Evidence map›Paper›PMID 30984541›Full record

ArticleFEBS open bio2019

Annexin A1 peptide and endothelial cell-conditioned medium modulate cervical tumorigenesis.

Laila Toniol Cardin, Janesly Prates, Bianca Rodrigues da Cunha, Eloiza Helena Tajara, Sonia Maria Oliani, Flávia Cristina Rodrigues-Lisoni

Open access · goldAbstract read
In one paragraph

Article in FEBS open bio, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. 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 2 institutions in 1 country.

Laila Toniol CardinInstitute of Bioscience, Humanities and Exact Science São Paulo State University (Unesp) São José do Rio Preto Brazil.
Janesly PratesInstitute of Bioscience, Humanities and Exact Science São Paulo State University (Unesp) São José do Rio Preto Brazil.
Bianca Rodrigues da CunhaDepartment of Molecular Biology School of Medicine of São José do Rio Preto São José do Rio Preto Brazil.
Eloiza Helena TajaraDepartment of Molecular Biology School of Medicine of São José do Rio Preto São José do Rio Preto Brazil.
Sonia Maria OlianiInstitute of Bioscience, Humanities and Exact Science São Paulo State University (Unesp) São José do Rio Preto Brazil.
Flávia Cristina Rodrigues-LisoniSchool of Engineering São Paulo State University (Unesp) Ilha Solteira Brazil.
Universidade Estadual Paulista (Unesp) · BRFaculdade de Medicina de São José do Rio Preto · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cervical cancer is one of the leading causes of cancer death in women worldwide, and its tumorigenesis can be influenced by the microenvironment. The anti-inflammatory protein annexin A1 (ANXA1) has been reported to be associated with cancer progression and metastasis, suggesting that it plays a role in regulating tumour cell proliferation. Here, we examined the effect of the N-terminal peptide Ac2-26 of ANXA1 on the HaCaT cell line (normal) and HeLa cell line (cervical cancer) co-cultured with endothelium cell-conditioned medium (HMC). Treatment with Ac2-26 decreased proliferation and increased motility of cervical cancer cells, but did not affect cellular morphology or viability. Combined HMC stimulus and Ac2-26 treatment resulted in an increase in apoptotic HeLa cells, upregulated expression of

Indexed as

Annexin A1Cell MovementCell ProliferationCell Transformation, NeoplasticDown-RegulationFemaleGene Expression Regulation, NeoplasticHeLa CellsHumansPeptidesUp-RegulationUterine Cervical NeoplasmsAnnexin A1annexin A1 peptide (2-26)ANXA1 protein, humanPeptidesANXA1carcinogenesiscervical cancerinflammationpeptide treatment

Identifiers

PMID30984541
PMCPMC6443877
OpenAlexW2911396514

What OpenQuestion holds

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LicenceCC BY
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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.