Cited by 31Adenosine and Purinergic SignalingCancer Immunotherapy and BiomarkersCancer, Hypoxia, and Metabolism

Oxygenation to improve cancer vaccines, adoptive cell transfer and blockade of immunological negative regulators

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Hatfield, Stephen M, Sitkovsky, Michail·2015·OncoImmunology

Abstract

Oxygenation of tumors weakens the tumor-protecting immunosuppressive signaling by A2A adenosine receptors in hypoxic and extracellular adenosine-rich microenvironments. This, in turn, unleashes the otherwise inhibited tumor-reactive T and natural killer (NK) cells. Oxygenation of tumors thus emerges as a novel checkpoint inhibitor of potential therapeutic value, but only in combination with cancer immunotherapies.

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Crossref · 10.1080/2162402x.2015.1052934

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Authors
Hatfield, S. M., & Sitkovsky, M.
Affiliations
Northeastern University (US)
Corresponding author
Sitkovsky, Michail
Venue
OncoImmunology
Published
2015-06
Volume
4
Issue
12
Pages
e1052934
ISSN
  • 2162-4011 (ISSN-L)
  • 2162-402X
OpenAlex
W2136374665
Cited by
31
References
9
Citations by year
2026: 3 · 2025: 3 · 2023: 1 · 2022: 6 · 2021: 6 · 2020: 2 · 2019: 5 · 2018: 4 · 2017: 1
FWCI
1.40
Type
journal article
Language
en
Open access
Licence
cc-by-nc
Locations
  • OncoImmunology (publishedVersion, cc-by-nc)
  • PubMed Central (publishedVersion, cc-by-nc)
  • PubMed (publishedVersion)
  • Digital Access to Scholarship at Harvard (DASH) (Harvard University) (submittedVersion, cc-by)
Funders
National Cancer Institute (R01CA111985)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Physiology › Adenosine and Purinergic Signaling
  • Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Hypoxia, and Metabolism
Keywords
tumor oxygenation, adenosine A2A receptor, tumor hypoxia, extracellular adenosine, tumor microenvironment, immunosuppression, cancer vaccines, adoptive cell transfer, immune checkpoint blockade, T cells, natural killer cells, cancer immunotherapy

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