Cargando…

Radioresistance of chordoma cells is associated with the ATM/ATR pathway, in which RAD51 serves as an important downstream effector

Surgery followed by radiotherapy is the standard treatment for chordomas, which are a rare but low-grade type of bone cancer arising from remnants of the embryonic notochord. However, disease recurrence following radiotherapy is common, most likely due to endogenous DNA repair mechanisms that promot...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Chao, Wang, Bing, Li, Lei, Li, Yawei, Li, Pengzhi, Lv, Guohua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5609200/
https://www.ncbi.nlm.nih.gov/pubmed/28962138
http://dx.doi.org/10.3892/etm.2017.4736
_version_ 1783265567436701696
author Zhang, Chao
Wang, Bing
Li, Lei
Li, Yawei
Li, Pengzhi
Lv, Guohua
author_facet Zhang, Chao
Wang, Bing
Li, Lei
Li, Yawei
Li, Pengzhi
Lv, Guohua
author_sort Zhang, Chao
collection PubMed
description Surgery followed by radiotherapy is the standard treatment for chordomas, which are a rare but low-grade type of bone cancer arising from remnants of the embryonic notochord. However, disease recurrence following radiotherapy is common, most likely due to endogenous DNA repair mechanisms that promote cell survival upon radiation strikes. The ataxia telangiectasia mutated/ataxia telangiectasia mutated and Rad3 related (ATM/ATR)-mediated pathway has a critical role in DNA repair mechanisms; however, it has rarely been investigated in chordomas. In the present study, the expression of signal molecules related to the ATM/ATR pathway in chordoma tissues and adjacent normal tissues were initially examined using immunohistochemistry and western blot analysis. Chordoma U-CH1 and U-CH2 cells were subsequently used to investigate cell responses to ionizing radiation and the potential protective actions mediated by the ATM/ATR pathway. Phosphorylated (p)-ATM, p-ATR, γ-H2A histone family, member X (H2AX) and RAD51 were significantly upregulated in chordoma tissues relative to adjacent normal tissues (P<0.05). No significant reductions were observed in the viability of U-CH1 and U-CH2 cells following exposure to low-dose (1 and 2 Gy) radiation. Radiation (1 and 2 Gy) triggered a significant upregulation in p-ATM, γ-H2AX and RAD51 expression in U-CH1 cells (P<0.05), as well as a significant upregulation in p-ATM, p-ATR and RAD51 levels in U-CH2 cells (P<0.05). RAD51 knockdown increased the responses of both U-CH1 and U-CH2 cells to 1 Gy radiation, as evidenced by the significantly decreased cell viability and increased apoptosis rate (P<0.05). Collectively, the results of the present study indicated that radioresistance of chordoma cells is associated with the ATM/ATR pathway, in which RAD51 serves as an important downstream effector. Thus, RAD51 presents a promising therapeutic target for improving the outcome of radiotherapy treatment in chordomas.
format Online
Article
Text
id pubmed-5609200
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-56092002017-09-28 Radioresistance of chordoma cells is associated with the ATM/ATR pathway, in which RAD51 serves as an important downstream effector Zhang, Chao Wang, Bing Li, Lei Li, Yawei Li, Pengzhi Lv, Guohua Exp Ther Med Articles Surgery followed by radiotherapy is the standard treatment for chordomas, which are a rare but low-grade type of bone cancer arising from remnants of the embryonic notochord. However, disease recurrence following radiotherapy is common, most likely due to endogenous DNA repair mechanisms that promote cell survival upon radiation strikes. The ataxia telangiectasia mutated/ataxia telangiectasia mutated and Rad3 related (ATM/ATR)-mediated pathway has a critical role in DNA repair mechanisms; however, it has rarely been investigated in chordomas. In the present study, the expression of signal molecules related to the ATM/ATR pathway in chordoma tissues and adjacent normal tissues were initially examined using immunohistochemistry and western blot analysis. Chordoma U-CH1 and U-CH2 cells were subsequently used to investigate cell responses to ionizing radiation and the potential protective actions mediated by the ATM/ATR pathway. Phosphorylated (p)-ATM, p-ATR, γ-H2A histone family, member X (H2AX) and RAD51 were significantly upregulated in chordoma tissues relative to adjacent normal tissues (P<0.05). No significant reductions were observed in the viability of U-CH1 and U-CH2 cells following exposure to low-dose (1 and 2 Gy) radiation. Radiation (1 and 2 Gy) triggered a significant upregulation in p-ATM, γ-H2AX and RAD51 expression in U-CH1 cells (P<0.05), as well as a significant upregulation in p-ATM, p-ATR and RAD51 levels in U-CH2 cells (P<0.05). RAD51 knockdown increased the responses of both U-CH1 and U-CH2 cells to 1 Gy radiation, as evidenced by the significantly decreased cell viability and increased apoptosis rate (P<0.05). Collectively, the results of the present study indicated that radioresistance of chordoma cells is associated with the ATM/ATR pathway, in which RAD51 serves as an important downstream effector. Thus, RAD51 presents a promising therapeutic target for improving the outcome of radiotherapy treatment in chordomas. D.A. Spandidos 2017-09 2017-07-09 /pmc/articles/PMC5609200/ /pubmed/28962138 http://dx.doi.org/10.3892/etm.2017.4736 Text en Copyright: © Zhang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Zhang, Chao
Wang, Bing
Li, Lei
Li, Yawei
Li, Pengzhi
Lv, Guohua
Radioresistance of chordoma cells is associated with the ATM/ATR pathway, in which RAD51 serves as an important downstream effector
title Radioresistance of chordoma cells is associated with the ATM/ATR pathway, in which RAD51 serves as an important downstream effector
title_full Radioresistance of chordoma cells is associated with the ATM/ATR pathway, in which RAD51 serves as an important downstream effector
title_fullStr Radioresistance of chordoma cells is associated with the ATM/ATR pathway, in which RAD51 serves as an important downstream effector
title_full_unstemmed Radioresistance of chordoma cells is associated with the ATM/ATR pathway, in which RAD51 serves as an important downstream effector
title_short Radioresistance of chordoma cells is associated with the ATM/ATR pathway, in which RAD51 serves as an important downstream effector
title_sort radioresistance of chordoma cells is associated with the atm/atr pathway, in which rad51 serves as an important downstream effector
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5609200/
https://www.ncbi.nlm.nih.gov/pubmed/28962138
http://dx.doi.org/10.3892/etm.2017.4736
work_keys_str_mv AT zhangchao radioresistanceofchordomacellsisassociatedwiththeatmatrpathwayinwhichrad51servesasanimportantdownstreameffector
AT wangbing radioresistanceofchordomacellsisassociatedwiththeatmatrpathwayinwhichrad51servesasanimportantdownstreameffector
AT lilei radioresistanceofchordomacellsisassociatedwiththeatmatrpathwayinwhichrad51servesasanimportantdownstreameffector
AT liyawei radioresistanceofchordomacellsisassociatedwiththeatmatrpathwayinwhichrad51servesasanimportantdownstreameffector
AT lipengzhi radioresistanceofchordomacellsisassociatedwiththeatmatrpathwayinwhichrad51servesasanimportantdownstreameffector
AT lvguohua radioresistanceofchordomacellsisassociatedwiththeatmatrpathwayinwhichrad51servesasanimportantdownstreameffector