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Efficacy of PD-1 Blockade Is Potentiated by Metformin-Induced Reduction of Tumor Hypoxia
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Abstract
Blockade of the coinhibitory checkpoint molecule PD-1 has emerged as an effective treatment for many cancers, resulting in remarkable responses. However, despite successes in the clinic, most patients do not respond to PD-1 blockade. Metabolic dysregulation is a common phenotype in cancer, but both patients and tumors are metabolically heterogeneous. We hypothesized that the deregulated oxidative energetics of tumor cells present a metabolic barrier to antitumor immunity through the generation of a hypoxic microenvironment and that normalization of tumor hypoxia might improve response to immunotherapy. We show that the murine tumor lines B16 and MC38 differed in their ability to consume oxygen and produce hypoxic environments, which correlated with their sensitivity to checkpoint blockade. Metformin, a broadly prescribed type II diabetes treatment, inhibited oxygen consumption in tumor cells in vitro and in vivo, resulting in reduced intratumoral hypoxia. Although metformin monotherapy had little therapeutic benefit in highly aggressive tumors, combination of metformin with PD-1 blockade resulted in improved intratumoral T-cell function and tumor clearance. Our data suggest tumor hypoxia acts as a barrier to immunotherapy and that remodeling the hypoxic tumor microenvironment has potential to convert patients resistant to immunotherapy into those that receive clinical benefit. Cancer Immunol Res; 5(1); 9–16. ©2016 AACR.
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“Current studies have focused on the role of hypoxia-induced metabolic reprogramming in causing T cell dysfunction and exhaustion16,19,52–55.”
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“As hypoxic microenvironment could provide tumor resistant to immunotherapy (42, 43), which has emerged as an effective therapy for CRC (44, 45), HRGS may have the potential to predict the outcome of the immunotherapy.”
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Prediction of immunotherapy efficacy and immunomodulatory role of hypoxia in colorectal cancer
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“Another study showed a correlation between the ability of mouse tumor cell lines to consume oxygen with their sensitivity to PD-1 checkpoint blockade [46], thus sug-”
BackgroundSantana-Krímskaya, S. E., Kawas, J. R., Zárate-Triviño, D. G., Ramos-Zayas, Y., Rodrı́guez-Padilla, C., & Franco-Molina, M. Á. (2022) · Research in Veterinary Science · doi:10.1016/j.rvsc.2022.08.026 · Cited by 10
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“22,23 Moreover, contrary to the long-held view that tumors are mostly glycolytic, oxidative phosphorylation active in many malignancies, representing a possible therapeutic target.”
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Redox Signaling Modulates Activity of Immune Checkpoint Inhibitors in Cancer Patients
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“Additionally, this would diminish intratumoural hypoxia [53].”
Facts and Hopes in Using Omics to Advance Combined Immunotherapy Strategies
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“Hypoxic stress was an important feature of tumor metabolism and prompted resistance to immunotherapy in cancers (24, 25).”
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“Interestingly, in that study metformin alone has also shown to increase the number of PD-1+ and Tim-3+ exhausted T cells in tumors [88] and this might have counter affected the cytotoxic activities of CD44 hi activated T cells in exerting the tumor control.”
InfluentialLlerena, P., Samarah, H., Nunes, K. L., Lin, Z., Bridgham, K., Tekumalla, S., Jain, A., Harshyne, L. A., Shukla, S. K., Vathiotis, I. A., et al. (2025) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-25-1098 · Cited by 8
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Beyond diabetes: harnessing the power of metformin in burn care
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The Role of Hypoxia in Brain Tumor Immune Responses
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“-e cytokines TNF-α, IL-2, and IFN-c secretion in CD8+ Tcells was significantly increased, and the immune response was enhanced by metformin synergized with PD-L1 MAb.”
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“Furthermore, given that hypoxia in the TME acts as a barrier to immunotherapy, a recent study determined that metformin led to reduction of tumor hypoxia which improved the efficacy of PD-1 blockade and could reduce immunotherapy resistance (133).”
BackgroundApplication of radiomics in lung immuno‐oncology
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Metadata
- Authors
- Scharping, N. E., Menk, A. V., Whetstone, R. D., Zeng, X., & Delgoffe, G. M.
- Affiliations
- University of Pittsburgh (US)
- UPMC Hillman Cancer Center (US)
- Corresponding author
- Delgoffe, Greg M.
- Venue
- Cancer Immunology Research
- Published
- 2017-01-01
- Volume
- 5
- Issue
- 1
- Pages
- 9-16
- ISSN
- 2326-6066 (ISSN-L)
- 2326-6074
- PMC
- PMC5340074
- OpenAlex
- W2560185130
- Cited by
- 520
- References
- 30
- Citations by year
- 2026: 34 · 2025: 53 · 2024: 49 · 2023: 72 · 2022: 85 · 2021: 79 · 2020: 69 · 2019: 38 · 2018: 30 · 2017: 11
- FWCI
- 14.18
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Cancer Immunology Research (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- UPCI (P30CA047904)
- Sidney Kimmel Foundation for Cancer Research (SKF-015-039)
- University of Pittsburgh Cancer Institute Skin Cancer (P50CA121973-08)
- University of Pittsburgh Cancer Institute Head and Neck Cancer SPORE (P50 CA097190)
- Cancer-AACR Innovative Research (SU2C-AACR-IRG-04-16)
- Topics
- Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Hypoxia, and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- anti-PD-1 therapy, metformin, tumor hypoxia, tumor microenvironment, cancer immunotherapy resistance, combination therapy, oxidative metabolism, T cell function, B16 melanoma, MC38 colon carcinoma, antitumor immunity
- MeSH terms
- Tumor Hypoxia, Antineoplastic Agents, Immunological, Animals, Cytotoxicity, Immunologic, Drug Synergism, Energy Metabolism, Melanoma, Experimental, Metformin, Oxygen Consumption, T-Lymphocytes, Cytokines, Lymphocytes, Tumor-Infiltrating, Mice, Tumor Microenvironment, Programmed Cell Death 1 Receptor
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