Evidence map›Paper›PMID 33072918›Full record

ArticleHeliyon2020

Anti-metastatic action of an

A M Sólimo, M C Soraires Santacruz, S Vanzulli, O Coggiola, E Bal de Kier Joffé, L Finkielsztein, M A Callero

Abstract read
In one paragraph

Article in Heliyon, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

7 authors.

A M SólimoUniversidad de Buenos Aires, Instituto de Oncología "Ángel H. Roffo", Área Investigación, Dpto. Inmunobiología, Ciudad Autónoma de Buenos Aires, Argentina.
M C Soraires SantacruzUniversidad de Buenos Aires, Facultad de Farmacia y Bioquímica, Departamento de Farmacología, Cátedra de Química Medicinal, Ciudad Autónoma de Buenos Aires, Argentina.
S VanzulliInstituto de Investigaciones Hematológicas (IIHEMA), Academia de Medicina, Ciudad Autónoma de Buenos Aires, Argentina.
O CoggiolaUniversidad de Buenos Aires, Instituto de Oncología "Ángel H. Roffo", Laboratorio Central, Buenos Aires, Argentina.
E Bal de Kier JofféUniversidad de Buenos Aires, Instituto de Oncología "Ángel H. Roffo", Área Investigación, Dpto. Inmunobiología, Ciudad Autónoma de Buenos Aires, Argentina.
L FinkielszteinUniversidad de Buenos Aires, Facultad de Farmacia y Bioquímica, Departamento de Farmacología, Cátedra de Química Medicinal, Ciudad Autónoma de Buenos Aires, Argentina.
M A CalleroUniversidad de Buenos Aires, Instituto de Oncología "Ángel H. Roffo", Área Investigación, Dpto. Inmunobiología, Ciudad Autónoma de Buenos Aires, Argentina.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAdvanced triple negative breast cancer (ATNBC) is defined by a lack of expression of hormones receptors as well as HER2/neu and its high probability of visceral metastasis. This pathology is associated with a poor prognosis. Previously, we found that T2, an

methodsIn order to deepen T2 action mode on ATNBC, we first confirmed T2 cytotoxicity on a panel of TNBC cells and then continued studying T2 effects

resultsWe found that T2 had a cytotoxic effect comparable to chemotherapeutics used in present treatment schemes for ATNBC. T2 treatment not only induced apoptosis, but it also down-modulated 4T1 invasive and metastatic-associated capacities, such as clonogenicity, migration and metallo-proteases activity. Moreover, this agent reduced the number of 4T1 cancer stem cells. Finally, T2 treatment induced a more differentiated cell phenotype and the overexpression of the metastasis suppressor gene NDRG-1.

conclusionThis study provided evidence that T2 not only exerted an anti-tumor activity but it also showed anti-invasive and anti-metastatic actions on ATNBC

Indexed as

BiochemistryCancer researchCell biologyInvasionMetastasisMolecular biologyOncologyStem cellsThiosemicarbazonesTriple negative breast cancer

Identifiers

PMID33072918
PMCPMC7548444

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.