Evidence map›Paper›PMID 26318853›Full record

ReviewCellular oncology (Dordrecht, Netherlands)2015

NF-κB signaling in cancer stem cells: a promising therapeutic target?

K Vazquez-Santillan, J Melendez-Zajgla, L Jimenez-Hernandez, G Martínez-Ruiz, V Maldonado

Abstract readReview
In one paragraph

Review in Cellular oncology (Dordrecht, Netherlands), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

62 citing papers in PubMed, 99 citations in OpenAlex.

  1. Article
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  3. Biomedical reports · 2025
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  7. Role of Sam68 in different types of cancer (Review).International journal of molecular medicine · 2025
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2 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

5 authors at 1 institution in 1 country.

K Vazquez-SantillanEpigenetics Laboratory, National Institute of Genomic Medicine, Periferico Sur 4809, Arenal Tepepan, Tlalpan, Mexico City, 14610, Mexico.
J Melendez-ZajglaFunctional Cancer Genomics laboratory, National Institute of Genomic Medicine, Periferico Sur 4809, Arenal Tepepan, Tlalpan, Mexico, Mexico City, 14610, Mexico.
L Jimenez-HernandezEpigenetics Laboratory, National Institute of Genomic Medicine, Periferico Sur 4809, Arenal Tepepan, Tlalpan, Mexico City, 14610, Mexico.
G Martínez-RuizFunctional Cancer Genomics laboratory, National Institute of Genomic Medicine, Periferico Sur 4809, Arenal Tepepan, Tlalpan, Mexico, Mexico City, 14610, Mexico.
V MaldonadoEpigenetics Laboratory, National Institute of Genomic Medicine, Periferico Sur 4809, Arenal Tepepan, Tlalpan, Mexico City, 14610, Mexico. vmaldonado@inmegen.gob.mx.ORCID http://orcid.org/0000-0003-4633-9694
National Institute of Genomic Medicine · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCancer stem cells (CSCs) are regulated by several signaling pathways that ultimately control their maintenance and expansion. NF-κB (nuclear factor kappa-light-chain-enhancer of activated B cells) forms a protein complex that controls DNA transcription and, as such, plays an important role in proliferation, inflammation, angiogenesis, invasion and metastasis. The NF-κB signaling pathway, which has been found to be constitutively activated in CSCs from a variety of cancers, participates in the maintenance, expansion, proliferation and survival of CSCs. Targeted disruption of this pathway may profoundly impair the adverse phenotype of CSCs and may provide a therapeutic opportunity to remove the CSC fraction. In particular, it may be attractive to use specific NF-κB inhibitors in chronic therapeutic schemes to reduce disease progression. Exceptional low toxicity profiles of these inhibitors are a prerequisite for use in combined treatment regimens and to avoid resistance.

conclusionAlthough still preliminary, recent evidence shows that such targeted strategies may be useful in adjuvant chemo-preventive settings.

Indexed as

Disease ProgressionHumansModels, BiologicalMolecular Targeted TherapyNeoplasmsNeoplastic Stem CellsNF-kappa BSignal TransductionNF-kappa BCancer stem cellsNF-κB signaling

Identifiers

PMID26318853
PMCPMC13004261
OpenAlexW1688235439

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.