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British Journal of Cancer
Article
License: CC BY NC SA
Data sources: UnpayWall
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PubMed Central
Other literature type . 2000
License: CC BY
Data sources: PubMed Central
British Journal of Cancer
Article . 2000 . Peer-reviewed
Data sources: Crossref
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Vascular endothelial growth factor-C (VEGF-C) expression in human colorectal cancer tissues

Authors: Akagi, K; Ikeda, Y; Miyazaki, M; Abe, T; Kinoshita, J; Maehara, Y; Sugimachi, K;

Vascular endothelial growth factor-C (VEGF-C) expression in human colorectal cancer tissues

Abstract

Vascular endothelial growth factor-C (VEGF-C) functions specifically to induce lymphangiogenesis. We examined the relationship between expression of VEGF-C and clinicopathological features in patients with colorectal cancer. The expression of VEGF-C in the 99 primary tumours and 18 metastatic lymph nodes from colorectal cancer patients was examined immunohistochemically. To verify VEGF-C mRNA expression, reverse transcriptase-polymerase chain reaction (RT-PCR) was carried out. The expression of VEGF-C correlated with lymphatic involvement, lymph nodes metastasis, and depth of invasion. On the other hand, correlations were nil with regard to gender of the patients, histologic type, venous involvement, and liver metastasis. The expression of VEGF-C in metastatic lymph nodes was fairly consistent with this expression in the primary tumour. Survival time was shorter for VEGF-C positive groups than for VEGF-C negative ones, but with no statistically significant difference. RT-PCR findings revealed that the expression of VEGF-C mRNA correlated mostly with that of VEGF-C protein expression. VEGF-C may play an important role in lymphatic spread of colorectal cancer.

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Keywords

Adult, Aged, 80 and over, Male, Adolescent, Reverse Transcriptase Polymerase Chain Reaction, Vascular Endothelial Growth Factor C, Regular Article, Endothelial Growth Factors, Middle Aged, Immunohistochemistry, Lymphatic Metastasis, Humans, Female, RNA, Messenger, Colorectal Neoplasms, Aged

  • BIP!
    Impact byBIP!
    selected citations
    These citations are derived from selected sources.
    This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    230
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 10%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Top 1%
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 1%
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
230
Top 10%
Top 1%
Top 1%
Green
hybrid
Related to Research communities
Cancer Research