Document Detail


Cell adhesion molecule expression within the microvasculature of human colorectal malignancies.
MedLine Citation:
PMID:  7517347     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
In situ expression of intercellular adhesion molecule-1 (ICAM-1), endothelial leukocyte adhesion molecule-1 (ELAM-1), and vascular cell adhesion molecule-1 (VCAM-1) was investigated in 20 human colorectal cancers using immunohistochemical techniques. Tumor microvessels, detected with endothelial marker Ulex Europaeus Agglutinin-I (UEAI), were consistently present within both stromal and glandular areas. Vessels expressing cell adhesion molecules (CAMs) were less frequent but more common within the tumor stroma. Although ICAM-1 and ELAM-1 vessel staining was present in all tumors, ICAM-1 staining was the most consistent with primary localization to stroma while ELAM-1 was variable with localization to both stroma and glandular areas. VCAM-1 staining was inconsistent and was rare in glandular areas. A significant increase in the number of vessels expressing CAMs with a concomitant decrease in the total number of vessels was noted in bowel muscularis adjacent to tumor compared to remote bowel. No relationship between number of vessels or frequency of CAM positive vessels and tumor site, grade, or stage was noted. These studies demonstrate enhanced microvascular expression of CAMs in close proximity to colorectal tumors despite decreases in total number of vessels, suggesting that factors within the tumor microenvironment effect tumor microvascular development. Correlation between these studies and previous microscopic studies suggest that vessels expressing CAMs play a role in immune cell infiltration and may provide new targets for anti-tumor therapies.
Authors:
H Nelson; P S Ramsey; J H Donohue; L E Wold
Related Documents :
25274627 - Post-translational glycoprotein modifications regulate colon cancer stem cells and colo...
8680027 - Practical study of the correlation between the shape of tumoral vessels (folberg) and t...
17354817 - Tumor therapeutic response and vessel tortuosity: preliminary report in metastatic brea...
10652587 - Quantification and distribution of neovascularization following microinjection of c6 gl...
20443837 - Sex modulates intestinal transformation by the tumor-suppressor gcc.
20969637 - Cancer death from non-muscle invasive bladder cancer: report of the japanese urological...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Clinical immunology and immunopathology     Volume:  72     ISSN:  0090-1229     ISO Abbreviation:  Clin. Immunol. Immunopathol.     Publication Date:  1994 Jul 
Date Detail:
Created Date:  1994-07-29     Completed Date:  1994-07-29     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0356637     Medline TA:  Clin Immunol Immunopathol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  129-36     Citation Subset:  IM    
Affiliation:
Department of Surgery, Mayo Clinic and Foundation, Rochester, Minnesota 55905.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Adenocarcinoma / blood supply
Cell Adhesion Molecules / biosynthesis*
Colorectal Neoplasms / blood supply*
E-Selectin
Endothelium, Vascular / immunology
Humans
Immunoenzyme Techniques
Intercellular Adhesion Molecule-1
Microcirculation / immunology
Vascular Cell Adhesion Molecule-1
Chemical
Reg. No./Substance:
0/Cell Adhesion Molecules; 0/E-Selectin; 0/Vascular Cell Adhesion Molecule-1; 126547-89-5/Intercellular Adhesion Molecule-1

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Inhibitory effects of (4-alkoxy-2, 3, 6-trimethylphenyl) glycopyranosides on histamine release induc...
Next Document:  Polyclonal in vitro T cell proliferation and T cell-dependent B cell differentiation supported by ac...