Evidence map›Paper›PMID 33334030›Full record

ReviewBiomolecules2020

New Actors Driving the Epithelial-Mesenchymal Transition in Cancer: The Role of Leptin.

Monserrat Olea-Flores, Juan C Juárez-Cruz, Miriam D Zuñiga-Eulogio, Erika Acosta, Eduardo García-Rodríguez, Ana E Zacapala-Gomez, Miguel A Mendoza-Catalán, Julio Ortiz-Ortiz, Carlos Ortuño-Pineda, Napoleón Navarro-Tito

Open access · goldAbstract readReview
In one paragraph

Review in Biomolecules, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

23 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Update on Adipose Tissue and Cancer.Endocrine reviews · 2023
    Article
  13. Article
  14. Review
  15. Review
  16. Predictive and prognostic value of leptin status in asthma.NPJ primary care respiratory medicine · 2023
    Article
  17. Article
  18. Heliyon · 2022
    Article
  19. Article
  20. Ribosomal Protein S6: A Potential Therapeutic Target against Cancer?International journal of molecular sciences · 2021
    Review
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 1 institution in 1 country.

Monserrat Olea-FloresLaboratorio de Biología Celular del Cáncer, Facultad de Ciencias Químico Biológicas, Universidad Autónoma de Guerrero, Chilpancingo 39090, Mexico.ORCID 0000-0003-1813-9062
Juan C Juárez-CruzLaboratorio de Biología Celular del Cáncer, Facultad de Ciencias Químico Biológicas, Universidad Autónoma de Guerrero, Chilpancingo 39090, Mexico.
Miriam D Zuñiga-EulogioLaboratorio de Biología Celular del Cáncer, Facultad de Ciencias Químico Biológicas, Universidad Autónoma de Guerrero, Chilpancingo 39090, Mexico.ORCID 0000-0003-2904-8350
Erika AcostaLaboratorio de Biología Celular del Cáncer, Facultad de Ciencias Químico Biológicas, Universidad Autónoma de Guerrero, Chilpancingo 39090, Mexico.ORCID 0000-0001-9390-5746
Eduardo García-RodríguezLaboratorio de Biología Celular del Cáncer, Facultad de Ciencias Químico Biológicas, Universidad Autónoma de Guerrero, Chilpancingo 39090, Mexico.
Ana E Zacapala-GomezLaboratorio de Biomedicina Molecular, Facultad de Ciencias Químico Biológicas, Universidad Autónoma de Guerrero, Chilpancingo 39090, Mexico.
Miguel A Mendoza-CatalánLaboratorio de Biomedicina Molecular, Facultad de Ciencias Químico Biológicas, Universidad Autónoma de Guerrero, Chilpancingo 39090, Mexico.ORCID 0000-0002-6247-8590
Julio Ortiz-OrtizLaboratorio de Biomedicina Molecular, Facultad de Ciencias Químico Biológicas, Universidad Autónoma de Guerrero, Chilpancingo 39090, Mexico.ORCID 0000-0003-3082-4716
Carlos Ortuño-PinedaLaboratorio de Ácidos Nucleicos y Proteinas, Facultad de Ciencias Químico Biológicas, Universidad Autónoma de Guerrero, Chilpancingo 39090, Mexico.
Napoleón Navarro-TitoLaboratorio de Biología Celular del Cáncer, Facultad de Ciencias Químico Biológicas, Universidad Autónoma de Guerrero, Chilpancingo 39090, Mexico.ORCID 0000-0003-4911-0545
Universidad Autónoma de Guerrero · MX

Funding

Consejo Nacional de Ciencia y Tecnología, CONACYT 239870
6 · The paper itself

Abstract

Leptin is a hormone secreted mainly by adipocytes; physiologically, it participates in the control of appetite and energy expenditure. However, it has also been linked to tumor progression in different epithelial cancers. In this review, we describe the effect of leptin on epithelial-mesenchymal transition (EMT) markers in different study models, including in vitro, in vivo, and patient studies and in various types of cancer, including breast, prostate, lung, and ovarian cancer. The different studies report that leptin promotes the expression of mesenchymal markers and a decrease in epithelial markers, in addition to promoting EMT-related processes such as cell migration and invasion and poor prognosis in patients with cancer. Finally, we report that leptin has the greatest biological relevance in EMT and tumor progression in breast, lung, prostate, esophageal, and ovarian cancer. This relationship could be due to the key role played by the enriched tumor microenvironment in adipose tissue. Together, these findings demonstrate that leptin is a key biomolecule that drives EMT and metastasis in cancer.

Indexed as

Epithelial-Mesenchymal TransitionAnimalsBiomarkers, TumorHumansLeptinModels, BiologicalNeoplasmsSignal TransductionBiomarkers, TumorLeptincancerEMTepithelial markersleptinmesenchymal markerssignaling pathways

Identifiers

PMID33334030
PMCPMC7765557
OpenAlexW3112887444

What Socratic 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 Socratic graph.