:  S Okamoto; A Hijikata; R Kikumoto; S Tonomura; H Hara; K Ninomiya; A Maruyama; M Sugano; Y Tamao
Journal:  Biochem Biophys Res Commun       Date:  1981-07-30       Impact factor: 3.575

6.  "Natural" killer cells in the mouse. I. Cytotoxic cells with specificity for mouse Moloney leukemia cells. Specificity and distribution according to genotype.

Authors:  R Kiessling; E Klein; H Wigzell
Journal:  Eur J Immunol       Date:  1975-02       Impact factor: 5.532

Review 7.  Role of plasma, platelets, and endothelial cells in tumor metastasis.

Authors:  G J Gasic
Journal:  Cancer Metastasis Rev       Date:  1984       Impact factor: 9.264

8.  Antibodies to plasminogen activator inhibit human tumor metastasis.

Authors:  L Ossowski; E Reich
Journal:  Cell       Date:  1983-12       Impact factor: 41.582

9.  Stimulation of endothelial cell prostacyclin production by thrombin, trypsin, and the ionophore A 23187.

Authors:  B B Weksler; C W Ley; E A Jaffe
Journal:  J Clin Invest       Date:  1978-11       Impact factor: 14.808

10.  Anticoagulants and experimental metastases-evaluation of antimetastatic effects in different model systems.

Authors:  B Maat; P Hilgard
Journal:  J Cancer Res Clin Oncol       Date:  1981       Impact factor: 4.553

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