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Role of Oct3/4 in Cervical Cancer Tumorigenesis

Cervical cancer (CC) is the fourth most common type of cancer that affects women. Compared to other types of cancer, CC has a high mortality rate in women worldwide. Several factors contribute to the development of CC, but persistent high-risk human papillomavirus infection is the main etiologic age...

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Autores principales: Clemente-Periván, Sayuri Itzel, Gómez-Gómez, Yazmín, Leyva-Vázquez, Marco Antonio, Lagunas-Martínez, Alfredo, Organista-Nava, Jorge, Illades-Aguiar, Berenice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7079573/
https://www.ncbi.nlm.nih.gov/pubmed/32219062
http://dx.doi.org/10.3389/fonc.2020.00247
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author Clemente-Periván, Sayuri Itzel
Gómez-Gómez, Yazmín
Leyva-Vázquez, Marco Antonio
Lagunas-Martínez, Alfredo
Organista-Nava, Jorge
Illades-Aguiar, Berenice
author_facet Clemente-Periván, Sayuri Itzel
Gómez-Gómez, Yazmín
Leyva-Vázquez, Marco Antonio
Lagunas-Martínez, Alfredo
Organista-Nava, Jorge
Illades-Aguiar, Berenice
author_sort Clemente-Periván, Sayuri Itzel
collection PubMed
description Cervical cancer (CC) is the fourth most common type of cancer that affects women. Compared to other types of cancer, CC has a high mortality rate in women worldwide. Several factors contribute to the development of CC, but persistent high-risk human papillomavirus infection is the main etiologic agent associated with the development of CC. Moreover, several studies reported that alterations in the expression of transcription factors present in a small subpopulation of cells within tumors called cancer stem cells (CSCs), which contribute to the development of CC by promoting tumorigenicity and metastasis. These transcription factors affect self-renewal and maintenance of pluripotency and differentiation in stem cells. OCT3/4 belongs to the family of transcription factors with the POU domain. It consists of five exons and can be edited by alternative splicing into three main transcripts: OCT3/4A, OCT3/4B, and OCT3/4B1. The OCT3/4 expression in CSCs promotes carcinogenesis and the development of malignant tumors, and the loss of expression leads to the loss of self-renewal and proliferation and favors apoptosis. This review describes the main roles of OCT3/4 in CC and its importance in several biological processes that contribute to the development of CC and may serve as molecular targets to improve prognosis of CC.
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spelling pubmed-70795732020-03-26 Role of Oct3/4 in Cervical Cancer Tumorigenesis Clemente-Periván, Sayuri Itzel Gómez-Gómez, Yazmín Leyva-Vázquez, Marco Antonio Lagunas-Martínez, Alfredo Organista-Nava, Jorge Illades-Aguiar, Berenice Front Oncol Oncology Cervical cancer (CC) is the fourth most common type of cancer that affects women. Compared to other types of cancer, CC has a high mortality rate in women worldwide. Several factors contribute to the development of CC, but persistent high-risk human papillomavirus infection is the main etiologic agent associated with the development of CC. Moreover, several studies reported that alterations in the expression of transcription factors present in a small subpopulation of cells within tumors called cancer stem cells (CSCs), which contribute to the development of CC by promoting tumorigenicity and metastasis. These transcription factors affect self-renewal and maintenance of pluripotency and differentiation in stem cells. OCT3/4 belongs to the family of transcription factors with the POU domain. It consists of five exons and can be edited by alternative splicing into three main transcripts: OCT3/4A, OCT3/4B, and OCT3/4B1. The OCT3/4 expression in CSCs promotes carcinogenesis and the development of malignant tumors, and the loss of expression leads to the loss of self-renewal and proliferation and favors apoptosis. This review describes the main roles of OCT3/4 in CC and its importance in several biological processes that contribute to the development of CC and may serve as molecular targets to improve prognosis of CC. Frontiers Media S.A. 2020-03-11 /pmc/articles/PMC7079573/ /pubmed/32219062 http://dx.doi.org/10.3389/fonc.2020.00247 Text en Copyright © 2020 Clemente-Periván, Gómez-Gómez, Leyva-Vázquez, Lagunas-Martínez, Organista-Nava and Illades-Aguiar. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Clemente-Periván, Sayuri Itzel
Gómez-Gómez, Yazmín
Leyva-Vázquez, Marco Antonio
Lagunas-Martínez, Alfredo
Organista-Nava, Jorge
Illades-Aguiar, Berenice
Role of Oct3/4 in Cervical Cancer Tumorigenesis
title Role of Oct3/4 in Cervical Cancer Tumorigenesis
title_full Role of Oct3/4 in Cervical Cancer Tumorigenesis
title_fullStr Role of Oct3/4 in Cervical Cancer Tumorigenesis
title_full_unstemmed Role of Oct3/4 in Cervical Cancer Tumorigenesis
title_short Role of Oct3/4 in Cervical Cancer Tumorigenesis
title_sort role of oct3/4 in cervical cancer tumorigenesis
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7079573/
https://www.ncbi.nlm.nih.gov/pubmed/32219062
http://dx.doi.org/10.3389/fonc.2020.00247
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