Evidence map›Paper›PMID 16698949›Full record

ArticleJournal of clinical pathology2007

Expression of KAI1 and tenascin, and microvessel density are closely correlated with liver metastasis of gastrointestinal adenocarcinoma.

Huachuan Zheng, Koichi Tsuneyama, Chunmei Cheng, Hiroyuki Takahashi, Zhengguo Cui, Kazuhiro Nomoto, Yoshihiro Murai, Yasuo Takano

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Article in Journal of clinical pathology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 25% of its field
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 19 citations in OpenAlex.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

8 authors at 2 institutions in 2 countries.

Huachuan ZhengDepartment of Pathology, Faculty of Medicine, University of Toyama, Toyama, Japan.
Koichi Tsuneyama
Chunmei Cheng
Hiroyuki Takahashi
Zhengguo Cui
Kazuhiro Nomoto
Yoshihiro Murai
Yasuo Takano
University of Toyama · JPUniversity of California, Davis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo seek good markers to predict invasion and metastasis of gastrointestinal adenocarcinoma (GIA).

methodsExpression of KAI1 and tenascin were examined on tissue microarrays containing gastric adenocarcinoma (n = 98), colorectal adenocarcinoma (n = 125), gastric adjacent non-cancerous mucosa (n = 95) and colorectal adjacent non-cancerous mucosa (n = 112) by immunostaining. Microvessel density (MVD) in GIA was labelled using anti-CD34 antibody by immunostaining. Expression of KAI1 and tenascin, and MVD were compared with clinicopathological features of tumours, including PTEN (phosphatase and tensin homology deleted from human chromosome 10) and EMMPRIN (extracellular matrix metalloproteinase inducer) expression.

resultsKAI1 expression was higher in GIAs than in their adjacent non-cancerous mucosa (p<0.05). KAI1 and tenascin expression showed a significantly negative association with liver metastasis of GIA (p<0.05), but not with depth of invasion, venous invasion or lymph node metastasis (p>0.05). A significantly negative relationship was observed between EMMPRIN and tenascin expression in GIA (p<0.05). MVD was positively correlated with depth of invasion, venous invasion, lymph node metastasis and liver metastasis of tumours (p<0.05), whereas it was negatively correlated with PTEN expression (p<0.05).

conclusionsUp-regulated KAI1 expression may play an important part in malignant transformation of gastrointestinal epithelial cells. Reduced expression of KAI1 and tenascin might underlie the molecular basis of liver metastasis of GIA. Angiogenesis is a key event in the invasion and metastasis of GIA. These markers might be used to indicate liver metastasis of GIA in clinicopathological practice.

Indexed as

AdenocarcinomaAdultAgedAged, 80 and overBiomarkers, TumorColorectal NeoplasmsFemaleHumansKangai-1 ProteinLiver NeoplasmsLymphatic MetastasisMaleMicrocirculationMiddle AgedNeoplasm InvasivenessNeoplasm ProteinsBiomarkers, TumorKangai-1 ProteinNeoplasm ProteinsTenascin

Identifiers

PMID16698949
PMCPMC1860584
OpenAlexW2151829000

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.