Evidence map›Paper›PMID 31052299›Full record

ArticleInternational journal of molecular sciences2019

β3-Adrenoreceptor Activity Limits Apigenin Efficacy in Ewing Sarcoma Cells: A Dual Approach to Prevent Cell Survival.

Amada Pasha, Marina Vignoli, Angela Subbiani, Alessio Nocentini, Silvia Selleri, Paola Gratteri, Annalisa Dabraio, Tommaso Casini, Luca Filippi, Ilaria Fotzi and 2 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Spotlight on ROS andOxidative medicine and cellular longevity · 2019
    Review
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 2 institutions in 1 country.

Amada PashaDivision of Pediatric Oncology/Hematology, Meyer University Children's Hospital, 50139 Florence, Italy. amanda.pasha@yahoo.it.
Marina VignoliDivision of Pediatric Oncology/Hematology, Meyer University Children's Hospital, 50139 Florence, Italy. marina.vignoli@unifi.it.
Angela SubbianiDivision of Pediatric Oncology/Hematology, Meyer University Children's Hospital, 50139 Florence, Italy. angela.subbiani@gmail.com.
Alessio NocentiniNEUROFARBA Department, Pharmaceutical and nutraceutical section, University of Florence, 50019 Sesto Fiorentino, Italy. alessio.nocentini@unifi.it.
Silvia SelleriNEUROFARBA Department, Pharmaceutical and nutraceutical section, University of Florence, 50019 Sesto Fiorentino, Italy. silvia.selleri@unifi.it.
Paola GratteriLaboratory of Molecular Modeling Cheminformatics & QSAR, NEUROFARBA Department, Pharmaceutical and nutraceutical section, University of Florence, 50019 Sesto Fiorentino, Italy. paola.gratteri@unifi.it.
Annalisa DabraioDivision of Pediatric Oncology/Hematology, Meyer University Children's Hospital, 50139 Florence, Italy. annalisa.d.92@gmail.com.
Tommaso CasiniDivision of Pediatric Oncology/Hematology, Meyer University Children's Hospital, 50139 Florence, Italy. tommaso.casini@meyer.it.
Luca FilippiNeonatal Intensive Care Unit, Medical Surgical Fetal-Neonatal Department, Meyer "University Children's Hospital, 50139 Florence, Italy. luca.filippi@meyer.it.
Ilaria FotziDivision of Pediatric Oncology/Hematology, Meyer University Children's Hospital, 50139 Florence, Italy. ilaria.fotzi@meyer.it.
Claudio FavreDivision of Pediatric Oncology/Hematology, Meyer University Children's Hospital, 50139 Florence, Italy. claudio.favre@meyer.it.
Maura CalvaniDivision of Pediatric Oncology/Hematology, Meyer University Children's Hospital, 50139 Florence, Italy. maura.calvani@meyer.it.
Meyer Children's Hospital · ITUniversity of Florence · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ewing Sarcoma (ES) is an aggressive paediatric tumour where oxidative stress and antioxidants play a central role in cancer therapy response. Inhibiting antioxidants expression, while at the same time elevating intracellular reactive oxygen species (ROS) levels, have been proposed as a valid strategy to overcome ES cancer progression. Flavonoid intake can affect free radical and nutritional status in children receiving cancer treatment, but it is not clear if it can arrest cancer progression. In particular, apigenin may enhance the effect of cytotoxic chemotherapy by inducing cell growth arrest, apoptosis, and by altering the redox state of the cells. Little is known about the use of apigenin in paediatric cancer. Recently, β3-adrenergic receptor (β3-AR) antagonism has been proposed as a possible strategy in cancer therapy for its ability to induce apoptosis by increasing intracellular levels of ROS. In this study we show that apigenin induces cell death in ES cells by modulating apoptosis, but not increasing ROS content. Since ES cells are susceptible to an increased oxidative stress to reduce cell viability, here we demonstrate that administration of β3-ARs antagonist, SR59230A, improves the apigenin effect on cell death, identifying β3-AR as a potential discriminating factor that could address the use of apigenin in ES.

Indexed as

Adrenergic beta-AgonistsAntineoplastic AgentsAntioxidantsApigeninApoptosisCell Line, TumorDrug SynergismHumansPropanolaminesReceptors, Adrenergic, beta-3Sarcoma, Ewing3-(2-ethylphenoxy)-1-(1,2,3,4-tetrahydronaphth-1-ylamino)-2-propanol oxalateAdrenergic beta-AgonistsAntineoplastic AgentsAntioxidantsApigeninPropanolaminesReceptors, Adrenergic, beta-3apigeninEwing Sarcomaβ3-adrenoreceptor

Identifiers

PMID31052299
PMCPMC6540192
OpenAlexW2943131817

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.