Advances in Pharmacological Sciences
Volume 2009 (2009), Article ID 862162, 6 pages
doi:10.1155/2009/862162
Research Article

Lectins from the Red Marine Algal Species Bryothamnion seaforthii and Bryothamnion triquetrum as Tools to Differentiate Human Colon Carcinoma Cells

1Curso de Medicina/Campus de Sobral , Universidade Federal do Ceará, Fortaleza 60020-181, Brazil
2Laboratoire de Chimie Biologique, UMR N. 8576 CNRS, Université des Sciences et Technologies de Lille, 59655 Lille, France
3Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, 53-114 Wroclaw, Poland
4BioMol-Lab, Departamento de Bioquímica e Biologia Molecular, Universidade Federal do Ceará, Fortaleza 6043, Brazil

Received 29 June 2009; Revised 8 September 2009; Accepted 18 September 2009

Academic Editor: Neal Davies

Copyright © 2009 Vicente P. T. Pinto et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. N. M. N. Alencar, E. H. Teixeira, A. M. S. Assreuy, B. S. Cavada, C. A. Flores, and R. A. Ribeiro, “Leguminous lectins as tools for studying the role of sugar residues in leukocyte recruitment,” Mediators of Inflammation, vol. 8, no. 2, pp. 107–113, 1999. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  2. J. L. Andrade, S. Arruda, T. Barbosa, et al., “Lectin-induced nitric oxide production,” Cellular Immunology, vol. 194, no. 1, pp. 98–102, 1999. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  3. M. Mazzuca, M. Lhermitte, J. J. Lafitte, and P. Roussel, “Use of lectins for detection of glycoconjugates in the glandular cells of the human bronchial mucosa,” Journal of Histochemistry and Cytochemistry, vol. 30, no. 9, pp. 956–966, 1982. View at Scopus
  4. C. Banchonglikitkul, J. D. Smart, R. V. Gibbs, and D. J. Cook, “Binding of some Diocleinae lectins to the mucosal surfaces of the eye and mouth,” British Journal of Biomedical Science, vol. 57, no. 1, pp. 7–12, 2000. View at Scopus
  5. V. Dhuna, J. S. Bains, S. S. Kamboj, J. Singh, S. Kamboj, and A. K. Saxena, “Purification and characterization of a lectin from Arisaema tortuosum schott having in-vitro anticancer activity against human cancer cell lines,” Journal of Biochemistry and Molecular Biology, vol. 38, no. 5, pp. 526–532, 2005. View at Scopus
  6. R. Mody, S. Joshi, and W. Chaney, “Use of lectins as diagnostic and therapeutic tools for cancer,” Journal of Pharmacological and Toxicological Methods, vol. 33, no. 1, pp. 1–10, 1995. View at Publisher · View at Google Scholar · View at Scopus
  7. I. Ofek, D. L. Hasty, and N. Sharon, “Anti-adhesion therapy of bacterial diseases: prospects and problems,” FEMS Immunology and Medical Microbiology, vol. 38, no. 3, pp. 181–191, 2003. View at Publisher · View at Google Scholar · View at Scopus
  8. Y. Lu and W. Chaney, “Induction of N-acetylglucosaminyltransferase V by elevated expression of activated or proto-Ha-ras oncogenes,” Molecular and Cellular Biochemistry, vol. 122, no. 1, pp. 85–92, 1993. View at Scopus
  9. Y. Lu, J. C. Pelling, and W. G. Chaney, “Tumor cell surface beta 1-6 branched oligosaccharides and lung metastasis,” Clinical and Experimental Metastasis, vol. 12, no. 1, pp. 47–54, 1994.
  10. R. A. Walker, “The use of lectins in histopathology,” Pathology Research and Practice, vol. 185, no. 6, pp. 826–835, 1989. View at Scopus
  11. S. S. Joshi, “Determination of lectin-mediated augmentation of natural killer cell-mediated cytotoxicity,” in Lectins and Glycobiology, H. J. Gabius and S. Gabius, Eds., pp. 376–379, Springer, New York, NY, USA, 1993.
  12. A. H. Sampaio, D. J. Rogers, C. J. Barwell, S. Saker-Sampaio, F. H. F. Costa, and M. V. Ramos, “A new isolation procedure and further characterisation of the lectin from the red marine alga Ptilota serrata,” Journal of Applied Phycology, vol. 10, no. 6, pp. 539–546, 1998. View at Publisher · View at Google Scholar · View at Scopus
  13. C. S. Nagano, H. Debray, K. S. Nascimento, et al., “HCA and HML isolated from the red marine algae Hypnea cervicornis and Hypnea musciformis define a novel lectin family,” Protein Science, vol. 14, no. 8, pp. 2167–2176, 2005. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  14. K. S. Nascimento, C. S. Nagano, E. V. Nunes, et al., “Isolation and characterization of a new agglutinin from the red marine alga Hypnea cervicornis J. Agardh,” Biochemistry and Cell Biology, vol. 84, no. 1, pp. 49–54, 2006. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  15. I. L. Ainouz, A. H. Sampaio, A. L. P. Freitas, N. M. B. Benevides, and S. Mapurunga, “Comparative study on hemagglutinins from the red algae Bryothamnion seaforthii and Bryothamnion triquetrum,” Revista Brasileira de Fisiologia Vegetal, vol. 7, no. 1, pp. 15–19, 1995.
  16. J. J. Calvete, F. H. F. Costa, S. Saker-Sampaio, et al., “The amino acid sequence of the agglutinin isolated from the red marine alga Bryothamnion triquetrum defines a novel lectin structure,” Cellular and Molecular Life Sciences, vol. 57, pp. 343–350, 2000.
  17. S. E. Baldus, K. Engelmann, and F.-G. Hanisch, “MUC1 and the MUCs: a family of human mucins with impact in cancer biology,” Critical Reviews in Clinical Laboratory Sciences, vol. 41, no. 2, pp. 189–231, 2004. View at Publisher · View at Google Scholar · View at PubMed
  18. C. Kieda, M. Paprocka, A. Krawczenko, et al., “New human microvascular endothelial cell lines with specific adhesion molecules phenotypes,” Endothelium, vol. 9, no. 4, pp. 247–261, 2002. View at Publisher · View at Google Scholar · View at Scopus
  19. D. Nowak, A. Krawczenko, D. Dus, and M. Malicka-Blaszkiewicz, “Actin in human colon adenocarcinoma cells with different metastatic potential,” Acta Biochimica Polonica, vol. 49, no. 4, pp. 823–828, 2002. View at Scopus
  20. A. Opolski, A. Laskowska, J. Madej, et al., “Metastatic potential of human CX-1 colon adenocarcinoma cells is dependent on the expression of sialosyl Lea antigen,” Clinical and Experimental Metastasis, vol. 16, no. 8, pp. 673–681, 1998. View at Publisher · View at Google Scholar · View at Scopus
  21. A. T. Florence, A. M. Hillery, N. Hussain, and P. U. Jani, “Factors affecting the oral uptake and translocation of polystyrene nanoparticles: histological and analytical evidence,” Journal of Drug Targeting, vol. 3, no. 1, pp. 65–70, 1995. View at Scopus
  22. I. L. Ainouz and A. H. Sampaio, “Screening of Brazilian marine algae for hemagglutinins,” Botanica Marina, vol. 34, no. 3, pp. 211–214, 1991. View at Publisher · View at Google Scholar
  23. I. L. Ainouz, A. H. Sampaio, N. M. B. Benevides, et al., “Agglutination of enzyme treated erythrocytes by Brazilian marine algal extracts,” Botanica Marina, vol. 35, no. 6, pp. 475–479, 1992.
  24. S. Hakomori, “Aberrant glycosylation in tumors and tumor-associated carbohydrate antigens,” Advances in Cancer Research, vol. 52, pp. 257–331, 1989. View at Scopus
  25. S. Itzkowitz, “Carbohydrate changes in colon carcinoma,” Acta Pathologica, Microbiologica et Immunologica Scandinavica, vol. 27, pp. 173–180, 1992.
  26. J. W. Dennis, “Changes in glycosylation with malignant transformation and tumor progression,” in Cell Surface Carbohydrates and Cell Development, M. Fukuda, Ed., pp. 161–194, CRC Press, Boca Raton, Fla, USA, 1991.
  27. A. P. Corfield, N. Myerscough, B. F. Warren, P. Durdey, C. Paraskeva, and R. Schauer, “Reduction of sialic acid O-acetylation in human colonic mucins in the adenoma-carcinoma sequence,” Glycoconjugate Journal, vol. 16, no. 6, pp. 307–317, 1999.
  28. M. C. Rose, “Mucins: structure, function, and role in pulmonary diseases,” American Journal of Physiology, vol. 263, no. 4, part 1, pp. L413–L429, 1992. View at Scopus
  29. M. D. Walsh, J. P. Young, B. A. Leggett, S. H. Williams, J. R. Jass, and M. A. McGuckin, “The MUC13 cell surface mucin is highly expressed by human colorectal carcinomas,” Human Pathology, vol. 38, no. 6, pp. 883–892, 2007. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  30. H. Ishizu, J. Kumagai, Y. Eishi, T. Takizawa, and M. Koike, “Mucin core protein expression by colorectal mucinous carcinomas with or without mucus hyperplasia,” Journal of Gastroenterology, vol. 39, no. 2, pp. 125–132, 2004. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  31. A. H. Sampaio, D. J. Rogers, and C. J. Barwell, “Isolation and characterization of the lectin from the green marine alga Ulva lactuca L.,” Botanica Marina, vol. 41, no. 4, pp. 427–433, 1998.
  32. R. F. Lima, D. N. Criddle, E. P. Souza, et al., “Red marine alga Bryothamnion triquetrum lectin induces endothelium-dependent relaxation of the rat aorta via release of nitric oxide,” Journal of Pharmacy and Pharmacology, vol. 56, no. 11, pp. 1415–1421, 2004. View at Publisher · View at Google Scholar · View at PubMed
  33. E. H. Teixeira, M. H. Napimoga, V. A. Carneiro, et al., “In vitro inhibition of oral streptococci binding to the acquired pellicle by algal lectins,” Journal of Applied Microbiology, vol. 103, no. 4, pp. 1001–1006, 2007. View at Publisher · View at Google Scholar · View at PubMed
  34. F. D. S. Bitencourt, J. G. Figueiredo, M. R. L. Mota, et al., “Antinociceptive and anti-inflammatory effects of a mucin-binding agglutinin isolated from the red marine alga Hypnea cervicornis,” Naunyn-Schmiedeberg's Archives of Pharmacology, vol. 377, no. 2, pp. 139–148, 2008. View at Publisher · View at Google Scholar · View at PubMed
  35. N. Horan, L. Yan, H. Isobe, G. M. Whitesides, and D. Kahne, “Nonstatistical binding of a protein to clustered carbohydrates,” Proceedings of the National Academy of Sciences of the United States of America, vol. 96, no. 21, pp. 11782–11786, 1999. View at Publisher · View at Google Scholar
  36. B. S. Cavada, T. Barbosa, S. Arruda, T. B. Grangeiro, and M. Barral-Netto, “Revisiting proteus: do minor changes in lectin structure matter in biological activity? Lessons from and potential biotechnological uses of the Diocleinae subtribe lectins,” Current Protein and Peptide Science, vol. 2, no. 2, pp. 123–135, 2001. View at Publisher · View at Google Scholar
  37. E. L. Heinrich, L. A. Y. Welty, L. R. Banner, and S. B. Oppenheimer, “Direct targeting of cancer cells: a multiparameter approach,” Acta Histochemica, vol. 107, no. 5, pp. 335–344, 2005. View at Publisher · View at Google Scholar · View at PubMed