Evidence map›Paper›PMID 32094378›Full record

ArticleScientific reports2020

MiR-23b-3p reduces the proliferation, migration and invasion of cervical cancer cell lines via the reduction of c-Met expression.

Gabriela Elizabeth Campos-Viguri, Oscar Peralta-Zaragoza, Hilda Jiménez-Wences, Alma Edith Longinos-González, Carlos Alberto Castañón-Sánchez, Miriam Ramírez-Carrillo, César López Camarillo, Eduardo Castañeda-Saucedo, Marco Antonio Jiménez-López, Dinorah Nashely Martínez-Carrillo and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.1field-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

31 citing papers in PubMed, 59 citations in OpenAlex.

  1. Review
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  3. Core microRNAs regulate neural crest delamination and condensation in the developing trigeminal ganglion.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  10. The Oncogenic Role ofInternational journal of molecular sciences · 2024
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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

11 authors at 4 institutions in 2 countries.

Gabriela Elizabeth Campos-ViguriLaboratorio de Investigación Clínica. Facultad de Ciencias Químico-Biológicas, Universidad Autónoma de Guerrero. Av. Lázaro Cárdenas S/N, Colonia Haciendita, Chilpancingo, 39070, Guerrero, México.
Oscar Peralta-ZaragozaDirección de Infecciones Crónicas y Cáncer; Centro de Investigación en Enfermedades Infecciosas. Instituto Nacional de Salud Pública. Av. Universidad No. 655, Cerrada los Pinos y Caminera. Colonia Santa María Ahuacatitlán, Cuernavaca, 62100, Morelos, México.
Hilda Jiménez-WencesLaboratorio de Investigación Clínica. Facultad de Ciencias Químico-Biológicas, Universidad Autónoma de Guerrero. Av. Lázaro Cárdenas S/N, Colonia Haciendita, Chilpancingo, 39070, Guerrero, México.
Alma Edith Longinos-GonzálezLaboratorio de Investigación Clínica. Facultad de Ciencias Químico-Biológicas, Universidad Autónoma de Guerrero. Av. Lázaro Cárdenas S/N, Colonia Haciendita, Chilpancingo, 39070, Guerrero, México.
Carlos Alberto Castañón-SánchezHospital Regional de Alta Especialidad de Oaxaca. Av. Aldama S/N, Colonia Centro, San Bartolo Coyotepec, 71256, Oaxaca, México.
Miriam Ramírez-CarrilloLaboratorio de Química de Productos Naturales, Facultad de Farmacia, Universidad Autónoma del Estado de Morelos. Av. Universidad No. 1001, Colonia Chamilpa, Cuernavaca, 62209, Morelos, México.
César López CamarilloPosgrado en Ciencias Genómicas, Universidad Autónoma de la Ciudad de México, Ciudad de México, México.
Eduardo Castañeda-SaucedoLaboratorio de Biología Celular del Cáncer. Facultad de Ciencias Químico-Biológicas, Universidad Autónoma de Guerrero. Av. Lázaro Cárdenas S/N, Colonia Haciendita, Chilpancingo, 39070, Guerrero, México.
Marco Antonio Jiménez-LópezInstituto Estatal de Cancerología "Dr. Arturo Beltrán Ortega". Av. Adolfo Ruiz Cortines, No. 128-A. Colonia Alta Progreso, Acapulco de Juárez, 39570, Guerrero, México.
Dinorah Nashely Martínez-CarrilloLaboratorio de Investigación Clínica. Facultad de Ciencias Químico-Biológicas, Universidad Autónoma de Guerrero. Av. Lázaro Cárdenas S/N, Colonia Haciendita, Chilpancingo, 39070, Guerrero, México.
Gloria Fernández-TilapaLaboratorio de Investigación Clínica. Facultad de Ciencias Químico-Biológicas, Universidad Autónoma de Guerrero. Av. Lázaro Cárdenas S/N, Colonia Haciendita, Chilpancingo, 39070, Guerrero, México. gferti@hotmail.com.
Universidad Autónoma de Guerrero · MXAsociación Española Contra el Cáncer · ESUniversidad Autónoma de la Ciudad de México · MXUniversidad Autónoma del Estado de Morelos · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malignant transformation and progression in cancer is associated with the altered expression of multiple miRNAs, which are considered as post-transcriptional regulators of genes participating in various cellular processes. Although, it has been proposed that miR-23b-3p acts as a tumor suppressor in cervical cancer (CC), not all the pathways through which it alters the cellular processes have been described. The present study examines whether miR-23b-3p directly represses the c-Met expression and that consequently modifies the proliferation, migration and invasion of C33A and CaSki cells. c-Met has five microRNA response elements (MREs) for miR-23b-3p in the 3'-UTR region. The ectopic overexpression of miR-23b-3p significantly reduces c-Met expression in C33A and CaSki cells. The overexpression of miR-23b-3p reduces proliferation, migration and invasion of CaSki cells and the proliferation and invasion in C33A cells. In CaSki cells, the activation of Gab1 and Fak, downstream of c-Met, is reduced in response to the overexpression of miR-23b-3p. Together, the results in the present study indicate that miR-23b-3p is a tumor suppressor that modulates the progression of CC via post-transcriptional regulation of the c-Met oncogene.

Indexed as

Gene Expression Regulation, Neoplastic3' Untranslated RegionsAlgorithmsCell Line, TumorCell MovementCell ProliferationFemaleHumansMicroRNAsNeoplasm InvasivenessNeoplasm MetastasisProto-Oncogene Proteins c-metResponse ElementsUterine Cervical Neoplasms3' Untranslated RegionsMET protein, humanMicroRNAsMIRN23b microRNA, humanProto-Oncogene Proteins c-met

Identifiers

PMID32094378
PMCPMC7039958
OpenAlexW3008492890

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.