Evidence map›Paper›PMID 32582965›Full record

ArticleMolecular medicine reports2020

Circulating extracellular vesicles from patients with breast cancer enhance migration and invasion via a Src‑dependent pathway in MDA‑MB‑231 breast cancer cells.

Javier Ramírez-Ricardo, Elizabeth Leal-Orta, Elia Martínez-Baeza, Carlos Ortiz-Mendoza, Fernando Breton-Mora, Analy Herrera-Torres, Irma Elizalde-Acosta, Pedro Cortes-Reynosa, Rocio Thompson-Bonilla, Eduardo Perez Salazar

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Exosome-Based Smart Drug Delivery Tool for Cancer Theranostics.ACS biomaterials science & engineering · 2023
    Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. The Biology and Function of Extracellular Vesicles in Cancer Development.Frontiers in cell and developmental biology · 2021
    Review
  13. Effects of Water Extract ofEvidence-based complementary and alternative medicine : eCAM · 2021
    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

10 authors at 2 institutions in 1 country.

Javier Ramírez-RicardoDepartament of Cell Biology, CINVESTAV‑IPN, Mexico City 07360, Mexico.
Elizabeth Leal-OrtaDepartament of Cell Biology, CINVESTAV‑IPN, Mexico City 07360, Mexico.
Elia Martínez-BaezaDepartament of Cell Biology, CINVESTAV‑IPN, Mexico City 07360, Mexico.
Carlos Ortiz-MendozaGeneral Hospital Tacuba‑ISSSTE, Mexico City 11410, Mexico.
Fernando Breton-MoraGeneral Hospital Dr. Fernando Quiroz‑ISSSTE, Mexico City 01140, Mexico.
Analy Herrera-TorresFirst October Regional Hospital‑ISSSTE, Mexico City 07760, Mexico.
Irma Elizalde-AcostaFirst October Regional Hospital‑ISSSTE, Mexico City 07760, Mexico.
Pedro Cortes-ReynosaDepartament of Cell Biology, CINVESTAV‑IPN, Mexico City 07360, Mexico.
Rocio Thompson-BonillaFirst October Regional Hospital‑ISSSTE, Mexico City 07760, Mexico.
Eduardo Perez SalazarDepartament of Cell Biology, CINVESTAV‑IPN, Mexico City 07360, Mexico.
Center for Research and Advanced Studies of the National Polytechnic Institute · MXInstitute for Social Security and Services for State Workers · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Triple negative breast cancer (TNBC) is a breast cancer subtype associated with high rates of metastasis, heterogeneity, drug resistance and a poor prognosis. Extracellular vesicles (EVs) are vesicles of endosomal and plasma membrane origin, and are secreted by healthy and cancer cells. In cancer, EVs contribute to tumor progression by mediating escape from the immune system surveillance, and are involved in extracellular matrix degradation, invasion, angiogenesis, migration and metastasis. Furthermore, EVs have been identified in several human fluids. However, the role of EVs from patients with breast cancer in the migration and invasion of human breast cancer cells is not fully understood. The present study investigated whether EVs isolated from Mexican patients with breast cancer can induce cellular processes related to invasion in breast cancer. Moreover, plasma fractions enriched in EVs and deprived of platelet‑derived EVs obtained from blood samples of 32 Mexican patients with biopsy‑diagnosed breast cancer at different clinical stages who had not received treatment were analyzed. Furthermore, one control group was included, which consisted of 20 Mexican healthy females. The present results demonstrated that EVs from women with breast cancer promote migration and invasion, and increase matrix metalloproteinase (MMP)‑2 and MMP‑9 secretion in TNBC MDA‑MB‑231 cells. In addition, it was found that EVs from patients with breast cancer induced Src and focal adhesion kinase activation, and focal adhesions assembly with an increase in focal adhesions number, while the migration and invasion was dependent on Src activity. Collectively, EVs from Mexican patients with breast cancer induce migration and invasion via a Src‑dependent pathway in TNBC MDA‑MB‑231 cells.

Indexed as

Signal TransductionAdolescentAdultAgedAged, 80 and overCase-Control StudiesCell MovementEpithelial-Mesenchymal TransitionExtracellular VesiclesFemaleGene Expression Regulation, NeoplasticHumansMatrix Metalloproteinase 2Matrix Metalloproteinase 9MCF-7 CellsMexicoMatrix Metalloproteinase 2Matrix Metalloproteinase 9MMP2 protein, humanMMP9 protein, humansrc-Family Kinasesbreast cancerextracellular vesiclesfocal adhesion kinaseinvasionMda-MB-231migrationSrc

Identifiers

PMID32582965
PMCPMC7411406
OpenAlexW3035828807

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.