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P68 RNA helicase as a molecular target for cancer therapy

The DEAD-box family of RNA helicase is known to be required in virtually all cellular processes involving RNA, and p68 is a prototypic one of the family. Reports have indicated that in addition to ATPase and RNA helicase ability, p68 can also function as a co-activator for transcription factors such...

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Autores principales: Dai, Ting-Yu, Cao, Liu, Yang, Zi-Chen, Li, Ya-Shu, Tan, Li, Ran, Xin-Ze, Shi, Chun-Meng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4431487/
https://www.ncbi.nlm.nih.gov/pubmed/25150365
http://dx.doi.org/10.1186/s13046-014-0064-y
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author Dai, Ting-Yu
Cao, Liu
Yang, Zi-Chen
Li, Ya-Shu
Tan, Li
Ran, Xin-Ze
Shi, Chun-Meng
author_facet Dai, Ting-Yu
Cao, Liu
Yang, Zi-Chen
Li, Ya-Shu
Tan, Li
Ran, Xin-Ze
Shi, Chun-Meng
author_sort Dai, Ting-Yu
collection PubMed
description The DEAD-box family of RNA helicase is known to be required in virtually all cellular processes involving RNA, and p68 is a prototypic one of the family. Reports have indicated that in addition to ATPase and RNA helicase ability, p68 can also function as a co-activator for transcription factors such as estrogen receptor alpha, tumor suppressor p53 and beta-catenin. More than that, post-translational modification of p68 including phosphorylation, acetylation, sumoylation, and ubiquitylation can regulate the coactivation effect. Furthermore, aberrant expression of p68 in cancers highlights that p68 plays an important role for tumorgenesis and development. In this review, we briefly introduce the function and modulation of p68 in cancer cells, and put forward envisagement about future study about p68.
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spelling pubmed-44314872015-05-15 P68 RNA helicase as a molecular target for cancer therapy Dai, Ting-Yu Cao, Liu Yang, Zi-Chen Li, Ya-Shu Tan, Li Ran, Xin-Ze Shi, Chun-Meng J Exp Clin Cancer Res Review The DEAD-box family of RNA helicase is known to be required in virtually all cellular processes involving RNA, and p68 is a prototypic one of the family. Reports have indicated that in addition to ATPase and RNA helicase ability, p68 can also function as a co-activator for transcription factors such as estrogen receptor alpha, tumor suppressor p53 and beta-catenin. More than that, post-translational modification of p68 including phosphorylation, acetylation, sumoylation, and ubiquitylation can regulate the coactivation effect. Furthermore, aberrant expression of p68 in cancers highlights that p68 plays an important role for tumorgenesis and development. In this review, we briefly introduce the function and modulation of p68 in cancer cells, and put forward envisagement about future study about p68. BioMed Central 2014-08-24 /pmc/articles/PMC4431487/ /pubmed/25150365 http://dx.doi.org/10.1186/s13046-014-0064-y Text en Copyright © 2014 Dai et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Dai, Ting-Yu
Cao, Liu
Yang, Zi-Chen
Li, Ya-Shu
Tan, Li
Ran, Xin-Ze
Shi, Chun-Meng
P68 RNA helicase as a molecular target for cancer therapy
title P68 RNA helicase as a molecular target for cancer therapy
title_full P68 RNA helicase as a molecular target for cancer therapy
title_fullStr P68 RNA helicase as a molecular target for cancer therapy
title_full_unstemmed P68 RNA helicase as a molecular target for cancer therapy
title_short P68 RNA helicase as a molecular target for cancer therapy
title_sort p68 rna helicase as a molecular target for cancer therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4431487/
https://www.ncbi.nlm.nih.gov/pubmed/25150365
http://dx.doi.org/10.1186/s13046-014-0064-y
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