Evidence map›Paper›PMID 18325046›Full record

ArticleCancer science2008

Expression of vasohibin as a novel endothelium-derived angiogenesis inhibitor in endometrial cancer.

Kousuke Yoshinaga, Kiyoshi Ito, Takuya Moriya, Satoru Nagase, Tadao Takano, Hitoshi Niikura, Nobuo Yaegashi, Yasufumi Sato

Open access · greenAbstract readComparative Study
In one paragraph

Article in Cancer science, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.9field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

30 citing papers in PubMed, 58 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Increased vasohibin-1 expression is associated with metastasis and poor prognosis of renal cell carcinoma patients.Laboratory investigation; a journal of technical methods and pathology · 2017
    Article
  5. Article
  6. The effect of Vasohibin-1 expression and tumor-associated macrophages on the angiogenesis in vitro and in vivo.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  7. Article
  8. A novel molecular marker of prognosis in colorectal cancer: Vasohibin-1.Medical oncology (Northwood, London, England) · 2014
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Vasohibin-1 expression is regulated by transforming growth factor-β/bone morphogenic protein signaling pathway between tumor-associated macrophages and pancreatic cancer cells.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2013
    Article
  14. Article
  15. Article
  16. Review
  17. The endometrial lymphatic vasculature: function and dysfunction.Reviews in endocrine & metabolic disorders · 2012
    Review
  18. Article
  19. Vasohibin-1 and vasohibin-2 expression in gastric cancer cells and TAMs.Medical oncology (Northwood, London, England) · 2012
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Kousuke YoshinagaDepartment of Gynecology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Kiyoshi Ito
Takuya Moriya
Satoru Nagase
Tadao Takano
Hitoshi Niikura
Nobuo Yaegashi
Yasufumi Sato
Tohoku University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have previously reported on vasohibin as a novel endothelium-derived vascular endothelial growth factor (VEGF)-inducible inhibitor of angiogenesis. The aim of our present study was to define the role of vasohibin in endometrioid endometrial adenocarcinoma. We collected 78 sections of endometrial carcinoma for assessment using immunohistochemistry. Twenty-seven were well differentiated (G1), 25 were moderately differentiated (G2), and 26 were poorly differentiated endometrioid adenocarcinomas (G3). We also included 12 sections of normal cyclic endometria, six of which were in the proliferative phase and six were in the secretory phase. We investigated the expression of vasohibin, and compared it to VEGF receptor-2 (VEGFR-2: KDR/flk-1), CD34, Ki-67, VEGF-A, and D2-40 (as a lymphatic vessel marker). We assessed the ratio of vasohibin- and VEGFR-2-positive vessels in the stroma of endometrial carcinoma. Immunohistochemical assessment was classified as negative or positive based on staining intensity. Vasohibin was selectively expressed on vascular endothelial cells in both cyclic endometria and endometrial carcinomas. Vasohibin was highly expressed in the normal functional endmetrium of the secretory phase, especially in the spiral artery, and was highly expressed in all grades of endometrioid adenocarcinomas. The stromal endothelial cells in G3 expressed vasohibin and VEGFR-2 more frequently than these in G1. In endometrioid adenocarcinomas, there was a significant correlation between the expression percentage of vasohibin and that of VEGFR-2 (P < 0.0001, r(2) = 0.591). This is the first study to elucidate the correlation between expression of vasohibin in the stromal endothelial cells and that of VEGFR-2 in human carcinomas.

Indexed as

AdenocarcinomaAngiogenesis InhibitorsCell Cycle ProteinsCell ProliferationEndometrial NeoplasmsEndothelial CellsEndotheliumFemaleHumansImmunohistochemistryMiddle AgedVascular Endothelial Growth Factor Receptor-2Angiogenesis InhibitorsCell Cycle ProteinsVascular Endothelial Growth Factor Receptor-2VASH1 protein, human

Identifiers

PMID18325046
PMCPMC11158585
OpenAlexW2095518272

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.