Decreased expression of Mac-2 (carbohydrate binding protein 35) and loss of its nuclear localization are associated with the neoplastic progression of colon carcinoma
AuthorsLotz, Margaret M.
Andrews, Charles W. Jr.
Korzelius, Cynthia A.
Lee, Edward C.
Steele, Glenn D. Jr.
Mercurio, Arthur M.
UMass Chan AffiliationsDepartment of Cancer Biology
Document TypeJournal Article
Amino Acid Sequence
Cell Transformation, Neoplastic
Molecular Sequence Data
Polymerase Chain Reaction
Amino Acids, Peptides, and Proteins
Digestive System Diseases
MetadataShow full item record
AbstractThe Mac-2 lectin (carbohydrate binding protein 35) is a soluble, 32- to 35-kDa phosphoprotein that binds galactose-containing glycoconjugates. We report here that the colonic epithelium is a major site of Mac-2 expression in vivo based on immunohistochemistry of human tissue specimens. In this epithelium, proliferating cells at the base of the crypts do not express Mac-2 but its expression increases with differentiation along the crypt-to-surface axis. Mac-2 expression is concentrated in the nuclei of these differentiated epithelial cells. The progression from normal mucosa to adenoma to carcinoma is associated with significant changes in Mac-2 nuclear localization and expression. In all adenomas (9/9) and carcinomas (13/13) examined, Mac-2 was not present in the nucleus but was localized in the cytoplasm. Sequencing of Mac-2 cDNAs from normal mucosa and carcinoma revealed no specific mutations that could account for this loss of nuclear localization. We also observed a 5- to 10-fold decrease in Mac-2 mRNA levels in cancer compared to normal mucosa as well as a significant reduction in the amount of Mac-2 protein expressed. These observations suggest that Mac-2 exclusion from the nucleus and its decreased expression may be related to the neoplastic progression of colon cancer.
Proc Natl Acad Sci U S A. 1993 Apr 15;90(8):3466-70.
Permanent Link to this Itemhttp://hdl.handle.net/20.500.14038/26290