Evidence map›Paper›PMID 39268158›Full record

ArticleOncology letters2024

Changes in the molecular nodes of the Notch and NRF2 pathways in cervical cancer tissues from the precursor stages to invasive carcinoma.

Jared E Limones-Gonzalez, Perla Aguilar Esquivel, Karla Vazquez-Santillan, Rosario Castro-Oropeza, Floria Lizarraga, Vilma Maldonado, Jorge Melendez-Zajgla, Patricia Piña-Sanchez, Gretel Mendoza-Almanza

Abstract read
In one paragraph

Article in Oncology letters, 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. Article
  2. Article
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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

9 authors.

Jared E Limones-GonzalezBiotechnology Laboratory, Autonomous University of Zacatecas, Zacatecas 98160, Mexico.
Perla Aguilar EsquivelDepartment of Pathology, Zacatecas General Hospital Luz González Cosío, Zacatecas 98160, Mexico.
Karla Vazquez-SantillanInnovation in Precision Medicine Laboratory, National Institute of Genomic Medicine, Mexico City 14610, Mexico.
Rosario Castro-OropezaMolecular Oncology Laboratory, Oncology Research Unit, XXI Century National Medical Center, IMSS, Mexico City 06720, Mexico.
Floria LizarragaEpigenetics Laboratory, National Institute of Genomic Medicine, Mexico City 14610, Mexico.
Vilma MaldonadoEpigenetics Laboratory, National Institute of Genomic Medicine, Mexico City 14610, Mexico.
Jorge Melendez-ZajglaFunctional Cancer Genomics Laboratory, National Institute of Genomic Medicine, Mexico City 14610, Mexico.
Patricia Piña-SanchezMolecular Oncology Laboratory, Oncology Research Unit, XXI Century National Medical Center, IMSS, Mexico City 06720, Mexico.
Gretel Mendoza-AlmanzaEpigenetics Laboratory, National Institute of Genomic Medicine, Mexico City 14610, Mexico.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer is a multifactorial disease characterized by the loss of control in the expression of genes known as cancer driver genes. Cancer driver genes trigger uncontrolled cell replication, which leads to the development of malignant tumors. A cluster of signal transduction pathways that contain cancer driver genes involved in cellular processes, such as cell proliferation, differentiation, apoptosis and dysregulated organ growth, are associated with cancer initiation and progression. In the present study, three signal transduction pathways involved in cervical cancer (CC) development were analyzed: The Hippo pathway (FAT atypical cadherin, yes-associated protein 1, SMAD4 and TEA domain family member 2), the Notch pathway [cellular-MYC, cAMP response element-binding binding protein (CREBBP), E1A-associated cellular p300 transcriptional co-activator protein and F-Box and WD repeat domain containing 7] and the nuclear factor erythroid 2-related factor 2 (NRF2) pathway [NRF2, kelch-like ECH-associated protein 1 (KEAP1), AKT and PIK3-catalytic subunit α]. Tumor samples from patients diagnosed with various stages of CC, including cervical intraepithelial neoplasia (CIN) 1, CIN 2, CIN 3,

Indexed as

cervical cancergene expression in cervical cancersignal transduction pathways

Identifiers

PMID39268158
PMCPMC11391250

What OpenQuestion holds

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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.