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The DOI matches its Crossref record; 74 of the 74 references it cites were found in a registry or an index.

Tumor aneuploidy correlates with markers of immune evasion and with reduced response to immunotherapy

Open access
Davoli, Teresa, Uno, Hajime, Wooten, Eric C., Elledge, Stephen J.·2017·Science

Abstract

Chromosomal chaos and tumor immunity: Cancer immunotherapy produces durable clinical responses in only a subset of patients. Identification of tumor characteristics that correlate with responses could lead to predictive biomarkers and shed light on causal mechanisms. Davoli et al. found that human tumors with extensive aneuploidy—i.e., that display a highly abnormal number of chromosomes and chromosomal segments—express fewer markers of the immune cells responsible for tumor destruction. In a retrospective analysis of clinical trial data, they found that melanoma patients with highly aneuploid tumors were less likely to benefit from immune checkpoint blockade therapy than patients whose tumors had a more normal karyotype. Thus, aneuploidy appears to enhance the ability of tumors to evade the immune system. Science , this issue p. 10.1126/science.aaf8399

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Metadata

Authors
Davoli, T., Uno, H., Wooten, E. C., & Elledge, S. J.
Venue
Science
Published
2017-01-20
Volume
355
Issue
6322
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2574604975
Cited by
1,360
References
74
FWCI
46.10
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Tumor aneuploidy correlates with markers of immune evasion and with reduced response to immunotherapy. https://app.cochat.ai/papers/10.1126/science.aaf8399
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Davoli, T., Uno, H., Wooten, E. C., & Elledge, S. J. (2017). Tumor aneuploidy correlates with markers of immune evasion and with reduced response to immunotherapy. Science. https://doi.org/10.1126/science.aaf8399

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.