Literature DB >> 3516383

Lewisx- and sialylated Lewisx-related antigen expression in human malignant and nonmalignant colonic tissues.

S H Itzkowitz, M Yuan, Y Fukushi, A Palekar, P C Phelps, A M Shamsuddin, B F Trump, S Hakomori, Y S Kim.   

Abstract

Biochemical studies have revealed that some normal cells express the LeX trisaccharide Gal beta 1----4(Fuc alpha 1----3)GlcNAc either on short-chain fucolipids or as a single immunodeterminant on glycolipid oligosaccharide side chains. Cancer cells, including those from colonic adenocarcinomas, express this antigen on longer type 2 blood group side chains as difucosylated or trifucosylated fucolipids. Moreover, sialylated forms of difucosylated LeX also accumulate in colon cancer but not in normal colonic mucosa. In the present study, six monoclonal antibodies which selectively recognize the various LeX-related antigens were used for immunohistochemical examination of these antigens in serial sections of human colonic tissue. All of these antigens were oncodevelopmental in human colon. Monoclonal antibodies anti-SSEA-1 and AH8-183, directed against short-chain, monofucosylated LeX, were unable to discriminate well between normal and malignant colonic tissue. However, the other four antibodies were much better at distinguishing cancer from normal tissue. FH6 was the most specific in that no normal tissues bound this antibody. However, FH6 failed to stain poorly differentiated cancers and some colloid-type carcinomas. FH4, which was also highly specific, stained almost all cancers, regardless of the degree of differentiation. FH4 primarily stained cancer cell cytoplasm, whereas the sialylated antigen defined by FH6 predominantly stained cell membranes. Differences were noted between the expression of LeX-related antigens in autopsied normal mucosa compared to mucosa of benign colonic diseases. Monoclonal antibodies recognizing long-chain polyfucosylated and sialylated LeX-related antigens appear to be useful tools for detection of colon cancer.

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Year:  1986        PMID: 3516383

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  38 in total

1.  Immunohistochemical expression of the sialyl Lewis x antigen on gastric cancer cells correlates with the presence of liver metastasis.

Authors:  M Tatsumi; A Watanabe; H Sawada; Y Yamada; Y Shino; H Nakano
Journal:  Clin Exp Metastasis       Date:  1998-11       Impact factor: 5.150

2.  Sialosylated Lewis chi expression in CD30-positive anaplastic large-cell lymphomas.

Authors:  K Kasai; Y Sato; S Kuwao; Y Kawakubo; H Inoue; T Kameya
Journal:  J Cancer Res Clin Oncol       Date:  1992       Impact factor: 4.553

Review 3.  Simple sugars to complex disease--mucin-type O-glycans in cancer.

Authors:  Matthew R Kudelka; Tongzhong Ju; Jamie Heimburg-Molinaro; Richard D Cummings
Journal:  Adv Cancer Res       Date:  2015-02-07       Impact factor: 6.242

4.  Blood group antigens, Lewisx and Lewisy in the diagnostic discrimination of malignant mesothelioma versus adenocarcinoma.

Authors:  D Jordon; J Jagirdar; M Kaneko
Journal:  Am J Pathol       Date:  1989-11       Impact factor: 4.307

5.  Co-expression of X-hapten-like antigen and antigen YH206 on mucin molecules.

Authors:  Y Hinoda; K Imai; T Ban; F Itoh; A Yachi
Journal:  Gastroenterol Jpn       Date:  1991-02

6.  Regulation of the oncodevelopmental expression of type 1 chain ABH and Lewis(b) blood group antigens in human colon by alpha-2-L-fucosylation.

Authors:  T F Orntoft; P Greenwell; H Clausen; W M Watkins
Journal:  Gut       Date:  1991-03       Impact factor: 23.059

Review 7.  Intervention of carbohydrate recognition by proteins and nucleic acids.

Authors:  P Sears; C H Wong
Journal:  Proc Natl Acad Sci U S A       Date:  1996-10-29       Impact factor: 11.205

Review 8.  Mucin glycoproteins in neoplasia.

Authors:  Y S Kim; J Gum; I Brockhausen
Journal:  Glycoconj J       Date:  1996-10       Impact factor: 2.916

9.  Altered expression of Lewis blood group and related antigens in fetal, normal adult and malignant tissues of the uterine endometrium.

Authors:  M Inoue; M Nakayama; O Tanizawa
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1990

10.  Core 3 synthase is down-regulated in colon carcinoma and profoundly suppresses the metastatic potential of carcinoma cells.

Authors:  Toshie Iwai; Takashi Kudo; Risa Kawamoto; Tomomi Kubota; Akira Togayachi; Toru Hiruma; Tomoko Okada; Toru Kawamoto; Kyoei Morozumi; Hisashi Narimatsu
Journal:  Proc Natl Acad Sci U S A       Date:  2005-03-08       Impact factor: 11.205

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