Premium
Western blot analysis of glycoproteins bearing lewis a and sialyl‐lewis a antigens in human colorectal mucosa
Author(s) -
Takabayashi Tsukasa,
Watanabe Masahiko,
Sakurai Yoichi,
Sugano Kokichi,
Kodaira Susumu,
Kitajima Masaki
Publication year - 1993
Publication title -
journal of surgical oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.201
H-Index - 111
eISSN - 1096-9098
pISSN - 0022-4790
DOI - 10.1002/jso.2930540208
Subject(s) - metastasis , glycoprotein , blot , antigen , pathology , colorectal cancer , western blot , sialyl lewis x , carcinoma , medicine , biology , microbiology and biotechnology , cancer , immunology , cell adhesion molecule , gene , biochemistry , selectin
Glycoproteins (GPs) bearing Lewis a and sialyl‐Lewis a antigens (Le a , sialyl‐Le a ) derived from human colorectal carcinomas and their surrounding non‐neoplastic mucosa (normal mucosa) were analyzed using Western blotting. GPs bearing Le a were detected mainly as segmental bands of Mr 310, 220, 160, and 80 kDa in 80% of the normal mucosa, but these GPs were detected predominantly as broad bands ranging from high to low molecular weight (MW) in 71% of the carcinoma tissues. GPs bearing sialyl‐Le a were detected only in 23% of the normal mucosa and limited on huge MW bands, i.e., more than 400 kDa, whereas these GPs were detected predominantly as broad bands in 49% of the carcinoma tissues. In the cases with lymph node metastasis, the MW of GPs bearing sialyl‐Le a varied over a wide range and were detected as broad bands, compared with the cases without metastasis. In conclusion, the MW of GPs bearing Le a and sialyl‐Le a in normal colorectal mucosa was different from that in colorectal carcinomas. That is, the MWs of GPs bearing Le a varied more in carcinoma tissues, and the GPs bearing sialyl‐Le a from carcinoma tissues had lower MWs than those from normal mucosa. It was, furthermore, suggested that the increased expression of lower MW GPs bearing sialyl‐Le a are associated with an increased metastatic potential of the tumor cells.© 1993 Wiley‐Liss, Inc.