Evidence map›Paper›PMID 33917317›Full record

ArticleCancers2021

Succinate Anaplerosis Has an Onco-Driving Potential in Prostate Cancer Cells.

Ana Carolina B Sant'Anna-Silva, Juan A Perez-Valencia, Marco Sciacovelli, Claude Lalou, Saharnaz Sarlak, Laura Tronci, Efterpi Nikitopoulou, Andras T Meszaros, Christian Frezza, Rodrigue Rossignol and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 26 citations in OpenAlex.

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  7. The bioenergetic landscape of cancer.Molecular metabolism · 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 3 countries.

Ana Carolina B Sant'Anna-SilvaDaniel Swarovski Research Laboratory, Department of Visceral, Transplant and Thoracic Surgery, Medical University Innsbruck, 6020 Innsbruck, Austria.
Juan A Perez-ValenciaInstitute of Human Genetics, Medical University Innsbruck, 6020 Innsbruck, Austria.ORCID 0000-0002-8282-1763
Marco SciacovelliMedical Research Council Cancer Unit, University of Cambridge, Cambridge CB2 0XZ, UK.
Claude LalouInstitut National de la Santé Et de la Recherche Médicale (INSERM) U1211, Bordeaux University, 33076 Bordeaux, France.
Saharnaz SarlakInstitut National de la Santé Et de la Recherche Médicale (INSERM) U1211, Bordeaux University, 33076 Bordeaux, France.
Laura TronciMedical Research Council Cancer Unit, University of Cambridge, Cambridge CB2 0XZ, UK.ORCID 0000-0002-1217-4046
Efterpi NikitopoulouMedical Research Council Cancer Unit, University of Cambridge, Cambridge CB2 0XZ, UK.
Andras T MeszarosDaniel Swarovski Research Laboratory, Department of Visceral, Transplant and Thoracic Surgery, Medical University Innsbruck, 6020 Innsbruck, Austria.
Christian FrezzaMedical Research Council Cancer Unit, University of Cambridge, Cambridge CB2 0XZ, UK.
Rodrigue RossignolInstitut National de la Santé Et de la Recherche Médicale (INSERM) U1211, Bordeaux University, 33076 Bordeaux, France.
Erich GnaigerDaniel Swarovski Research Laboratory, Department of Visceral, Transplant and Thoracic Surgery, Medical University Innsbruck, 6020 Innsbruck, Austria.
Helmut KlockerDepartment of Surgery, Division of Experimental Urology, University Hospital for Urology, Medical University Innsbruck, 6020 Innsbruck, Austria.ORCID 0000-0001-7732-9443
Innsbruck Medical University · ATUniversity of Cambridge · GBInserm · FRUniversity Hospital Innsbruck · AT

Funding

Medical Research Council MC_UP_1101/3Medical Research Council MC_UU_12022/6TRANSMIT (Translating the Role of Mitochondria in Tumorigenesis) H2020-MSCA-ITN-2016/722605
6 · The paper itself

Abstract

Tumor cells display metabolic alterations when compared to non-transformed cells. These characteristics are crucial for tumor development, maintenance and survival providing energy supplies and molecular precursors. Anaplerosis is the property of replenishing the TCA cycle, the hub of carbon metabolism, participating in the biosynthesis of precursors for building blocks or signaling molecules. In advanced prostate cancer, an upshift of succinate-driven oxidative phosphorylation via mitochondrial Complex II was reported. Here, using untargeted metabolomics, we found succinate accumulation mainly in malignant cells and an anaplerotic effect contributing to biosynthesis, amino acid, and carbon metabolism. Succinate also stimulated oxygen consumption. Malignant prostate cells displayed higher mitochondrial affinity for succinate when compared to non-malignant prostate cells and the succinate-driven accumulation of metabolites induced expression of mitochondrial complex subunits and their activities. Moreover, extracellular succinate stimulated migration, invasion, and colony formation. Several enzymes linked to accumulated metabolites in the malignant cells were found upregulated in tumor tissue datasets, particularly NME1 and SHMT2 mRNA expression. High expression of the two genes was associated with shorter disease-free survival in prostate cancer cohorts. Moreover,

Indexed as

anaplerosiscancer metabolismmitochondriaprostate cancersuccinate

Identifiers

PMID33917317
PMCPMC8038717
OpenAlexW3143251005

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.