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Expression of Lewis antigenic determinants in colorectal adenocarcinomas.

Abstract
Expression of type 1 and type 2 chain Lewis antigens was studied in 32 rectal adenocarcinoma specimens; the results were correlated with the patients' Lewis phenotype and secretor status. In addition, the pattern of expression of these antigens was analyzed in adjacent and distant normal mucosa. We used an indirect immunofluorescence technique with p-phenylenediamine counterstaining (Oriol technique) and a panel of monoclonal antibodies directed against the different antigenic specificities. Normal distal colonic mucosa only expresses monofucosylated structures (Lea and X) arising from activity of the alpha 1-3,4-fucosyltransferase coded by the Le gene. Rectal adenocarcinomas also show Lea and X, but also reexpress blood group antigens ABH and exhibit difucosylated determinants (Leb and Y). The accumulation of mono- and difucosylated type 2 chain in neoplastic processes, independently of the Le and Se genes, could be due to the enzymes coded by reactivation of the H and X genes. Blood group antigens form a complex signal code, genetically regulated, which intervenes in differentiation, growth and cellular recognition processes, and which may undergo important modifications during malignant transformation. These alterations could be useful in the diagnosis and prognosis of some types of carcinoma.
AuthorsE Blasco, J Torrado, A Cosme, E Alvarez, A Zugasti, A Gutierrez-Hoyos, J I Arenas
JournalExperimental cell biology (Exp Cell Biol) Vol. 57 Issue 3 Pg. 153-8 ( 1989) ISSN: 0304-3568 [Print] Switzerland
PMID2476347 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Biomarkers, Tumor
  • Epitopes
  • Lewis Blood Group Antigens
Topics
  • Adenocarcinoma (blood, pathology)
  • Biomarkers, Tumor (blood)
  • Colorectal Neoplasms (blood, pathology)
  • Epitopes (immunology)
  • Fluorescent Antibody Technique
  • Humans
  • Intestinal Mucosa (immunology, pathology)
  • Lewis Blood Group Antigens (immunology)
  • Phenotype
  • Rectum (immunology, pathology)

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