Evidence map›Paper›PMID 26525902›Full record

ArticleBMC cancer2015

Reprogramming energy metabolism and inducing angiogenesis: co-expression of monocarboxylate transporters with VEGF family members in cervical adenocarcinomas.

Céline Pinheiro, Eduardo A Garcia, Filipa Morais-Santos, Marise A R Moreira, Fábio M Almeida, Luiz F Jubé, Geraldo S Queiroz, Élbio C Paula, Maria A Andreoli, Luisa L Villa and 2 more

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 22% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Endometriosis and the Hallmarks of Cancer.Reproductive sciences (Thousand Oaks, Calif.) · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. COVID-19 and oral cancer: Critical viewpoint.World journal of clinical oncology · 2022
    Article
  11. GLUT1, LDHA, and MCT4 Expression Is Deregulated in Cervical Cancer and Precursor Lesions.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2022
    Article
  12. Review
  13. Potential of NovelFrontiers in pharmacology · 2022
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. How do cancer cells replenish their fuel supply?Cancer reports (Hoboken, N.J.) · 2018
    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

12 authors at 4 institutions in 2 countries.

Céline PinheiroLife and Health Sciences Research Institute (ICVS), School of Health Sciences, University of Minho, Braga, 4710-057, Portugal. celinepinheiro@gmail.com.
Eduardo A GarciaBarretos School of Health Sciences, Dr. Paulo Prata - FACISB, Barretos, São Paulo, Brazil. eduardoag@gmail.com.
Filipa Morais-SantosLife and Health Sciences Research Institute (ICVS), School of Health Sciences, University of Minho, Braga, 4710-057, Portugal. filipasantos@ecsaude.uminho.pt.
Marise A R MoreiraDepartment of Pathology of the School of Medicine of the Federal University of Goiás, Goiânia, Go, Brazil. marisemoreira7@gmail.com.
Fábio M AlmeidaDepartment of Pathology of the School of Medicine of the Federal University of Goiás, Goiânia, Go, Brazil. fabim12@gmail.com.
Luiz F JubéHospital Araújo Jorge, Goiânia, Go, Brazil. lfjube@hotmail.com.
Geraldo S QueirozHospital Araújo Jorge, Goiânia, Go, Brazil. geraldoestudantedelogosofia@yahoo.com.br.
Élbio C PaulaHospital Araújo Jorge, Goiânia, Go, Brazil. elcanpa@yahoo.com.br.
Maria A AndreoliInstituto Nacional de Ciência e Tecnologia do HPV (INCT-HPV), Sao Paulo, Brazil. mandreoli@incthpv.org.br.
Luisa L VillaInstituto Nacional de Ciência e Tecnologia do HPV (INCT-HPV), Sao Paulo, Brazil. luisa.villa@icesp.org.br.
Adhemar Longatto-FilhoLife and Health Sciences Research Institute (ICVS), School of Health Sciences, University of Minho, Braga, 4710-057, Portugal. longatto16@hotmail.com.
Fátima BaltazarLife and Health Sciences Research Institute (ICVS), School of Health Sciences, University of Minho, Braga, 4710-057, Portugal. fbaltazar@ecsaude.uminho.pt.
Hospital Araújo Jorge · BRUniversidade Federal de Goiás · BRUniversity of Minho · PTHospital de Câncer de Barretos · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDeregulation of cellular energetic metabolism was recently pointed out as a hallmark of cancer cells. This deregulation involves a metabolic reprogramming that leads to a high production of lactate. Lactate efflux, besides contributing for the glycolytic flux, also acts in the extracellular matrix, contributing for cancer malignancy, by, among other effects, induction of angiogenesis. However, studies on the interplay between cancer metabolism and angiogenesis are scarce. Therefore, the aim of the present study was to evaluate the metabolic and vascular molecular profiles of cervical adenocarcinomas, their co-expression, and their relation to the clinical and pathological behavior.

methodsThe immunohistochemical expression of metabolism-related proteins (MCT1, MCT4, CD147, GLUT1 and CAIX) as well as VEGF family members (VEGF-A, VEGF-C, VEGF-D, VEGFR-1, VEGFR-2 and VEGFR-3) was assessed in a series of 232 cervical adenocarcinomas. The co-expression among proteins was assessed and the expression profiles were associated with patients' clinicopathological parameters.

resultsAmong the metabolism-related proteins, MCT4 and CAIX were the most frequently expressed in cervical adenocarcinomas while CD147 was the less frequently expressed protein. Overall, VEGF family members showed a strong and extended expression with VEGF-C and VEGFR-2 as the most frequently expressed and VEGFR-1 as the less expressed member. Co-expression of MCT isoforms with VEGF family members was demonstrated. Finally, MCT4 was associated with parametrial invasion and HPV18 infection, CD147 and GLUT1 with distant metastasis, CAIX with tumor size and HPV18 infection, and VEGFR-1 with local and lymphnode metastasis.

conclusionsThe results herein presented provide additional evidence for a crosstalk between deregulating cellular energetics and inducing angiogenesis. Also, the metabolic remodeling and angiogenic switch are relevant to cancer progression and aggressiveness in adenocarcinomas.

Indexed as

AdenocarcinomaAngiogenesis Inducing AgentsEnergy MetabolismFemaleGene Expression Regulation, NeoplasticHumansLymphatic MetastasisMiddle AgedMonocarboxylic Acid TransportersNeoplasm ProteinsNeovascularization, PathologicUterine Cervical NeoplasmsVascular Endothelial Growth Factor AAngiogenesis Inducing AgentsMonocarboxylic Acid TransportersNeoplasm ProteinsVascular Endothelial Growth Factor A

Identifiers

PMID26525902
PMCPMC4630851
OpenAlexW1930815067

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.