Literature DB >> 10651313

In vivo treatment of rats with unfractionated heparin (UFH) or low molecular weight heparin (LMWH) does not affect experimentally induced colon carcinoma metastasis.

S M Smorenburg1, R Vink, M te Lintelo, W Tigchelaar, A Maas, H R Büller, C J van Noorden.   

Abstract

Recent randomized trials have suggested that treatment with low molecular weight heparin (LMWH) improves survival of cancer patients with venous thromboembolism, as compared to treatment with unfractionated heparin (UFH). Experimental studies have shown that UFH has activities besides its anticoagulant function which may affect progression of malignancy, including stimulation of new blood vessel formation. In contrast, LMWH has been suggested to inhibit angiogenesis. In the present study, we compared quantitatively the effects of treatment with UFH, LMWH or placebo on the development of experimentally induced colon carcinoma metastases in rat liver and on tumor-associated angiogenesis. It is shown that UFH and LMWH in therapeutic dosages neither affect development of metastases nor tumor blood vessel formation in this animal model. These results indicate that heparins do not affect colon cancer metastasis in liver. Further studies in other animal models are required to establish the mechanisms by which heparins potentially affect cancer.

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Year:  1999        PMID: 10651313     DOI: 10.1023/a:1006648429914

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


  39 in total

1.  Lower mortality in cancer patients treated with low-molecular-weight versus standard heparin.

Authors:  D Green; R D Hull; R Brant; G F Pineo
Journal:  Lancet       Date:  1992-06-13       Impact factor: 79.321

Review 2.  Inhibition of metastases by anticoagulants.

Authors:  M Hejna; M Raderer; C C Zielinski
Journal:  J Natl Cancer Inst       Date:  1999-01-06       Impact factor: 13.506

3.  Automated amidolytic method for determining heparin, a heparinoid, and a low-Mr heparin fragment, based on their anti-Xa activity.

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Journal:  Clin Chem       Date:  1984-06       Impact factor: 8.327

4.  Heparin and angiogenesis: a low-molecular-weight fraction inhibits and a high-molecular-weight fraction stimulates angiogenesis systemically.

Authors:  K Norrby
Journal:  Haemostasis       Date:  1993-03

5.  Low-molecular-weight heparins and unfractionated heparin in the treatment of patients with acute venous thromboembolism: results of a meta-analysis.

Authors:  S Siragusa; B Cosmi; F Piovella; J Hirsh; J S Ginsberg
Journal:  Am J Med       Date:  1996-03       Impact factor: 4.965

Review 6.  Heparanases and tumor metastasis.

Authors:  M Nakajima; T Irimura; G L Nicolson
Journal:  J Cell Biochem       Date:  1988-02       Impact factor: 4.429

7.  Interferon treatment of a transplantable rat colon adenocarcinoma: importance of tumor site.

Authors:  R L Marquet; D L Westbroek; J Jeekel
Journal:  Int J Cancer       Date:  1984-05-15       Impact factor: 7.396

8.  alpha2-Macroglobulin is mainly produced by cancer cells and not by hepatocytes in rats with colon carcinoma metastases in liver.

Authors:  S M Smorenburg; P Griffini; A B Tiggelman; A F Moorman; W Boers; J F Van Noorden
Journal:  Hepatology       Date:  1996-03       Impact factor: 17.425

9.  Variations in the size and sulfation of heparin modulate the effect of heparin on the binding of VEGF165 to its receptors.

Authors:  S Soker; D Goldstaub; C M Svahn; I Vlodavsky; B Z Levi; G Neufeld
Journal:  Biochem Biophys Res Commun       Date:  1994-09-15       Impact factor: 3.575

10.  Heparin oligosaccharides: inhibitors of the biological activity of bFGF on Caco-2 cells.

Authors:  G C Jayson; J T Gallagher
Journal:  Br J Cancer       Date:  1997       Impact factor: 7.640

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  5 in total

Review 1.  Impact of venous thromboembolism and anticoagulation on cancer and cancer survival.

Authors:  Nicole M Kuderer; Thomas L Ortel; Charles W Francis
Journal:  J Clin Oncol       Date:  2009-09-08       Impact factor: 44.544

2.  Modest anti-cancer activity of a bile acid acylated heparin derivative in a PC14PE6 induced orthotopic lung cancer model.

Authors:  Zheng Yun Cui; Min Jae Park; Jeeyun Lee; Jin Seok Ahn; Myung Ju Ahn; Soo Won Seo; Jin Woo Park; Youngro Byun; Keunchil Park
Journal:  Cancer Res Treat       Date:  2009-06-30       Impact factor: 4.679

3.  Clinical use of the low-molecular-weight heparins in cancer patients: focus on the improved patient outcomes.

Authors:  Bo H Chao; Lisa Lepeak; Ticiana Leal; H Ian Robins
Journal:  Thrombosis       Date:  2011-04-12

4.  Unfractionated heparin displaces sFlt-1 from the placental extracellular matrix.

Authors:  Kyle H Moore; Heather Chapman; Eric M George
Journal:  Biol Sex Differ       Date:  2020-06-29       Impact factor: 5.027

5.  The direct oral anticoagulants rivaroxaban and dabigatran do not inhibit orthotopic growth and metastasis of human breast cancer in mice.

Authors:  Jeroen T Buijs; El H Laghmani; Rob F P van den Akker; Chris Tieken; Esther M Vletter; Kim M van der Molen; Juliette J Crooijmans; Chantal Kroone; Sylvia E Le Dévédec; Gabri van der Pluijm; Henri H Versteeg
Journal:  J Thromb Haemost       Date:  2019-04-29       Impact factor: 5.824

  5 in total

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