Evidence map›Paper›PMID 35055064›Full record

ArticleInternational journal of molecular sciences2022

Hypoxia Marker Carbonic Anhydrase IX Is Present in Abdominal Aortic Aneurysm Tissue and Plasma.

Katarina Grossmannova, Monika Barathova, Petra Belvoncikova, Viliam Lauko, Lucia Csaderova, Jan Tomka, Tomas Dulka, Jaromir Pastorek, Juraj Madaric

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
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  4. Review
  5. Progress of Section "Biochemistry" in 2022.International journal of molecular sciences · 2023
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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

9 authors at 3 institutions in 1 country.

Katarina GrossmannovaDepartment of Cancer Biology, Institute of Virology, Biomedical Research Center, Slovak Academy of Sciences, Dúbravská Cesta 9, 84505 Bratislava, Slovakia.
Monika BarathovaDepartment of Cancer Biology, Institute of Virology, Biomedical Research Center, Slovak Academy of Sciences, Dúbravská Cesta 9, 84505 Bratislava, Slovakia.
Petra BelvoncikovaDepartment of Cancer Biology, Institute of Virology, Biomedical Research Center, Slovak Academy of Sciences, Dúbravská Cesta 9, 84505 Bratislava, Slovakia.
Viliam LaukoDepartment of Laboratory Medicine, National Institute of Cardiovascular Disease, Pod Krásnou Hôrkou 1, 83101 Bratislava, Slovakia.
Lucia CsaderovaDepartment of Cancer Biology, Institute of Virology, Biomedical Research Center, Slovak Academy of Sciences, Dúbravská Cesta 9, 84505 Bratislava, Slovakia.
Jan TomkaDepartment of Vascular Surgery, National Institute of Cardiovascular Disease, Pod Krásnou Hôrkou 1, 83101 Bratislava, Slovakia.
Tomas DulkaDepartment of Vascular Surgery, National Institute of Cardiovascular Disease, Pod Krásnou Hôrkou 1, 83101 Bratislava, Slovakia.
Jaromir PastorekMABPRO, a.s., Dúbravská Cesta 2, 84104 Bratislava, Slovakia.
Juraj MadaricDepartment of Angiology, National Institute of Cardiovascular Disease, Pod Krásnou Hôrkou 1, 83101 Bratislava, Slovakia.
National Institute of Cardiovascular Diseases · SKInstitute of Virology of the Slovak Academy of Sciences · SKBiomedical Research Center of the Slovak Academy of Sciences · SK

Funding

Research & Developmental Support Agency APVV-16-0343Slovak Scientific Grant Agency VEGA 2/0061/21Slovak Scientific Grant Agency VEGA 2/0064/18Slovak Scientific Grant Agency VEGA 2/0090/20
6 · The paper itself

Abstract

Abdominal aortic aneurysms (AAA) are a significant cause of premature deaths worldwide. Since there is no specific treatment for reducing AAA progression, it is crucial to understand the pathogenesis leading to aneurysm wall weakening/remodeling and identify new proteins involved in this process which could subsequently serve as novel therapeutic targets. In this study, we analyzed the presence of the hypoxia-related proteins carbonic anhydrase IX (CA IX), hypoxia-inducible factor 1α (HIF-1α), and AKT as the key molecule in the phosphoinositide-3-kinase pathway in the AAA wall. Additionally, we used a blood-based assay to examine soluble CA IX (s-CA IX) levels in the plasma of AAA patients. Using western blotting, we detected CA IX protein in 12 out of 15 AAA tissue samples. Immunohistochemistry staining proved CA IX expression in the media of the aneurysmal wall. Evaluation of phosphorylated (p-AKT) and total AKT showed elevated levels of both forms in AAA compared to normal aorta. Using ELISA, we determined the concentration of s-CA IX >20 pg/mL in 13 out of 15 AAA patients. Results obtained from in silico analysis of

Indexed as

BiomarkersAgedAged, 80 and overAortic Aneurysm, AbdominalCarbonic Anhydrase IXDisease SusceptibilityFemaleGene ExpressionGene Expression ProfilingHumansHypoxiaHypoxia-Inducible Factor 1, alpha SubunitImmunohistochemistryMaleProto-Oncogene Proteins c-aktBiomarkersCarbonic Anhydrase IXHypoxia-Inducible Factor 1, alpha SubunitProto-Oncogene Proteins c-aktabdominal aortic aneurysmcarbonic anhydrase IXhypoxiahypoxia-inducible factor 1

Identifiers

PMID35055064
PMCPMC8778372
OpenAlexW4205310235

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Registered trials

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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.