Evidence map›Paper›PMID 39335585›Full record

ReviewBiomedicines2024

Non-Coding RNAs and Innate Immune Responses in Cancer.

Carlos Romero Díaz, María Teresa Hernández-Huerta, Laura Pérez-Campos Mayoral, Miriam Emily Avendaño Villegas, Edgar Zenteno, Margarito Martínez Cruz, Eduardo Pérez-Campos Mayoral, María Del Socorro Pina Canseco, Gabriel Mayoral Andrade, Manuel Ángeles Castellanos and 6 more

Abstract readReview
In one paragraph

Review in Biomedicines, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

16 authors.

Carlos Romero DíazTecnológico Nacional de México/IT Oaxaca, Oaxaca 68030, Mexico.
María Teresa Hernández-HuertaConsejo Nacional de Humanidades, Ciencias y Tecnologías (CONAHCyT), Facultad de Medicina y Cirugía, Universidad Autónoma "Benito Juárez" de Oaxaca (UABJO), Oaxaca 68020, Mexico.ORCID 0000-0003-2182-2540
Laura Pérez-Campos MayoralCentro de Investigación, Facultad de Medicina UNAM-UABJO, Universidad Autónoma "Benito Juárez" de Oaxaca (UABJO), Oaxaca 68020, Mexico.ORCID 0000-0003-4140-4661
Miriam Emily Avendaño VillegasTecnológico Nacional de México/IT Oaxaca, Oaxaca 68030, Mexico.ORCID 0000-0002-4871-8658
Edgar ZentenoFacultad de Medicina, Universidad Nacional Autónoma de Mexico, Ciudad de México 04510, Mexico.ORCID 0000-0001-5603-4072
Margarito Martínez CruzTecnológico Nacional de México/IT Oaxaca, Oaxaca 68030, Mexico.
Eduardo Pérez-Campos MayoralCentro de Investigación, Facultad de Medicina UNAM-UABJO, Universidad Autónoma "Benito Juárez" de Oaxaca (UABJO), Oaxaca 68020, Mexico.
María Del Socorro Pina CansecoCentro de Investigación, Facultad de Medicina UNAM-UABJO, Universidad Autónoma "Benito Juárez" de Oaxaca (UABJO), Oaxaca 68020, Mexico.
Gabriel Mayoral AndradeCentro de Investigación, Facultad de Medicina UNAM-UABJO, Universidad Autónoma "Benito Juárez" de Oaxaca (UABJO), Oaxaca 68020, Mexico.
Manuel Ángeles CastellanosFacultad de Medicina, Universidad Nacional Autónoma de Mexico, Ciudad de México 04510, Mexico.ORCID 0000-0002-6496-9465
José Manuel Matías SalvadorHospital General Dr. Aurelio Valdivieso, Oaxaca 68040, Mexico.
Eli Cruz ParadaTecnológico Nacional de México/IT Oaxaca, Oaxaca 68030, Mexico.ORCID 0000-0001-7578-1305
Alexis Martínez BarrasFacultad de Ingeniería, Universidad Autónoma de Querétaro, Querétaro 76017, Mexico.
Jaydi Nora Cruz FernándezCentro de Investigación, Facultad de Medicina UNAM-UABJO, Universidad Autónoma "Benito Juárez" de Oaxaca (UABJO), Oaxaca 68020, Mexico.
Daniel Scott-AlgaraUnité de Biologie Cellulaire des Lymphocytes and Direction of International Affairs, Institut Pasteur, 75015 Paris, France.ORCID 0000-0003-1851-503X
Eduardo Pérez-CamposTecnológico Nacional de México/IT Oaxaca, Oaxaca 68030, Mexico.ORCID 0000-0001-6720-7952

Funding

French National Agency for Research on AIDS, Viral Hepatitis, and emerging and re-emerging infectious diseases ANRS MIE
6 · The paper itself

Abstract

Non-coding RNAs (ncRNAs) and the innate immune system are closely related, acting as defense mechanisms and regulating gene expression and innate immunity. Both are modulators in the initiation, development and progression of cancer. We aimed to review the major types of ncRNAs, including small interfering RNAs (siRNAs), microRNAs (miRNAs), piwi-interacting RNAs (piRNAs), and long non-coding RNAs (lncRNAs), with a focus on cancer, innate immunity, and inflammation. We found that ncRNAs are closely related to innate immunity, epigenetics, chronic inflammation, and cancer and share properties such as inducibility, specificity, memory, and transfer. These similarities and interrelationships suggest that ncRNAs and modulators of trained immunity, together with the control of chronic inflammation, can be combined to develop novel therapeutic approaches for personalized cancer treatment. In conclusion, the close relationship between ncRNAs, the innate immune system, and inflammation highlights their importance in cancer pathways and their potential as targets for novel therapeutic strategies.

Indexed as

cancerchronic inflammationepimutationimmune-inducibleinheritancemiRNApiRNAsiRNAspecificitytrained immunitytransfer

Identifiers

PMID39335585
PMCPMC11429077

What OpenQuestion holds

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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.