Source:http://linkedlifedata.com/resource/pubmed/id/15471558
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
2004-10-8
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pubmed:abstractText |
We have previously demonstrated significantly decreased immunoreactivity of hepatocyte growth factor activator inhibitor type 1 (HAI-1), an integral membrane protein that exhibits potent inhibitory activity against hepatocyte growth factor activator (HGFA) and matriptase, in colorectal adenocarcinomas. In this report, we describe further detailed analysis of HAI-1 expression in colorectal adenocarcinoma by using three kinds of anti-HAI-1 antibodies, each of which recognizes a distinct epitope of the HAI-1 molecule, and also by in-situ hybridization for HAI-1 mRNA. The results indicated that the decreased immunoreactivity of HAI-1 in colorectal carcinoma cells is largely a result of enhanced ectodomain shedding of HAI-1 in these cells. In contrast, immunoreactivity of mature membrane-form HAI-1 was paradoxically en-hanced in cancer cells at the invasion front, showing intense cell-stroma interactions and/or sprouting invasion. This finding indicates that these invading cells showed decreased ectodomain shedding of HAI-1 and consequently might require the existence of the membrane-form HAI-1. Of particular interest was the observation of a possible inverse correlation between paradoxical up-regulation of membrane-form HAI-1 expression and membrane-associated E-cadherin in these cells. These membrane-form HAI-1-positive sprouting cancer cells were also negative for MIB-1 immunohistochemically, indicating a low-proliferating population. All these results suggest that HAI-1 may mediate diverse functions in regard to the progression of colorectal carcinomas, and the immunoreactivity of membrane-form HAI-1 may serve as a marker of invading cancer cells.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Cadherins,
http://linkedlifedata.com/resource/pubmed/chemical/Epitopes,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin G,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Glycoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Peptide Fragments,
http://linkedlifedata.com/resource/pubmed/chemical/Proteinase Inhibitory Proteins...,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/SPINT1 protein, human
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1347-9032
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
95
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
728-35
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:15471558-Adenocarcinoma,
pubmed-meshheading:15471558-Adult,
pubmed-meshheading:15471558-Aged,
pubmed-meshheading:15471558-Aged, 80 and over,
pubmed-meshheading:15471558-Animals,
pubmed-meshheading:15471558-Cadherins,
pubmed-meshheading:15471558-Cell Membrane,
pubmed-meshheading:15471558-Colorectal Neoplasms,
pubmed-meshheading:15471558-Disease Progression,
pubmed-meshheading:15471558-Epitopes,
pubmed-meshheading:15471558-Female,
pubmed-meshheading:15471558-Humans,
pubmed-meshheading:15471558-Immunoglobulin G,
pubmed-meshheading:15471558-In Situ Hybridization,
pubmed-meshheading:15471558-Male,
pubmed-meshheading:15471558-Membrane Glycoproteins,
pubmed-meshheading:15471558-Middle Aged,
pubmed-meshheading:15471558-Neoplasm Invasiveness,
pubmed-meshheading:15471558-Peptide Fragments,
pubmed-meshheading:15471558-Proteinase Inhibitory Proteins, Secretory,
pubmed-meshheading:15471558-RNA, Messenger,
pubmed-meshheading:15471558-Rabbits
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pubmed:year |
2004
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pubmed:articleTitle |
Paradoxically enhanced immunoreactivity of hepatocyte growth factor activator inhibitor type 1 (HAI-1) in cancer cells at the invasion front.
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pubmed:affiliation |
Second Department of Pathology, Faculty of Medicine, University of Miyazaki, Kiyotake, Miyazaki 889-1692, Japan.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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