Evidence map›Paper›PMID 28886304›Full record

ReviewCancer biology & therapy2017

The roles of vasohibin and its family members: Beyond angiogenesis modulators.

Hua Du, Jing Zhao, Ling Hai, Jing Wu, Hua Yi, Yonghong Shi

Open access · hybridAbstract readReview
In one paragraph

Review in Cancer biology & therapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

20 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Life science alliance · 2020
    Article
  16. Review
  17. Review
  18. A review on vasohibin and ocular neovascularization.International journal of ophthalmology · 2020
    Review
  19. 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

6 authors at 1 institution in 1 country.

Hua Dua The Department of Pathology Affiliated Hospital , Inner Mongolia Medical University Hohhot City, Inner Mongolia Autonomous Region , R. P. of China.
Jing Zhaoa The Department of Pathology Affiliated Hospital , Inner Mongolia Medical University Hohhot City, Inner Mongolia Autonomous Region , R. P. of China.
Ling Haia The Department of Pathology Affiliated Hospital , Inner Mongolia Medical University Hohhot City, Inner Mongolia Autonomous Region , R. P. of China.
Jing Wua The Department of Pathology Affiliated Hospital , Inner Mongolia Medical University Hohhot City, Inner Mongolia Autonomous Region , R. P. of China.
Hua Yia The Department of Pathology Affiliated Hospital , Inner Mongolia Medical University Hohhot City, Inner Mongolia Autonomous Region , R. P. of China.
Yonghong Shia The Department of Pathology Affiliated Hospital , Inner Mongolia Medical University Hohhot City, Inner Mongolia Autonomous Region , R. P. of China.
Inner Mongolia Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vasohibin-1 is an intrinsic angiogenesis inhibitor, and is expressed in endothelial cells via induction by pro-angiogenesis factors. It is known to inhibit several processes of angiogenesis, with different mechanisms from extrinsic angiogenesis inhibitors. Vasohibin-2 is mainly expressed by mononuclear cells which have been mobilized from bone marrow. It not only promotes angiogenesis, but also modulates the releases of FGF-2 and VEGF, which are the two major inducers for vasohibin1. Hypoxic environment induces the expression of hypoxia-inducible Factor 1α with a result of VEGF release nearly in all tumor cell lines and tissues. However, it has been observed that hypoxia reduces the inducible effects of VEGF on vasohibin, which indicates that a complicated mechanism exists in the angiogenesis. Vasohibin and its family members play important roles in both the physiological and pathological procedures, in contrary but complementary patterns. Furthermore, human aortic smooth muscle cells and fibroblast have also been detected to express vasohibin on a moderate to weak scale range. Recently, the results of an increasing number of studies in vivo have shown that vasohibin can also be detected in several cancers, and is associated with micro-vessel densities, histology grades, invasions, poor clinical features, metastasis, and dissemination in abdominal cavities, as well as EMT. In more recent reports, it has been confirmed that, along with being angiogenesis regulators, a variety of other roles have been associated with this family. The focus of this study was the upstream regulatory mechanisms of vasohibin expressions, and their role in regard to the downstream target proteins of vasohibin, especially in carcinoma. Vasohibin is considered to be an original angiogenesis inhibitor, and has a much broader significance in pathological processes. It can be taken as an independent prognostic factor, as well as a potential strategy for cancer therapy programs.

Indexed as

Angiogenesis Modulating AgentsCell Cycle ProteinsHumansAngiogenesis Modulating AgentsCell Cycle ProteinsVASH1 protein, humanangiogenesisangiogenesis inhibitorcarcinogenesisgrowth and differentiation regulating factorsnatural anticancer compoundsprognostic markertumors

Identifiers

PMID28886304
PMCPMC5710674
OpenAlexW2752782732

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.