Evidence map›Paper›PMID 35736489›Full record

ArticleMetabolites2022

Evaluation of Syrosingopine, an MCT Inhibitor, as Potential Modulator of Tumor Metabolism and Extracellular Acidification.

Chloe Buyse, Nicolas Joudiou, Aude Warscotte, Elena Richiardone, Lionel Mignion, Cyril Corbet, Bernard Gallez

Open access · goldAbstract read
In one paragraph

Article in Metabolites, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

26 citing papers in PubMed, 37 citations in OpenAlex.

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  17. 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

7 authors at 1 institution in 1 country.

Chloe BuyseLouvain Drug Research Institute, Biomedical Magnetic Resonance (REMA), Université Catholique de Louvain (UCLouvain), 1200 Brussels, Belgium.ORCID 0000-0002-5281-7106
Nicolas JoudiouLouvain Drug Research Institute, Nuclear and Electron Spin Technologies (NEST) Platform, Université Catholique de Louvain (UCLouvain), 1200 Brussels, Belgium.ORCID 0000-0002-6760-7400
Aude WarscotteLouvain Drug Research Institute, Biomedical Magnetic Resonance (REMA), Université Catholique de Louvain (UCLouvain), 1200 Brussels, Belgium.
Elena RichiardonePole of Pharmacology and Therapeutics (FATH), Institut de Recherche Expérimentale et Clinique (IREC), Université Catholique de Louvain (UCLouvain), 1200 Brussels, Belgium.
Lionel MignionLouvain Drug Research Institute, Biomedical Magnetic Resonance (REMA), Université Catholique de Louvain (UCLouvain), 1200 Brussels, Belgium.ORCID 0000-0002-9426-8600
Cyril CorbetPole of Pharmacology and Therapeutics (FATH), Institut de Recherche Expérimentale et Clinique (IREC), Université Catholique de Louvain (UCLouvain), 1200 Brussels, Belgium.ORCID 0000-0001-8795-9131
Bernard GallezLouvain Drug Research Institute, Biomedical Magnetic Resonance (REMA), Université Catholique de Louvain (UCLouvain), 1200 Brussels, Belgium.ORCID 0000-0002-5708-1302
UCLouvain · BE

Funding

Fonds National de la Recherche Scientifique FNRS 7463520Fonds National de la Recherche Scientifique FNRS J008220F
6 · The paper itself

Abstract

Extracellular acidification has been shown to be an important characteristic of invasive tumors, as it promotes invasion and migration but also resistance to treatments. Targeting transporters involved in the regulation of tumor pH constitutes a promising anti-tumor approach, as it would disrupt cellular pH homeostasis and negatively impact tumor growth. In this study, we evaluated the impact of syrosingopine, an inhibitor of MCT1 and MCT4, as a modulator of tumor metabolism and extracellular acidification in human breast cancer (MDA-MB-231) and pharyngeal squamous cell carcinoma (FaDu) cell models. In both models in vitro, we observed that exposure to syrosingopine led to a decrease in the extracellular acidification rate, intracellular pH, glucose consumption, lactate secretion and tumor cell proliferation with an increase in the number of late apoptotic/necrotic cells. However, in vivo experiments using the MDA-MB-231 model treated with a daily injection of syrosingopine did not reveal any significant change in extracellular pH (pHe) (as measured using CEST-MRI) or primary tumor growth. Overall, our study suggests that targeting MCT could lead to profound changes in tumor cell metabolism and proliferation, and it warrants further research to identify candidates without off-target effects.

Indexed as

CEST-MRIMCTpHeproliferationsyrosingopinetumor metabolism

Identifiers

PMID35736489
PMCPMC9230831
OpenAlexW4283022582

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.