Evidence map›Paper›PMID 31966368›Full record

ArticleInternational journal of clinical and experimental pathology2017

Leptin induces partial epithelial-mesenchymal transition in a FAK-ERK dependent pathway in MCF10A mammary non-tumorigenic cells.

Alfredo Villanueva-Duque, Miriam Daniela Zuniga-Eulogio, Jose Dena-Beltran, Eduardo Castaneda-Saucedo, Mercedes Calixto-Galvez, Miguel Angel Mendoza-Catalán, Carlos Ortuno-Pineda, Napoleon Navarro-Tito

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2017. 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
1.0field-weighted citation impact, top 28% 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, 16 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Alfredo Villanueva-DuqueLaboratorio de Biología Celular del Cancer, FCQB, Universidad Autónoma de Guerrero Mexico.
Miriam Daniela Zuniga-EulogioLaboratorio de Biología Celular del Cancer, FCQB, Universidad Autónoma de Guerrero Mexico.
Jose Dena-BeltranLaboratorio de Biología Celular del Cancer, FCQB, Universidad Autónoma de Guerrero Mexico.
Eduardo Castaneda-SaucedoLaboratorio de Biología Celular del Cancer, FCQB, Universidad Autónoma de Guerrero Mexico.
Mercedes Calixto-GalvezLaboratorio de Biología Celular del Cancer, FCQB, Universidad Autónoma de Guerrero Mexico.
Miguel Angel Mendoza-CatalánLaboratorio de Biomedicina Molecular, FCQB, Universidad Autónoma de Guerrero Mexico.
Carlos Ortuno-PinedaLaboratorio de Acidos Nucleicos y Proteinas, FCQB, Universidad Autónoma de Guerrero Mexico.
Napoleon Navarro-TitoLaboratorio de Biología Celular del Cancer, FCQB, Universidad Autónoma de Guerrero Mexico.
Universidad Autónoma de Guerrero · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epithelial-mesenchymal transition (EMT) is a biological process involved in different steps of tumor progression and metastasis of breast cancer cells. Epidemiological studies suggest a link between obesity and the progression of breast cancer. Leptin is an adipocyte-secreted hormone which can promote cell migration and invasion as part of EMT in breast cancer cells. We investigated the effect of leptin on expression of EMT markers in MCF10A cells, as well as, the role of FAK and ERK in this process. We found that leptin induces morphological changes from an epithelial phenotype towards a mesenchymal phenotype and promotes cell migration in MCF10A cells. Moreover, leptin induces an increase in vimentin expression, changes in the cellular localization of E-cadherin and increase in FAK and ERK phosphorylation. Furthermore, using FAK and ERK chemical inhibitors we show that leptin regulates EMT markers in a FAK and ERK dependent manner. In conclusion, leptin promotes vimentin expression and cell migration in a FAK and ERK dependent pathway in the non-tumorigenic epithelial cell line MCF10A.

Indexed as

breast cancercell migrationEMTLeptin

Identifiers

PMID31966368
PMCPMC6965759
OpenAlexW3026049133

What OpenQuestion holds

Textmetadata
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.