The DOI matches its Crossref record; 44 of the 44 references it cites were found in a registry or an index.
The Tumor Microenvironment Represses T Cell Mitochondrial Biogenesis to Drive Intratumoral T Cell Metabolic Insufficiency and Dysfunction
Open accessAbstract
Although tumor-specific T cells recognize cancer cells, they are often rendered dysfunctional due to an immunosuppressive microenvironment. Here we showed that T cells demonstrated persistent loss of mitochondrial function and mass when infiltrating murine and human tumors, an effect specific to the tumor microenvironment and not merely caused by activation. Tumor-infiltrating T cells showed a progressive loss of PPAR-gamma coactivator 1α (PGC1α), which programs mitochondrial biogenesis, induced by chronic Akt signaling in tumor-specific T cells. Reprogramming tumor-specific T cells through enforced expression of PGC1α resulted in superior intratumoral metabolic and effector function. Our data support a model in which signals in the tumor microenvironment repress T cell oxidative metabolism, resulting in effector cells with metabolic needs that cannot be met. Our studies also suggest that modulation or reprogramming of the altered metabolism of tumor-infiltrating T cells might represent a potential strategy to reinvigorate dysfunctional T cells for cancer treatment.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Exhausted T cells and tumor-infiltrating NK cells also exhibit dysregulated mitochondrial biogenesis, a mechanism that has created interest in using strategies to improve mitochondrial biogenesis to promote tumor immunity (Scharping et al., 2016; Zheng et al., 2019).”
From Hallmarks of response, resistance, and toxicity to immune checkpoint blockade (2021) · cites this paper as Scharping et al., 2016
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Molecular and cellular insights into T cell exhaustion
Wherry, E. J., & Kurachi, M. (2015) · Nature Reviews Immunology · doi:10.1038/nri3862 · Cited by 4,652
Metabolic Competition in the Tumor Microenvironment Is a Driver of Cancer Progression
Chang, C.-H., Qiu, J., O’Sullivan, D., Buck, M. D., Noguchi, T., Curtis, J. D., Chen, Q., Gindin, M., Gubin, M. M., van der Windt, G. J. W., et al. (2015) · Cell · doi:10.1016/j.cell.2015.08.016 · Cited by 3,331
Regulatory T cells prevent catastrophic autoimmunity throughout the lifespan of mice
Kim, J. M., Rasmussen, J. P., & Rudensky, A. Y. (2006) · Nature Immunology · doi:10.1038/ni1428 · Cited by 1,827
Mitochondria as sensors and regulators of calcium signalling
Rizzuto, R., De Stefani, D., Raffaello, A., & Mammucari, C. (2012) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3412 · Cited by 1,781
Woo, S.-R., Turnis, M. E., Goldberg, M. V., Bankoti, J., Selby, M., Nirschl, C. J., Bettini, M. L., Gravano, D. M., Vogel, P., Liu, C. L., et al. (2012) · Cancer Research · doi:10.1158/0008-5472.can-11-1620 · Cited by 1,647
Mitochondrial respiratory capacity is a critical regulator of CD8+ T cell memory development
van der Windt, G. J. W., Everts, B., Chang, C.-H., Curtis, J. D., Freitas, T. C., Amiel, E., Pearce, E. J., & Pearce, E. L. (2012) · Immunity · doi:10.1016/j.immuni.2011.12.007 · Cited by 1,540
Phosphoenolpyruvate Is a Metabolic Checkpoint of Anti-tumor T Cell Responses
Ho, P.-C., Bihuniak, J. D., Macintyre, A. N., Staron, M., Liu, X., Amezquita, R., Tsui, Y.-C., Cui, G., Micevic, G., Perales, J. C., et al. (2015) · Cell · doi:10.1016/j.cell.2015.08.012 · Cited by 1,462
PGC-1 coactivators: inducible regulators of energy metabolism in health and disease
Finck, B. N. (2006) · Journal of Clinical Investigation · doi:10.1172/jci27794 · Cited by 1,461
Fueling Immunity: Insights into Metabolism and Lymphocyte Function
Pearce, E. L., Poffenberger, M. C., Chang, C.-H., & Jones, R. G. (2013) · Science · doi:10.1126/science.1242454 · Cited by 1,363
Combination cancer immunotherapy and new immunomodulatory targets
Mahoney, K. M., Rennert, P. D., & Freeman, G. J. (2015) · Nature Reviews Drug Discovery · doi:10.1038/nrd4591 · Cited by 1,294
Research works printed but not linked: 1
- Scarpulla, 2011, Metabolic control of mitochondrial biogenesis through the PGC-1 family regulatory network. Biochimica et Biophysica Acta (BBA) -, Molecular Cell Research, 1813, 1269
Cited by
Sorted by citations
Items 301–400 of 847
Rezvan, A., Romain, G., Fathi, M., Heeke, D., Martinez-Paniagua, M. A., An, X., Bandey, I. N., Montalvo, M. J., Adolacion, J. R. T., Saeedi, A., et al. (2024) · Nature Cancer · doi:10.1038/s43018-024-00768-3 · Cited by 39
Targeting chromosomal instability in patients with cancer
Al-Rawi, D. H., Lettera, E., Li, J., Bona, M. D., & Bakhoum, S. F. W. (2024) · Nature Reviews Clinical Oncology · doi:10.1038/s41571-024-00923-w · Cited by 41
Regulation of mTOR, Metabolic Fitness, and Effector Functions by Cytokines in Natural Killer Cells
Viel, S., Besson, L., Marotel, M., Walzer, T., & Marçais, A. (2017) · Cancers · doi:10.3390/cancers9100132 · Cited by 38
Yaghoubizadeh, M., Pishkar, L., & Basati, G. (2019) · Gastrointestinal Tumors · doi:10.1159/000503995 · Cited by 39
Akagi, J., & Baba, H. (2020) · Oncology Letters · doi:10.3892/ol.2020.12121 · Cited by 40
Amino acids and RagD potentiate mTORC1 activation in CD8 + T cells to confer antitumor immunity
Zhang, Y., Hu, H., Liu, W., Yan, S., Li, Y., Tan, L., Chen, Y., Liu, J., Peng, Z., Yuan, Y., et al. (2021) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2020-002137 · Cited by 37
Liu, X., Zhao, Y., Wu, X., Liu, Z., & Liu, X. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.931104 · Cited by 41
Targeting T-cell metabolism to boost immune checkpoint inhibitor therapy
Li, H., Zhao, A., Li, M., Shi, L., Han, Q., & Hou, Z. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1046755 · Cited by 42
Xu, N., Zhu, Y., Han, Y., Liu, Q., Tong, L., Li, Y., Chen, Z., Shao, S., He, W., Li, M., et al. (2025) · Nature Metabolism · doi:10.1038/s42255-025-01347-1 · Cited by 47
Oxygen-dependent regulation of immune checkpoint mechanisms
Ohta, A. (2018) · International Immunology · doi:10.1093/intimm/dxy038 · Cited by 38
T-cell Exhaustion in Organ Transplantation
Angeletti, A., Cantarelli, C., Riella, L. V., Fribourg, M., & Cravedi, P. (2021) · Transplantation · doi:10.1097/tp.0000000000003851 · Cited by 39
Immunotherapy: an emerging modality to checkmate brain metastasis
Ahmad, A., Κhan, P., Rehman, A. U., Batra, S. K., & Nasser, M. W. (2023) · Molecular Cancer · doi:10.1186/s12943-023-01818-7 · Cited by 38
Dimitri, A. J., Baxter, A. E., Chen, G. M., Hopkins, C. R., Rouin, G. T., Huang, H., Kong, W., Holliday, C., Wiebking, V., Bartoszek, R. L., et al. (2024) · Science Advances · doi:10.1126/sciadv.adp9371 · Cited by 42
Li, Y., Zhang, Q., Wu, M., Zhang, P., Huang, L., Ai, X., Yang, Z., Shen, Q., Wang, Y., Wang, P., et al. (2022) · International Journal of Biological Sciences · doi:10.7150/ijbs.70013 · Cited by 37
Xu, T., Liu, Z., Huang, L., Jing, J., & Liu, X. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1057850 · Cited by 38
Mitochondrial Metabolism in T-Cell Exhaustion
Li, F., Yu, F., Yin, Z., & Wang, Y. J. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26157400 · Cited by 42
Glucometabolic Reprogramming in the Hepatocellular Carcinoma Microenvironment: Cause and Effect
Tian, H., Zhu, X., Lv, Y., Jiao, Y., & Wang, G. (2020) · Cancer Management and Research · doi:10.2147/cmar.s258196 · Cited by 39
Immunometabolic reprogramming, another cancer hallmark
Kumar, V., & Stewart, J. H. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1125874 · Cited by 37
Magalhaes, I., Yogev, O., Mattsson, J., & Schurich, A. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02309 · Cited by 34
The Ups and Downs of Metabolism during the Lifespan of a T Cell
Balyan, R., Gautam, N., & Gascoigne, N. R. J. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21217972 · Cited by 36
Sadeghirad, H., Monkman, J. H., Tan, C. W., Liu, N., Yunis, J., Donovan, M. L., Moradi, A., Jhaveri, N., Perry, C., Adams, M. N., et al. (2024) · Journal of Translational Medicine · doi:10.1186/s12967-024-05409-y · Cited by 35
Metabolic profiles of regulatory T cells in the tumour microenvironment
Rao, D., Verburg, F., Renner, K., Peeper, D. S., Lacroix, R., & Blank, C. U. (2021) · Cancer Immunology Immunotherapy · doi:10.1007/s00262-021-02881-z · Cited by 43
Hickman, T. L., Choi, E., Whiteman, K. R., Muralidharan, S., Pai, T., Johnson, T., Parikh, A. B., Friedman, T., Gilbert, M., Shen, B., et al. (2022) · PLoS ONE · doi:10.1371/journal.pone.0266980 · Cited by 36
Metabolic reprogramming of CAR T cells: a new frontier in cancer immunotherapy
Frlic, T., & Pavlin, M. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1688995 · Cited by 38
Mitochondria as Playmakers of CAR T-cell Fate and Longevity
Rostamian, H., Khakpoor-Koosheh, M., Fallah-Mehrjardi, K., Mirzaei, H. R., & Brown, C. E. (2021) · Cancer Immunology Research · doi:10.1158/2326-6066.cir-21-0110 · Cited by 34
Mitochondrial regulation in the tumor microenvironment: targeting mitochondria for immunotherapy
Ahn, M., Ali, A., & Seo, J. H. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1453886 · Cited by 33
Insights Into the Role of Mitochondrial Ion Channels in Inflammatory Response
Ponnalagu, D., & Singh, H. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00258 · Cited by 32
Arming a killer: mitochondrial regulation of CD8+ T cell cytotoxicity
Lisci, M., & Griffiths, G. M. (2022) · Trends in Cell Biology · doi:10.1016/j.tcb.2022.05.007 · Cited by 29
Repas, J., Zupin, M., Vodlan, M., Veranič, P., Gole, B., Potočnik, U., & Pavlin, M. (2022) · Cancers · doi:10.3390/cancers14051343 · Cited by 32
In Vitro Modeling of Tumor–Immune System Interaction
Mengus, C., Muraro, M. G., Mele, V., Amicarella, F., Manfredonia, C., Foglietta, F., Muenst, S. E., Soysal, S. D., Iezzi, G., & Spagnoli, G. C. (2017) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.7b00077 · Cited by 32
Chen, Z., Zhu, Z., Hu, T., Yao, C., & Wu, T. (2025) · Cellular and Molecular Immunology · doi:10.1038/s41423-025-01378-4 · Cited by 37
Metabolic and Mitochondrial Functioning in Chimeric Antigen Receptor (CAR)—T Cells
Rad, S. M. A. H., Halpin, J. C., Mollaei, M., Smith‐Bell, S. W., Hirankarn, N., & McLellan, A. D. (2021) · Cancers · doi:10.3390/cancers13061229 · Cited by 31
Tian, H., Wang, G., Wang, Q., Zhang, B., Jiang, G., Li, H., Chai, D., Fang, L., Wang, M., & Zheng, J. (2022) · Cancer Science · doi:10.1111/cas.15261 · Cited by 33
Drug delivery for metabolism targeted cancer immunotherapy
Khodaei, T., Inamdar, S., Suresh, A. P., & Acharya, A. P. (2022) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2022.114242 · Cited by 30
Evolving CAR-T-Cell Therapy for Cancer Treatment: From Scientific Discovery to Cures
Majumder, A. (2023) · Cancers · doi:10.3390/cancers16010039 · Cited by 35
Single‐cell transcriptomics identify TNFRSF1B as a novel T‐cell exhaustion marker for ovarian cancer
Gao, Y., Shi, H., Zhao, H., Yao, M., He, Y., Jiang, M., Li, J., Li, Z., Su, S., Liu, T., et al. (2023) · Clinical and Translational Medicine · doi:10.1002/ctm2.1416 · Cited by 29
Hu, W., Li, F., Liang, Y., Liu, S., Wang, S., Shen, C., Zhao, Y., Wang, H., & Zhang, Y. (2025) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2024-010540 · Cited by 32
Tumour microenvironment on mitochondrial dynamics and chemoresistance in cancer
Han, Y., Cho, U., Kim, S., Park, I. S., Cho, J., Dhanasekaran, D. N., & Song, Y. S. (2018) · Free Radical Research · doi:10.1080/10715762.2018.1459594 · Cited by 28
Peeters, M. J. W., Aehnlich, P., Pizzella, A., Mølgaard, K., Seremet, T., Met, Ö., Rasmussen, L. J., Straten, P. T., & Desler, C. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.718863 · Cited by 29
P2RX7 Enhances Tumor Control by CD8+ T Cells in Adoptive Cell Therapy
Wanhainen, K. M., Peng, C., Zhou, M. H., Macedo, B. D. G., O’Flanagan, S. D., Yang, T., Kelekar, A., Burbach, B. J., da Silva, H. B., & Jameson, S. C. (2022) · Cancer Immunology Research · doi:10.1158/2326-6066.cir-21-0691 · Cited by 29
Coengineering specificity, safety, and function into T cells for cancer immunotherapy
Attianese, G. M. P. G., Ash, S., & Irving, M. B. (2023) · Immunological Reviews · doi:10.1111/imr.13252 · Cited by 29
Shafqat, A., Omer, M. H., Ahmed, E. N., Mushtaq, A. H., Ijaz, E., Ahmed, Z., AlKattan, K. M., & Yaqinuddin, A. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1200941 · Cited by 32
Ascierto, P. A., Bifulco, C. B., Buonaguro, L., Emens, L. A., Ferris, R. L., Fox, B. A., Delgoffe, G. M., Galon, J., Gridelli, C., Merlano, M. C., et al. (2019) · Journal for ImmunoTherapy of Cancer · doi:10.1186/s40425-019-0798-3 · Cited by 28
Self-citationThe future of cryoablation: An abscopal effect
Chen, J., Qian, W., Mu, F., Niu, L., Du, D., & Xu, K. (2020) · Cryobiology · doi:10.1016/j.cryobiol.2020.02.010 · Cited by 28
Harnessing Metabolic Reprogramming to Improve Cancer Immunotherapy
Liang, Y., Tan, Y., Chen, G., Fan, J., & Zhang, J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221910268 · Cited by 29
Innate and Adaptive Immune Cell Metabolism in Tumor Microenvironment
Wu, D. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-94-024-1170-6_7 · Cited by 27
Genetically engineering glycolysis in T cells increases their antitumor function
Zur-Toledano, R., Atar, O., Barliya, T., Hoogi, S., Abramovich, I., Gottlieb, E., Ron‐Harel, N., & Cohen, C. J. (2024) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2023-008434 · Cited by 27
A Mitochondrial Polymorphism Alters Immune Cell Metabolism and Protects Mice from Skin Inflammation
Schilf, P., Künstner, A., Olbrich, M. R., Waschina, S., Fuchs, B., Galuska, C. E., Braun, A., Neuschütz, K., Seutter, M., Bieber, K., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22031006 · Cited by 27
LDHB Overexpression Can Partially Overcome T Cell Inhibition by Lactic Acid
Decking, S.-M., Bruß, C., Babl, N., Bittner, S., Klobuch, S., Thomas, S., Feuerer, M., Hoffmann, P., Dettmer, K., Oefner, P. J., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23115970 · Cited by 27
Deng, X., Chen, D., Sun, X., Dong, J., & Huang, J. (2022) · Journal of Food Science · doi:10.1111/1750-3841.16228 · Cited by 27
Synthetic Biology: Immunotherapy by Design
Brenner, J., Cho, J. H., Wong, N. M. L., & Wong, W. W. (2018) · Annual Review of Biomedical Engineering · doi:10.1146/annurev-bioeng-062117-121147 · Cited by 26
Sun, S., Xu, H., Zhao, W., Li, Q., Yuan, Y., Zhang, G., Li, S., Wang, B., Zhang, W., Gao, X., et al. (2023) · Cancer Letters · doi:10.1016/j.canlet.2023.216511 · Cited by 28
Liu, Y., Xu, C., Zhang, L., Xu, G., Yang, Z., Xiang, L., Jiao, K., Chen, Z., Zhang, X., & Liu, Y. (2024) · Science Advances · doi:10.1126/sciadv.adi7764 · Cited by 27
Han, P., Chu, S., Shen, J., Li, L., Zhang, Y., Wang, S., Chen, Y., Ma, Y., Tang, X., Gao, C., et al. (2025) · Cell Metabolism · doi:10.1016/j.cmet.2025.09.010 · Cited by 30
Mangal, J. L., Handlos, J. L., Esrafili, A., Inamdar, S., Mcmillian, S., Wankhede, M., Gottardi, R., & Acharya, A. P. (2021) · Cancers · doi:10.3390/cancers13051123 · Cited by 26
Qian, C., & Cao, X. (2021) · Cellular and Molecular Immunology · doi:10.1038/s41423-021-00709-5 · Cited by 26
Impact of Drp1-Mediated Mitochondrial Dynamics on T Cell Immune Modulation
Song, J., Yi, X., Gao, R.-L., Sun, L., Wu, Z., Zhang, S., Huang, L., Han, C., & Ma, J. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.873834 · Cited by 29
LEF1 Drives a Central Memory Program and Supports Antitumor Activity of Natural Killer T Cells
Ngai, H., Barragán, G. A., Tian, G., Balzeau, J. C., Zhang, C., Courtney, A. N., Guo, L., Xu, X. Y., Wood, M. S., Drabek, J. M., et al. (2022) · Cancer Immunology Research · doi:10.1158/2326-6066.cir-22-0333 · Cited by 26
Filling the Tank: Keeping Antitumor T Cells Metabolically Fit for the Long Haul
Delgoffe, G. M. (2016) · Cancer Immunology Research · doi:10.1158/2326-6066.cir-16-0244 · Cited by 26
Self-citationTumor Immune Microenvironment in Gynecologic Cancers
Margul, D. J., Yu, C., & AlHilli, M. M. (2023) · Cancers · doi:10.3390/cancers15153849 · Cited by 24
Metabolic plasticity of T cell fate decision
Pan, X., Wang, J., Zhang, L., Li, G., & Huang, B. (2023) · Chinese Medical Journal · doi:10.1097/cm9.0000000000002989 · Cited by 26
CD8+ T-cell exhaustion: Impediment to triple-negative breast cancer (TNBC) immunotherapy
Feng, D., Pu, D., Ren, J., Liu, M., Zhang, Z., Liu, Z., & Li, J. (2024) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2024.189193 · Cited by 26
Tejero, J. D., Hesterberg, R. S., Drápela, S., Ilter, D., Raizada, D., Lazure, F., Kashfi, H., Liu, M., Silvane, L., Avram, D., et al. (2024) · Oncogene · doi:10.1038/s41388-024-03191-1 · Cited by 26
Admasu, T. D., & Yu, J. S. (2025) · Aging Cell · doi:10.1111/acel.70055 · Cited by 30
Barriers and solutions for CAR-T therapy in solid tumors
Tu, Z., Chen, Y., Zhang, Z., Meng, W., & Li, L. (2025) · Cancer Gene Therapy · doi:10.1038/s41417-025-00931-7 · Cited by 32
Receptor signaling, transcriptional, and metabolic regulation of T cell exhaustion
Balkhi, M. Y. (2020) · OncoImmunology · doi:10.1080/2162402x.2020.1747349 · Cited by 26
Tinkering under the Hood: Metabolic Optimisation of CAR-T Cell Therapy
Jenkins, Y. R., Zabkiewicz, J., Ottmann, O. G., & Jones, N. (2021) · Antibodies · doi:10.3390/antib10020017 · Cited by 24
Cooke, J. P., & Lai, L. (2023) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2023.115118 · Cited by 25
Prospects of molecular hydrogen in cancer prevention and treatment
Zhou, W., Zhang, J., Chen, W., & Miao, C. (2024) · Journal of Cancer Research and Clinical Oncology · doi:10.1007/s00432-024-05685-7 · Cited by 25
Understanding and overcoming resistance to immunotherapy in genitourinary cancers
Evans, S. T., Jani, Y. C., Jansen, C. S., Yıldırım, A., Kalemoglu, E., & Bilen, M. A. (2024) · Cancer Biology & Therapy · doi:10.1080/15384047.2024.2342599 · Cited by 24
T cell exhaustion and senescence for ovarian cancer immunotherapy
Zhao, J., Wang, Z., Tian, Y., Ning, J., & Ye, H. (2024) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2024.07.001 · Cited by 26
Zhu, Z., Luo, Y., Lou, G., Yihunie, K. D., Wizzard, S., DeVilbiss, A., Muh, S., Ma, C., Shinde, S. S., Hoar, J., et al. (2024) · Science Immunology · doi:10.1126/sciimmunol.adk2954 · Cited by 25
Metabolic immunoengineering approaches to enhance CD8+ T cell-based cancer immunotherapy
Feng, B., Li, R., Li, W., & Tang, L. (2024) · Cell Systems · doi:10.1016/j.cels.2024.11.010 · Cited by 27
Ruffin, A. T., Casey, A. N., Kunning, S. R., MacFawn, I., Liu, Z., Arora, C., Rohatgi, A., Kemp, F., Lampenfeld, C., Somasundaram, A., et al. (2025) · Science Translational Medicine · doi:10.1126/scitranslmed.adh1315 · Cited by 24
Self-citationRodríguez‐Berriguete, G., Puliyadi, R., Machado, N., Barberis, A., Prevo, R., McLaughlin, M., Buffa, F. M., Harrington, K. J., & Higgins, G. S. (2024) · Cell Death and Disease · doi:10.1038/s41419-023-06405-8 · Cited by 25
Current Advances and Challenges in CAR-T Therapy for Hematological and Solid Tumors
Zhang, G., Bai, M., Du, H., Yuan, Y., Wang, Y., Fan, W., Zhu, H., Wu, D., He, P., & Xue, B. (2025) · ImmunoTargets and Therapy · doi:10.2147/itt.s519616 · Cited by 26
The multifaceted impact of stress on immune function
Balcerowska, M., & Kwaśnik, P. (2025) · Molecular Biology Reports · doi:10.1007/s11033-025-11134-6 · Cited by 23
T Cell Exhaustion in Cancer Immunotherapy: Heterogeneity, Mechanisms, and Therapeutic Opportunities
Yang, Y. P., Yao, X., Wang, Q., Yang, M., Li, R., Qin, J., Zhuang, J., & Sun, C. (2026) · Advanced Science · doi:10.1002/advs.202520634 · Cited by 27
Translating In Vitro T Cell Metabolic Findings to In Vivo Tumor Models of Nutrient Competition
Ecker, C., & Riley, J. L. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2018.07.009 · Cited by 22
Resistance mechanisms in melanoma to immuneoncologic therapy with checkpoint inhibitors
Fenton, S. E., Sosman, J. A., & Chandra, S. (2019) · Cancer Drug Resistance · doi:10.20517/cdr.2019.28 · Cited by 28
Directing T-Cell Immune Responses for Cancer Vaccination and Immunotherapy
Smith, P. L., Piadel, K., & Dalgleish, A. G. (2021) · Vaccines · doi:10.3390/vaccines9121392 · Cited by 24
Regulation of immune cell metabolism in health and disease: Special focus on T and B cell subsets
Chakraborty, S., Khamaru, P., & Bhattacharyya, A. (2022) · Cell Biology International · doi:10.1002/cbin.11867 · Cited by 24
C1QBP regulates mitochondrial plasticity to impact tumor progression and antitumor immune response
Wang, Q., Chai, D., Sobhani, N., Sun, N., Neeli, P. K., Zheng, J., & Tian, H. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.1012112 · Cited by 29
Roselle, C., Horikawa, I., Chen, L., Kelly, A. R., Gonzales, D. M., Da, T., Wellhausen, N., Rommel, P. C., Baker, D., Suhoski, M. M., et al. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2317735121 · Cited by 24
Nicotinamide Inhibits T Cell Exhaustion and Increases Differentiation of CD8 Effector T Cells
Alavi, S., Emran, A. A., Tseng, H., Tiffen, J. C., McGuire, H. M., & Hersey, P. (2022) · Cancers · doi:10.3390/cancers14020323 · Cited by 22
Metabolism heterogeneity in melanoma fuels deactivation of immunotherapy: Predict before protect
Zhang, X., Tai, Z., Miao, F., Huang, H., Zhu, Q., Bao, L., & Chen, Z. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.1046102 · Cited by 22
Nirschl, C. J., Brodkin, H. R., Domonkos, C., Dwyer, C. J., Hicklin, D. J., Ismail, N. S., Seidel‐Dugan, C., Steiner, P., Steuert, Z., Sullivan, J. M., et al. (2023) · Cancer Immunology Research · doi:10.1158/2326-6066.cir-22-0705 · Cited by 22
Augustin, R. C., Huang, Z., Ding, F., Zhai, S., McArdle, J., Santisi, A., Davis, M., Sander, C., Davar, D., Kirkwood, J. M., et al. (2023) · Frontiers in Oncology · doi:10.3389/fonc.2023.1075823 · Cited by 24
Self-citationHuang, X., Sun, Y., Song, J., Huang, Y., Shi, H., Qian, A., Cao, Y., Zhou, Y., & Wang, Q. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1301452 · Cited by 22
Begum, H. M., Ta, H. P., Zhou, H., Ando, Y., Kang, D. S., Nemes, K., Mariano, C. F., Hao, J., Yu, M., & Shen, K. (2019) · Scientific Reports · doi:10.1038/s41598-019-47593-8 · Cited by 22
The tumor immune microenvironment and T-cell-related immunotherapies in colorectal cancer
Liu, C., Qifeng, J., & Shaolei, Y. (2024) · Discover Oncology · doi:10.1007/s12672-024-01117-7 · Cited by 22
Focusing on CD8+ T-cell phenotypes: improving solid tumor therapy
Yao, Z., Zeng, Y., Liu, C., Jin, H., Wang, H., Zhang, Y., Ding, C., Chen, G., & Wu, D. (2024) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-024-03195-5 · Cited by 27
Jacobs, C. F., Peters, F. S., Camerini, E., Cretenet, G., Rietveld, J. M., Schomakers, B. V., van Weeghel, M., Hahn, N., Verberk, S. G. S., den Bossche, J. V., et al. (2025) · Cellular and Molecular Immunology · doi:10.1038/s41423-025-01262-1 · Cited by 23
Reprogramming T-Cell Metabolism for Better Anti-Tumor Immunity
Ping, Y., Shen, C., Huang, B., & Zhang, Y. (2022) · Cells · doi:10.3390/cells11193103 · Cited by 22
Modulation of T cell function and survival by the tumor microenvironment
Mani, N. L., Andrews, D., & Obeng, R. C. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1191774 · Cited by 22
Anderson, K. G., Braun, D. A., Buqué, A., Gitto, S. B., Guerriero, J. L., Horton, B. L., Keenan, B. P., Kim, T. S., Overacre-Delgoffe, A. E., Ruella, M., et al. (2023) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2022-006533 · Cited by 22
Pfister, F., Dörrie, J., Schaft, N., Buchele, V., Unterweger, H., Carnell, L. R., Schreier, P., Stein, R. A., Kubánková, M., Guck, J. R., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1223695 · Cited by 21
Advances in reprogramming of energy metabolism in tumor T cells
Xuekai, L., Yan, S., Chu, J., Yifei, S., Wu, X., Wenyuan, Z., Han, S., & Xi, Y. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1347181 · Cited by 23
Stem‐like T cells in cancer and autoimmunity
Schnell, A. (2024) · Immunological Reviews · doi:10.1111/imr.13356 · Cited by 22
Mitochondrial metabolism: Inducer or therapeutic target in tumor immune-resistance?
Kopecka, J., Gazzano, E., Castella, B., Salaroglio, I. C., Mungo, E., Massaia, M., & Riganti, C. (2019) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2019.05.008 · Cited by 21
Metadata
- Authors
- Scharping, N. E., Menk, A. V., Moreci, R. S., Whetstone, R. D., Dadey, R. E., Watkins, S. C., Ferris, R. L., & Delgoffe, G. M.
- Affiliations
- University of Pittsburgh (US)
- UPMC Hillman Cancer Center (US)
- Corresponding author
- Delgoffe, Greg M.
- ORCID
- Venue
- Immunity
- Publisher
- Elsevier BV
- Published
- 2016-08
- Volume
- 45
- Issue
- 2
- Pages
- 374-388
- ISSN
- 1074-7613 (ISSN-L)
- PMC
- PMC5207350
- OpenAlex
- W4294138012
- Cited by
- 848
- References
- 44
- Citations by year
- 2026: 136 · 2025: 111 · 2024: 113 · 2023: 97 · 2022: 109 · 2021: 90 · 2020: 76 · 2019: 42 · 2018: 33 · 2017: 34 · 2016: 7
- FWCI
- 20.82
- Type
- journal article
- Language
- en
- Update notices
- erratum (2016-09-20)
- Open access
- bronze
- doi.org
- Licence
- Locations
- Immunity (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (1s10od016236-01)
- National Cancer Institute (P50CA121973, P50CA097190, P30CA047904)
- Topics
- Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Immune cells in cancer
- Keywords
- tumor microenvironment, PGC-1α, Akt signaling, T cell metabolism, oxidative metabolism, tumor-infiltrating T cells, T cell dysfunction, immunosuppression, metabolic reprogramming, cancer immunotherapy
- MeSH terms
- Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha, Animals, Colonic Neoplasms, Humans, Mice, Inbred C57BL, Mice, Transgenic, Mitochondria, Neoplasms, Experimental, T-Lymphocytes, Signal Transduction, Lymphocytes, Tumor-Infiltrating, Oxidative Stress, Cell Line, Tumor, PPAR gamma, Oncogene Protein v-akt, Mice, Tumor Microenvironment, Cellular Reprogramming
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review