DNA Damage and Repair Biomarkers of Immunotherapy Response

DNA-damaging agents are widely used in clinical oncology and exploit deficiencies in tumor DNA repair. Given the expanding role of immune checkpoint blockade as a therapeutic strategy, the interaction of tumor DNA damage with the immune system has recently come into focus, and it is now clear that t...

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Vydáno v:Cancer discovery Ročník 7; číslo 7; s. 675
Hlavní autoři: Mouw, Kent W, Goldberg, Michael S, Konstantinopoulos, Panagiotis A, D'Andrea, Alan D
Médium: Journal Article
Jazyk:angličtina
Vydáno: United States 01.07.2017
Témata:
Antineoplastic Agents - immunology
Antineoplastic Agents - therapeutic use
Biomarkers, Tumor - genetics
Biomarkers, Tumor - immunology
DNA Damage - drug effects
DNA Damage - immunology
DNA Repair - drug effects
DNA Repair - immunology
Genomic Instability - drug effects
Genomic Instability - immunology
Humans
Immunotherapy - adverse effects
Neoplasms - genetics
Neoplasms - immunology
Neoplasms - therapy
ISSN:2159-8290, 2159-8290
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Shrnutí:DNA-damaging agents are widely used in clinical oncology and exploit deficiencies in tumor DNA repair. Given the expanding role of immune checkpoint blockade as a therapeutic strategy, the interaction of tumor DNA damage with the immune system has recently come into focus, and it is now clear that the tumor DNA repair landscape has an important role in driving response to immune checkpoint blockade. Here, we summarize the mechanisms by which DNA damage and genomic instability have been found to shape the antitumor immune response and describe clinical efforts to use DNA repair biomarkers to guide use of immune-directed therapies. Only a subset of patients respond to immune checkpoint blockade, and reliable predictive biomarkers of response are needed to guide therapy decisions. DNA repair deficiency is common among tumors, and emerging experimental and clinical evidence suggests that features of genomic instability are associated with response to immune-directed therapies.
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ISSN:2159-8290
2159-8290
DOI:10.1158/2159-8290.CD-17-0226