Evidence map›Paper›PMID 26059764›Full record

ArticleAngiogenesis2015

Hypoxia-induced expression of phosducin-like 3 regulates expression of VEGFR-2 and promotes angiogenesis.

Srimathi Srinivasan, Vipul Chitalia, Rosana D Meyer, Edward Hartsough, Manisha Mehta, Itrat Harrold, Nicole Anderson, Hui Feng, Lois E H Smith, Yan Jiang and 2 more

Open access · greenAbstract read
In one paragraph

Article in Angiogenesis, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

29 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
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  6. Article
  7. Novel Drugs with High Efficacy against Tumor Angiogenesis.International journal of molecular sciences · 2022
    Review
  8. Article
  9. Article
  10. Targeting macrophages in cancer immunotherapy.Signal transduction and targeted therapy · 2021
    Article
  11. Article
  12. Article
  13. Review
  14. The role of microenvironment in tumor angiogenesis.Journal of experimental & clinical cancer research : CR · 2020
    Review
  15. Article
  16. Article
  17. Article
  18. Calcium Permeable Channels in Cancer Hallmarks.Frontiers in pharmacology · 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

12 authors at 5 institutions in 1 country.

Srimathi SrinivasanDepartments of Pathology and Ophthalmology, Boston University School of Medicine, Boston, MA, 02118, USA.
Vipul ChitaliaRenal Section, Department of Medicine, Boston Medical Center, Boston University School of Medicine, Boston, MA, USA.
Rosana D MeyerDepartments of Pathology and Ophthalmology, Boston University School of Medicine, Boston, MA, 02118, USA.
Edward HartsoughDepartments of Pathology and Ophthalmology, Boston University School of Medicine, Boston, MA, 02118, USA.
Manisha MehtaDepartments of Pathology and Ophthalmology, Boston University School of Medicine, Boston, MA, 02118, USA.
Itrat HarroldSection of Hematology and Medical Oncology, Department of Pharmacology and Experimental Therapeutics, The Center for Cancer Research, Boston University School of Medicine, Boston, MA, USA.
Nicole AndersonSection of Hematology and Medical Oncology, Department of Pharmacology and Experimental Therapeutics, The Center for Cancer Research, Boston University School of Medicine, Boston, MA, USA.
Hui FengSection of Hematology and Medical Oncology, Department of Pharmacology and Experimental Therapeutics, The Center for Cancer Research, Boston University School of Medicine, Boston, MA, USA.
Lois E H SmithDepartment of Ophthalmology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Yan JiangDepartment of Biochemistry and Center for Biomedical Mass Spectrometry, School of Medicine, Boston University Medical Campus, Boston, MA, USA.
Catherine E CostelloDepartment of Biochemistry and Center for Biomedical Mass Spectrometry, School of Medicine, Boston University Medical Campus, Boston, MA, USA.
Nader RahimiDepartments of Pathology and Ophthalmology, Boston University School of Medicine, Boston, MA, 02118, USA. nrahimi@bu.edu.
Boston University · USUniversity School · USBoston Medical Center · USCenter for Cancer Research · USHarvard University · US

Funding

XI INTERNATIONAL SYMPOSIUM ON AMYLOIDOSISP41RR010888 · NCRR · BOSTON UNIVERSITY MEDICAL CAMPUS · PI ZAIA, JOSEPH · 1996 to 2011
$18.6M
Dietary control of angiogenesis in retinopathy modelsR01EY017017 · NEI · BOSTON CHILDREN'S HOSPITAL · PI Zhongjie Fu, Lois Smith · 2006 to 2026
$11.8M
Mass Spectrometry Resource for Biology and MedicineP41GM104603 · NIGMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI COSTELLO, CATHERINE E. · 2012 to 2017
$10.4M
Novel therapies to inhibit Diabetic RetinopathyR24EY024864 · NEI · UNIVERSITY OF CALIFORNIA-IRVINE · PI KERN, TIMOTHY S · 2015 to 2019
$8.1M
Mouse Neurodevelopmental Behavior CoreU54HD090255 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI POMEROY, SCOTT LOREN · 2016 to 2020
$5.2M
Role of c-Cbl in Colon cancerR01CA175382 · NCI · BOSTON MEDICAL CENTER · PI CHITALIA, VIPUL C · 2014 to 2018
$1.8M
Role of Protein Ubiquitination in AngiogenesisR01EY017955 · NEI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI RAHIMI, NADER · 2008 to 2010
$1.2M
Role of Wnt signaling in uremia-induced entothelial dysfunctionK08DK080946 · NIDDK · BOSTON MEDICAL CENTER · PI CHITALIA, VIPUL C · 2009 to 2013
$746k
LTQ MASS SPECTROMETER: STRUCTURAL BIOLOGYS10RR020946 · NCRR · BOSTON UNIVERSITY MEDICAL CAMPUS · PI ZAIA, JOSEPH · 2006 to 2006
$497k
Overcoming the resistance to anti-angiogenesis therapyR21CA191970 · NCI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI RAHIMI, NADER · 2015 to 2016
$392k
IGPR-1 in colon cancer chemotherapyR21CA193958 · NCI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI RAHIMI, NADER · 2015 to 2016
$392k
STRUCTURAL CHARACTERIZATION OF THE APOPROTEIN E RECEPTORR01HL028178 · NHLBI · J. DAVID GLADSTONE INSTITUTES · PI INNERARITY, THOMAS L. · 1986 to 1988
–
NCI NIH HHS R01 CA175382NCI NIH HHS R21 CA191970NCI NIH HHS R21 CA193958NCRR NIH HHS P41 RR010888NCRR NIH HHS P41RR010888NCRR NIH HHS S10 RR020946NEI NIH HHS R01 EY017017NEI NIH HHS R01 EY017955NEI NIH HHS R01EY017955NEI NIH HHS R24 EY024864NHLBI NIH HHS HHSN268201000031CNHLBI NIH HHS N01 HV028178NICHD NIH HHS U54 HD090255NIDDK NIH HHS DK080946NIDDK NIH HHS K08 DK080946NIGMS NIH HHS GM104603NIGMS NIH HHS P41 GM104603
6 · The paper itself

Abstract

Expression and activation of vascular endothelial growth factor receptor 2 (VEGFR-2) by VEGF ligands are the main events in the stimulation of pathological angiogenesis. VEGFR-2 expression is generally low in the healthy adult blood vessels, but its expression is markedly increased in the pathological angiogenesis. In this report, we demonstrate that phosducin-like 3 (PDCL3), a recently identified chaperone protein involved in the regulation of VEGFR-2 expression, is required for angiogenesis in zebrafish and mouse. PDCL3 undergoes N-terminal methionine acetylation, and this modification affects PDCL3 expression and its interaction with VEGFR-2. Expression of PDCL3 is regulated by hypoxia, the known stimulator of angiogenesis. The mutant PDCL3 that is unable to undergo N-terminal methionine acetylation was refractory to the effect of hypoxia. The siRNA-mediated silencing of PDCL3 decreased VEGFR-2 expression resulting in a decrease in VEGF-induced VEGFR-2 phosphorylation, whereas PDCL3 over-expression increased VEGFR-2 protein. Furthermore, we show that PDCL3 protects VEGFR-2 from misfolding and aggregation. The data provide new insights for the chaperone function of PDCL3 in angiogenesis and the roles of hypoxia and N-terminal methionine acetylation in PDCL3 expression and its effect on VEGFR-2.

Indexed as

Gene Expression RegulationNeovascularization, PhysiologicAnimalsCarrier ProteinsHEK293 CellsHumansHuman Umbilical Vein Endothelial CellsHypoxiaMiceMolecular ChaperonesNerve Tissue ProteinsProtein FoldingVascular Endothelial Growth Factor Receptor-2Carrier ProteinsKDR protein, humanKdr protein, mouseMolecular ChaperonesNerve Tissue ProteinsPDCL3 protein, humanVascular Endothelial Growth Factor Receptor-2AngiogenesisChaperone proteinHypoxiaN-terminal methionine acetylationPDCL3Protein ubiquitinationVEGFR-2

Identifiers

PMID26059764
PMCPMC4600037
OpenAlexW1790297113

What OpenQuestion holds

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LicenceTDM
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.