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OCT4B Isoform Promotes Anchorage-Independent Growth of Glioblastoma Cells
OCT4, also known as POU5F1 (POU domain class 5 transcription factor 1), is a transcription factor that acts as a master regulator of pluripotency in embryonic stem cells and is one of the reprogramming factors required for generating induced pluripotent stem cells. The human OCT4 encodes three isofo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society for Molecular and Cellular Biology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6399006/ https://www.ncbi.nlm.nih.gov/pubmed/30622231 http://dx.doi.org/10.14348/molcells.2018.0311 |
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author | Choi, Sang-Hun Kim, Jun-Kyum Jeon, Hee-Young Eun, Kiyoung Kim, Hyunggee |
author_facet | Choi, Sang-Hun Kim, Jun-Kyum Jeon, Hee-Young Eun, Kiyoung Kim, Hyunggee |
author_sort | Choi, Sang-Hun |
collection | PubMed |
description | OCT4, also known as POU5F1 (POU domain class 5 transcription factor 1), is a transcription factor that acts as a master regulator of pluripotency in embryonic stem cells and is one of the reprogramming factors required for generating induced pluripotent stem cells. The human OCT4 encodes three isoforms, OCT4A, OCT4B, and OCT4B1, which are generated by alternative splicing. Currently, the functions and expression patterns of OCT4B remain largely unknown in malignancies, especially in human glioblastomas. Here, we demonstrated the function of OCT4B in human glioblastomas. Among the isoform of OCT4B, OCT4B-190 (OCT4B(19kDa)) was highly expressed in human glioblastoma stem cells and glioblastoma cells and was mainly detected in the cytoplasm rather than the nucleus. Overexpression of OCT4B(19kDa) promoted colony formation of glioblastoma cells when grown in soft agar culture conditions. Clinical data analysis revealed that patients with gliomas that expressed OCT4B at high levels had a poorer prognosis than patients with gliomas that expressed OCT4B at low levels. Thus, OCT4B(19kDa) may play a crucial role in regulating cancer cell survival and adaption in a rigid environment. |
format | Online Article Text |
id | pubmed-6399006 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Korean Society for Molecular and Cellular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-63990062019-03-07 OCT4B Isoform Promotes Anchorage-Independent Growth of Glioblastoma Cells Choi, Sang-Hun Kim, Jun-Kyum Jeon, Hee-Young Eun, Kiyoung Kim, Hyunggee Mol Cells Article OCT4, also known as POU5F1 (POU domain class 5 transcription factor 1), is a transcription factor that acts as a master regulator of pluripotency in embryonic stem cells and is one of the reprogramming factors required for generating induced pluripotent stem cells. The human OCT4 encodes three isoforms, OCT4A, OCT4B, and OCT4B1, which are generated by alternative splicing. Currently, the functions and expression patterns of OCT4B remain largely unknown in malignancies, especially in human glioblastomas. Here, we demonstrated the function of OCT4B in human glioblastomas. Among the isoform of OCT4B, OCT4B-190 (OCT4B(19kDa)) was highly expressed in human glioblastoma stem cells and glioblastoma cells and was mainly detected in the cytoplasm rather than the nucleus. Overexpression of OCT4B(19kDa) promoted colony formation of glioblastoma cells when grown in soft agar culture conditions. Clinical data analysis revealed that patients with gliomas that expressed OCT4B at high levels had a poorer prognosis than patients with gliomas that expressed OCT4B at low levels. Thus, OCT4B(19kDa) may play a crucial role in regulating cancer cell survival and adaption in a rigid environment. Korean Society for Molecular and Cellular Biology 2019-02-28 2019-01-02 /pmc/articles/PMC6399006/ /pubmed/30622231 http://dx.doi.org/10.14348/molcells.2018.0311 Text en © The Korean Society for Molecular and Cellular Biology. All rights reserved. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/. |
spellingShingle | Article Choi, Sang-Hun Kim, Jun-Kyum Jeon, Hee-Young Eun, Kiyoung Kim, Hyunggee OCT4B Isoform Promotes Anchorage-Independent Growth of Glioblastoma Cells |
title | OCT4B Isoform Promotes Anchorage-Independent Growth of Glioblastoma Cells |
title_full | OCT4B Isoform Promotes Anchorage-Independent Growth of Glioblastoma Cells |
title_fullStr | OCT4B Isoform Promotes Anchorage-Independent Growth of Glioblastoma Cells |
title_full_unstemmed | OCT4B Isoform Promotes Anchorage-Independent Growth of Glioblastoma Cells |
title_short | OCT4B Isoform Promotes Anchorage-Independent Growth of Glioblastoma Cells |
title_sort | oct4b isoform promotes anchorage-independent growth of glioblastoma cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6399006/ https://www.ncbi.nlm.nih.gov/pubmed/30622231 http://dx.doi.org/10.14348/molcells.2018.0311 |
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