author_facet Fast, Olivia G.
Gentry, Brittany
Strouth, Liah
Niece, Madison B.
Beckford, Floyd A.
Shell, Steven M.
Fast, Olivia G.
Gentry, Brittany
Strouth, Liah
Niece, Madison B.
Beckford, Floyd A.
Shell, Steven M.
author Fast, Olivia G.
Gentry, Brittany
Strouth, Liah
Niece, Madison B.
Beckford, Floyd A.
Shell, Steven M.
spellingShingle Fast, Olivia G.
Gentry, Brittany
Strouth, Liah
Niece, Madison B.
Beckford, Floyd A.
Shell, Steven M.
Bioscience Reports
Polynuclear ruthenium organometallic compounds induce DNA damage in human cells identified by the nucleotide excision repair factor XPC
Cell Biology
Molecular Biology
Biochemistry
Biophysics
author_sort fast, olivia g.
spelling Fast, Olivia G. Gentry, Brittany Strouth, Liah Niece, Madison B. Beckford, Floyd A. Shell, Steven M. 0144-8463 1573-4935 Portland Press Ltd. Cell Biology Molecular Biology Biochemistry Biophysics http://dx.doi.org/10.1042/bsr20190378 <jats:title>Abstract</jats:title> <jats:p>Ruthenium organometallic compounds represent an attractive avenue in developing alternatives to platinum-based chemotherapeutic agents. While evidence has been presented indicating ruthenium-based compounds interact with isolated DNA in vitro, it is unclear what effect these compounds exert in cells. Moreover, the antibiotic efficacy of polynuclear ruthenium organometallic compounds remains uncertain. In the present study, we report that exposure to polynuclear ruthenium organometallic compounds induces recruitment of damaged DNA sensing protein Xeroderma pigmentosum Group C into chromatin-immobilized foci. Additionally, we observed one of the tested polynuclear ruthenium organometallic compounds displayed increased cytotoxicity against human cells deficient in nucleotide excision repair (NER). Taken together, these results suggest that polynuclear ruthenium organometallic compounds induce DNA damage in cells, and that cellular resistance to these compounds may be influenced by the NER DNA repair phenotype of the cells.</jats:p> Polynuclear ruthenium organometallic compounds induce DNA damage in human cells identified by the nucleotide excision repair factor XPC Bioscience Reports
doi_str_mv 10.1042/bsr20190378
facet_avail Online
Free
finc_class_facet Biologie
Chemie und Pharmazie
Physik
format ElectronicArticle
fullrecord blob:ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTA0Mi9ic3IyMDE5MDM3OA
id ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTA0Mi9ic3IyMDE5MDM3OA
institution DE-D275
DE-Bn3
DE-Brt1
DE-Zwi2
DE-D161
DE-Gla1
DE-Zi4
DE-15
DE-Pl11
DE-Rs1
DE-105
DE-14
DE-Ch1
DE-L229
imprint Portland Press Ltd., 2019
imprint_str_mv Portland Press Ltd., 2019
issn 0144-8463
1573-4935
issn_str_mv 0144-8463
1573-4935
language English
mega_collection Portland Press Ltd. (CrossRef)
match_str fast2019polynuclearrutheniumorganometalliccompoundsinducednadamageinhumancellsidentifiedbythenucleotideexcisionrepairfactorxpc
publishDateSort 2019
publisher Portland Press Ltd.
recordtype ai
record_format ai
series Bioscience Reports
source_id 49
title Polynuclear ruthenium organometallic compounds induce DNA damage in human cells identified by the nucleotide excision repair factor XPC
title_unstemmed Polynuclear ruthenium organometallic compounds induce DNA damage in human cells identified by the nucleotide excision repair factor XPC
title_full Polynuclear ruthenium organometallic compounds induce DNA damage in human cells identified by the nucleotide excision repair factor XPC
title_fullStr Polynuclear ruthenium organometallic compounds induce DNA damage in human cells identified by the nucleotide excision repair factor XPC
title_full_unstemmed Polynuclear ruthenium organometallic compounds induce DNA damage in human cells identified by the nucleotide excision repair factor XPC
title_short Polynuclear ruthenium organometallic compounds induce DNA damage in human cells identified by the nucleotide excision repair factor XPC
title_sort polynuclear ruthenium organometallic compounds induce dna damage in human cells identified by the nucleotide excision repair factor xpc
topic Cell Biology
Molecular Biology
Biochemistry
Biophysics
url http://dx.doi.org/10.1042/bsr20190378
publishDate 2019
physical
description <jats:title>Abstract</jats:title> <jats:p>Ruthenium organometallic compounds represent an attractive avenue in developing alternatives to platinum-based chemotherapeutic agents. While evidence has been presented indicating ruthenium-based compounds interact with isolated DNA in vitro, it is unclear what effect these compounds exert in cells. Moreover, the antibiotic efficacy of polynuclear ruthenium organometallic compounds remains uncertain. In the present study, we report that exposure to polynuclear ruthenium organometallic compounds induces recruitment of damaged DNA sensing protein Xeroderma pigmentosum Group C into chromatin-immobilized foci. Additionally, we observed one of the tested polynuclear ruthenium organometallic compounds displayed increased cytotoxicity against human cells deficient in nucleotide excision repair (NER). Taken together, these results suggest that polynuclear ruthenium organometallic compounds induce DNA damage in cells, and that cellular resistance to these compounds may be influenced by the NER DNA repair phenotype of the cells.</jats:p>
container_issue 7
container_start_page 0
container_title Bioscience Reports
container_volume 39
format_de105 Article, E-Article
format_de14 Article, E-Article
format_de15 Article, E-Article
format_de520 Article, E-Article
format_de540 Article, E-Article
format_dech1 Article, E-Article
format_ded117 Article, E-Article
format_degla1 E-Article
format_del152 Buch
format_del189 Article, E-Article
format_dezi4 Article
format_dezwi2 Article, E-Article
format_finc Article, E-Article
format_nrw Article, E-Article
_version_ 1792332903716225027
geogr_code not assigned
last_indexed 2024-03-01T14:04:15.559Z
geogr_code_person not assigned
openURL url_ver=Z39.88-2004&ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fvufind.svn.sourceforge.net%3Agenerator&rft.title=Polynuclear+ruthenium+organometallic+compounds+induce+DNA+damage+in+human+cells+identified+by+the+nucleotide+excision+repair+factor+XPC&rft.date=2019-07-31&genre=article&issn=1573-4935&volume=39&issue=7&jtitle=Bioscience+Reports&atitle=Polynuclear+ruthenium+organometallic+compounds+induce+DNA+damage+in+human+cells+identified+by+the+nucleotide+excision+repair+factor+XPC&aulast=Shell&aufirst=Steven%C2%A0M.&rft_id=info%3Adoi%2F10.1042%2Fbsr20190378&rft.language%5B0%5D=eng
SOLR
_version_ 1792332903716225027
author Fast, Olivia G., Gentry, Brittany, Strouth, Liah, Niece, Madison B., Beckford, Floyd A., Shell, Steven M.
author_facet Fast, Olivia G., Gentry, Brittany, Strouth, Liah, Niece, Madison B., Beckford, Floyd A., Shell, Steven M., Fast, Olivia G., Gentry, Brittany, Strouth, Liah, Niece, Madison B., Beckford, Floyd A., Shell, Steven M.
author_sort fast, olivia g.
container_issue 7
container_start_page 0
container_title Bioscience Reports
container_volume 39
description <jats:title>Abstract</jats:title> <jats:p>Ruthenium organometallic compounds represent an attractive avenue in developing alternatives to platinum-based chemotherapeutic agents. While evidence has been presented indicating ruthenium-based compounds interact with isolated DNA in vitro, it is unclear what effect these compounds exert in cells. Moreover, the antibiotic efficacy of polynuclear ruthenium organometallic compounds remains uncertain. In the present study, we report that exposure to polynuclear ruthenium organometallic compounds induces recruitment of damaged DNA sensing protein Xeroderma pigmentosum Group C into chromatin-immobilized foci. Additionally, we observed one of the tested polynuclear ruthenium organometallic compounds displayed increased cytotoxicity against human cells deficient in nucleotide excision repair (NER). Taken together, these results suggest that polynuclear ruthenium organometallic compounds induce DNA damage in cells, and that cellular resistance to these compounds may be influenced by the NER DNA repair phenotype of the cells.</jats:p>
doi_str_mv 10.1042/bsr20190378
facet_avail Online, Free
finc_class_facet Biologie, Chemie und Pharmazie, Physik
format ElectronicArticle
format_de105 Article, E-Article
format_de14 Article, E-Article
format_de15 Article, E-Article
format_de520 Article, E-Article
format_de540 Article, E-Article
format_dech1 Article, E-Article
format_ded117 Article, E-Article
format_degla1 E-Article
format_del152 Buch
format_del189 Article, E-Article
format_dezi4 Article
format_dezwi2 Article, E-Article
format_finc Article, E-Article
format_nrw Article, E-Article
geogr_code not assigned
geogr_code_person not assigned
id ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTA0Mi9ic3IyMDE5MDM3OA
imprint Portland Press Ltd., 2019
imprint_str_mv Portland Press Ltd., 2019
institution DE-D275, DE-Bn3, DE-Brt1, DE-Zwi2, DE-D161, DE-Gla1, DE-Zi4, DE-15, DE-Pl11, DE-Rs1, DE-105, DE-14, DE-Ch1, DE-L229
issn 0144-8463, 1573-4935
issn_str_mv 0144-8463, 1573-4935
language English
last_indexed 2024-03-01T14:04:15.559Z
match_str fast2019polynuclearrutheniumorganometalliccompoundsinducednadamageinhumancellsidentifiedbythenucleotideexcisionrepairfactorxpc
mega_collection Portland Press Ltd. (CrossRef)
physical
publishDate 2019
publishDateSort 2019
publisher Portland Press Ltd.
record_format ai
recordtype ai
series Bioscience Reports
source_id 49
spelling Fast, Olivia G. Gentry, Brittany Strouth, Liah Niece, Madison B. Beckford, Floyd A. Shell, Steven M. 0144-8463 1573-4935 Portland Press Ltd. Cell Biology Molecular Biology Biochemistry Biophysics http://dx.doi.org/10.1042/bsr20190378 <jats:title>Abstract</jats:title> <jats:p>Ruthenium organometallic compounds represent an attractive avenue in developing alternatives to platinum-based chemotherapeutic agents. While evidence has been presented indicating ruthenium-based compounds interact with isolated DNA in vitro, it is unclear what effect these compounds exert in cells. Moreover, the antibiotic efficacy of polynuclear ruthenium organometallic compounds remains uncertain. In the present study, we report that exposure to polynuclear ruthenium organometallic compounds induces recruitment of damaged DNA sensing protein Xeroderma pigmentosum Group C into chromatin-immobilized foci. Additionally, we observed one of the tested polynuclear ruthenium organometallic compounds displayed increased cytotoxicity against human cells deficient in nucleotide excision repair (NER). Taken together, these results suggest that polynuclear ruthenium organometallic compounds induce DNA damage in cells, and that cellular resistance to these compounds may be influenced by the NER DNA repair phenotype of the cells.</jats:p> Polynuclear ruthenium organometallic compounds induce DNA damage in human cells identified by the nucleotide excision repair factor XPC Bioscience Reports
spellingShingle Fast, Olivia G., Gentry, Brittany, Strouth, Liah, Niece, Madison B., Beckford, Floyd A., Shell, Steven M., Bioscience Reports, Polynuclear ruthenium organometallic compounds induce DNA damage in human cells identified by the nucleotide excision repair factor XPC, Cell Biology, Molecular Biology, Biochemistry, Biophysics
title Polynuclear ruthenium organometallic compounds induce DNA damage in human cells identified by the nucleotide excision repair factor XPC
title_full Polynuclear ruthenium organometallic compounds induce DNA damage in human cells identified by the nucleotide excision repair factor XPC
title_fullStr Polynuclear ruthenium organometallic compounds induce DNA damage in human cells identified by the nucleotide excision repair factor XPC
title_full_unstemmed Polynuclear ruthenium organometallic compounds induce DNA damage in human cells identified by the nucleotide excision repair factor XPC
title_short Polynuclear ruthenium organometallic compounds induce DNA damage in human cells identified by the nucleotide excision repair factor XPC
title_sort polynuclear ruthenium organometallic compounds induce dna damage in human cells identified by the nucleotide excision repair factor xpc
title_unstemmed Polynuclear ruthenium organometallic compounds induce DNA damage in human cells identified by the nucleotide excision repair factor XPC
topic Cell Biology, Molecular Biology, Biochemistry, Biophysics
url http://dx.doi.org/10.1042/bsr20190378