Source:http://linkedlifedata.com/resource/pubmed/id/17785951
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2007-9-5
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pubmed:abstractText |
Angiopoietins are endothelial growth factors, which play crucial roles in normal vascular development and tumor angiogenesis. We examined the expression profiles of angiopoietin-1 (Ang-1), angiopoietin-2 (Ang-2), vascular endothelial growth factor (VEGF), and Tie-2, a receptor for Ang-1 and Ang-2, in both colorectal adenocarcinoma and adjacent normal tissues, as judged by histology, in order to elucidate their relationships with microvascular density (MVD) and clinicopathologic properties. Higher MVD was associated with a lower degree of differentiation of colorectal adenocarcinoma. Immunohistochemical analysis revealed that the expression of Ang-2 and VEGF was significantly increased in colorectal adenocarcinoma compared to adjacent normal tissues (p < 0.01), and the expression of Ang-2 positively correlated with that of VEGF (r = 0.997, p < 0.01). In contrast, the expression of Ang-1 was lower in adenocarcinoma tissues than in adjacent normal tissues (p < 0.01), while there was no significant difference in Tie-2 expression in both tissues. Moreover, MVD was increased in Ang-2- and VEGF-expressing adenocarcinoma tissues compared to the Ang-2- and VEGF-negative tissues, respectively (p < 0.01). Importantly, MVD was lower in Ang-1-expressing adenocarcinoma tissues relative to Ang-1-negative tissues (p < 0.01). Furthermore, expression of Ang-2 as well as VEGF was significantly up-regulated in colorectal adenocarcinoma with diameters > or = 5 cm or with lymph-node metastases (p < 0.01). In conclusion, the increased expression of Ang-2 and the decreased expression of Ang-1 may be responsible for blood vessel formation and rapid growth of the colorectal adenocarcinoma.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0040-8727
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
213
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
33-40
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:17785951-Adenocarcinoma,
pubmed-meshheading:17785951-Adult,
pubmed-meshheading:17785951-Aged,
pubmed-meshheading:17785951-Angiopoietin-1,
pubmed-meshheading:17785951-Angiopoietin-2,
pubmed-meshheading:17785951-Colorectal Neoplasms,
pubmed-meshheading:17785951-Female,
pubmed-meshheading:17785951-Humans,
pubmed-meshheading:17785951-Immunohistochemistry,
pubmed-meshheading:17785951-Male,
pubmed-meshheading:17785951-Microcirculation,
pubmed-meshheading:17785951-Middle Aged,
pubmed-meshheading:17785951-Neoplasm Staging,
pubmed-meshheading:17785951-Neovascularization, Pathologic,
pubmed-meshheading:17785951-Receptor, TIE-2,
pubmed-meshheading:17785951-Vascular Endothelial Growth Factor A
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pubmed:year |
2007
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pubmed:articleTitle |
Expression of angiopoietin-2 is correlated with vascularization and tumor size in human colorectal adenocarcinoma.
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pubmed:affiliation |
Department of Gastroenterology, Zhongnan Hospital of Wuhan University, Wuhan 430071, Hubei Province, China.
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pubmed:publicationType |
Journal Article
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