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ZATT, TDP2, and SUMO2: Breaking the tie that binds TOP2 to DNA

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ZATT, TDP2, and SUMO2: Breaking the tie that binds TOP2 to DNA. / Hall, Steven Robert; Goralski, Kerry B.
In: Translational Cancer Research, Vol. 7, No. 4, 26.04.2018, p. 1412-16.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Hall, SR & Goralski, KB 2018, 'ZATT, TDP2, and SUMO2: Breaking the tie that binds TOP2 to DNA', Translational Cancer Research, vol. 7, no. 4, pp. 1412-16. https://doi.org/10.21037/tcr.2018.02.03

APA

Hall, S. R., & Goralski, K. B. (2018). ZATT, TDP2, and SUMO2: Breaking the tie that binds TOP2 to DNA. Translational Cancer Research, 7(4), 1412-16. https://doi.org/10.21037/tcr.2018.02.03

Vancouver

Hall SR, Goralski KB. ZATT, TDP2, and SUMO2: Breaking the tie that binds TOP2 to DNA. Translational Cancer Research. 2018 Apr 26;7(4):1412-16. doi: 10.21037/tcr.2018.02.03

Author

Hall, Steven Robert ; Goralski, Kerry B. / ZATT, TDP2, and SUMO2: Breaking the tie that binds TOP2 to DNA. In: Translational Cancer Research. 2018 ; Vol. 7, No. 4. pp. 1412-16.

Bibtex

@article{e1a5d6742e774638976f9ab097f887f4,
title = "ZATT, TDP2, and SUMO2: Breaking the tie that binds TOP2 to DNA",
abstract = "Invited Editorial Article. First paragraph: {"}Type II topoisomerase (TOP2) poisons are widely used chemotherapeutics that work by disrupting the cycle of TOP2-DNA interactions that are required for DNA synthesis, gene expression, and the maintenance of genome integrity. Schellenberg et al.{\textquoteright}s recent Science paper, entitled “ZATT (ZNF451)-mediated resolution of topoisomerase 2 DNA protein cross-links” provides a major advancement in the understanding of the mechanisms that regulate TOP2-DNA interactions, and how they can inhibit the anticancer effects of TOP2 poisons. Through these new insights, promising new therapeutic targets have been identified.{"}",
author = "Hall, {Steven Robert} and Goralski, {Kerry B}",
year = "2018",
month = apr,
day = "26",
doi = "10.21037/tcr.2018.02.03",
language = "English",
volume = "7",
pages = "1412--16",
journal = "Translational Cancer Research",
number = "4",

}

RIS

TY - JOUR

T1 - ZATT, TDP2, and SUMO2: Breaking the tie that binds TOP2 to DNA

AU - Hall, Steven Robert

AU - Goralski, Kerry B

PY - 2018/4/26

Y1 - 2018/4/26

N2 - Invited Editorial Article. First paragraph: "Type II topoisomerase (TOP2) poisons are widely used chemotherapeutics that work by disrupting the cycle of TOP2-DNA interactions that are required for DNA synthesis, gene expression, and the maintenance of genome integrity. Schellenberg et al.’s recent Science paper, entitled “ZATT (ZNF451)-mediated resolution of topoisomerase 2 DNA protein cross-links” provides a major advancement in the understanding of the mechanisms that regulate TOP2-DNA interactions, and how they can inhibit the anticancer effects of TOP2 poisons. Through these new insights, promising new therapeutic targets have been identified."

AB - Invited Editorial Article. First paragraph: "Type II topoisomerase (TOP2) poisons are widely used chemotherapeutics that work by disrupting the cycle of TOP2-DNA interactions that are required for DNA synthesis, gene expression, and the maintenance of genome integrity. Schellenberg et al.’s recent Science paper, entitled “ZATT (ZNF451)-mediated resolution of topoisomerase 2 DNA protein cross-links” provides a major advancement in the understanding of the mechanisms that regulate TOP2-DNA interactions, and how they can inhibit the anticancer effects of TOP2 poisons. Through these new insights, promising new therapeutic targets have been identified."

U2 - 10.21037/tcr.2018.02.03

DO - 10.21037/tcr.2018.02.03

M3 - Journal article

VL - 7

SP - 1412

EP - 1416

JO - Translational Cancer Research

JF - Translational Cancer Research

IS - 4

ER -