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

cervical cancer gene expression in cervical cancer signal transduction pathways

Journal

Oncology letters
ISSN: 1792-1082
Titre abrégé: Oncol Lett
Pays: Greece
ID NLM: 101531236

Informations de publication

Date de publication:
Nov 2024
Historique:
received: 28 03 2024
accepted: 24 06 2024
medline: 13 9 2024
pubmed: 13 9 2024
entrez: 13 9 2024
Statut: epublish

Résumé

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,

Identifiants

pubmed: 39268158
doi: 10.3892/ol.2024.14655
pii: OL-28-5-14655
pmc: PMC11391250
doi:

Types de publication

Journal Article

Langues

eng

Pagination

522

Informations de copyright

Copyright: © Limones-Gonzalez et al.

Déclaration de conflit d'intérêts

The authors declare that they have no competing interests.

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Auteurs

Jared E Limones-Gonzalez (JE)

Biotechnology Laboratory, Autonomous University of Zacatecas, Zacatecas 98160, Mexico.

Perla Aguilar Esquivel (P)

Department of Pathology, Zacatecas General Hospital Luz González Cosío, Zacatecas 98160, Mexico.

Karla Vazquez-Santillan (K)

Innovation in Precision Medicine Laboratory, National Institute of Genomic Medicine, Mexico City 14610, Mexico.

Rosario Castro-Oropeza (R)

Molecular Oncology Laboratory, Oncology Research Unit, XXI Century National Medical Center, IMSS, Mexico City 06720, Mexico.

Floria Lizarraga (F)

Epigenetics Laboratory, National Institute of Genomic Medicine, Mexico City 14610, Mexico.

Vilma Maldonado (V)

Epigenetics Laboratory, National Institute of Genomic Medicine, Mexico City 14610, Mexico.

Jorge Melendez-Zajgla (J)

Functional Cancer Genomics Laboratory, National Institute of Genomic Medicine, Mexico City 14610, Mexico.

Patricia Piña-Sanchez (P)

Molecular Oncology Laboratory, Oncology Research Unit, XXI Century National Medical Center, IMSS, Mexico City 06720, Mexico.

Gretel Mendoza-Almanza (G)

Epigenetics Laboratory, National Institute of Genomic Medicine, Mexico City 14610, Mexico.

Classifications MeSH