Cargando…

High expression of octamer transcription factor 1 in cervical cancer

Cervical carcinoma is the second most prevalent malignancy in females worldwide. The crucial etiologic factors involved in the development of cervical carcinoma include infection with papillomavirus, and the structural or functional mutation of oncogenes and tumor suppressor genes. The abnormal chan...

Descripción completa

Detalles Bibliográficos
Autores principales: XIAO, SONGSHU, LIAO, SHAN, ZHOU, YANHONG, JIANG, BIN, LI, YUERAN, XUE, MIN
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4049708/
https://www.ncbi.nlm.nih.gov/pubmed/24932254
http://dx.doi.org/10.3892/ol.2014.2023
_version_ 1782319855054094336
author XIAO, SONGSHU
LIAO, SHAN
ZHOU, YANHONG
JIANG, BIN
LI, YUERAN
XUE, MIN
author_facet XIAO, SONGSHU
LIAO, SHAN
ZHOU, YANHONG
JIANG, BIN
LI, YUERAN
XUE, MIN
author_sort XIAO, SONGSHU
collection PubMed
description Cervical carcinoma is the second most prevalent malignancy in females worldwide. The crucial etiologic factors involved in the development of cervical carcinoma include infection with papillomavirus, and the structural or functional mutation of oncogenes and tumor suppressor genes. The abnormal change of octamer transcription factor 1 (OCT1) is associated with tumor progression and a poor patient survival rate. However, little is known regarding the effect of OCT1 in cervical cancer. In the present study, flow cytometry, western blot analysis and quantitative polymerase chain reaction (qPCR) were peformed to identify differentially expressed OCT1 in cervical cancer tissue and adjacent non-cancerous tissues. The normalized OCT1 gene expression in cervical cancer was 5.98 times higher compared with the adjacent non-cancerous tissues. Western blot analysis and flow cytometry assessed the levels of OCT1 protein. The results of these two differential techniques showed that the protein expression level of OCT1 was greater in cervical cancer tissues, which corresponded with the qPCR results. Finally, as OCT1 is a potential target gene for microRNA (miR)-1467, -1185, -4493 and -3919, their expression levels were analyzed in cervical cancer tissues and adjacent non-cancerous tissues; they were downregulated by ~45% in the cervical cancer samples. The results of the present study showed that OCT1 is highly expressed in cervical cancer tissues and indicated that OCT-1 may be significant in cervical cancer.
format Online
Article
Text
id pubmed-4049708
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-40497082014-06-13 High expression of octamer transcription factor 1 in cervical cancer XIAO, SONGSHU LIAO, SHAN ZHOU, YANHONG JIANG, BIN LI, YUERAN XUE, MIN Oncol Lett Articles Cervical carcinoma is the second most prevalent malignancy in females worldwide. The crucial etiologic factors involved in the development of cervical carcinoma include infection with papillomavirus, and the structural or functional mutation of oncogenes and tumor suppressor genes. The abnormal change of octamer transcription factor 1 (OCT1) is associated with tumor progression and a poor patient survival rate. However, little is known regarding the effect of OCT1 in cervical cancer. In the present study, flow cytometry, western blot analysis and quantitative polymerase chain reaction (qPCR) were peformed to identify differentially expressed OCT1 in cervical cancer tissue and adjacent non-cancerous tissues. The normalized OCT1 gene expression in cervical cancer was 5.98 times higher compared with the adjacent non-cancerous tissues. Western blot analysis and flow cytometry assessed the levels of OCT1 protein. The results of these two differential techniques showed that the protein expression level of OCT1 was greater in cervical cancer tissues, which corresponded with the qPCR results. Finally, as OCT1 is a potential target gene for microRNA (miR)-1467, -1185, -4493 and -3919, their expression levels were analyzed in cervical cancer tissues and adjacent non-cancerous tissues; they were downregulated by ~45% in the cervical cancer samples. The results of the present study showed that OCT1 is highly expressed in cervical cancer tissues and indicated that OCT-1 may be significant in cervical cancer. D.A. Spandidos 2014-06 2014-04-02 /pmc/articles/PMC4049708/ /pubmed/24932254 http://dx.doi.org/10.3892/ol.2014.2023 Text en Copyright © 2014, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
XIAO, SONGSHU
LIAO, SHAN
ZHOU, YANHONG
JIANG, BIN
LI, YUERAN
XUE, MIN
High expression of octamer transcription factor 1 in cervical cancer
title High expression of octamer transcription factor 1 in cervical cancer
title_full High expression of octamer transcription factor 1 in cervical cancer
title_fullStr High expression of octamer transcription factor 1 in cervical cancer
title_full_unstemmed High expression of octamer transcription factor 1 in cervical cancer
title_short High expression of octamer transcription factor 1 in cervical cancer
title_sort high expression of octamer transcription factor 1 in cervical cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4049708/
https://www.ncbi.nlm.nih.gov/pubmed/24932254
http://dx.doi.org/10.3892/ol.2014.2023
work_keys_str_mv AT xiaosongshu highexpressionofoctamertranscriptionfactor1incervicalcancer
AT liaoshan highexpressionofoctamertranscriptionfactor1incervicalcancer
AT zhouyanhong highexpressionofoctamertranscriptionfactor1incervicalcancer
AT jiangbin highexpressionofoctamertranscriptionfactor1incervicalcancer
AT liyueran highexpressionofoctamertranscriptionfactor1incervicalcancer
AT xuemin highexpressionofoctamertranscriptionfactor1incervicalcancer