C-Jun Transcription Factor Oncogenic Activation in Oral Carcinoma.

Détails

ID Serval
serval:BIB_3B3C75617D0C
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
C-Jun Transcription Factor Oncogenic Activation in Oral Carcinoma.
Périodique
Maedica
Auteur⸱e⸱s
Mastronikolis N., Chrysovergis A., Papanikolaou V., Derka S., Asimakopoulos A.D., Mastronikoli S., Tsiambas E., Manaios L., Papouliakos S., Ragos V., Fotiades P., Pantos P., Stathopoulos P., Kyrodimos E.
ISSN
1841-9038 (Print)
ISSN-L
1841-9038
Statut éditorial
Publié
Date de publication
06/2024
Peer-reviewed
Oui
Volume
19
Numéro
2
Pages
350-354
Langue
anglais
Notes
Publication types: Journal Article ; Review
Publication Status: ppublish
Résumé
Oral carcinogenetic is based on a variety of genomic imbalances (gross chromosome or specific gene alterations) that drive the normal oral mucosa to its neoplastic/dysplastic epithelial form and finally to a totally malignant tissue transformation. In this multi-step procedure, down-regulation of suppressor genes combined with overactivation of oncogenes are two crucial and partially early genetic events involved in the onset and progression of neoplastic/malignant epithelia transformation. More specifically, deregulation of strong transcription factors negatively affects the normal expression of a broad spectrum of genes that are involved in cell proliferation and signalling transduction to the nucleus.
The purpose of the current molecular review was to explore the c-Jun (chromosome location: 1p32-p31) transcription factor transformation mechanisms to oncogene in oral squamous cell carcinoma (OSCC).
A systematic review of the literature was carried out by searching in PubMed international database. The year 2010 was set as a prominent time limit for the publication date of the articles in the majority of them, whereas specific references of great importance and historical value in the field of the c-Jun gene discovery and analysis were also included. The following keywords were used: c-Jun, oncogene, signaling pathway, oral, carcinoma, transcription. A pool of 45 important articles were selected for the present study at the basis of combining molecular knowledge with new targeted therapeutic strategies.
C-Jun - as a part of the c-Jun/c-Fos transcription factors' complex -critically regulates the expression levels in a variety of genes inside the cellular microenvironment. A broad spectrum of malignancies, including OSCC, demonstrate c-Jun alterations driving the gene to its oncogenic phenotype. Interestingly, c-Jun oncogenic activation is mediated by high-risk human papilloma virus (HR-HPV) persistent infection in significant subsets of these malignancies.
C-Jun was the first oncogene - acting as a strong transcription factor - that was discovered and cloned 35 years ago. C-Jun is the living history of oncogenes and its discovery marks a significant step in the evolution of molecular biology.
Pubmed
Création de la notice
30/08/2024 15:18
Dernière modification de la notice
05/09/2024 9:00
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