Evidence map›Paper›PMID 32498717›Full record

ArticleJournal of experimental & clinical cancer research : CR2020

Inhibition of lysine acetyltransferases impairs tumor angiogenesis acting on both endothelial and tumor cells.

Marta Di Martile, Chiara Gabellini, Marianna Desideri, Marta Matraxia, Valentina Farini, Elisabetta Valentini, Simone Carradori, Cristiana Ercolani, Simonetta Buglioni, Daniela Secci and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 38% 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, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. 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

13 authors at 6 institutions in 2 countries.

Marta Di MartilePreclinical Models and New Therapeutic Agents Unit, Department of Research and Advanced Technologies, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Chiara GabelliniUnit of Cell and Developmental Biology, Department of Biology, University of Pisa, Pisa, Italy.
Marianna DesideriPreclinical Models and New Therapeutic Agents Unit, Department of Research and Advanced Technologies, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Marta MatraxiaInstitute of Molecular Biology and Pathology, National Research Council, Rome, Italy.
Valentina FariniPreclinical Models and New Therapeutic Agents Unit, Department of Research and Advanced Technologies, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Elisabetta ValentiniPreclinical Models and New Therapeutic Agents Unit, Department of Research and Advanced Technologies, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Simone CarradoriDepartment of Pharmacy, University "G. d'Annunzio" of Chieti-Pescara, Chieti, Italy.
Cristiana ErcolaniPathology Unit, Department of Research and Advanced Technologies, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Simonetta BuglioniPathology Unit, Department of Research and Advanced Technologies, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Daniela SecciDepartment of Chemistry and Technologies of Drugs, "Sapienza" University, Rome, Italy.
Massimiliano AndreazzoliUnit of Cell and Developmental Biology, Department of Biology, University of Pisa, Pisa, Italy.
Donatella Del BufaloPreclinical Models and New Therapeutic Agents Unit, Department of Research and Advanced Technologies, IRCCS Regina Elena National Cancer Institute, Rome, Italy. donatella.delbufalo@ifo.gov.it.
Daniela TrisciuoglioPreclinical Models and New Therapeutic Agents Unit, Department of Research and Advanced Technologies, IRCCS Regina Elena National Cancer Institute, Rome, Italy. daniela.trisciuoglio@uniroma1.it.ORCID http://orcid.org/0000-0002-7007-7914
Istituti di Ricovero e Cura a Carattere Scientifico · ITInstitute of Molecular Biology and Pathology · ITUniversity of Pisa · ITNational Cancer Institute · MYSapienza University of Rome · ITUniversity of Chieti-Pescara · IT

Funding

AIRC IG18560Regione Lazio 15438 MITOIM
6 · The paper itself

Abstract

backgroundUnderstanding the signalling pathways involved in angiogenesis, and developing anti-angiogenic drugs are one of the major focuses on cancer research. Herein, we assessed the effect of CPTH6, a lysine acetyltransferase inhibitor and anti-tumoral compound, on angiogenesis-related properties of both endothelial and cancer cells.

methodsThe in vitro effect of CPTH6 on protein acetylation and anti-angiogenic properties on endothelial and lung cancer cells was evaluated via wound healing, trans-well invasion and migration, tube formation, immunoblotting and immunofluorescence. Matrigel plug assay, zebrafish embryo and mouse xenograft models were used to evaluate in vivo anti-angiogenic effect of CPTH6.

resultsCPTH6 impaired in vitro endothelial angiogenesis-related functions, and decreased the in vivo vascularization both in mice xenografts and zebrafish embryos. Mechanistically, CPTH6 reduced α-tubulin acetylation and induced accumulation of acetylated microtubules in the perinuclear region of endothelial cells. Interestingly, CPTH6 also affected the angiogenesis-related properties of lung cancer cells, and conditioned media derived from CPTH6-treated lung cancer cells impaired endothelial cells morphogenesis. CPTH6 also modulated the VEGF/VEGFR2 pathway, and reshaped cytoskeletal organization of lung cancer cells. Finally, anti-migratory effect of CPTH6, dependent on α-tubulin acetylation, was also demonstrated by genetic approaches in lung cancer cells.

conclusionOverall, this study indicates that α-tubulin acetylation could play a role in the anti-angiogenic effect of CPTH6 and, more in general, it adds information to the role of histone acetyltransferases in tumor angiogenesis, and proposes the inhibition of these enzymes as an antiangiogenic therapy of cancer.

Indexed as

Angiogenesis InhibitorsAnimalsApoptosisCell DifferentiationCell MovementCell ProliferationHumansHuman Umbilical Vein Endothelial CellsLung NeoplasmsLysine AcetyltransferasesMiceMice, Inbred NODMice, SCIDNeovascularization, PathologicSignal TransductionThiazoles3-methylcyclopentylidene-(4-(4'-chlorophenyl)thiazol-2-yl)hydrazoneAngiogenesis InhibitorsKDR protein, humanLysine AcetyltransferasesThiazolesVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-2VEGFA protein, humanAcetylationEndothelial cellsLung cancer cellsTubulin

Identifiers

PMID32498717
PMCPMC7273677
OpenAlexW3033281519

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.