Evidence map›Paper›PMID 41195272›Full record

ReviewFrontiers in oncology2025

Long noncoding RNAs involved in therapeutic response: implications for cervical cancer drug resistance.

Samuel Trujano-Camacho, Carlos Contreras-Romero, Verónica García-Castillo, David Sánchez-Marín, Mercedes Olvera-Valencia, Mauricio Rodríguez-Dorantes, Oscar Peralta-Zaragoza, David Cantú de León, Eduardo López-Urrutia, Carlos Pérez-Plasencia

Abstract readReview
In one paragraph

Review in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

10 authors.

Samuel Trujano-CamachoLaboratorio de Genómica, Unidad de Biomedicina, Facultad de Estudios Superiores-Iztacala (FES-IZTACALA), Universidad Nacional Autónoma de México (UNAM), Tlalnepantla, Mexico.
Carlos Contreras-RomeroLaboratorio de Diagnóstico Molecular Genelab, Cuahutémoc, Mexico.
Verónica García-CastilloLaboratorio de Genómica, Unidad de Biomedicina, Facultad de Estudios Superiores-Iztacala (FES-IZTACALA), Universidad Nacional Autónoma de México (UNAM), Tlalnepantla, Mexico.
David Sánchez-MarínPosgrado en Ciencias Biológicas, Facultad de Medicina, Universidad Nacional Autónoma de México (UNAM), Coyoacan, Mexico.
Mercedes Olvera-ValenciaLaboratorio de Virus y Cáncer, Dirección de Investigación, Instituto Nacional de Cancerología, México City, Mexico.
Mauricio Rodríguez-DorantesLaboratorio de Oncogenómica, Instituto Nacional de Medicina Genómica, Tlalpan, Mexico.
Oscar Peralta-ZaragozaDirección de Infecciones Crónicas y Cáncer, Centro de Investigación Sobre Enfermedades Infecciosas, Instituto Nacional de Salud Pública, Cuernavaca, Mexico.
David Cantú de LeónDirección de Investigación, Instituto Nacional de Cancerología, México City, Mexico.
Eduardo López-UrrutiaLaboratorio de Genómica, Unidad de Biomedicina, Facultad de Estudios Superiores-Iztacala (FES-IZTACALA), Universidad Nacional Autónoma de México (UNAM), Tlalnepantla, Mexico.
Carlos Pérez-PlasenciaLaboratorio de Genómica, Unidad de Biomedicina, Facultad de Estudios Superiores-Iztacala (FES-IZTACALA), Universidad Nacional Autónoma de México (UNAM), Tlalnepantla, Mexico.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cervical cancer (CC) remains among the top causes of death for women worldwide, especially in low-income countries, where screening strategies are less widespread. Treatment strategies are mainly based on DNA-damaging agents, though resistance mechanisms still pose a substantial challenge. Among the cellular components that mediate treatment resistance, long non-coding RNAs (lncRNAs) stand out because of their broad regulatory effects. They are involved in virtually all drug resistance mechanisms, such as drug efflux, DNA repair, evasion of cell death, and aberrant epigenetic modifications. Although resistance mechanisms are fundamentally similar in most cancers, the underlying regulatory networks vary substantially. Here, we review the literature for lncRNAs involved in treatment resistance mechanisms in general, and then focus on lncRNAs that mediate resistance in CC. We found a broad area of opportunity in lncRNA research in resistant CC, as the lncRNAs involved are still to be described. These master regulators are promising candidates for response markers and therapeutic targets. May this compilation serve as the basis for further descriptions of the regulatory roles of lncRNA in CC treatment resistance.

Indexed as

cancercervical cancerchemoresistancelncRNAsnon-coding RNAs

Identifiers

PMID41195272
PMCPMC12582941

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.