chondroitin has been researched along with Skin-Neoplasms* in 5 studies
5 other study(ies) available for chondroitin and Skin-Neoplasms
Article | Year |
---|---|
Localization and characterization of melanoma-associated glycosaminoglycans: differential expression of chondroitin and heparan sulfate epitopes in melanoma.
Glycosaminoglycans (GAGs) are anionic polysaccharides present on cells and in the extracellular matrix (ECM). They likely play a role in tumor formation because of their capacity to bind and modulate a variety of proteins including growth factors, cytokines, and proteases. Using a panel of (human) phage display-derived anti-GAG antibodies, the location and expression of GAG epitopes in human cutaneous melanocytic lesions was studied. Antibodies EW4E1 and EW4G2 identified a melanoma-associated chondroitin sulfate/heparan sulfate epitope, whereas antibody EW4B7 recognized a melanoma-associated heparan sulfate epitope. These antibodies showed a high reactivity with blood vessels and ECM in cutaneous melanoma tumors, whereas their reactivity with nevi was very low. Using a set of defined oligosaccharides it was established that sulfate groups are of main importance in the binding to the antibodies and that glycomimetics can mimic natural oligosaccharides. In xenografts of melanoma cell line MeL57, a strong association of GAG epitopes with an injected fluorescent fluid flow tracer was observed. In uveal melanoma antibody, EW4E1 proved to be a sensitive probe for the detection of the geometry of ECM structures, known to have prognostic value. Taken together, data indicate that in melanoma a defined set and location of GAG epitopes are present with possible functional significance. Topics: Animals; Antibodies; Chondroitin; Epitopes; Heparitin Sulfate; Humans; Melanoma; Mice; Mice, Inbred BALB C; Mice, Nude; Neoplasm Transplantation; Oligosaccharides; Peptide Library; Rats; Rats, Wistar; Skin Neoplasms; Transplantation, Heterologous; Uveal Neoplasms | 2003 |
Systemic hyalinosis or fibromatosis hyalinica multiplex juvenilis as a congenital syndrome. A new entity based on the inborn error of the acid mucopolysaccharide metabolism in connective tissue cells?
Topics: Bone Diseases; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chondroitin; Connective Tissue; Gingival Hypertrophy; Glycosaminoglycans; Histocytochemistry; Humans; Infant; Infant, Newborn; Joint Diseases; Male; Methods; Skin; Skin Diseases; Skin Neoplasms; Staining and Labeling; Syndrome | 1973 |
[Mucopolysaccharidosis of the Pfaundler-Hurler type with spastic tetraparesis and retinitis pigmentosa of two adult sisters].
Topics: Adult; Carbohydrate Metabolism, Inborn Errors; Chondroitin; Eczema; Female; Fibroma; Glycosaminoglycans; Hip Dislocation, Congenital; Humans; Mucopolysaccharidosis I; Muscle Spasticity; Nevus, Pigmented; Psoriasis; Quadriplegia; Retinitis Pigmentosa; Skin Neoplasms; Syndrome | 1972 |
Biochemical changes in 9,10-dimethyl-1,2-benzanthracene painted mouse skin.
Topics: Animals; Benz(a)Anthracenes; Carbazoles; Chondroitin; Electrophoresis; Female; Heparin; Hyaluronic Acid; Mice; Neoplasms, Experimental; Phenols; Skin; Skin Neoplasms; Water | 1968 |
DERMATOLOGIC ASPECTS OF MAST CELL ACTIVITY.
Topics: Chondroitin; Coloring Agents; Cushing Syndrome; Dermatology; Erythema Multiforme; Heparin; Hexosamines; Histocytochemistry; Humans; Hyaluronic Acid; Hydroxyproline; Inflammation; Mast Cells; Myxedema; Pigmentation Disorders; Scleroderma, Systemic; Skin Neoplasms; Staining and Labeling; Urticaria; Wound Healing | 1964 |