@article{aparicio_dna_2014,
	title = {{DNA} double-strand break repair pathway choice and cancer},
	volume = {19},
	issn = {1568-7856},
	doi = {10.1016/j.dnarep.2014.03.014},
	abstract = {Since DNA double-strand breaks (DSBs) contribute to the genomic instability that drives cancer development, DSB repair pathways serve as important mechanisms for tumor suppression. Thus, genetic lesions, such as BRCA1 and BRCA2 mutations, that disrupt DSB repair are often associated with cancer susceptibility. In addition, recent evidence suggests that DSB "mis-repair", in which DSBs are resolved by an inappropriate repair pathway, can also promote genomic instability and presumably tumorigenesis. This notion has gained currency from recent cancer genome sequencing studies which have uncovered numerous chromosomal rearrangements harboring pathological DNA repair signatures. In this perspective, we discuss the factors that regulate DSB repair pathway choice and their consequences for genome stability and cancer.},
	language = {eng},
	journal = {DNA repair},
	author = {Aparicio, Tomas and Baer, Richard and Gautier, Jean},
	month = jul,
	year = {2014},
	keywords = {53BP1–BRCA1, BRCA1 Protein, DNA Breaks, Double-Stranded, DNA End-Joining Repair, DNA Repair, DNA double strand break, DNA ends, Genomic Instability, Humans, Intracellular Signaling Peptides and Proteins, Microhomology-mediated end joining, Neoplasms, Recombination, Genetic, Repair pathway choice, Resection, Signal Transduction, Tumor Suppressor p53-Binding Protein 1, carcinogenesis},
	pages = {169--175},
}

{"_id":"f5g9ioYCh5EaqSP3v","bibbaseid":"aparicio-baer-gautier-dnadoublestrandbreakrepairpathwaychoiceandcancer-2014","author_short":["Aparicio, T.","Baer, R.","Gautier, J."],"bibdata":{"bibtype":"article","type":"article","title":"DNA double-strand break repair pathway choice and cancer","volume":"19","issn":"1568-7856","doi":"10.1016/j.dnarep.2014.03.014","abstract":"Since DNA double-strand breaks (DSBs) contribute to the genomic instability that drives cancer development, DSB repair pathways serve as important mechanisms for tumor suppression. Thus, genetic lesions, such as BRCA1 and BRCA2 mutations, that disrupt DSB repair are often associated with cancer susceptibility. In addition, recent evidence suggests that DSB \"mis-repair\", in which DSBs are resolved by an inappropriate repair pathway, can also promote genomic instability and presumably tumorigenesis. This notion has gained currency from recent cancer genome sequencing studies which have uncovered numerous chromosomal rearrangements harboring pathological DNA repair signatures. In this perspective, we discuss the factors that regulate DSB repair pathway choice and their consequences for genome stability and cancer.","language":"eng","journal":"DNA repair","author":[{"propositions":[],"lastnames":["Aparicio"],"firstnames":["Tomas"],"suffixes":[]},{"propositions":[],"lastnames":["Baer"],"firstnames":["Richard"],"suffixes":[]},{"propositions":[],"lastnames":["Gautier"],"firstnames":["Jean"],"suffixes":[]}],"month":"July","year":"2014","keywords":"53BP1–BRCA1, BRCA1 Protein, DNA Breaks, Double-Stranded, DNA End-Joining Repair, DNA Repair, DNA double strand break, DNA ends, Genomic Instability, Humans, Intracellular Signaling Peptides and Proteins, Microhomology-mediated end joining, Neoplasms, Recombination, Genetic, Repair pathway choice, Resection, Signal Transduction, Tumor Suppressor p53-Binding Protein 1, carcinogenesis","pages":"169–175","bibtex":"@article{aparicio_dna_2014,\n\ttitle = {{DNA} double-strand break repair pathway choice and cancer},\n\tvolume = {19},\n\tissn = {1568-7856},\n\tdoi = {10.1016/j.dnarep.2014.03.014},\n\tabstract = {Since DNA double-strand breaks (DSBs) contribute to the genomic instability that drives cancer development, DSB repair pathways serve as important mechanisms for tumor suppression. Thus, genetic lesions, such as BRCA1 and BRCA2 mutations, that disrupt DSB repair are often associated with cancer susceptibility. In addition, recent evidence suggests that DSB \"mis-repair\", in which DSBs are resolved by an inappropriate repair pathway, can also promote genomic instability and presumably tumorigenesis. This notion has gained currency from recent cancer genome sequencing studies which have uncovered numerous chromosomal rearrangements harboring pathological DNA repair signatures. In this perspective, we discuss the factors that regulate DSB repair pathway choice and their consequences for genome stability and cancer.},\n\tlanguage = {eng},\n\tjournal = {DNA repair},\n\tauthor = {Aparicio, Tomas and Baer, Richard and Gautier, Jean},\n\tmonth = jul,\n\tyear = {2014},\n\tkeywords = {53BP1–BRCA1, BRCA1 Protein, DNA Breaks, Double-Stranded, DNA End-Joining Repair, DNA Repair, DNA double strand break, DNA ends, Genomic Instability, Humans, Intracellular Signaling Peptides and Proteins, Microhomology-mediated end joining, Neoplasms, Recombination, Genetic, Repair pathway choice, Resection, Signal Transduction, Tumor Suppressor p53-Binding Protein 1, carcinogenesis},\n\tpages = {169--175},\n}\n\n","author_short":["Aparicio, T.","Baer, R.","Gautier, J."],"key":"aparicio_dna_2014","id":"aparicio_dna_2014","bibbaseid":"aparicio-baer-gautier-dnadoublestrandbreakrepairpathwaychoiceandcancer-2014","role":"author","urls":{},"keyword":["53BP1–BRCA1","BRCA1 Protein","DNA Breaks","Double-Stranded","DNA End-Joining Repair","DNA Repair","DNA double strand break","DNA ends","Genomic Instability","Humans","Intracellular Signaling Peptides and Proteins","Microhomology-mediated end joining","Neoplasms","Recombination","Genetic","Repair pathway choice","Resection","Signal Transduction","Tumor Suppressor p53-Binding Protein 1","carcinogenesis"],"metadata":{"authorlinks":{}}},"bibtype":"article","biburl":"https://bibbase.org/zotero/tplas","dataSources":["YLgywGcXWx96vKKaB"],"keywords":["53bp1–brca1","brca1 protein","dna breaks","double-stranded","dna end-joining repair","dna repair","dna double strand break","dna ends","genomic instability","humans","intracellular signaling peptides and proteins","microhomology-mediated end joining","neoplasms","recombination","genetic","repair pathway choice","resection","signal transduction","tumor suppressor p53-binding protein 1","carcinogenesis"],"search_terms":["dna","double","strand","break","repair","pathway","choice","cancer","aparicio","baer","gautier"],"title":"DNA double-strand break repair pathway choice and cancer","year":2014}