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Broken by the Cut: A Journey into the Role of Topoisomerase II in DNA Fragility
by
Atkin, Naomi
, Raimer, Heather
, Wang, Yuh-Hwa
in
Adducts
/ Androgens
/ Binding sites
/ CCCTC-Binding Factor - metabolism
/ Cell cycle
/ Chromatin - metabolism
/ Cytotoxicity
/ Deoxyribonucleic acid
/ DNA
/ DNA - chemistry
/ DNA - metabolism
/ DNA Breaks, Double-Stranded - drug effects
/ DNA damage
/ DNA Repair - drug effects
/ DNA topoisomerase
/ DNA topoisomerase (ATP-hydrolysing)
/ DNA Topoisomerases, Type II - genetics
/ DNA Topoisomerases, Type II - metabolism
/ Enhancers
/ Enzymes
/ Gene expression
/ genes
/ Genomes
/ Humans
/ leukemia
/ Leukemia, Myeloid, Acute - drug therapy
/ mutation
/ Papillary thyroid cancer
/ Proteins
/ Review
/ RNA polymerase
/ therapeutics
/ Thyroid Cancer, Papillary - drug therapy
/ Thyroid gland
/ thyroid neoplasms
/ Topoisomerase II Inhibitors - pharmacology
/ Torsion, Mechanical
/ torsional stress
/ Transcription
/ transcription (genetics)
/ Translocation
2019
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Broken by the Cut: A Journey into the Role of Topoisomerase II in DNA Fragility
by
Atkin, Naomi
, Raimer, Heather
, Wang, Yuh-Hwa
in
Adducts
/ Androgens
/ Binding sites
/ CCCTC-Binding Factor - metabolism
/ Cell cycle
/ Chromatin - metabolism
/ Cytotoxicity
/ Deoxyribonucleic acid
/ DNA
/ DNA - chemistry
/ DNA - metabolism
/ DNA Breaks, Double-Stranded - drug effects
/ DNA damage
/ DNA Repair - drug effects
/ DNA topoisomerase
/ DNA topoisomerase (ATP-hydrolysing)
/ DNA Topoisomerases, Type II - genetics
/ DNA Topoisomerases, Type II - metabolism
/ Enhancers
/ Enzymes
/ Gene expression
/ genes
/ Genomes
/ Humans
/ leukemia
/ Leukemia, Myeloid, Acute - drug therapy
/ mutation
/ Papillary thyroid cancer
/ Proteins
/ Review
/ RNA polymerase
/ therapeutics
/ Thyroid Cancer, Papillary - drug therapy
/ Thyroid gland
/ thyroid neoplasms
/ Topoisomerase II Inhibitors - pharmacology
/ Torsion, Mechanical
/ torsional stress
/ Transcription
/ transcription (genetics)
/ Translocation
2019
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Do you wish to request the book?
Broken by the Cut: A Journey into the Role of Topoisomerase II in DNA Fragility
by
Atkin, Naomi
, Raimer, Heather
, Wang, Yuh-Hwa
in
Adducts
/ Androgens
/ Binding sites
/ CCCTC-Binding Factor - metabolism
/ Cell cycle
/ Chromatin - metabolism
/ Cytotoxicity
/ Deoxyribonucleic acid
/ DNA
/ DNA - chemistry
/ DNA - metabolism
/ DNA Breaks, Double-Stranded - drug effects
/ DNA damage
/ DNA Repair - drug effects
/ DNA topoisomerase
/ DNA topoisomerase (ATP-hydrolysing)
/ DNA Topoisomerases, Type II - genetics
/ DNA Topoisomerases, Type II - metabolism
/ Enhancers
/ Enzymes
/ Gene expression
/ genes
/ Genomes
/ Humans
/ leukemia
/ Leukemia, Myeloid, Acute - drug therapy
/ mutation
/ Papillary thyroid cancer
/ Proteins
/ Review
/ RNA polymerase
/ therapeutics
/ Thyroid Cancer, Papillary - drug therapy
/ Thyroid gland
/ thyroid neoplasms
/ Topoisomerase II Inhibitors - pharmacology
/ Torsion, Mechanical
/ torsional stress
/ Transcription
/ transcription (genetics)
/ Translocation
2019
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Broken by the Cut: A Journey into the Role of Topoisomerase II in DNA Fragility
Journal Article
Broken by the Cut: A Journey into the Role of Topoisomerase II in DNA Fragility
2019
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Overview
DNA topoisomerase II (TOP2) plays a critical role in many processes such as replication and transcription, where it resolves DNA structures and relieves torsional stress. Recent evidence demonstrated the association of TOP2 with topologically associated domains (TAD) boundaries and CCCTC-binding factor (CTCF) binding sites. At these sites, TOP2 promotes interactions between enhancers and gene promoters, and relieves torsional stress that accumulates at these physical barriers. Interestingly, in executing its enzymatic function, TOP2 contributes to DNA fragility through re-ligation failure, which results in persistent DNA breaks when unrepaired or illegitimately repaired. Here, we discuss the biological processes for which TOP2 is required and the steps at which it can introduce DNA breaks. We describe the repair processes that follow removal of TOP2 adducts and the resultant broken DNA ends, and present how these processes can contribute to disease-associated mutations. Furthermore, we examine the involvement of TOP2-induced breaks in the formation of oncogenic translocations of leukemia and papillary thyroid cancer, as well as the role of TOP2 and proteins which repair TOP2 adducts in other diseases. The participation of TOP2 in generating persistent DNA breaks and leading to diseases such as cancer, could have an impact on disease treatment and prevention.
Publisher
MDPI AG,MDPI
Subject
/ CCCTC-Binding Factor - metabolism
/ DNA
/ DNA Breaks, Double-Stranded - drug effects
/ DNA topoisomerase (ATP-hydrolysing)
/ DNA Topoisomerases, Type II - genetics
/ DNA Topoisomerases, Type II - metabolism
/ Enzymes
/ genes
/ Genomes
/ Humans
/ leukemia
/ Leukemia, Myeloid, Acute - drug therapy
/ mutation
/ Proteins
/ Review
/ Thyroid Cancer, Papillary - drug therapy
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