The DOI matches its Crossref record; 71 of the 71 references it cites were found in a registry or an index.
Oxygen, a source of life and stress
Abstract
Oxygen is an essential element in the survival of complex organisms, however the level of oxygen, low or high, can be a source of stress depending on the biological context. Low levels of oxygen in tissues (hypoxia) can be the consequence of a number of pathophysiological conditions including ischemic disorders and cancer while relative, higher levels (hyperoxia) can lead to retinopathy of prematurity. The local oxygen environment and oxygen consumption dictate vascular homeostasis, vaso‐proliferation and vaso‐cessation, which is deregulated in these diseases through oxygen‐dependent growth factors. In this review, we will introduce aspects of the physiology and biology of oxygen partial pressure and the molecular mechanisms implicated in oxygen sensing. We will outline the regulation and function of the key operator in cellular signalling of hypoxia, the transcription factor, hypoxia‐inducible factor. In addition, we will focus on cancer cell hypoxia and on its role in driving cell metabolism, pH regulation and survival.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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
“A master regulator of hypoxia and oxygen homeostasis is HIF-1 (26,27).”
From Adipose tissue remodeling and obesity (2011) · cites this paper as [27]
Citations
Cites
Targeting HIF-1 for cancer therapy
Semenza, G. L. (2003) · Nature Reviews Cancer · doi:10.1038/nrc1187 · Cited by 6,717
Why Do Cancers Have High Aerobic Glycolysis?
Gatenby, R. A., & Gillies, R. J. (2004) · Nature reviews. Cancer · doi:10.1038/nrc1478 · Cited by 4,784
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
Angiogenesis as a therapeutic target
Ferrara, N., & Kerbel, R. S. (2005) · Nature · doi:10.1038/nature04483 · Cited by 2,653
HIF-1 mediates adaptation to hypoxia by actively downregulating mitochondrial oxygen consumption
Papandreou, I., Cairns, R. A., Fontana, L., Lim, A. L., & Denko, N. C. (2006) · Cell Metabolism · doi:10.1016/j.cmet.2006.01.012 · Cited by 2,267
TIGAR, a p53-Inducible Regulator of Glycolysis and Apoptosis
Bensaad, K., Tsuruta, A., Selak, M. A., Vidal, M. N. C., Nakano, K., Bartrons, R., Gottlieb, E., & Vousden, K. H. (2006) · Cell · doi:10.1016/j.cell.2006.05.036 · Cited by 2,019
Ras, PI(3)K and mTOR signalling controls tumour cell growth
Shaw, R. J., & Cantley, L. C. (2006) · Nature · doi:10.1038/nature04869 · Cited by 2,019
Hypoxia signalling in cancer and approaches to enforce tumour regression
Pouysségur, J., Dayan, F., & Mazure, N. M. (2006) · Nature · doi:10.1038/nature04871 · Cited by 1,676
Self-citationp53 Regulates Mitochondrial Respiration
Matoba, S., Kang, J.-G., Patino, W. D., Wragg, A., Boehm, M., Gavrilova, O., Hurley, P. J., Bunz, F., & Hwang, P. M. (2006) · Science · doi:10.1126/science.1126863 · Cited by 1,650
Fantin, V. R., St-Pierre, J., & Leder, P. (2006) · Cancer Cell · doi:10.1016/j.ccr.2006.04.023 · Cited by 1,635
Flagged first, then by citations
Research works printed but not linked: 1
- 2001 John Wiley & Sons Ltd J. Pouyssegur A. Franchi G. Pages Novartis Found Symposium 186 196
Cited by
Sorted by citations
Items 201–300 of 380
Potential therapeutic applications of medical gases in cancer treatment
Bazzal, A. A., Hoteit, B. H., Chokor, M., Safawi, A., Zibara, Z., Rizk, F., Kawssan, A., Danaf, N., Msheik, L. B., & Hamdar, H. (2025) · Medical Gas Research · doi:10.4103/mgr.medgasres-d-24-00089 · Cited by 18
Dutour, A., Pasello, M., Farrow, L., Amer, M. H., Entz‐Werlé, N., Nathrath, M., Scotlandi, K., Mittnacht, S., & Gomez‐Brouchet, A. (2025) · Cancer and Metastasis Reviews · doi:10.1007/s10555-025-10257-3 · Cited by 21
Oxygen concentration modulates colibactin production
Bossuet‐Greif, N., Guyonnet, C., Chagneau, C. V., Tang-Fichaux, M., Pénary, M., Loubet, D., Branchu, P., Oswald, É., & Nougayrède, J. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2222437 · Cited by 21
Said, H. M. (1994) · Oncology Reports · doi:10.3892/or_00000023 · Cited by 18
Role of the HBx oncoprotein in carbonic anhydrase 9 induction
Holotnakova, T., Tylková, L., Takáčová, M., Kopáček, J., Petrík, J., Pastoreková, S., & Pastorek, J. (2009) · Journal of Medical Virology · doi:10.1002/jmv.21671 · Cited by 18
Cytoprotective effects of endothelin‐1 on mesenchymal stem cells: an in vitro study
Pourjafar, M., Saidijam, M., Mansouri, K., Malih, S., Nejad, T. R., Shabab, N., & Najafi, R. (2016) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/1440-1681.12590 · Cited by 18
Zhang, S., Ren, J.-Y., & Yang, B. (2021) · World Journal of Stem Cells · doi:10.4252/wjsc.v13.i11.1625 · Cited by 19
Hypoxia induced phosphorylation of estrogen receptor at serine 118 in the absence of ligand
Park, J., & Lee, Y. (2017) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2017.08.013 · Cited by 17
Hydroxylation of the NOTCH1 intracellular domain regulates Notch signaling dynamics
Ferrante, F., Giaimo, B. D., Friedrich, T., Sugino, T., Mertens, D., Kugler, S. J., Gahr, B. M., Just, S., Pan, L., Bartkuhn, M., et al. (2022) · Cell Death and Disease · doi:10.1038/s41419-022-05052-9 · Cited by 17
Trauma-Hemorrhage and Hypoxia Differentially Influence Kupffer Cell Phagocytic Capacity
Hsieh, C.-H., Nickel, E. A., Hsu, J.-T., Schwacha, M. G., Bland, K. I., & Chaudry, I. H. (2009) · Annals of Surgery · doi:10.1097/sla.0b013e3181b0ebf8 · Cited by 17
CXCR3: Latest evidence for the involvement of chemokine signaling in bone cancer pain
Guo, G., & Gao, F. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.02.003 · Cited by 17
Direct phosphorylation events involved in HIF-α regulation: the role of GSK-3β
Mennerich, D., Dimova, E. Y., & Kietzmann, T. (2014) · Hypoxia · doi:10.2147/hp.s60703 · Cited by 17
Weighing the Risk: effects of Obesity on the Mammary Gland and Breast Cancer Risk
Hillers‐Ziemer, L. E., & Arendt, L. M. (2020) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1007/s10911-020-09452-5 · Cited by 18
Development of the 99mTc-Hydroxamamide Complex as a Probe Targeting Carbonic Anhydrase IX
Iikuni, S., Tanimura, K., Watanabe, H., Shimizu, Y., Saji, H., & Ono, M. (2019) · Molecular Pharmaceutics · doi:10.1021/acs.molpharmaceut.8b01120 · Cited by 16
Lee, H. H., & Cho, H. (2022) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.2201.01010 · Cited by 16
Burr, R., & Espenshade, P. J. (2017) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2017.08.043 · Cited by 16
No effect of acute normobaric hypoxia on plasma triglyceride levels in fasting healthy men
Mahat, B., Chassé, É., Lindon, C., Mauger, J., & Imbeault, P. (2018) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2017-0505 · Cited by 16
The Role of Macrophage Migration Inhibitory Factor in Adipose-Derived Stem Cells Under Hypoxia
Hofmann, E., Soppert, J., Ruhl, T., Gousopoulos, E., Gerra, S., Storti, G., Tian, Y., Brandhofer, M., Schweizer, R., Song, S. Y., et al. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.638448 · Cited by 15
Sun, B., Long, Y., Xu, G., Chen, J., Wu, G., Liu, B., & Gao, Y. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1534009 · Cited by 15
Yang, W., Luo, C., Lai, L., & Ouyang, Q. (2015) · Biomicrofluidics · doi:10.1063/1.4929406 · Cited by 15
Hepatocyte growth factor and interferon‐γ inducible protein‐10 are related to visceral adiposity
Faber, D. R., van der Graaf, Y., Westerink, J., Kanhai, D. A., Monajemi, H., Visseren, F. L. J., & on behalf of the SMART study Group (2013) · European Journal of Clinical Investigation · doi:10.1111/eci.12054 · Cited by 15
Bisht, G., Zaidi, M. G. H., & Rayamajhi, S. (2017) · International Journal of Polymeric Materials · doi:10.1080/00914037.2016.1263949 · Cited by 15
Nano/Microcarriers in Drug Delivery: Moving the Timeline to Contemporary
Vujačić, A., & Novaković, J. G. (2022) · Current Medicinal Chemistry · doi:10.2174/0929867329666220821193938 · Cited by 16
Oxygen Sensing, Cardiac Ischemia, HIF-1α and Some Emerging Concepts
Goswami, S. K., & Das, D. K. (2010) · Current Cardiology Reviews · doi:10.2174/157340310793566136 · Cited by 15
A mRNA-Responsive G-Quadruplex-Based Drug Release System
Yaku, H., Murashima, T., Miyoshi, D., & Sugimoto, N. (2015) · Sensors · doi:10.3390/s150409388 · Cited by 15
Role of proton pumps in tumorigenesis
Kobliakov, V. A. (2017) · Biochemistry (Moscow) · doi:10.1134/s0006297917040010 · Cited by 15
Cullberg, K. B., Foldager, C. B., Lind, M., Richelsen, B., & Pedersen, S. B. (2014) · Journal of Functional Foods · doi:10.1016/j.jff.2014.02.015 · Cited by 14
Oxygen – the forgotten nutrient
Trayhurn, P. (2017) · Journal of Nutritional Science · doi:10.1017/jns.2017.53 · Cited by 14
YANG, C.-Q., XU, J.-H., YAN, D.-D., LIU, B.-L., LIU, K., & HUANG, F. (2017) · Chinese Journal of Natural Medicines · doi:10.1016/s1875-5364(17)30095-x · Cited by 14
Muscle Stem Cell Microenvironment and Functions in Muscle Regeneration
Li, W., Chen, M., & Zhang, L. (2025) · Biomolecules · doi:10.3390/biom15060765 · Cited by 13
Oxygen in Metabolic Dysfunction and Its Therapeutic Relevance
López-Pascual, A., Trayhurn, P., Martínez, J. A., & González‐Muniesa, P. (2021) · Antioxidants and Redox Signaling · doi:10.1089/ars.2019.7901 · Cited by 14
Metabolic Dialogue Shapes Immune Response in the Tumor Microenvironment
Gao, F., Shah, R., Xin, G., & Wang, R. (2025) · European Journal of Immunology · doi:10.1002/eji.202451102 · Cited by 15
Nakata, E., Hirose, H., Gerelbaatar, K., Arafiles, J. V. V., Zhang, Z., Futaki, S., & Morii, T. (2021) · Chemical Science · doi:10.1039/d1sc01575c · Cited by 13
Ahn, N., & Kim, K. (2014) · Physical Activity and Nutrition · doi:10.5717/jenb.2014.18.3.311 · Cited by 13
Ueda, M., Ogawa, K., Miyano, A., Ono, M., Kizaka‐Kondoh, S., & Saji, H. (2013) · Molecular Imaging and Biology · doi:10.1007/s11307-013-0647-6 · Cited by 13
Inflammatory response to acute hypoxia in humans
Burki, N. K., & Tetenta, S. (2013) · Pulmonary Pharmacology & Therapeutics · doi:10.1016/j.pupt.2013.05.008 · Cited by 13
Gilani, K., & Vafakhah, M. (2010) · Archives of Advances in Biosciences · doi:10.22037/jps.v1i2.1616 · Cited by 13
Acidity of Microenvironment as a Further Driver of Tumor Metabolic Reprogramming
Peppicelli, S., Andreucci, E., Ruzzolini, J., Margheri, F., Laurenzana, A., Bianchini, F., & Calorini, L. (2017) · Journal of Clinical & Cellular Immunology · doi:10.4172/2155-9899.1000485 · Cited by 13
Wang, S., Gusenoff, J. A., Rubin, J. P., & Kokai, L. E. (2019) · Plastic & Reconstructive Surgery Global Open · doi:10.1097/gox.0000000000002275 · Cited by 13
Cell Shape and Cardiosphere Differentiation: A Revelation by Proteomic Profiling
Kawaguchi, N., Machida, M., Hatta, K., Nakanishi, T., & Takagaki, Y. (2013) · Biochemistry Research International · doi:10.1155/2013/730874 · Cited by 12
Devaux, J. B. L., Hedges, C. P., Birch, N. P., Herbert, N. A., Renshaw, G. M. C., & Hickey, A. J. (2023) · Journal of Comparative Physiology B · doi:10.1007/s00360-023-01495-4 · Cited by 12
Rapid effects of hypoxia on H+ homeostasis in articular chondrocytes
Gibson, J. S., McCartney, D., Sumpter, J., Fairfax, T. P. A., Milner, P., Edwards, H. L., & Wilkins, R. J. (2009) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-009-0695-6 · Cited by 12
Study of Tumor Growth under Hyperthermia Condition
Zhu, Q., Zhang, A., Liu, P., & Xu, L. X. (2012) · Computational and Mathematical Methods in Medicine · doi:10.1155/2012/198145 · Cited by 12
Radioprotective Activity and Preliminary Mechanisms of N-oxalyl-d-phenylalanine (NOFD) In Vitro
Meng, Y., Yang, F., Long, W., & Xu, W. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms20010037 · Cited by 12
Li, Y., Zhong, W., & Tang, X. (2021) · Stem Cells International · doi:10.1155/2021/9929128 · Cited by 12
Wang, T., Meng, J., Li, L., & Zhang, G. (2016) · PLoS ONE · doi:10.1371/journal.pone.0166057 · Cited by 12
HIF-1α Pathway in COVID-19: A Scoping Review of Its Modulation and Related Treatments
da Silva, F. P. G., Matte, R., Wiedmer, D. B., da Silva, A. P. G., Menin, R. M., Barbosa, F. B., Meneguzzi, T. A. M., Pereira, S. B., Fausto, A. T., Klug, L., et al. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26094202 · Cited by 11
Bath, C. (2013) · Acta Ophthalmologica · doi:10.1111/aos.12157 · Cited by 11
Jara, N., Ramírez, E., Ferrada, L., Salazar, K., Espinoza, F., González‐Chavarría, I., & Nualart, F. (2021) · Journal of Cellular Physiology · doi:10.1002/jcp.30264 · Cited by 11
Oxidative Stress and Drug Resistance in Cancer
Trachootham, D., Zhang, W., & Huang, P. (2009) · Springer eBooks · doi:10.1007/978-0-387-89445-4_7 · Cited by 12
Prenatal stress, anxiety and depression: a mechanism involving CRH peptide family.
Fan, J., Chen, X., & Du, J.-Z. (2014) · PubMed · Cited by 11
Hypoxia in Mesenchymal Stem Cell
Widowati, W., Rihibiha, D. D., Khiong, K., Widodo, M. A., Sumitro, S. B., & Bachtiar, I. (2017) · InTech eBooks · doi:10.5772/65510 · Cited by 11
The Influence of Winter Swimming on Oxidative Stress Indicators in the Blood of Healthy Males
Wesołowski, R., Mila-Kierzenkowska, C., Pawłowska, M., Szewczyk‐Golec, K., Saletnik, Ł., Sutkowy, P., & Woźniak, A. (2023) · Metabolites · doi:10.3390/metabo13020143 · Cited by 10
Mekki, M. S., Mougel, A., Vinchent, A., Paquet, C., Copin, M., Leroy, C., Kherrouche, Z., Bonte, J., Melnyk, O., Vicogne, J., et al. (2018) · Oncotarget · doi:10.18632/oncotarget.25472 · Cited by 10
Younes, N., Mohamed, O., & Rizk, N. M. (2022) · Nutrients · doi:10.3390/nu14214600 · Cited by 12
Optical oxygen sensing with quantum dot conjugates
Lemon, C. M. (2018) · Pure and Applied Chemistry · doi:10.1515/pac-2018-0303 · Cited by 10
Iikuni, S., Watanabe, H., Shimizu, Y., Nakamoto, Y., & Ono, M. (2020) · PLoS ONE · doi:10.1371/journal.pone.0243327 · Cited by 9
Reyal, J. (2009) · Medical Hypotheses · doi:10.1016/j.mehy.2009.09.002 · Cited by 9
Memetimin, H., Izumi, Y., Nakayama, Y., Kohda, Y., Inoue, H., Nonoguchi, H., & Tomita, K. (2009) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.90520.2008 · Cited by 9
Bourguignon, M., Yaghi, L., Flajollet, S., Krawice-Radanne, I., Rouas‐Freiss, N., Lugrin, D., Richalet, J., Carosella, E. D., & Moreau, P. (2010) · Human Immunology · doi:10.1016/j.humimm.2010.08.011 · Cited by 9
Cao, Y., Ma, W., Ji, W., Yu, P., Wu, F., Wu, H., & Mao, L. (2019) · ACS Applied Bio Materials · doi:10.1021/acsabm.9b00100 · Cited by 9
Hypoxia drives HIF2-dependent reversible macrophage cell cycle entry
Meng, B., Zhao, N., Mlčochová, P., Ferreira, I. A. T. M., Ortmann, B. M., Davis, T., Wit, N., Rehwinkel, J., Cook, S. J., Maxwell, P. H., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114471 · Cited by 8
Pumklin, J., Bhalang, K., & Pavasant, P. (2016) · Odontology · doi:10.1007/s10266-015-0223-4 · Cited by 8
Wetzel, G., Relja, B., Klarner, A., Henrich, D. M., Dehne, N., Brühne, B., Lehnert, M., & Marzi, İ. (2014) · Mediators of Inflammation · doi:10.1155/2014/930419 · Cited by 8
Jagannathan, L., Jose, C. C., Arita, A., Kluz, T., Sun, H., Zhang, X., Yao, Y., Kartashov, A. V., Barski, A., Costa, M., et al. (2015) · Journal of Cellular Physiology · doi:10.1002/jcp.25262 · Cited by 8
Hypoxia Regulation of Stem Cell
Liu, Y., Tsai, A., Yuan, X., Li, Y., & Ma, T. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-802734-9.00018-4 · Cited by 8
Distinct hypoxic regulation of preadipocyte factor-1 (Pref-1) in preadipocytes and mature adipocytes
Moon, Y., Lee, S., Park, B., & Park, H. (2017) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2017.11.008 · Cited by 8
Liu, R., Zhang, S., Ren, G., Jin, P., Zeng, H., Yin, Y., Wang, T., Zhang, M., & Mao, L. (2025) · Angewandte Chemie International Edition · doi:10.1002/anie.202501901 · Cited by 7
In vitro/In vivo oxygen electrochemical nanosensor for bioanalysis
Vaneev, A. N., Gorelkin, P. V., Akasov, R., Timoshenko, R. V., Lopatukhina, E. V., Garanina, A. S., Abakumova, T. O., Aleksandrin, V., Salikhov, S. V., Edwards, C. R. W., et al. (2024) · Journal of Electroanalytical Chemistry · doi:10.1016/j.jelechem.2024.118796 · Cited by 7
Effect of oxygen levels in cellular activity
Figueiredo, S. M., Sousa, F. O. C., Lopes, M., Quinta-Ferreira, R. M., & Quinta-Ferreira, M. E. (2020) · Energy Reports · doi:10.1016/j.egyr.2020.11.145 · Cited by 7
Tarhan, D., & Dursun, Ş. (2022) · Journal of Trace Elements in Medicine and Biology · doi:10.1016/j.jtemb.2022.126951 · Cited by 7
Bolli, R., Dasari, C., Arshia, A., Devadoss, D., Guo, Y., Ashraf, U., & Li, Q. (2021) · Stem Cell Reviews and Reports · doi:10.1007/s12015-020-10106-6 · Cited by 7
Molecular Design of pH-Responsive Helix Peptides That Can Damage Tumor Cells Selectively
Sakurai, H., Nishimura, K., Yamamoto, S., Maruyama, T., & Tamura, A. (2021) · ACS Applied Bio Materials · doi:10.1021/acsabm.0c01407 · Cited by 7
Where in the Tissues of Danio rerio Is More H 2 O 2 Produced During Acute Hypoxia?
Sergeeva, A. D., Panova, A. S., Ivanova, A. D., Khramova, Y. V., Morozova, K. I., Kotova, D. A., Guryleva, A. V., Хохлов, Д. Д., Kelmanson, I. V., Vasilev, A. V., et al. (2024) · Antioxidants and Redox Signaling · doi:10.1089/ars.2024.0563 · Cited by 7
The Use of Patient-Derived Organoids in the Study of Molecular Metabolic Adaptation in Breast Cancer
Glibetić, N., Bowman, S., Skaggs, T., & Weichhaus, M. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms251910503 · Cited by 6
Primary cilia as antennas for oxygen
Schneider, P., Fandrey, J., & Leu, T. (2024) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00298.2024 · Cited by 6
Xiao, W., Sun, G., Fan, T., Liu, J., Zhang, N., Zhao, L., & Zhong, R. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20246308 · Cited by 6
Block of Voltage-Gated Sodium Channels as a Potential Novel Anti-cancer Mechanism of TIC10
Fuchs, E., Messerer, D. A. C., Karpel‐Massler, G., Fauler, M., Zimmer, T., Jungwirth, B., & Föhr, K. J. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.737637 · Cited by 6
Padmini, E., Parasuraman, P., & Tharani, J. (2016) · Fish Physiology and Biochemistry · doi:10.1007/s10695-015-0185-z · Cited by 6
The role of tissue oxygenation in obesity-related cardiometabolic complications
Li, G., Meex, R. C. R., & Goossens, G. H. (2024) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-024-09910-z · Cited by 5
Papel del adipocito en la expresión del factor inducible por hipoxia (HIF) asociado a la obesidad
Reyes, H. J. N., Cortés, P., Cruz, A. G., Ugalde, M. C. N., Pizaña-Venegas, A., Jimenez, C. H., & RoblesI, R. R. (2011) · NCT Neumología y Cirugía de Tórax · Cited by 5
Adipose Stem Cells: From Liposuction to Adipose Tissue Engineering
Yoshimura, K., Eto, H., D, H. K. M., Doi, K., & Suga, H. (2011) · Springer eBooks · doi:10.1007/978-3-642-20012-0_7 · Cited by 5
Kalinina, S., & Rück, A. C. (2016) · Photonics and Lasers in Medicine · doi:10.1515/plm-2016-0026 · Cited by 5
Tsiapalis, D., Ribeiro, S., Pieri, A. D., Sallent, I., Guillaumin, S., Gaspar, D., Korntner, S. H., Bayon, Y., Gomes, M. E., Reis, R. L., et al. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.11140-7 · Cited by 6
Hypoxia Preconditioning of Bone Marrow Mesenchymal Stem Cells Before Implantation in Orthopaedics
Tsiapalis, D., & Zeugolis, D. I. (2019) · Journal of the American Academy of Orthopaedic Surgeons · doi:10.5435/jaaos-d-19-00044 · Cited by 5
Organics Modified Mesoporous Silica for Controlled Drug Delivery Systems
Fu, J., Zhao, Y., Zhu, Y., & Chen, F. (2013) · Wiley eBooks · doi:10.1002/9781118644591.ch7 · Cited by 5
Zhou, N., Zheng, W., Peng, L., Gao, S., Shi, Y., Cao, M., Xu, Y., Sun, B., & Li, X. (2023) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgad710 · Cited by 4
Coupling of the energetic and purinergic activities of ATP in ischemic and hypoxic disease states
Ehringer, W. D., & Smith, K. H. (2025) · Biosystems · doi:10.1016/j.biosystems.2025.105544 · Cited by 4
Michalak, K. P., & Nawrocka-Bogusz, H. (2011) · Journal of Physics Conference Series · doi:10.1088/1742-6596/329/1/012024 · Cited by 4
Tardelli, L. P., Breda, L., Marques, L. F., Lima, N. C. G. C., Camargo, T. F., Scherer, B. R., Moreira, N. F., Dias, J. F., Dalia, R. A., Thomazini, B. F., et al. (2018) · Journal of Nutrition & Intermediary Metabolism · doi:10.1016/j.jnim.2018.08.003 · Cited by 4
Rashid, I., Baisvar, V. S., Singh, M., Srivastava, P., Kumar, R., Kushwaha, B., & Pathak, A. K. (2019) · Molecular Biology Reports · doi:10.1007/s11033-019-04617-w · Cited by 4
Passive and Active Targeting for Solid Tumors
More, M. P., Deshmukh, P. K., Patil, P. O., Nangare, S., Tade, R. S., Patil, A., Pandey, A. P., Mutalik, S., Patil, P. B., Khan, Z. G., et al. (2022) · Environmental chemistry for a sustainable world · doi:10.1007/978-3-031-14848-4_5 · Cited by 4
Impact of the hypoxic microenvironment on spermatogonial stem cells in culture
Gille, A., Givelet, M., Pehlic, D., Lapoujade, C., Lassalle, B., Barroca, V., Bemelmans, A., Borderie, D., Moison, D., Livera, G., et al. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1293068 · Cited by 4
Loncaric, D., Stanković, B., Ghousein, A., Vreća, M., Spasovski, V., Villacreces, A., Debeissat, C., Grosset, C. F., Ivanović, Z., & Pavlović, S. (2019) · Archives of Biological Sciences · doi:10.2298/abs181117001l · Cited by 4
The effect of platinum nanoparticles on the physicochemical properties of daunorubicin
Zakrzewski, M., Bełdzińska, P., Gajdowska, F., Gołuński, G., Gackowska, K., Strankowska, J., Jamrógiewicz, M., Wyrzykowski, D., Grzyb, K., Gutowska‐Owsiak, D., et al. (2025) · RSC Advances · doi:10.1039/d5ra02827b · Cited by 3
Nanomodulation and nanotherapeutics of tumor-microenvironment
Dubey, R., Garg, S. S., & Gupta, J. (2022) · OpenNano · doi:10.1016/j.onano.2022.100099 · Cited by 3
Nakata, E., Gerelbaatar, K., Asif, M., Konishi, H., Shibano, Y., Lin, P., & Morii, T. (2023) · Chemistry · doi:10.3390/chemistry5030125 · Cited by 3
Correlated oxygen-sensing PLIM, cell metabolism FLIM and applications
Rück, A., Kalinina, S., Schäfer, P., von Einem, B., & Arnim, C. A. F. V. (2017) · Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE · doi:10.1117/12.2253714 · Cited by 3
Targeting the Tumor Microenvironment in Osteosarcoma: A Pathway to Overcome Therapeutic Resistance
Pandi, K., Cheriyan, B. V., Sooriyaprakash, R., Sakthivel, P., & Thirupathi, R. (2024) · Biomedical & Pharmacology Journal · doi:10.13005/bpj/3022 · Cited by 3
A Multichamber Gas System to Examine the Effect of Multiple Oxygen Conditions on Cell Culture
Khoury, S., Khalil, T. H., Palzur, E., & Srouji, S. (2020) · Tissue Engineering Part C Methods · doi:10.1089/ten.tec.2020.0288 · Cited by 3
Metadata
- Authors
- Brahimi-Horn, M. C., & Pouysségur, J.
- Affiliations
- Centre National de la Recherche Scientifique (FR)
- Corresponding author
- Brahimi-Horn, M. Christiane
- ORCID
- Pouysségur, Jacques
- Venue
- FEBS Letters
- Publisher
- Wiley
- Published
- 2007-06-19
- Volume
- 581
- Issue
- 19
- Pages
- 3582-3591
- ISSN
- 0014-5793 (ISSN-L)
- 1873-3468
- OpenAlex
- W1983199304
- Cited by
- 383
- References
- 71
- Citations by year
- 2026: 3 · 2025: 12 · 2024: 14 · 2023: 14 · 2022: 16 · 2021: 23 · 2020: 20 · 2019: 28 · 2018: 20 · 2017: 26 · 2016: 22 · 2015: 18 · 2014: 24 · 2013: 37 · 2012: 13
- FWCI
- 1.88
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- FEBS Letters (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Funders
- Institut National de la Santé et de la Recherche Médicale
- Centre National de la Recherche Scientifique
- 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
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Angiogenesis and VEGF in Cancer
- Keywords
- oxygen, hypoxia, hyperoxia, hypoxia-inducible factor, oxygen sensing, oxygen partial pressure, cellular metabolism, pH control, retinopathy of prematurity, ischemic disorders, vascular homeostasis
- MeSH terms
- Acidosis, Hypoxia, Glucose, Humans, Neoplasms, Oxygen, Partial Pressure, Signal Transduction, Heat-Shock Response, Hypoxia-Inducible Factor 1
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