The DOI matches its Crossref record; 233 of the 233 references it cites were found in a registry or an index.
Cellular adaptation to hypoxia through hypoxia inducible factors and beyond
Open accessAbstract
Molecular oxygen (O 2) sustains intracellular bioenergetics and is consumed by numerous biochemical reactions, making it essential for most species on Earth. Accordingly, decreased oxygen concentration (hypoxia) is a major stressor that generally subverts life of aerobic species and is a prominent feature of pathological states encountered in bacterial infection, inflammation, wounds, cardiovascular defects and cancer. Therefore, key adaptive mechanisms to cope with hypoxia have evolved in mammals. Systemically, these adaptations include increased ventilation, cardiac output, blood vessel growth and circulating red blood cell numbers. On a cellular level, ATP-consuming reactions are suppressed, and metabolism is altered until oxygen homeostasis is restored. A critical question is how mammalian cells sense oxygen levels to coordinate diverse biological outputs during hypoxia. The best-studied mechanism of response to hypoxia involves hypoxia inducible factors (HIFs), which are stabilized by low oxygen availability and control the expression of a multitude of genes, including those involved in cell survival, angiogenesis, glycolysis and invasion/metastasis. Importantly, changes in oxygen can also be sensed via other stress pathways as well as changes in metabolite levels and the generation of reactive oxygen species by mitochondria. Collectively, this leads to cellular adaptations of protein synthesis, energy metabolism, mitochondrial respiration, lipid and carbon metabolism as well as nutrient acquisition. These mechanisms are integral inputs into fine-tuning the responses to hypoxic stress.
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
“Cancer hypoxia and the induced adaptation mechanisms are two of the major causes of therapy resistance.”
From Hypoxia Signaling in Cancer: From Basics to Clinical Practice (2021) · cites this paper as [5]
In the citing paper
“However, chronic hypoxia is the most typical form of hypoxia in tumor tissues [5].”
From Hypoxia Signaling in Cancer: From Basics to Clinical Practice (2021) · cites this paper as [5]
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
1 retracted
Mitochondrial Autophagy Is an HIF-1-dependent Adaptive Metabolic Response to Hypoxia
Zhang, H., Bosch-Marce, M., Shimoda, L. A., Tan, Y. S., Baek, J. H., Wesley, J. B., Gonzalez, F. J., & Semenza, G. L. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m800102200 · Cited by 1,601
RetractedRepertoires of Autophagy in the Pathogenesis of Ocular Diseases
Li, Y., Jiang, Q. L., Cao, G.-F., Yao, J., & Yan, B. (2015) · Cellular Physiology and Biochemistry · doi:10.1159/000373980 · Cited by 16,351
A role for mitochondria in nlrp3 inflammasome activation
Zhou, R., Yazdi, A. S., Menu, P., & Tschopp, J. (2011) · Nature · doi:10.1038/nature09663 · Cited by 5,602
Control of inositol 1,4,5-trisphosphate-induced Ca2+ release by cytosolic Ca2+
Bootman, M. D., Missiaen, L., Parys, J. B., SMEDT, H. D., & Casteels, R. (1995) · Biochemical Journal · doi:10.1042/bj3060445 · Cited by 5,131
Targeting Hypoxia-Inducible Factors for the Treatment of Anemia in Chronic Kidney Disease Patients
Locatelli, F., Fishbane, S. N., Block, G. A., & Macdougall, I. C. (2017) · American Journal of Nephrology · doi:10.1159/000455166 · Cited by 4,836
Mitochondria, Oxidants, and Aging
Balaban, R. S., Nemoto, S., & Finkel, T. (2005) · Cell · doi:10.1016/j.cell.2005.02.001 · Cited by 4,388
The unfolded protein response: controlling cell fate decisions under ER stress and beyond
Hetz, C. A. (2012) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3270 · Cited by 4,223
Yoshida, H., Matsui, T., Yamamoto, A., Okada, T., & Mori, K. (2001) · Cell · doi:10.1016/s0092-8674(01)00611-0 · Cited by 4,054
Kim, J.-W., Tchernyshyov, I., Semenza, G. L., & Dang, C. V. (2006) · Cell Metabolism · doi:10.1016/j.cmet.2006.02.002 · Cited by 3,905
Mutation of the mouse klotho gene leads to a syndrome resembling ageing
Kuro-o, M., Matsumura, Y., Aizawa, H., Kawaguchi, H., Suga, T., Utsugi, T., Ohyama, Y., Kurabayashi, M., Kaname, T., Kume, E., et al. (1997) · Nature · doi:10.1038/36285 · Cited by 3,837
Research works printed but not linked: 1
- Hernansanz-Agustín, P. et al. Mitochondrial Na+ import controls oxidative phosphorylation and hypoxic redox signalling. bioRxiv https://doi.org/10.1101/385690 (2018). · DOI
Cited by
Sorted by citations
Items 101–200 of 1,000
Pearce, L., Davidson, S. M., & Yellon, D. M. (2021) · Basic Research in Cardiology · doi:10.1007/s00395-021-00852-0 · Cited by 66
Advancing glioblastoma treatment by targeting metabolism
Zhao, J., Ma, X.-M., Gao, P., Han, X., Zhao, P., Xie, F., & Liu, M. (2024) · Neoplasia · doi:10.1016/j.neo.2024.100985 · Cited by 70
Flores‐Opazo, M., Kopinke, D., Helmbacher, F., Fernández‐Verdejo, R., Tuñón‐Suárez, M., Lynch, G. S., & Contreras, O. (2024) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2024.101277 · Cited by 66
Song, C.-C., Pantopoulos, K., Chen, G., Zhong, C.-C., Zhao, T., Zhang, D.-G., & Luo, Z. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-022-04423-x · Cited by 65
Hypoxia Conditioning for High-Altitude Pre-acclimatization
Burtscher, M., Millet, G. P., & Burtscher, J. (2022) · Journal of Science in Sport and Exercise · doi:10.1007/s42978-021-00150-0 · Cited by 68
Fang, J., Chen, J., Zheng, J.-L., Zeng, H.-X., Chen, J.-G., Wu, C.-H., Cai, J.-L., Wang, Z., & Zhuang, S. (2023) · Cancer Research · doi:10.1158/0008-5472.can-22-1844 · Cited by 65
Zhu, K., Wang, L., Xiao, Y., Zhang, X., You, G., Chen, Y., Wang, Q., Zhao, L., Zhou, H., & Chen, G. (2024) · Journal of Nanobiotechnology · doi:10.1186/s12951-024-02606-1 · Cited by 65
Disease Mechanisms of Perioperative Organ Injury
Conrad, C., & Eltzschig, H. K. (2020) · Anesthesia & Analgesia · doi:10.1213/ane.0000000000005191 · Cited by 63
3D-printed oxygen-releasing scaffolds improve bone regeneration in mice
Farris, A. L., Lambrechts, D., Zhou, Y., Zhang, N. Y., Sarkar, N., Moorer, M. C., Rindone, A. N., Nyberg, E. L., Perdomo‐Pantoja, A., Burris, S. J., et al. (2021) · Biomaterials · doi:10.1016/j.biomaterials.2021.121318 · Cited by 63
Novel insights into anticancer mechanisms of elesclomol: More than a prooxidant drug
Gao, J., Wu, X., Huang, S., Zhao, Z., He, W., & Song, M. L. (2023) · Redox Biology · doi:10.1016/j.redox.2023.102891 · Cited by 66
Salidroside: An Overview of Its Promising Potential and Diverse Applications
Liang, K., Ma, S., Luo, K., Wang, R., Xiao, C., Zhang, X., Gao, Y., & Li, M. (2024) · Pharmaceuticals · doi:10.3390/ph17121703 · Cited by 62
Dynamic investigation of hypoxia-induced L-lactylation
Gao, J., Liu, R., Huang, K., Li, Z., Sheng, X., Chakraborty, K., Han, C., Zhang, D., Becker, L., & Zhao, Y. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2404899122 · Cited by 69
Targeting hypoxia signaling pathways in angiogenesis
Monaci, S., Coppola, F., Filippi, I., Falsini, A., Carraro, F., & Naldini, A. (2024) · Frontiers in Physiology · doi:10.3389/fphys.2024.1408750 · Cited by 64
Metabolic programs drive function of therapeutic NK cells in hypoxic tumor environments
Kennedy, P. R., Arvindam, U. S., Phung, S. K., Ettestad, B., Feng, X., Li, Y., Kile, Q. M., Hinderlie, P., Khaw, M. J., Huang, R., et al. (2024) · Science Advances · doi:10.1126/sciadv.adn1849 · Cited by 62
Applications and enhancement strategies of ROS-based non-invasive therapies in cancer treatment
Guo, Q., Tang, Y., Wang, S., & Xia, X. (2025) · Redox Biology · doi:10.1016/j.redox.2025.103515 · Cited by 61
Anemia and Its Connections to Inflammation in Older Adults: A Review
Wacka, E., Nicikowski, J., Jarmużek, P., & Zembroń-Łacny, A. (2024) · Journal of Clinical Medicine · doi:10.3390/jcm13072049 · Cited by 64
Song, M., & Grabocka, E. (2020) · Reviews of physiology, biochemistry and pharmacology · doi:10.1007/112_2020_37 · Cited by 61
The Role of Hypoxia and SRC Tyrosine Kinase in Glioblastoma Invasiveness and Radioresistance
Torrisi, F., Vicario, N., Spitale, F. M., Cammarata, F. P., Minafra, L., Salvatorelli, L., Russo, G. I., Cuttone, G., Valable, S., Gulino, R., et al. (2020) · Cancers · doi:10.3390/cancers12102860 · Cited by 59
Histone H3 proline 16 hydroxylation regulates mammalian gene expression
Liu, X., Wang, J., Boyer, J. A., Gong, W., Zhao, S., Xie, L., Wu, Q., Zhang, C., Jain, K., Guo, Y., et al. (2022) · Nature Genetics · doi:10.1038/s41588-022-01212-x · Cited by 60
Regulation of Metabolic Plasticity in Cancer Stem Cells and Implications in Cancer Therapy
Papadaki, S., & Magklara, A. (2022) · Cancers · doi:10.3390/cancers14235912 · Cited by 62
Ruan, H., Zhang, Q., Zhang, Y., Li, S., & Ran, X. (2024) · Critical Care · doi:10.1186/s13054-024-04885-4 · Cited by 60
Regulation of Oxygen Homeostasis at the Intestinal Epithelial Barrier Site
Konjar, Š., Pavšič, M., & Veldhoen, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22179170 · Cited by 58
USP14 maintains HIF1-α stabilization via its deubiquitination activity in hepatocellular carcinoma
Lv, C., Wang, S., Lin, L., Wang, C., Zeng, K., Meng, Y., Sun, G., Wei, S., Liu, Y., & Zhao, Y. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-04089-6 · Cited by 57
Metabolic regulation of T cells in the tumor microenvironment by nutrient availability and diet
Zhao, S., Peralta, R. M., Avina-Ochoa, N., Delgoffe, G. M., & Kaech, S. M. (2021) · Seminars in Immunology · doi:10.1016/j.smim.2021.101485 · Cited by 58
Factors Determining Epithelial-Mesenchymal Transition in Cancer Progression
Tomecka, P., Kunachowicz, D., Górczyńska, J., Gebuza, M., Kuźnicki, J., Skinderowicz, K., & Choromańska, A. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25168972 · Cited by 62
The human zinc-binding cysteine proteome
Burger, N., Mittenbühler, M. J., Xiao, H., Shin, S.-H., Wei, S. M., Henze, E. K., Schindler, S., Mehravar, S., Wood, D. M., Petrocelli, J. J., et al. (2024) · Cell · doi:10.1016/j.cell.2024.11.025 · Cited by 60
Qin, S., Xu, Y., Li, H., Chen, H., & Yuan, Z. (2022) · Biomaterials Science · doi:10.1039/d1bm00317h · Cited by 56
Hypoxia signaling: Challenges and opportunities for cancer therapy
Ivan, M., Fishel, M. L., Tudoran, O. M., Pollok, K. E., Wu, X., & Smith, P. J. (2021) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2021.10.002 · Cited by 57
D’Aiuto, N., Hochmann, J., Millán, M., Paolo, A. D., Bologna‐Molina, R. E., Sotelo-Silveira, J. R., & Arocena, M. (2022) · Scientific Reports · doi:10.1038/s41598-022-26205-y · Cited by 58
Poison cassette exon splicing ofSRSF6regulates nuclear speckle dispersal and the response to hypoxia
Machado, C. D. O. F., Schafranek, M., Brüggemann, M., Cañás, M. C. H., Keller, M., Liddo, A. D., Brezski, A., Blümel, N., Arnold, B., Bremm, A., et al. (2023) · Nucleic Acids Research · doi:10.1093/nar/gkac1225 · Cited by 59
Han, X., Burrows, M., Kim, L. C., Xu, J. P., Vostrejs, W., Le, T. N. V., Poltorack, C. D., Jiang, Y., Cukierman, E., Stanger, B. Z., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114972 · Cited by 56
Self-citationKip, A. M., Soons, Z., Mohren, R., Duivenvoorden, A. A. M., Röth, A. A. J., Cillero-Pastor, B., Neumann, U. P., Dejong, C. H. C., Heeren, R. M. A., Olde Damink, S. W. M., et al. (2021) · Cell Death & Disease · doi:10.1038/s41419-020-03379-9 · Cited by 55
Tamamouna, V., Rahman, M. M., Petersson, M., Charalambous, I., Kux, K., Mainor, H., Bolender, V., Isbilir, B., Edgar, B. A., & Pitsouli, C. (2021) · Nature Cell Biology · doi:10.1038/s41556-021-00674-1 · Cited by 57
Supraphysiological Oxygen Levels in Mammalian Cell Culture: Current State and Future Perspectives
Alva, R., Gardner, G. L., Liang, P., & Stuart, J. A. (2022) · Cells · doi:10.3390/cells11193123 · Cited by 62
Chen, Y., Jiao, D., Liu, Y., Xu, X., Wang, Y., Luo, X., Saiyin, H., Li, Y., Gao, K., Chen, Y., et al. (2023) · Cell Death and Differentiation · doi:10.1038/s41418-023-01205-1 · Cited by 55
The interplay between autophagy and cGAS-STING signaling and its implications for cancer
Schmid, M., Fischer, P., Engl, M., Widder, J., Gruber, S., & Slade, D. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1356369 · Cited by 61
Signaling Paradigms of H2S-Induced Vasodilation: A Comprehensive Review
Munteanu, C., Popescu, C., Vlădulescu-Trandafir, A.-I., & Onose, G. (2024) · Antioxidants · doi:10.3390/antiox13101158 · Cited by 57
Tumour hypoxia in driving genomic instability and tumour evolution
Suvac, A., Ashton, J., & Bristow, R. G. (2025) · Nature reviews. Cancer · doi:10.1038/s41568-024-00781-9 · Cited by 60
Metabolism and Signaling of Plant Mitochondria in Adaptation to Environmental Stresses
Barreto, P. L. M., Koltun, A., Nonato, J. V. A., Yassitepe, J. É. D. C. T., Maia, I. G., & Arruda, P. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231911176 · Cited by 54
Fleischer, J. R., Schmitt, A. M., Haas, G., Xu, X., Zeisberg, E. M., Bohnenberger, H., Küffer, S., Teuwen, L.-A. M. N., Karras, P. J., Beißbarth, T., et al. (2023) · Molecular Cancer · doi:10.1186/s12943-023-01713-1 · Cited by 55
Baik, A. H., Haribowo, A. G., Chen, X., Queliconi, B. B., Barrios, A. M., Garg, A., Maishan, M., Campos, A. R., Matthay, M. A., & Jain, I. H. (2023) · Molecular Cell · doi:10.1016/j.molcel.2023.02.013 · Cited by 57
Reactive oxygen species in tendon injury and repair
Kračun, D., Görlach, A., Snedeker, J. G., & Buschmann, J. (2025) · Redox Biology · doi:10.1016/j.redox.2025.103568 · Cited by 54
Oxidative stress and antioxidant therapeutic mechanisms
Liu, H. F., Jiao, Y., Wang, P., Chen, Y., Xu, M., Zhang, X., Zheng, X., & Yang, Z. (2025) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2025.108962 · Cited by 61
Tian, X., Yan, T., Liu, F., Liu, Q., Zhao, J., Xiong, H., & Jiang, S. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.991052 · Cited by 53
Gharib, E., & Robichaud, G. A. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25179463 · Cited by 55
Hippocampal neurons respond to brain activity with functional hypoxia
Butt, U. J., Steixner-Kumar, A. A., Depp, C., Sun, T., Hassouna, I. A., Wüstefeld, L., Arinrad, S., Zillmann, M. R., Schopf, N., Garcia‐Agudo, L. F., et al. (2021) · Molecular Psychiatry · doi:10.1038/s41380-020-00988-w · Cited by 53
Hypoxia Conditioning as a Promising Therapeutic Target in Parkinson's Disease?
Burtscher, J., Syed, M. M. K., Lashuel, H. A., & Millet, G. P. (2021) · Movement Disorders · doi:10.1002/mds.28544 · Cited by 53
Huang, M., Yang, L., Peng, X., Wei, S., Fan, Q., Yang, S., Li, X., Li, B., Jin, H., Wu, B., et al. (2020) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-020-01698-5 · Cited by 54
Common methods in mitochondrial research (Review)
Yin, Y., & Shen, H. (2022) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2022.5182 · Cited by 52
Identification of oleoylethanolamide as an endogenous ligand for HIF-3α
Diao, X., Ye, F., Zhang, M., Ren, X., Tian, X., Lu, J., Sun, X., Hou, Z., Chen, X., Li, F., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-30338-z · Cited by 51
Gene transcription and chromatin regulation in hypoxia
Batie, M., & Rocha, S. (2020) · Biochemical Society Transactions · doi:10.1042/bst20191106 · Cited by 52
Genetic diversity and selection of Tibetan sheep breeds revealed by whole-genome resequencing
Tian, D., Han, B., Li, X., Liu, D., Zhou, B., Zhao, C., Zhang, N., Wang, L., Pei, Q., & Zhao, K. (2023) · Animal Bioscience · doi:10.5713/ab.22.0432 · Cited by 51
Ghosh, M. C., Zhang, D., Ollivierre, W. H., Noguchi, A. C., Springer, D., Linehan, W. M., & Rouault, T. A. (2020) · Blood · doi:10.1182/blood.2020009138 · Cited by 54
Molecular Mechanisms Involved in Hypoxia-Induced Alterations in Bone Remodeling
Usategui‐Martín, R., Rigual, R. J., Ruiz‐Mambrilla, M., Fernández-Gómez, J. M., Dueñas, A., & Pérez‐Castrillón, J. L. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23063233 · Cited by 51
Tao, P., Lv, Z., Zheng, X.-K., Jiang, H., Liu, S., Wang, H., Wong, W., & Zhao, Q. (2022) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.2c02854 · Cited by 50
Arias, C., Sepúlveda, P., Castillo, R. L., & Salazar, L. A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24043073 · Cited by 53
Tumor Cells and Cancer-Associated Fibroblasts: An Updated Metabolic Perspective
Gentric, G., & Mechta‐Grigoriou, F. (2021) · Cancers · doi:10.3390/cancers13030399 · Cited by 52
Tang, Y., Hou, Y., Zeng, Y., Hu, Y., Zhang, Y., Wang, X., & Meng, X. (2021) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2021.174617 · Cited by 50
Li, J., Yang, P., Chen, F., Tan, Y., Huang, C., Shen, H., Peng, C., Feng, Y., & Sun, Y. (2021) · Clinical and Translational Medicine · doi:10.1002/ctm2.349 · Cited by 49
Hypoxia adaptation in the cornea: Current animal models and underlying mechanisms
Pang, K., Lennikov, A., & Yang, M. (2021) · Animal Models and Experimental Medicine · doi:10.1002/ame2.12192 · Cited by 49
Wang, D., Zhang, H., Liao, X., Li, J., Zeng, J., Wang, Y., Zhang, M., Ma, X., Wang, X., Ren, F., et al. (2024) · Journal of Nanobiotechnology · doi:10.1186/s12951-024-02663-6 · Cited by 49
Wang, X., Zhao, D. H., Xie, H., & Hu, Y. (2020) · Cancer Letters · doi:10.1016/j.canlet.2020.11.007 · Cited by 49
Tumor‐Homing Phage Nanofibers for Nanozyme‐Enhanced Targeted Breast Cancer Therapy
Yang, T., Zhang, Q., Miao, Y., Lyu, Y., Xu, Y., Yang, M., & Mao, C. (2024) · Advanced Materials · doi:10.1002/adma.202403756 · Cited by 49
Photosynthetic Microorganisms for the Oxygenation of Advanced 3D Bioprinted Tissues
Ortega, J. S., Corrales-Orovio, R., Ralph, P., Egaña, J. T., & Gentile, C. (2023) · Acta Biomaterialia · doi:10.1016/j.actbio.2022.05.009 · Cited by 47
Genetically Encoded ATP Biosensors for Direct Monitoring of Cellular ATP Dynamics
White, D., & Yang, Q. (2022) · Cells · doi:10.3390/cells11121920 · Cited by 48
Understanding the tumor microenvironment in head and neck squamous cell carcinoma
Sadeghirad, H., Shiravand, Y., Radfar, P., Ladwa, R., Perry, C., Han, X., Warkiani, M. E., Adams, M. N., Hughes, B. G. M., O'Byrne, K. J., et al. (2022) · Clinical & Translational Immunology · doi:10.1002/cti2.1397 · Cited by 52
Notch signaling, hypoxia, and cancer
Guo, M., Niu, Y., Xie, M., Liu, X., & Li, X. (2023) · Frontiers in Oncology · doi:10.3389/fonc.2023.1078768 · Cited by 48
Fang, K., Sun, M., Leng, Z., Chu, Y., Zhao, Z., Li, Z., Zhang, Y., Xu, A., Zhang, Z., Zhang, L., et al. (2023) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-023-02623-2 · Cited by 49
Wang, Z., & Yang, L. (2024) · Pharmacological Research · doi:10.1016/j.phrs.2024.107150 · Cited by 49
Chen, S., Liu, X., Zhang, W., Li, B., Liu, F., Zhang, Y., & Han, Y. (2025) · ACS Nano · doi:10.1021/acsnano.5c07535 · Cited by 49
USP5 promotes breast cancer cell proliferation and metastasis by stabilizing HIF2α
Huang, W., Liu, X., Zhang, Y., Deng, M., Li, G., Chen, G., Li, Y., Jin, L., Liu, T., Wang, Y., et al. (2022) · Journal of Cellular Physiology · doi:10.1002/jcp.30686 · Cited by 46
Microbiota-assisted iron uptake promotes immune tolerance in the intestine
Zhu, L., Li, G., Liang, Z., Qi, T., Deng, K., Yu, J., Peng, Y., Zheng, J., Song, Y., & Chang, X. (2023) · Nature Communications · doi:10.1038/s41467-023-38444-2 · Cited by 47
He, L., Wang, L., Yu, X., Tang, Y., Jiang, Z. L., Yang, G., Liu, Z., & Li, W. (2024) · Nature Communications · doi:10.1038/s41467-024-52607-9 · Cited by 50
Tajaldini, M., Saeedi, M., Amiriani, T., Amiriani, A., Sedighi, S., Zadeh, F. M., Dehghan, M. H., Jahanshahi, M., Zanjan, M. G., Khalili, P., et al. (2022) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2022.175087 · Cited by 46
Wang, Y.-J., Yang, B., Lai, Q., Shi, J., Peng, J., Zhang, Y., Hu, K., Li, Y., Peng, J.-W., Yang, Z.-Z., et al. (2020) · RNA Biology · doi:10.1080/15476286.2020.1804697 · Cited by 45
SIRT1/PGC-1α/PPAR-γ Correlate With Hypoxia-Induced Chemoresistance in Non-Small Cell Lung Cancer
Xu, R., Luo, X., Ye, X., Li, H., Liu, H., Du, Q., & Zhai, Q. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.682762 · Cited by 44
Regulation of chromatin accessibility by hypoxia and HIF
Batie, M., Frost, J., Shakir, D., & Rocha, S. (2022) · Biochemical Journal · doi:10.1042/bcj20220008 · Cited by 48
Wang, Y., Liu, X., Huang, W., Liang, J., & Chen, Y. (2022) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2022.108303 · Cited by 44
NADH Ties One-Carbon Metabolism to Cellular Respiration
Maynard, A. G., & Kanarek, N. (2020) · Cell Metabolism · doi:10.1016/j.cmet.2020.03.012 · Cited by 44
Resistance of Hypoxic Cells to Ionizing Radiation Is Mediated in Part via Hypoxia-Induced Quiescence
Menegakis, A., Klompmaker, R., Vennin, C., Arbusà, A., Damen, M. P. F., van den Broek, B., Zips, D., van Rheenen, J., Krenning, L., & Medema, R. H. (2021) · Cells · doi:10.3390/cells10030610 · Cited by 44
Mitochondrial Redox Metabolism: The Epicenter of Metabolism during Cancer Progression
Choudhury, F. K. (2021) · Antioxidants · doi:10.3390/antiox10111838 · Cited by 44
Xu, R., You, Y., Zheng, W., Ma, L., Chang, Y., Pan, S., He, Y., Zhou, M., Xu, Z., Chen, T., et al. (2024) · Advanced Functional Materials · doi:10.1002/adfm.202313122 · Cited by 43
Sun, Y., Xu, L., Liu, X., Shen, Y., Zhang, Y., Gu, N., & Xiong, F. (2021) · Chemical Engineering Journal · doi:10.1016/j.cej.2021.132303 · Cited by 43
Sartini, S., Massobrio, L., Cutuli, O., Campodonico, P., Bernini, C., Sartini, M., Cristina, M. L., Castellani, L., Ceschi, L., Spadaro, M., et al. (2021) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph182111534 · Cited by 42
Cuproptosis: Advances in Stimulus‐Responsive Nanomaterials for Cancer Therapy
Lu, J., Miao, Y., & Li, Y. (2024) · Advanced Healthcare Materials · doi:10.1002/adhm.202400652 · Cited by 42
Wang, S., Zhang, X., Chen, Q., Wu, H., Cao, S., Zhao, S., Li, G., Wang, J., Gong, Y., Wang, X., et al. (2024) · Journal of Advanced Research · doi:10.1016/j.jare.2024.12.026 · Cited by 42
Sukkar, S. G., & Bassetti, M. (2020) · Nutrition · doi:10.1016/j.nut.2020.110967 · Cited by 42
Macropinocytosis and Cancer: From Tumor Stress to Signaling Pathways
Lambies, G., & Commisso, C. (2022) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-3-030-94004-1_2 · Cited by 43
Metabolic Adaptation-Mediated Cancer Survival and Progression in Oxidative Stress
Tang, Y., Zhang, Z., Chen, Y., Qin, S., Zhou, L., Gao, W., & Shen, Z. (2022) · Antioxidants · doi:10.3390/antiox11071324 · Cited by 47
Cancer Metastasis‐on‐a‐Chip for Modeling Metastatic Cascade and Drug Screening
Brooks, A., Zhang, Y., Chen, J., & Zhao, C. (2024) · Advanced Healthcare Materials · doi:10.1002/adhm.202302436 · Cited by 41
Pecze, L., Randi, E. B., & Szabó, C. (2020) · Molecular Medicine · doi:10.1186/s10020-020-00225-8 · Cited by 43
Hypoxia in Cell Reprogramming and the Epigenetic Regulations
Nakamura, N., Shi, X., Darabi, R., & Li, Y. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.609984 · Cited by 41
Electrospun Fibers Improving Cellular Respiration via Mitochondrial Protection
Chen, W., Zheng, D., Chen, Y., Ruan, H., Zhang, Y., Chen, X., Shen, H., Deng, L., Cui, W., & Chen, H. (2021) · Small · doi:10.1002/smll.202104012 · Cited by 41
Tong, B., Liao, Z., Liu, H., Ke, W., Lei, C., Zhang, W., Liang, H., Wang, H., He, Y., Lei, J., et al. (2023) · ACS Nano · doi:10.1021/acsnano.2c10351 · Cited by 40
Naas, S., Schiffer, M., & Schödel, J. (2023) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00201.2023 · Cited by 46
Immunoregulatory orchestrations in osteoarthritis and mesenchymal stromal cells for therapy
Jiang, T., Su, S., Tian, R., Jiao, Y., Zheng, S., Liu, T., Yu, Y., Hua, P., Cao, X., Xing, Y., et al. (2025) · Journal of Orthopaedic Translation · doi:10.1016/j.jot.2025.08.009 · Cited by 40
Tackling cuproptosis: from metabolic rewiring to therapeutic exploitation in cancer
Hao, Q., Gan, Y., & Zhou, X. (2026) · Cellular and Molecular Immunology · doi:10.1038/s41423-026-01387-x · Cited by 43
Multimodal Functional Imaging for Cancer/Tumor Microenvironments Based on MRI, EPRI, and PET
Matsumoto, K., Mitchell, J. B., & Krishna, M. C. (2021) · Molecules · doi:10.3390/molecules26061614 · Cited by 40
Remodeling of the Lamina Cribrosa: Mechanisms and Potential Therapeutic Approaches for Glaucoma
Strickland, R. G., Garner, M. A., Gross, A. K., & Girkin, C. A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23158068 · Cited by 40
Molecular basis and clinical implications of HIFs in cardiovascular diseases
Hu, Y., Lu, H., Li, H., & Ge, J. (2022) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2022.09.004 · Cited by 42
Metadata
- Authors
- Lee, P., Chandel, N. S., & Simon, M. C.
- Affiliations
- University of Pennsylvania (US)
- Northwestern University (US)
- Corresponding author
- Lee, Pearl
- Chandel, Navdeep S.
- Simon, M. Celeste
- Venue
- Nature Reviews Molecular Cell Biology
- Published
- 2020-03-06
- Volume
- 21
- Issue
- 5
- Pages
- 268-283
- ISSN
- 1471-0072 (ISSN-L)
- 1471-0080
- PMC
- PMC7222024
- OpenAlex
- W3009721059
- Cited by
- 1,272
- References
- 233
- Citations by year
- 2026: 207 · 2025: 275 · 2024: 209 · 2023: 201 · 2022: 186 · 2021: 137 · 2020: 55
- FWCI
- 14.94
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature Reviews Molecular Cell Biology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Cancer Institute (F32CA217185, P01CA104838, R35CA197532, R01CA158301, R35CA220483)
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (T32AR053461)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Hypoxia, and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Health Sciences › Medicine › Hematology › Erythropoietin and Anemia Treatment
- Keywords
- hypoxia, hypoxia-inducible factor, cellular adaptation, oxygen sensing, energy metabolism, glycolysis, angiogenesis, reactive oxygen species, mitochondrial respiration, nutrient uptake, protein synthesis, cancer, cardiovascular disease, inflammation, wound healing, transcriptional response
- MeSH terms
- Adenosine Triphosphate, Energy Metabolism, Humans, Mitochondria, Oxygen, Signal Transduction, Cell Hypoxia, Reactive Oxygen Species, Oxidative Stress
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