Evidence map›Paper›PMID 35163250›Full record

ArticleInternational journal of molecular sciences2022

Blockade of β2-Adrenergic Receptor Reduces Inflammation and Oxidative Stress in Clear Cell Renal Cell Carcinoma.

Virginia Albiñana, Lucía Recio-Poveda, Pilar González-Peramato, Luis Martinez-Piñeiro, Luisa María Botella, Angel M Cuesta

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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. β-Adrenoceptors in Cancer: Old Players and New Perspectives.Handbook of experimental pharmacology · 2024
    Review
  10. Sympathetic Nervous System and Atherosclerosis.International journal of molecular sciences · 2023
    Review
  11. 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 4 institutions in 1 country.

Virginia AlbiñanaCentro de Investigaciones Biológicas Margaritas Salas, 28040 Madrid, Spain.
Lucía Recio-PovedaCentro de Investigaciones Biológicas Margaritas Salas, 28040 Madrid, Spain.
Pilar González-PeramatoDepartment of Pathology, La Paz University Hospital, Autonomous University of Madrid, 28029 Madrid, Spain.
Luis Martinez-PiñeiroDepartment of Urology, Instituto de Investigación IdiPaz, 28029 Madrid, Spain.
Luisa María BotellaCentro de Investigaciones Biológicas Margaritas Salas, 28040 Madrid, Spain.ORCID 0000-0002-6310-2245
Angel M CuestaDepartment of Biochemistry and Molecular Biology, Faculty of Pharmacy, Complutense University of Madrid, 28040 Madrid, Spain.ORCID 0000-0002-6596-9600
Instituto de Salud Carlos III · ESHospital La Paz Institute for Health Research · ESUniversidad Autónoma de Madrid · ESUniversidad Complutense de Madrid · ES

Funding

Alianza Española de pacientes y familiares de von Hippel Lindau AVHL lab 109Centre for Biomedical Network Research on Rare Diseases U-707Ministry of Economy, Industry and Competitiveness SAF-2017-83351RProyecto Intramural Especial CSIC PIE-201820E073
6 · The paper itself

Abstract

Von Hippel-Lindau (VHL) syndrome is a rare inherited cancer disease where the lack of VHL protein triggers the development of multisystemic tumors such us retinal hemangioblastomas (HBs), CNS-HBs, and clear cell renal cell carcinoma (ccRCC). Since standard therapies in VHL have shown limited response, leaving surgery as the only possible treatment, targeting of the β2-adrenergic receptor (ADRB2) has shown therapeutic antitumor benefits on VHL-retinal HBs (clinical trial), VHL-CNS HBs, and VHL-ccRCC (in vitro and in vivo). In the present study, we wanted to look deep into the effects of the ADRB2 blockers propranolol and ICI-118,551 on two main aspects of cancer progression: (i) the changes on the inflammatory response of ccRCC cells; and (ii) the modulation on the Warburg effect (glycolytic metabolism), concretely, on the expression of genes involved in the cell reactive oxygen species (ROS) balance and levels. Accordingly, in vitro studies with primary VHL-ccRCC and 786-O cells measuring ROS levels, ROS-expression of detoxifying enzymes, and the expression of p65/NF-κB targets by RT-PCR were carried out. Furthermore, histological analyses of ccRCC samples from heterotopic mouse xenografts were performed. The obtained results show that ADRB2 blockade in ccRCC cells reduces the level of oxidative stress and stabilizes the inflammatory response. Thus, these data further support the idea of targeting ADRB2 as a promising strategy for the treatment of VHL and other non-VHL tumors.

Indexed as

AnimalsCarcinoma, Renal CellCell Line, TumorGene Expression Regulation, NeoplasticHemangioblastomaHumansInflammationKidney NeoplasmsMaleMiceOxidative StressPropanolaminesPropranololReceptors, Adrenergic, beta-2Signal Transductionvon Hippel-Lindau DiseaseICI 118551PropanolaminesPropranololReceptors, Adrenergic, beta-2Von Hippel-Lindau Tumor Suppressor Proteincancer therapyccRCChemangioblastomaICI-118,551inflammatory cytokinespropranololreactive oxygen species (ROS)von Hippel-Lindauβ-adrenergic receptorβ-blocker

Identifiers

PMID35163250
PMCPMC8835934
OpenAlexW4210273142

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.