Dysregulated human Tyrosyl-DNA phosphodiesterase I acts as cellular toxin
Tyrosyl-DNA phosphodiesterase I (TDP1) hydrolyzes the drug-stabilized 3'phospho-tyrosyl bond formed between DNA topoisomerase I (TOPO1) and DNA. TDP1-mediated hydrolysis uses a nucleophilic histidine (Hisnuc) and a general acid/base histidine (Hisgab). A Tdp1Hisgab to Arg mutant identified in patients with the autosomal recessive neurodegenerative disease SCAN1 causes stabilization of the TDP1-DNA intermediate. Based on our previously reported Hisgab-substitutions inducing yeast toxicity (Gajewski et al. J. Mol. Biol. 415, 741-758, 2012), we propose that converting TDP1 into a cellular poison by stabilizing the covalent enzyme-DNA intermediate is a novel therapeutic strategy for cancer treatment. Here, we analyzed the toxic effects of two TDP1 catalytic mutants in HEK293 cells. Expression of human Tdp1HisnucAla and Tdp1HisgabAsn mutants results in stabilization of the covalent TDP1-DNA intermediate and induces cytotoxicity. Moreover, these mutants display reduced in vitro catalytic activity compared to wild type. Co-treatment of Tdp1mutant with topotecan shows more than additive cytotoxicity. Overall, these results support the hypothesis that stabilization of the TDP1-DNA covalent intermediate is a potential anti-cancer therapeutic strategy.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2016 |
---|---|
Erschienen: |
2016 |
Enthalten in: |
Zur Gesamtaufnahme - volume:7 |
---|---|
Enthalten in: |
Oncotarget - 7(2016), 52 vom: 27. Dez., Seite 86660-86674 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Cuya, Selma M [VerfasserIn] |
---|
Links: |
---|
Anmerkungen: |
Date Completed 22.02.2018 Date Revised 20.09.2019 published: Print Citation Status MEDLINE |
---|
doi: |
10.18632/oncotarget.13528 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM266608043 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM266608043 | ||
003 | DE-627 | ||
005 | 20231224214914.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231224s2016 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.18632/oncotarget.13528 |2 doi | |
028 | 5 | 2 | |a pubmed24n0888.xml |
035 | |a (DE-627)NLM266608043 | ||
035 | |a (NLM)27893431 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Cuya, Selma M |e verfasserin |4 aut | |
245 | 1 | 0 | |a Dysregulated human Tyrosyl-DNA phosphodiesterase I acts as cellular toxin |
264 | 1 | |c 2016 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 22.02.2018 | ||
500 | |a Date Revised 20.09.2019 | ||
500 | |a published: Print | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Tyrosyl-DNA phosphodiesterase I (TDP1) hydrolyzes the drug-stabilized 3'phospho-tyrosyl bond formed between DNA topoisomerase I (TOPO1) and DNA. TDP1-mediated hydrolysis uses a nucleophilic histidine (Hisnuc) and a general acid/base histidine (Hisgab). A Tdp1Hisgab to Arg mutant identified in patients with the autosomal recessive neurodegenerative disease SCAN1 causes stabilization of the TDP1-DNA intermediate. Based on our previously reported Hisgab-substitutions inducing yeast toxicity (Gajewski et al. J. Mol. Biol. 415, 741-758, 2012), we propose that converting TDP1 into a cellular poison by stabilizing the covalent enzyme-DNA intermediate is a novel therapeutic strategy for cancer treatment. Here, we analyzed the toxic effects of two TDP1 catalytic mutants in HEK293 cells. Expression of human Tdp1HisnucAla and Tdp1HisgabAsn mutants results in stabilization of the covalent TDP1-DNA intermediate and induces cytotoxicity. Moreover, these mutants display reduced in vitro catalytic activity compared to wild type. Co-treatment of Tdp1mutant with topotecan shows more than additive cytotoxicity. Overall, these results support the hypothesis that stabilization of the TDP1-DNA covalent intermediate is a potential anti-cancer therapeutic strategy | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a DNA repair | |
650 | 4 | |a DNA topoisomerases | |
650 | 4 | |a DNA-adducts | |
650 | 4 | |a TDP1 | |
650 | 4 | |a biochemistry | |
650 | 7 | |a Topotecan |2 NLM | |
650 | 7 | |a 7M7YKX2N15 |2 NLM | |
650 | 7 | |a DNA |2 NLM | |
650 | 7 | |a 9007-49-2 |2 NLM | |
650 | 7 | |a Phosphoric Diester Hydrolases |2 NLM | |
650 | 7 | |a EC 3.1.4.- |2 NLM | |
650 | 7 | |a tyrosyl-DNA phosphodiesterase |2 NLM | |
650 | 7 | |a EC 3.1.4.- |2 NLM | |
650 | 7 | |a DNA Topoisomerases, Type I |2 NLM | |
650 | 7 | |a EC 5.99.1.2 |2 NLM | |
700 | 1 | |a Comeaux, Evan Q |e verfasserin |4 aut | |
700 | 1 | |a Wanzeck, Keith |e verfasserin |4 aut | |
700 | 1 | |a Yoon, Karina J |e verfasserin |4 aut | |
700 | 1 | |a van Waardenburg, Robert C A M |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Oncotarget |d 2010 |g 7(2016), 52 vom: 27. Dez., Seite 86660-86674 |w (DE-627)NLM199620113 |x 1949-2553 |7 nnns |
773 | 1 | 8 | |g volume:7 |g year:2016 |g number:52 |g day:27 |g month:12 |g pages:86660-86674 |
856 | 4 | 0 | |u http://dx.doi.org/10.18632/oncotarget.13528 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 7 |j 2016 |e 52 |b 27 |c 12 |h 86660-86674 |