Evidence map›Paper›PMID 30257666›Full record

ArticleBMC cancer2018

Molecular iodine inhibits the expression of stemness markers on cancer stem-like cells of established cell lines derived from cervical cancer.

Gabriele Davide Bigoni-Ordóñez, Elizabeth Ortiz-Sánchez, Pedro Rosendo-Chalma, Heriberto A Valencia-González, Carmen Aceves, Alejandro García-Carrancá

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.8field-weighted citation impact, top 22% 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

18 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
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  3. SF1, a Standardised Fraction fromThe Malaysian journal of medical sciences : MJMS · 2025
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  16. Targeting cancer stem cell pathways for cancer therapy.Signal transduction and targeted therapy · 2020
    Review
  17. Article
  18. Cancer stem cell impact on clinical oncology.World journal of stem cells · 2018
    Review
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

6 authors at 3 institutions in 1 country.

Gabriele Davide Bigoni-OrdóñezDivisión de Investigación Básica, Laboratory of Virus and Cancer, Instituto Nacional de Cancerología, Secretaria de Salud, Av. San Fernando No. 22, Sección XVI, Tlalpan, 14080, Ciudad de México, CP, Mexico.
Elizabeth Ortiz-SánchezDivisión de Investigación Básica, Laboratory of Virus and Cancer, Instituto Nacional de Cancerología, Secretaria de Salud, Av. San Fernando No. 22, Sección XVI, Tlalpan, 14080, Ciudad de México, CP, Mexico.
Pedro Rosendo-ChalmaDivisión de Investigación Básica, Laboratory of Virus and Cancer, Instituto Nacional de Cancerología, Secretaria de Salud, Av. San Fernando No. 22, Sección XVI, Tlalpan, 14080, Ciudad de México, CP, Mexico.
Heriberto A Valencia-GonzálezDivisión de Investigación Básica, Laboratory of Virus and Cancer, Instituto Nacional de Cancerología, Secretaria de Salud, Av. San Fernando No. 22, Sección XVI, Tlalpan, 14080, Ciudad de México, CP, Mexico.
Carmen AcevesInstituto de Neurobiología, Universidad Nacional Autónoma de México, Boulevard Juriquilla 3001, Juriquilla. Campus-Juriquilla., Querétaro, 76230, Qro, Mexico. caracev@unam.mx.
Alejandro García-CarrancáDivisión de Investigación Básica, Laboratory of Virus and Cancer, Instituto Nacional de Cancerología, Secretaria de Salud, Av. San Fernando No. 22, Sección XVI, Tlalpan, 14080, Ciudad de México, CP, Mexico. carranca@biomedicas.unam.mx.ORCID http://orcid.org/0000-0003-1220-5014
Secretaria de Salud · MXInstituto Nacional de Cancerología · MXUniversidad Nacional Autónoma de México · MX

Funding

CONACYT 0253804CONACYT 414125
6 · The paper itself

Abstract

backgroundCancer stem cells (CSC) are characterized by deregulated self-renewal, tumorigenicity, metastatic potential, aberrant stemness signaling pathways, resistance to conventional therapy, and the ability to give rise to a progeny of proliferating cells that constitute the bulk of tumors. Targeting CSC will provide novel treatments for cancer. Different investigations have focused on developing complementary approaches that involve natural compounds that decrease chemo-resistance and reduce the side effects of conventional therapies. Since, it has been reported that molecular iodine (I

methodsHeLa and SiHa cervical cancer cells were treated with 200uM I

resultsIn the present study, monolayer and CSC-enriched cultures (cervospheres) from cervical cancer-derived cell lines, HeLa and SiHa, showed that 200uM I

conclusionsAll this data led us to suggest a clinical potential use of I

Indexed as

AnimalsAntineoplastic AgentsBiomarkers, TumorCell Line, TumorCell ProliferationCell SurvivalFemaleGene Expression Regulation, NeoplasticHeLa CellsHumansIodineKruppel-Like Factor 4MiceNeoplastic Stem CellsUterine Cervical NeoplasmsXenograft Model Antitumor AssaysAntineoplastic AgentsBiomarkers, TumorIodineKLF4 protein, humanKlf4 protein, mouseKruppel-Like Factor 4Cervical cancer stem cellsMolecular iodinePPAR gammaStemness markers

Identifiers

PMID30257666
PMCPMC6158890
OpenAlexW2894083008

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.