Evidence map›Paper›PMID 23723256›Full record

ArticleCirculation2013

Androgen receptor promotes sex-independent angiogenesis in response to ischemia and is required for activation of vascular endothelial growth factor receptor signaling.

Sumiko Yoshida, Ken-Ichi Aihara, Yasumasa Ikeda, Yuka Sumitomo-Ueda, Ryoko Uemoto, Kazue Ishikawa, Takayuki Ise, Shusuke Yagi, Takashi Iwase, Yasuhiro Mouri and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in Circulation, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing 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

37 citing papers in PubMed, 69 citations in OpenAlex.

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  19. Estrogen-related receptor α is involved in angiogenesis and skeletal muscle revascularization in hindlimb ischemia.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  20. Gender Differences in Gastric Cancer Survival: 99,922 Cases Based on the SEER Database.Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract · 2020
    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

19 authors at 3 institutions in 1 country.

Sumiko YoshidaDepartment of Medicine and Bioregulatory Sciences, University of Tokushima Graduate School of Health Biosciences, 3-18-15 Kuramoto-cho Tokushima 770-8503, Japan. toshio.matsumoto@tokushima-u.ac.jp
Ken-Ichi Aihara
Yasumasa Ikeda
Yuka Sumitomo-Ueda
Ryoko Uemoto
Kazue Ishikawa
Takayuki Ise
Shusuke Yagi
Takashi Iwase
Yasuhiro Mouri
Matomo Sakari
Takahiro Matsumoto
Ken-Ichi Takeyama
Masashi Akaike
Mitsuru Matsumoto
Masataka Sata
Kenneth Walsh
Shigeaki Kato
Toshio Matsumoto
The University of Tokyo · JPTokushima University · JPMatsumoto University · JP

Funding

Muscle loss and metabolic dysfunction associated with agingR01AG034972 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI WALSH, KENNETH · 2010 to 2014
$1.6M
NIA NIH HHS R01 AG034972
6 · The paper itself

Abstract

backgroundHypoandrogenemia is associated with an increased risk of ischemic diseases. Because actions of androgens are exerted through androgen receptor (AR) activation, we studied hind-limb ischemia in AR knockout mice to elucidate the role of AR in response to ischemia. METHODS AND

resultsBoth male and female AR knockout mice exhibited impaired blood flow recovery, more cellular apoptosis, and a higher incidence of autoamputation after ischemia. In ex vivo and in vivo angiogenesis studies, AR-deficient vascular endothelial cells showed reduced angiogenic capability. In ischemic limbs of AR knockout mice, reductions in the phosphorylation of the Akt protein kinase and endothelial nitric oxide synthase were observed despite a robust increase in hypoxia-inducible factor 1α and vascular endothelial cell growth factor (VEGF) gene expression. In in vitro studies, siRNA-mediated ablation of AR in vascular endothelial cells blunted VEGF-stimulated phosphorylation of Akt and endothelial nitric oxide synthase. Immunoprecipitation experiments documented an association between AR and kinase insert domain protein receptor that promoted the recruitment of downstream signaling components.

conclusionsThese results document a physiological role of AR in sex-independent angiogenic potency and provide evidence of novel cross-talk between the androgen/AR signaling and VEGF/kinase insert domain protein receptor signaling pathways.

Indexed as

Amputation StumpsAnimalsApoptosisCapillariesFemaleFeminizationHindlimbHumansHuman Umbilical Vein Endothelial CellsIschemiaMaleMiceMice, KnockoutMuscle, SkeletalNeovascularization, PhysiologicNitric Oxide Synthase Type IIIAkt1 protein, mouseNitric Oxide Synthase Type IIINos3 protein, mousePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktProto-Oncogene Proteins pp60(c-src)Receptors, AndrogenVascular Endothelial Growth Factor Receptor-2Akt1 protein, mouseangiogenesis inducing agentsnitric oxide synthase type IIIreceptors, androgenvascular endothelial growth factor receptor-2

Identifiers

PMID23723256
PMCPMC3933182
OpenAlexW1983118275

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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.