Evidence map›Paper›PMID 25881671›Full record

ReviewClinical science (London, England : 1979)2015

PEDF and its roles in physiological and pathological conditions: implication in diabetic and hypoxia-induced angiogenic diseases.

Xuemin He, Rui Cheng, Siribhinya Benyajati, Jian-xing Ma

Abstract readReview
In one paragraph

Review in Clinical science (London, England : 1979), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
–field-weighted citation impact
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

79 citing papers in PubMed.

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19 more citing papers are in PubMed but not listed here.

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

4 authors.

Xuemin He*Department of Physiology, The University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Rui Cheng*Department of Physiology, The University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Siribhinya Benyajati*Department of Physiology, The University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Jian-xing Ma*Department of Physiology, The University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pigment epithelium-derived factor (PEDF) is a broadly expressed multifunctional member of the serine proteinase inhibitor (serpin) family. This widely studied protein plays critical roles in many physiological and pathophysiological processes, including neuroprotection, angiogenesis, fibrogenesis and inflammation. The present review summarizes the temporal and spatial distribution patterns of PEDF in a variety of developing and adult organs, and discusses its functions in maintaining physiological homoeostasis. The major focus of the present review is to discuss the implication of PEDF in diabetic and hypoxia-induced angiogenesis, and the pathways mediating PEDF's effects under these conditions. Furthermore, the regulatory mechanisms of PEDF expression, function and degradation are also reviewed. Finally, the therapeutic potential of PEDF as an anti-angiogenic drug is briefly summarized.

Indexed as

AdultAngiogenesis InhibitorsDiabetes MellitusEye ProteinsGene Expression ProfilingHumansHypoxiaNeovascularization, PathologicNeovascularization, PhysiologicNerve Growth FactorsPigment Epithelium-Derived FactorSerpinsSignal TransductionAngiogenesis InhibitorsEye ProteinsNerve Growth FactorsPigment Epithelium-Derived FactorSerpins

Identifiers

PMID25881671
PMCPMC4557399

What OpenQuestion holds

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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.