Evidence map›Paper›PMID 29137304›Full record

ArticleOncotarget2017

Monocarboxylate transporter 1 (MCT1), a tool to stratify acute myeloid leukemia (AML) patients and a vehicle to kill cancer cells.

Filipa Lopes-Coelho, Carolina Nunes, Sofia Gouveia-Fernandes, Rita Rosas, Fernanda Silva, Paula Gameiro, Tânia Carvalho, Maria Gomes da Silva, José Cabeçadas, Sérgio Dias and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed, 26 citations in OpenAlex.

  1. Glucose and Lactate, Starters or Intermediates of Cancer Metabolic Rewiring.Advances in experimental medicine and biology · 2026
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  5. Exploring monocarboxylate transporter inhibition for cancer treatment.Exploration of targeted anti-tumor therapy · 2024
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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

12 authors at 4 institutions in 1 country.

Filipa Lopes-CoelhoCentro de Estudos de Doenças Crónicas da Faculdade de Ciências Médicas da Universidade NOVA (CEDOC-FCM-UNL), Lisbon, Portugal.
Carolina NunesCentro de Estudos de Doenças Crónicas da Faculdade de Ciências Médicas da Universidade NOVA (CEDOC-FCM-UNL), Lisbon, Portugal.
Sofia Gouveia-FernandesCentro de Estudos de Doenças Crónicas da Faculdade de Ciências Médicas da Universidade NOVA (CEDOC-FCM-UNL), Lisbon, Portugal.
Rita RosasInstituto de Tecnologia Química e Biológica António Xavier (ITQB Nova), Oeiras, Portugal.
Fernanda SilvaCentro de Estudos de Doenças Crónicas da Faculdade de Ciências Médicas da Universidade NOVA (CEDOC-FCM-UNL), Lisbon, Portugal.
Paula GameiroServiço de Hemato-Oncologia, IPOLFG, Lisbon, Portugal.
Tânia CarvalhoInstituto de Medicina Molecular da Universidade de Lisboa, Lisbon, Portugal.
Maria Gomes da SilvaServiço de Hemato-Oncologia, IPOLFG, Lisbon, Portugal.
José CabeçadasServiço de Anatomia Patológica, IPOLFG, Lisbon, Portugal.
Sérgio DiasInstituto de Medicina Molecular da Universidade de Lisboa, Lisbon, Portugal.
Luís G GonçalvesInstituto de Tecnologia Química e Biológica António Xavier (ITQB Nova), Oeiras, Portugal.
Jacinta SerpaCentro de Estudos de Doenças Crónicas da Faculdade de Ciências Médicas da Universidade NOVA (CEDOC-FCM-UNL), Lisbon, Portugal.
Instituto Português de Oncologia de Coimbra Francisco Gentil · PTInstituto de Biologia Experimental e Tecnológica · PTUniversidade Nova de Lisboa · PTUniversity of Lisbon · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dysregulation of glucose/lactate dynamics plays a role in cancer progression, and MCTs are key elements in metabolic remodeling. VEGF is a relevant growth factor in the maintenance of bone marrow microenvironment and it is also important in hematological diseases. Our aim was to investigate the role of VEGF in the metabolic adaptation of Acute myeloid leukemia (AML) cells by evaluating the metabolic profiles and cell features according to the AML lineage and testing lactate as a metabolic coin. Our

Indexed as

BM microenvironmentlactateMCT1metabolic switchVEGF

Identifiers

PMID29137304
PMCPMC5669930
OpenAlexW2746910349

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.