Cartilage aggrecan undergoes significant compositional and structural alterations during laryngeal cancer

Biochimica et Biophysica Acta - General Subjects

Volumn 1760, Issue 7, 2006, Pages 1046-1053

  Skandalis, Spyros S ^a   Theocharis, Achilleas D ^a   Vynios, Demitrios H ^a   Papageorgakopoulou, Nickoletta ^a   Hjerpe, Anders ^b   Karamanos, Nikos K ^a   Theocharis, Dimitrios A ^c  

^a Section of Organic Chemistry   (Greece)

^b KAROLINSKA INSTITUTE   (Sweden)

^c UNIVERSITY OF PATRAS   (Greece)

Author keywords

Aggrecan degradation; Aggregable aggrecan; Cartilage; Laryngeal cancer; Proteoglycans

Indexed keywords

AGGRECAN;

ADULT; AGED; ARTICLE; CANCER STAGING; CARTILAGE; CARTILAGE DEGENERATION; CONTROLLED STUDY; HUMAN; HUMAN TISSUE; HYDRODYNAMICS; LARYNX CANCER; LARYNX CARTILAGE; MALE; PHYSICAL CHEMISTRY; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN DOMAIN; PROTEIN STRUCTURE; SQUAMOUS CELL CARCINOMA;

ADULT; AGGRECANS; CARCINOMA, SQUAMOUS CELL; CARTILAGE; EXTRACELLULAR MATRIX PROTEINS; GENE EXPRESSION REGULATION, NEOPLASTIC; GLYCOSAMINOGLYCANS; HUMANS; IMMUNOHISTOCHEMISTRY; LARYNGEAL NEOPLASMS; LECTINS, C-TYPE; MALE; MIDDLE AGED; PEPTIDES; PROTEIN BINDING; PROTEIN STRUCTURE, TERTIARY; PROTEOCHONDROITIN SULFATES;

EID: 33745102282     PISSN: 03044165     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbagen.2006.02.007     Document Type: Article

References (30)

1. Sessions R.B., Harrison L.B., and Forastiere A.A. Tumors of the larynx and hypopharynx. In: DeVita V.T., Hellman S., and Rosenberg S.A. (Eds). Cancer Principles and Practice of Oncology. 6th ed. (2001), Lippincott Williams and Wilkins, Philadelphia 861-886
2. Dudhia J. Aggrecan, aging and assembly in articular cartilage. Cell. Mol. Life Sci. 62 (2005) 2241-2256
3. Skandalis S.S., Theocharis A.D., Vynios D.H., Theocharis D.A., and Papageorgakopoulou N. Proteoglycans in human laryngeal cartilage. Identification of proteoglycan types in successive cartilage extracts with particular reference to aggregating proteoglycans. Biochimie 86 (2004) 221-229
4. Mankin H.J., and Lippiello L. Biochemical and metabolic abnormalities in articular cartilage from osteo-arthritic human hips. J. Bone Joint Surg. Am. 52 (1970) 424-434
5. Martel-Pelletier J. Pathophysiology of osteoarthritis. Osteoarthr. Cartil. 7 (1999) 371-373
6. Goldring M.B. The role of the chondrocyte in osteoarthritis. Arthritis Rheum. 43 (2000) 1916-1926
7. Arner E.C. Aggrecanase-mediated cartilage degradation. Curr. Opin. Pharmacol. 2 (2002) 322-329
8. Skandalis S.S., Theocharis D.A., Papageorgakopoulou N., and Vynios D.H. The extractability of extracellular matrix components as a marker of cartilage remodeling in laryngeal squamous cell carcinoma. Biochim. Biophys. Acta 1721 (2005) 81-88
9. Skandalis S.S., Theocharis A.D., Theocharis D.A., Papadas T., Vynios D.H., and Papageorgakopoulou N. Matrix proteoglycans are markedly affected in advanced laryngeal squamous cell carcinoma. Biochim. Biophys. Acta 28 (2004) 152-161
10. Grigoreas G.H., Anagnostides S.T., and Vynios D.H. A solid-phase assay for the quantitative analysis of hyaluronic acid at the nanogram level. Anal. Biochem. 320 (2003) 179-184
11. Bitter T., and Muir H. A modified uronic acid carbazole reaction. Anal. Biochem. 4 (1962) 330-334
12. Farndale R.W., Buttle D.J., and Barrett A. Improved quantitation and discrimination of sulfated glycosaminoglycans by use of dimethylmethylene blue. Biochim. Biophys. Acta 883 (1986) 173-177
13. Bradford M.M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72 (1976) 248-254
14. Karamanos N.K., Syrokou A., Vanky P., Nurminen M., and Hjerpe A. Determination of 24 variously sulfated galactosaminoglycan and hyaluronan derived disaccharides by high-performance liquid chromatography. Anal. Biochem. 221 (1994) 189-199
15. Sajdera S.W., and Hascall V.C. Protein polysaccharide complex from bovine nasal cartilage. A comparison of low and high shear extraction procedures. J. Biol. Chem. 244 (1969) 77-87
16. Oegema T.R., Hascall V.C., and Dziewiatkowski D.D. Isolation and characterization of proteoglycans from the Swarm rat chondrosarcoma. J. Biol. Chem. 250 (1975) 6151-6159
17. Aletras A.J., and Tsiganos C.P. In situ interaction of cartilage proteoglycans with matrix proteins. Biochim. Biophys. Acta 840 (1985) 170-179
18. Yanagishita M., and Hascall V.C. Characterization of low buoyant density dermatan sulfate proteoglycans synthesized by rat ovarian granulose cells in culture. J. Biol. Chem. 258 (1983) 12847-12856
19. Theocharis A.D., Vynios D.H., Papageorgakopoulou N., Skandalis S.S., and Theocharis D.A. Altered content composition and structure of glycosaminoglycans and proteoglycans in gastric carcinoma. Int. J. Biochem. Cell Biol. 35 (2003) 376-390
20. Theocharis A.D., Karamanos N.K., Papageorgakopoulou N., Tsiganos C.P., and Theocharis D.A. Isolation and characterization of matrix proteoglycans from human nasal cartilage. Compositional and structural comparison between normal and scoliotic tissues. Biochim. Biophys. Acta 1569 (2002) 117-126
21. Theocharis D.A., Papageorgakopoulou N., Vynios D.H., Anagnostides S.Th., and Tsiganos C.P. Determination and structural characterization of dermatan sulfate in the presence of other galactosaminoglycans. J. Chromatogr., B, Biomed. Sci. Appl. 754 (2001) 297-309
22. Tsara M.E., Papageorgakopoulou N., Karavias D.D., and Theocharis D.A. Distribution and changes of glycosaminoglycans in neoplasias of rectum. Anticancer Res. 15 (1995) 2107-2112
23. Theocharis D.A., and Tsiganos C.P. Age-related changes of proteoglycans subunits from sheep nasal cartilage. Int. J. Biochem. 17 (1985) 479-484
24. Laemmli U.K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227 (1970) 680-685
25. Schwartz G.J., and Wenig B.L. Clinical considerations for neoplasms of the larynx. Head and Neck Pathology with Clinical Correlations (1998), Churchill Livingstone, Philadelphia 330-360
26. Cumming G.J., Handley C.J., and Preston B.N. Permeability of composite chondrocyte-culture-millipore membranes to solutes of varying size and shape. Biochem. J. 181 (1979) 257-266
27. Sztrolovics R., Recklie A.D., Roughley P.J., and Mort J.S. Hyaluronate degradation as an alternative mechanism for proteoglycan release from cartilage during interleukin-1b-stimulated catabolism. Biochem. J. 362 (2002) 473-479
28. Tortorella M.D., Pratta M., Liu R.Q., Austin J., Ross O.H., Abbaszade I., Burn T., and Arner E. Sites of aggrecan cleavage by recombinant human aggrecanase-1 (ADAMTS-4). J. Biol. Chem. 275 (2000) 18566-18573
29. Sandy J.D., Thompson V., Doege K., and Verscharen C. The intermediates of aggrecanase-dependent cleavage of aggrecan in rat chondrosarcoma cells treated with interleukin-1. Biochem. J. 351 (2000) 161-166
30. Nagase H., and Kashiwagi M. Aggrecanases and cartilage matrix degradation. Arthritis Res. Ther. 5 (2003) 94-103