Evidence map›Paper›PMID 36235125›Full record

ArticleMolecules (Basel, Switzerland)2022

Fermentation Extract of Naringenin Increases the Expression of Estrogenic Receptor β and Modulates Genes Related to the p53 Signalling Pathway, miR-200c and miR-141 in Human Colon Cancer Cells Exposed to BPA.

Sara Julietta Lozano-Herrera, Gabriel Luna-Bárcenas, Ramón Gerardo Guevara-González, Rocio Campos-Vega, Juan Carlos Solís-Sáinz, Ana Gabriela Hernández-Puga, Haydé Azeneth Vergara-Castañeda

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
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  12. Antiproliferative Activity and Impact on Human Gut Microbiota of NewInternational journal of molecular sciences · 2023
    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

7 authors at 2 institutions in 1 country.

Sara Julietta Lozano-HerreraAdvanced Biomedical Research Center, School of Medicine, Universidad Autónoma de Querétaro, Querétaro 76140, Qro., Mexico.ORCID 0000-0002-4406-3463
Gabriel Luna-BárcenasCinvestav-Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Unidad Querétaro, Querétaro 76230, Qro., Mexico.ORCID 0000-0002-1162-6928
Ramón Gerardo Guevara-GonzálezBiosystems Engineering Group, School of Engineering, Autonomous University of Queretaro-Campus Amazcala, Highway Amazcala-Chichimequillas S/N, Km 1, Amazcala, El Marques, Querétaro 76265, Qro., Mexico.
Rocio Campos-VegaResearch and Graduate Studies in Food Science, School of Chemistry, Universidad Autónoma de Querétaro, Querétaro 76010, Qro., Mexico.
Juan Carlos Solís-SáinzAdvanced Biomedical Research Center, School of Medicine, Universidad Autónoma de Querétaro, Querétaro 76140, Qro., Mexico.
Ana Gabriela Hernández-PugaAdvanced Biomedical Research Center, School of Medicine, Universidad Autónoma de Querétaro, Querétaro 76140, Qro., Mexico.ORCID 0000-0001-9040-3521
Haydé Azeneth Vergara-CastañedaAdvanced Biomedical Research Center, School of Medicine, Universidad Autónoma de Querétaro, Querétaro 76140, Qro., Mexico.ORCID 0000-0001-8926-2223
Autonomous University of Queretaro · MXCentro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional · MX

Funding

Autonomous University of Queretaro FME201805Consejo Nacional de Ciencia y Tecnología 2016/286926
6 · The paper itself

Abstract

The estrogenic receptor beta (ERβ) protects against carcinogenesis by stimulating apoptosis. Bisphenol A (BPA) is related to promoting cancer, and naringenin has chemoprotective activities both can bind to ERβ. Naringenin in the colon is metabolized by the microbiota. Cancer involves genetic and epigenetic mechanisms, including miRNAs. The objective of the present study was to evaluate the co-exposure effect of colonic in vitro fermented extract of naringenin (FEN) and BPA, to elucidate molecular effects in HT-29 colon cancer cell line. For this, we quantified genes related to the p53 signaling pathway as well as ERβ, miR-200c, and miR-141. As an important result, naringenin (IC50 250 µM) and FEN (IC50 37%) promoted intrinsic pathways of apoptosis through phosphatase and tensin homolog (PTEN) (+2.70, +1.72-fold, respectively) and CASP9 (+3.99, +2.03-fold, respectively) expression. BPA decreased the expression of PTEN (-3.46-fold) gene regulated by miR-200. We suggest that once co-exposed, cells undergo a greater stress forcing them to mediate other extrinsic apoptosis mechanisms associated with death domain FASL. In turn, these findings are related to the increase of ERβ (5.3-fold with naringenin and 13.67-fold with FEN) gene expression, important in the inhibition of carcinogenic development.

Indexed as

Colonic NeoplasmsMicroRNAsBenzhydryl CompoundsBisphenol A CompoundsCell ProliferationEstrogen Receptor betaFermentationFlavanonesHumansPhenolsSignal TransductionTensinsTumor Suppressor Protein p53Benzhydryl Compoundsbisphenol ABisphenol A CompoundsEstrogen Receptor betaFlavanonesMicroRNAsMIRN141 microRNA, humannaringeninPhenolsTensinsTumor Suppressor Protein p53BPAcolon cancerERβfermented extract of naringeninmiR-141miR-200c

Identifiers

PMID36235125
PMCPMC9572342
OpenAlexW4303958962

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.