Evidence map›Paper›PMID 32722549›Full record

ArticleInternational journal of molecular sciences2020

An In Vitro Model of Mast Cell Recruitment and Activation by Breast Cancer Cells Supports Anti-Tumoral Responses.

Angélica Aponte-López, Jennifer Enciso, Samira Muñoz-Cruz, Ezequiel M Fuentes-Pananá

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

8 citing papers in PubMed, 16 citations in OpenAlex.

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  8. Mast cell density in the primary tumor predicts lymph node metastases in patients with breast cancer.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    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

4 authors at 2 institutions in 1 country.

Angélica Aponte-LópezUnidad de Investigación en Virología y Cáncer, Hospital Infantil de Mexico Federico Gómez, Ciudad de Mexico 06720, Mexico.ORCID 0000-0003-2823-6739
Jennifer EncisoPrograma de Doctorado en Ciencias Biomédicas, Universidad Nacional Autónoma de Mexico (UNAM), Ciudad de Mexico 04510, Mexico.
Samira Muñoz-CruzUnidad de Investigación Médica en Enfermedades Infecciosas y Parasitarias, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Ciudad de Mexico 06720, Mexico.ORCID 0000-0002-9547-2515
Ezequiel M Fuentes-PananáUnidad de Investigación en Virología y Cáncer, Hospital Infantil de Mexico Federico Gómez, Ciudad de Mexico 06720, Mexico.ORCID 0000-0003-2872-0459
Hospital Infantil de México Federico Gómez · MXMexican Social Security Institute · MX

Funding

Consejo Nacional de Ciencia y Tecnología 223678Hospital Infantil de Mexico "Federico Gómez" HIM-2017-014Instituto Mexicano del Seguro Social FIS/IMSS/PROT/G18/1829
6 · The paper itself

Abstract

Breast cancer (BrC) affects millions of women yearly. Mast cells (MCs) are common components of breast tumors with documented agonistic and antagonistic roles in tumor progression. Understanding the participation of MCs in BrC may lead to new therapies to control tumor growth. In this study, we looked into mechanistic models of MC responses triggered by BrC cells (BrCC), assessing both early degranulation and late transcriptional activities. We used aggressive and non-aggressive BrCC to model the progressive staging of the disease over HMC1 and LAD-2 human MC lines. We found that both MC lines were chemoattracted by all BrCC, but their activation was preferentially induced by aggressive lines, finding differences in their active transcriptional programs, both at basal level and after stimulation. Among those genes with altered expression were down-regulated

Indexed as

Gene Expression Regulation, NeoplasticModels, BiologicalBreast NeoplasmsDatabases, FactualDisease-Free SurvivalFemaleHumansMast CellsMCF-7 CellsNeoplasm ProteinsSurvival RateNeoplasm Proteinsanti-tumor functionsbreast cancerIFNγmast cellstumor stroma

Identifiers

PMID32722549
PMCPMC7432939
OpenAlexW3044893228

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.