» Articles » PMID: 12087470

Periodate-treated, Non-anticoagulant Heparin-carrying Polystyrene (NAC-HCPS) Affects Angiogenesis and Inhibits Subcutaneous Induced Tumour Growth and Metastasis to the Lung

Overview
Journal Br J Cancer
Specialty Oncology
Date 2002 Jun 28
PMID 12087470
Citations 23
Authors
Affiliations
Soon will be listed here.
Abstract

Periodate-treated, non-anticoagulant heparin-carrying polystyrene consists of about ten periodate-oxidized, alkaline-degraded low molecular weight-heparin chains linked to a polystyrene core and has a markedly lower anti-coagulant activity than heparin. In this study, we evaluated the effect of non-anticoagulant heparin-carrying polystyrene on tumour growth and metastasis. Non-anticoagulant heparin-carrying polystyrene has a higher activity to inhibit vascular endothelial growth factor-165-, fibroblast growth factor-2- or hepatocyte growth factor-induced human microvascular endothelial cell growth than heparin, ten periodate-oxidized-heparin and ten periodate-oxidized-low molecular weight-heparin, which is probably due to the heparin-clustering effect of non-anticoagulant heparin-carrying polystyrene. Non-anticoagulant heparin-carrying polystyrene inhibited human microvascular endothelial cell, B16 melanoma and Lewis lung cancer cell adhesion to Matrigel-coated plates. Non-anticoagulant heparin-carrying polystyrene also showed strong inhibitory activities in the tubular formation of endothelial cells on Matrigel and B16-melanoma and Lewis lung cancer cell invasion in a Matrigel-coated chamber assay. In vivo studies showed that growth of subcutaneous induced tumours and lung metastasis of B16-melanoma and Lewis lung cancer cells were more effectively inhibited by non-anticoagulant heparin-carrying polystyrene than ten periodate-oxidized-heparin and ten periodate-oxidized-low molecular weight-heparin. Furthermore, non-anticoagulant heparin-carrying polystyrene markedly reduced the number of CD34-positive vessels in subcutaneous Lewis lung cancer tumours, indicating a strong inhibition of angiogenesis. These results suggest that non-anticoagulant heparin-carrying polystyrene has an inhibitory activity on angiogenesis and tumour invasion and may be very useful in cancer therapy.

Citing Articles

Towards an emerging role for anticoagulants in cancer therapy: a systematic review and meta-analysis.

Asmael Al-Azzawi H, Hamza S, Paolini R, Arshad F, Patini R, OReilly L Front Oral Health. 2024; 5:1495942.

PMID: 39568788 PMC: 11576436. DOI: 10.3389/froh.2024.1495942.


Concomitant heparin use promotes skin graft donor site healing by basic fibroblast growth factor: A pilot prospective randomized controlled study.

Kohyama K, Kato H, Okada H, Ishihara T, Yasue Y, Kamidani R Contemp Clin Trials Commun. 2024; 42:101375.

PMID: 39398328 PMC: 11470421. DOI: 10.1016/j.conctc.2024.101375.


Low molecular weight heparin synergistically enhances the efficacy of adoptive and anti-PD-1-based immunotherapy by increasing lymphocyte infiltration in colorectal cancer.

Quan Y, He J, Zou Q, Zhang L, Sun Q, Huang H J Immunother Cancer. 2023; 11(8).

PMID: 37597850 PMC: 10441131. DOI: 10.1136/jitc-2023-007080.


Non-anticoagulant heparin derivatives for COVID-19 treatment.

Cao M, Qiao M, Sohail M, Zhang X Int J Biol Macromol. 2022; 226:974-981.

PMID: 36528145 PMC: 9749384. DOI: 10.1016/j.ijbiomac.2022.12.090.


Glycosaminoglycans: Carriers and Targets for Tailored Anti-Cancer Therapy.

Berdiaki A, Neagu M, Giatagana E, Kuskov A, Tsatsakis A, N Tzanakakis G Biomolecules. 2021; 11(3).

PMID: 33800172 PMC: 8001210. DOI: 10.3390/biom11030395.


References
1.
Ishihara M, Saito Y, Yura H, Ono K, Ishikawa K, Hattori H . Heparin-carrying polystyrene to mediate cellular attachment and growth via interaction with growth factors. J Biomed Mater Res. 2000; 50(2):144-52. DOI: 10.1002/(sici)1097-4636(200005)50:2<144::aid-jbm8>3.0.co;2-s. View

2.
Basbaum C, Werb Z . Focalized proteolysis: spatial and temporal regulation of extracellular matrix degradation at the cell surface. Curr Opin Cell Biol. 1996; 8(5):731-8. DOI: 10.1016/s0955-0674(96)80116-5. View

3.
Dvorak H, Harvey V, Estrella P, Brown L, McDonagh J, Dvorak A . Fibrin containing gels induce angiogenesis. Implications for tumor stroma generation and wound healing. Lab Invest. 1987; 57(6):673-86. View

4.
Gogly B, Hornebeck W, Groult N, Godeau G, Pellat B . Influence of heparin(s) on the interleukin-1-beta-induced expression of collagenase, stromelysin-1, and tissue inhibitor of metalloproteinase-1 in human gingival fibroblasts. Biochem Pharmacol. 1998; 56(11):1447-54. DOI: 10.1016/s0006-2952(98)00257-3. View

5.
Fransson L, Carlstedt I . Alkaline and smith degradation of oxidized dermatan sulphate-chondroitin sulphate copolymers. Carbohydr Res. 1974; 36(2):349-58. DOI: 10.1016/s0008-6215(00)83056-6. View