Evidence map›Paper›PMID 34426652›Full record

ArticleCancer gene therapy2022

Cholenic acid derivative UniPR1331 impairs tumor angiogenesis via blockade of VEGF/VEGFR2 in addition to Eph/ephrin.

Marco Rusnati, Giulia Paiardi, Chiara Tobia, Chiara Urbinati, Alessio Lodola, Pasqualina D'Ursi, Miriam Corrado, Riccardo Castelli, Rebecca C Wade, Massimiliano Tognolini and 1 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Cancer gene therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 46% 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

4 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 3 countries.

Marco RusnatiExperimental Oncology and Immunology, Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Giulia PaiardiExperimental Oncology and Immunology, Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Chiara TobiaExperimental Oncology and Immunology, Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Chiara UrbinatiExperimental Oncology and Immunology, Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Alessio LodolaDepartment of Food and Drug, University of Parma, Parma, Italy.ORCID http://orcid.org/0000-0002-8675-1002
Pasqualina D'UrsiInstitute for Biomedical Technologies, National Research Council (ITB-CNR), Segrate, MI, Italy.
Miriam CorradoDepartment of Food and Drug, University of Parma, Parma, Italy.
Riccardo CastelliDepartment of Food and Drug, University of Parma, Parma, Italy.
Rebecca C WadeMolecular and Cellular Modeling Group, Heidelberg Institute for Theoretical Studies, Heidelberg, Germany.
Massimiliano TognoliniDepartment of Food and Drug, University of Parma, Parma, Italy.
Paola ChiodelliExperimental Oncology and Immunology, Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy. paola.chiodelli@unibs.it.ORCID http://orcid.org/0000-0002-8702-0623
University of Brescia · ITUniversity of Parma · ITHeidelberg Institute for Theoretical Studies · DEHeidelberg University · DENational Academies of Sciences, Engineering, and Medicine · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Angiogenesis, the formation of new blood vessels from preexisting ones, is crucial for tumor growth and metastatization, and is considered a promising therapeutic target. Unfortunately, drugs directed against a specific proangiogenic growth factor or receptor turned out to be of limited benefit for oncology patients, likely due to the high biochemical redundancy of the neovascularization process. In this scenario, multitarget compounds that are able to simultaneously tackle different proangiogenic pathways are eagerly awaited. UniPR1331 is a 3β-hydroxy-Δ

Indexed as

EphrinsVascular Endothelial Growth Factor Receptor-2Angiogenesis InhibitorsAnimalsEndothelial CellsNeovascularization, PathologicVascular Endothelial Growth Factor AZebrafishAngiogenesis InhibitorsEphrinsVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-2

Identifiers

PMID34426652
PMCPMC9293752
OpenAlexW3194002753

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.