Targeting DNA-PKcs and ATM with miR-101 sensitizes tumors to radiation.

<h4>Background</h4>Radiotherapy kills tumor-cells by inducing DNA double strand breaks (DSBs). However, the efficient repair of tumors frequently prevents successful treatment. Therefore, identifying new practical sensitizers is an essential step towards successful radiotherapy. In this...

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Autores principales: Dan Yan, Wooi Loon Ng, Xiangming Zhang, Ping Wang, Zhaobin Zhang, Yin-Yuan Mo, Hui Mao, Chunhai Hao, Jeffrey J Olson, Walter J Curran, Ya Wang
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Publicado: Public Library of Science (PLoS) 2010
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Acceso en línea:https://doaj.org/article/b73c1458c96f4e3b9d79b60678b2b336
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spelling oai:doaj.org-article:b73c1458c96f4e3b9d79b60678b2b3362021-12-02T20:20:20ZTargeting DNA-PKcs and ATM with miR-101 sensitizes tumors to radiation.1932-620310.1371/journal.pone.0011397https://doaj.org/article/b73c1458c96f4e3b9d79b60678b2b3362010-07-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20617180/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Background</h4>Radiotherapy kills tumor-cells by inducing DNA double strand breaks (DSBs). However, the efficient repair of tumors frequently prevents successful treatment. Therefore, identifying new practical sensitizers is an essential step towards successful radiotherapy. In this study, we tested the new hypothesis: identifying the miRNAs to target DNA DSB repair genes could be a new way for sensitizing tumors to ionizing radiation.<h4>Principal findings</h4>HERE, WE CHOSE TWO GENES: DNA-PKcs (an essential factor for non-homologous end-joining repair) and ATM (an important checkpoint regulator for promoting homologous recombination repair) as the targets to search their regulating miRNAs. By combining the database search and the bench work, we picked out miR-101. We identified that miR-101 could efficiently target DNA-PKcs and ATM via binding to the 3'- UTR of DNA-PKcs or ATM mRNA. Up-regulating miR-101 efficiently reduced the protein levels of DNA-PKcs and ATM in these tumor cells and most importantly, sensitized the tumor cells to radiation in vitro and in vivo.<h4>Conclusions</h4>These data demonstrate for the first time that miRNAs could be used to target DNA repair genes and thus sensitize tumors to radiation. These results provide a new way for improving tumor radiotherapy.Dan YanWooi Loon NgXiangming ZhangPing WangZhaobin ZhangYin-Yuan MoHui MaoChunhai HaoJeffrey J OlsonWalter J CurranYa WangPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 5, Iss 7, p e11397 (2010)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Dan Yan
Wooi Loon Ng
Xiangming Zhang
Ping Wang
Zhaobin Zhang
Yin-Yuan Mo
Hui Mao
Chunhai Hao
Jeffrey J Olson
Walter J Curran
Ya Wang
Targeting DNA-PKcs and ATM with miR-101 sensitizes tumors to radiation.
description <h4>Background</h4>Radiotherapy kills tumor-cells by inducing DNA double strand breaks (DSBs). However, the efficient repair of tumors frequently prevents successful treatment. Therefore, identifying new practical sensitizers is an essential step towards successful radiotherapy. In this study, we tested the new hypothesis: identifying the miRNAs to target DNA DSB repair genes could be a new way for sensitizing tumors to ionizing radiation.<h4>Principal findings</h4>HERE, WE CHOSE TWO GENES: DNA-PKcs (an essential factor for non-homologous end-joining repair) and ATM (an important checkpoint regulator for promoting homologous recombination repair) as the targets to search their regulating miRNAs. By combining the database search and the bench work, we picked out miR-101. We identified that miR-101 could efficiently target DNA-PKcs and ATM via binding to the 3'- UTR of DNA-PKcs or ATM mRNA. Up-regulating miR-101 efficiently reduced the protein levels of DNA-PKcs and ATM in these tumor cells and most importantly, sensitized the tumor cells to radiation in vitro and in vivo.<h4>Conclusions</h4>These data demonstrate for the first time that miRNAs could be used to target DNA repair genes and thus sensitize tumors to radiation. These results provide a new way for improving tumor radiotherapy.
format article
author Dan Yan
Wooi Loon Ng
Xiangming Zhang
Ping Wang
Zhaobin Zhang
Yin-Yuan Mo
Hui Mao
Chunhai Hao
Jeffrey J Olson
Walter J Curran
Ya Wang
author_facet Dan Yan
Wooi Loon Ng
Xiangming Zhang
Ping Wang
Zhaobin Zhang
Yin-Yuan Mo
Hui Mao
Chunhai Hao
Jeffrey J Olson
Walter J Curran
Ya Wang
author_sort Dan Yan
title Targeting DNA-PKcs and ATM with miR-101 sensitizes tumors to radiation.
title_short Targeting DNA-PKcs and ATM with miR-101 sensitizes tumors to radiation.
title_full Targeting DNA-PKcs and ATM with miR-101 sensitizes tumors to radiation.
title_fullStr Targeting DNA-PKcs and ATM with miR-101 sensitizes tumors to radiation.
title_full_unstemmed Targeting DNA-PKcs and ATM with miR-101 sensitizes tumors to radiation.
title_sort targeting dna-pkcs and atm with mir-101 sensitizes tumors to radiation.
publisher Public Library of Science (PLoS)
publishDate 2010
url https://doaj.org/article/b73c1458c96f4e3b9d79b60678b2b336
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