Evidence map›Paper›PMID 25032859›Full record

ArticleCell death & disease2014

Breast cancer stem cells rely on fermentative glycolysis and are sensitive to 2-deoxyglucose treatment.

D Ciavardelli, C Rossi, D Barcaroli, S Volpe, A Consalvo, M Zucchelli, A De Cola, E Scavo, R Carollo, D D'Agostino and 7 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 161 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
161citing papers in PubMed, 1 pooled it
8.0field-weighted citation impact, top 2% 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

161 citing papers in PubMed, 1 synthesis or guideline pooled it, 268 citations in OpenAlex.

  1. PGC1α-Mediated Metabolic Reprogramming Drives the Stemness of Pancreatic Precursor Lesions.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Pooled it
  2. Review
  3. Article
  4. The metabolic profiles of cancer stem cells.Stem cell research & therapy · 2026
    Review
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101 more citing papers are in PubMed but not listed here.

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

17 authors at 5 institutions in 1 country.

D Ciavardelli1] School of Human and Social Science, 'Kore' University of Enna, Enna, Italy [2] Center of Excellence on Aging (Ce.S.I.), 'G. d'Annunzio' Foundation, Chieti, Italy.
C Rossi1] Center of Excellence on Aging (Ce.S.I.), 'G. d'Annunzio' Foundation, Chieti, Italy [2] Department of Experimental and Clinical Sciences, 'G. d'Annunzio' University of Chieti-Pescara, Chieti, Italy.
D Barcaroli1] Center of Excellence on Aging (Ce.S.I.), 'G. d'Annunzio' Foundation, Chieti, Italy [2] Department of Experimental and Clinical Sciences, 'G. d'Annunzio' University of Chieti-Pescara, Chieti, Italy.
S VolpeDepartment of Surgical and Oncological Sciences, Laboratory of Cellular and Molecular Pathophysiology, University of Palermo, Palermo, Italy.
A Consalvo1] Center of Excellence on Aging (Ce.S.I.), 'G. d'Annunzio' Foundation, Chieti, Italy [2] Department of Experimental and Clinical Sciences, 'G. d'Annunzio' University of Chieti-Pescara, Chieti, Italy.
M Zucchelli1] Center of Excellence on Aging (Ce.S.I.), 'G. d'Annunzio' Foundation, Chieti, Italy [2] Department of Experimental and Clinical Sciences, 'G. d'Annunzio' University of Chieti-Pescara, Chieti, Italy.
A De Cola1] Center of Excellence on Aging (Ce.S.I.), 'G. d'Annunzio' Foundation, Chieti, Italy [2] Department of Experimental and Clinical Sciences, 'G. d'Annunzio' University of Chieti-Pescara, Chieti, Italy.
E ScavoDepartment of Surgical and Oncological Sciences, Laboratory of Cellular and Molecular Pathophysiology, University of Palermo, Palermo, Italy.
R CarolloDepartment of Surgical and Oncological Sciences, Laboratory of Cellular and Molecular Pathophysiology, University of Palermo, Palermo, Italy.
D D'Agostino1] Center of Excellence on Aging (Ce.S.I.), 'G. d'Annunzio' Foundation, Chieti, Italy [2] Department of Experimental and Clinical Sciences, 'G. d'Annunzio' University of Chieti-Pescara, Chieti, Italy.
F Forlì1] Center of Excellence on Aging (Ce.S.I.), 'G. d'Annunzio' Foundation, Chieti, Italy [2] Department of Experimental and Clinical Sciences, 'G. d'Annunzio' University of Chieti-Pescara, Chieti, Italy.
S D'AguannoIRCCS S. Lucia, Rome, Italy.
M TodaroDepartment of Surgical and Oncological Sciences, Laboratory of Cellular and Molecular Pathophysiology, University of Palermo, Palermo, Italy.
G StassiDepartment of Surgical and Oncological Sciences, Laboratory of Cellular and Molecular Pathophysiology, University of Palermo, Palermo, Italy.
C Di IlioDepartment of Experimental and Clinical Sciences, 'G. d'Annunzio' University of Chieti-Pescara, Chieti, Italy.
V De Laurenzi1] Center of Excellence on Aging (Ce.S.I.), 'G. d'Annunzio' Foundation, Chieti, Italy [2] Department of Experimental and Clinical Sciences, 'G. d'Annunzio' University of Chieti-Pescara, Chieti, Italy.
A Urbani1] IRCCS S. Lucia, Rome, Italy [2] Department of Internal Medicine, University of Rome 'Tor Vergata', Rome, Italy.
University of Chieti-Pescara · ITUniversity of Palermo · ITFondazione Santa Lucia · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITUniversità degli Studi di Enna Kore · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A number of studies suggest that cancer stem cells are essential for tumour growth, and failure to target these cells can result in tumour relapse. As this population of cells has been shown to be resistant to radiation and chemotherapy, it is essential to understand their biology and identify new therapeutic approaches. Targeting cancer metabolism is a potential alternative strategy to counteract tumour growth and recurrence. Here we applied a proteomic and targeted metabolomic analysis in order to point out the main metabolic differences between breast cancer cells grown as spheres and thus enriched in cancer stem cells were compared with the same cells grown in adherent differentiating conditions. This integrated approach allowed us to identify a metabolic phenotype associated with the stem-like condition and shows that breast cancer stem cells (BCSCs) shift from mitochondrial oxidative phosphorylation towards fermentative glycolysis. Functional validation of proteomic and metabolic data provide evidences for increased activities of key enzymes of anaerobic glucose fate such as pyruvate kinase M2 isoform, lactate dehydrogenase and glucose 6-phopshate dehydrogenase in cancer stem cells as well as different redox status. Moreover, we show that treatment with 2-deoxyglucose, a well known inhibitor of glycolysis, inhibits BCSC proliferation when used alone and shows a synergic effect when used in combination with doxorubicin. In conclusion, we suggest that inhibition of glycolysis may be a potentially effective strategy to target BCSCs.

Indexed as

GlycolysisBreast NeoplasmsCell Line, TumorDeoxyglucoseFemaleHumansL-Lactate DehydrogenaseNeoplastic Stem CellsOxidative PhosphorylationPyruvate KinaseDeoxyglucoseL-Lactate DehydrogenasePyruvate Kinase

Identifiers

PMID25032859
PMCPMC4123079
OpenAlexW2028303721

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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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.