Evidence map›Paper›PMID 37417334›Full record

ReviewInternational journal of molecular medicine2023

Epstein‑Barr virus as a promoter of tumorigenesis in the tumor microenvironment of breast cancer (Review).

José Damián Gómez-Archila, José Arellano-Galindo, Carmen Palacios-Reyes, Ana María Espinosa-García, Patricia García Alonso-Themann, Juan Xicohtencatl-Cortes, Sara A Ochoa, Ariadnna Cruz-Córdova, Icela Palma-Lara

Open access · hybridAbstract readReview
In one paragraph

Review in International journal of molecular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.2field-weighted citation impact, top 18% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. 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

9 authors at 5 institutions in 1 country.

José Damián Gómez-ArchilaLaboratorio de Morfología Molecular, Unidad de Posgrado, Escuela Superior de Medicina, Instituto Politécnico Nacional, Ciudad de México 11340, Mexico.
José Arellano-GalindoLaboratorio de Virología Clínica y Experimental, Unidad de Investigación en Enfermedades Infecciosas, Hospital Infantil de México Federico Gómez, Ciudad de México 06720, Mexico.
Carmen Palacios-ReyesDepartamento de Investigación, Hospital Juárez de México, Ciudad de México 07760, Mexico.
Ana María Espinosa-GarcíaServicio de Farmacología Clínica, Hospital General de México, Ciudad de México 06720, Mexico.
Patricia García Alonso-ThemannInstituto Nacional de Perinatología, Ciudad de México 11000, Mexico.
Juan Xicohtencatl-CortesLaboratorio de Bacteriología Intestinal, Hospital Infantil de México Federico Gómez, Ciudad de México 06720, Mexico.
Sara A OchoaLaboratorio de Bacteriología Intestinal, Hospital Infantil de México Federico Gómez, Ciudad de México 06720, Mexico.
Ariadnna Cruz-CórdovaLaboratorio de Bacteriología Intestinal, Hospital Infantil de México Federico Gómez, Ciudad de México 06720, Mexico.
Icela Palma-LaraLaboratorio de Morfología Molecular, Unidad de Posgrado, Escuela Superior de Medicina, Instituto Politécnico Nacional, Ciudad de México 11340, Mexico.
Hospital Infantil de México Federico Gómez · MXInstituto Politécnico Nacional · MXHospital General de México · MXHospital Juárez de México · MXInstituto Nacional de Perinatología · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epstein‑Barr virus (EBV) is an oncovirus associated with various neoplasms, including breast cancer (BC). EBV‑associated oncogenesis requires the action of several viral molecules, such as EBV nuclear antigen 3C, latent membrane protein 1, microRNAs and long non‑coding RNAs, which are able of manipulating the cellular machinery, inducing an evasion of the immune system, blocking apoptosis processes, promoting cell survival and metastasis. The risk of developing cancer is associated with epigenetic alterations and alterations in various signaling pathways. The activation of all these molecules can modify the expression of EBV proteins with oncogenic activity, influencing the oncogenic process. It is clear that BC, being multifactorial, presents a greater complexity; in numerous cases, the infection associated with EBV may be crucial for this neoplasia, if particular conditions for both the virus and host are present. In the present review, all these variables are analyzed in an aim to improve the understanding of the participation of EBV in BC.

Indexed as

Breast NeoplasmsEpstein-Barr Virus InfectionsCarcinogenesisCell Transformation, NeoplasticFemaleHerpesvirus 4, HumanHumansTumor Microenvironmentbreast cancercytokinesEpstein‑Barr virushuman papillomavirustumor microenvironment1

Identifiers

PMID37417334
PMCPMC10373119
OpenAlexW4383370423

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.