The attenuation of experimental lung metastasis by a bile acid acylated-heparin derivative

Kyeongsoon Park, Seok Ki Lee, Dai Hyun Son, Soo Ah Park, Kwang Meyung Kim, Hyo Won Chang, Eun jeong Jeong, Rang Woon Park, In-San Kim, Ick Chan Kwon, Youngro Byun, Sang Yoon Kim

Research output: Contribution to journalArticle

31 Citations (Scopus)

Abstract

The inhibitory efficacies of new bile acid acylated-heparin derivative (heparin-DOCA) were evaluated on experimental lung metastasis. We evaluated the effect of heparin-DOCA on intercellular interactions including those between B16F10 and thrombin-activated platelets and TNF-α-activated HUVECs, and between B16F10 and immobilized mouse P-selectin. In addition, the inhibitory effects of heparin-DOCA on adhesion and invasion of B16F10 to Matrigel were studied. In an animal mouse study, the blood clot formation and the retention of red fluorescence protein (RFP)-B16F10 in lungs were assessed after heparin-DOCA and RFP-B16F10 intravenous administration. Furthermore, we investigated the anti-metastatic effect of heparin-DOCA against lung metastasis induced by B16F10 and SCC7. Heparin-DOCA inhibited intercellular interactions between B16F10 and activated platelets or activated HUVECs by blocking P- and E-selectin-mediated interactions. Moreover, it reduced adhesion and invasion of B16F10 to ECM, thereby affecting the reduction of early retention of B16F10 in the lung. Heparin-DOCA attenuated lung colony formation on the surfaces and in interior of the lung, and attenuated metastasis by B16F10 and SCC7. These results suggest that heparin-DOCA may have potentials as therapeutic agent that prevents tumor metastasis and progression.

Original languageEnglish
Pages (from-to)2667-2676
Number of pages10
JournalBiomaterials
Volume28
Issue number16
DOIs
Publication statusPublished - 2007 Jun 1
Externally publishedYes

Fingerprint

Desoxycorticosterone Acetate
Bile Acids and Salts
Heparin
Neoplasm Metastasis
Derivatives
Lung
Acids
P-Selectin
Platelets
Blood Platelets
Adhesion
Fluorescence
Proteins
Military electronic countermeasures
E-Selectin
Thrombin
Intravenous Administration
Tumors
Animals
Thrombosis

Keywords

  • Adhesion
  • B16F10 melanoma
  • Bile acid acylated-heparin derivative
  • Invasion
  • Lung metastasis

ASJC Scopus subject areas

  • Biotechnology
  • Bioengineering
  • Biomedical Engineering

Cite this

Park, K., Ki Lee, S., Hyun Son, D., Ah Park, S., Kim, K. M., Won Chang, H., ... Kim, S. Y. (2007). The attenuation of experimental lung metastasis by a bile acid acylated-heparin derivative. Biomaterials, 28(16), 2667-2676. https://doi.org/10.1016/j.biomaterials.2007.02.001

The attenuation of experimental lung metastasis by a bile acid acylated-heparin derivative. / Park, Kyeongsoon; Ki Lee, Seok; Hyun Son, Dai; Ah Park, Soo; Kim, Kwang Meyung; Won Chang, Hyo; Jeong, Eun jeong; Park, Rang Woon; Kim, In-San; Kwon, Ick Chan; Byun, Youngro; Kim, Sang Yoon.

In: Biomaterials, Vol. 28, No. 16, 01.06.2007, p. 2667-2676.

Research output: Contribution to journalArticle

Park, K, Ki Lee, S, Hyun Son, D, Ah Park, S, Kim, KM, Won Chang, H, Jeong, EJ, Park, RW, Kim, I-S, Kwon, IC, Byun, Y & Kim, SY 2007, 'The attenuation of experimental lung metastasis by a bile acid acylated-heparin derivative', Biomaterials, vol. 28, no. 16, pp. 2667-2676. https://doi.org/10.1016/j.biomaterials.2007.02.001
Park, Kyeongsoon ; Ki Lee, Seok ; Hyun Son, Dai ; Ah Park, Soo ; Kim, Kwang Meyung ; Won Chang, Hyo ; Jeong, Eun jeong ; Park, Rang Woon ; Kim, In-San ; Kwon, Ick Chan ; Byun, Youngro ; Kim, Sang Yoon. / The attenuation of experimental lung metastasis by a bile acid acylated-heparin derivative. In: Biomaterials. 2007 ; Vol. 28, No. 16. pp. 2667-2676.
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