Evidence map›Paper›PMID 24237221›Full record

ReviewAnti-cancer agents in medicinal chemistry2014

Chemical metabolic inhibitors for the treatment of blood-borne cancers.

Martin Villalba, Nuria Lopez-Royuela, Ewelina Krzywinska, Moeez G Rathore, Robert A Hipskind, Houda Haouas, Nerea Allende-Vega

Abstract readReview
In one paragraph

Review in Anti-cancer agents in medicinal chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

22 citing papers in PubMed, 30 citations in OpenAlex.

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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 2 institutions in 3 countries.

Martin Villalba
Nuria Lopez-Royuela
Ewelina Krzywinska
Moeez G Rathore
Robert A Hipskind
Houda Haouas
Nerea Allende-VegaINSERM U1040, Institut de Recherche en Biothérapie, 80, avenue Augustin Fliche. 34295 Montpellier Cedex 5, France. martin.villalba@inserm.fr.
National Institute of Applied Science and Technology · TNInstitut National de Recherche en Santé Publique · ML

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor cells, including leukemic cells, remodel their bioenergetic system in favor of aerobic glycolysis. This process is called "the Warburg effect" and offers an attractive pharmacological target to preferentially eliminate malignant cells. In addition, recent results show that metabolic changes can be linked to tumor immune evasion. Mouse models demonstrate the importance of this metabolic remodeling in leukemogenesis. Some leukemias, although treatable, remain incurable and resistance to chemotherapy produces an elevated percentage of relapse in most leukemia cases. Several groups have targeted the specific metabolism of leukemia cells in preclinical and clinical studies to improve the prognosis of these patients, i.e. using L-asparaginase to treat pediatric acute lymphocytic leukemia (ALL). Additional metabolic drugs that are currently being used to treat other diseases or tumors could also be exploited for leukemia, based on preclinical studies. Finally, we discuss the potential use of several metabolic drugs in combination therapies, including immunomodulatory drugs (IMiDs) or immune cell-based therapies, to increase their efficacy and reduce side effects in the treatment of hematological cancers.

Indexed as

AnimalsAntineoplastic AgentsCell TransplantationCombined Modality TherapyGlutamineGlycolysisHistocompatibility Antigens Class IHistone DeacetylasesHumansImmunomodulationKiller Cells, NaturalLeukemiaOxidative PhosphorylationSirtuinsT-Lymphocytes, CytotoxicAntineoplastic AgentsGlutamineHistocompatibility Antigens Class IHistone DeacetylasesSirtuins

Identifiers

PMID24237221
PMCPMC5055580
OpenAlexW2136853910

What OpenQuestion holds

Textmetadata
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.