Evidence map›Paper›PMID 33167334›Full record

ReviewMolecules (Basel, Switzerland)2020

Targeting Lipid Peroxidation for Cancer Treatment.

Sofia M Clemente, Oscar H Martínez-Costa, Maria Monsalve, Alejandro K Samhan-Arias

Open access · goldAbstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
8.1field-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

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 95 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Programmed cell death pathways in huntington's disease: spotlight on ferroptosis and pyroptosis.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Targeting inflammation as cancer therapy.Journal of hematology & oncology · 2024
    Review
  17. Article
  18. The role of TRPV4 in programmed cell deaths.Molecular biology reports · 2024
    Review
  19. Article
  20. Article
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

4 authors at 2 institutions in 2 countries.

Sofia M ClementeDepartamento de Química, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, 2829-516 Caparica, Portugal.
Oscar H Martínez-CostaDepartamento de Bioquímica, Facultad de Medicina, Universidad Autónoma de Madrid (UAM), c/Arturo Duperier 4, 28029 Madrid, Spain.ORCID 0000-0003-4893-2205
Maria MonsalveInstituto de Investigaciones Biomédicas 'Alberto Sols' (CSIC-UAM), c/Arturo Duperier 4, 28029 Madrid, Spain.ORCID 0000-0003-2796-1453
Alejandro K Samhan-AriasDepartamento de Bioquímica, Facultad de Medicina, Universidad Autónoma de Madrid (UAM), c/Arturo Duperier 4, 28029 Madrid, Spain.ORCID 0000-0001-9602-4848
Instituto de Investigaciones Biomédicas Sols-Morreale · ESUniversidade Nova de Lisboa · PT

Funding

Horizon 2020 Framework Programme MSCA GA 721236-TREATMENTMinisterio de Ciencia, Innovación y Universidades RTI2018-093864-B-I00
6 · The paper itself

Abstract

Cancer is one of the highest prevalent diseases in humans. The chances of surviving cancer and its prognosis are very dependent on the affected tissue, body location, and stage at which the disease is diagnosed. Researchers and pharmaceutical companies worldwide are pursuing many attempts to look for compounds to treat this malignancy. Most of the current strategies to fight cancer implicate the use of compounds acting on DNA damage checkpoints, non-receptor tyrosine kinases activities, regulators of the hedgehog signaling pathways, and metabolic adaptations placed in cancer. In the last decade, the finding of a lipid peroxidation increase linked to 15-lipoxygenases isoform 1 (15-LOX-1) activity stimulation has been found in specific successful treatments against cancer. This discovery contrasts with the production of other lipid oxidation signatures generated by stimulation of other lipoxygenases such as 5-LOX and 12-LOX, and cyclooxygenase (COX-2) activities, which have been suggested as cancer biomarkers and which inhibitors present anti-tumoral and antiproliferative activities. These findings support the previously proposed role of lipid hydroperoxides and their metabolites as cancer cell mediators. Depletion or promotion of lipid peroxidation is generally related to a specific production source associated with a cancer stage or tissue in which cancer originates. This review highlights the potential therapeutical use of chemical derivatives to stimulate or block specific cellular routes to generate lipid hydroperoxides to treat this disease.

Indexed as

Lipid PeroxidationArachidonate 12-LipoxygenaseArachidonate 15-LipoxygenaseCyclooxygenase 2DNA DamageFerroptosisHumansHydrogen PeroxideInhibitory Concentration 50IronKineticsLipid PeroxidesNAD(P)H Dehydrogenase (Quinone)NanoparticlesNeoplasmsSignal TransductionArachidonate 12-LipoxygenaseArachidonate 15-LipoxygenaseCyclooxygenase 2Fenton's reagentHydrogen PeroxideIronLipid PeroxidesNAD(P)H Dehydrogenase (Quinone)cancerCOXFenton reactionferroptosisironLOXnanoparticlesperoxides

Identifiers

PMID33167334
PMCPMC7663840
OpenAlexW3096804594

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.