The DOI matches its Crossref record; 71 of the 71 references it cites were found in a registry or an index.
Genetic Screen for Cell Fitness in High or Low Oxygen Highlights Mitochondrial and Lipid Metabolism
Open accessAbstract
Human cells are able to sense and adapt to variations in oxygen levels. Historically, much research in this field has focused on hypoxia-inducible factor (HIF) signaling and reactive oxygen species (ROS). Here, we perform genome-wide CRISPR growth screens at 21%, 5%, and 1% oxygen to systematically identify gene knockouts with relative fitness defects in high oxygen (213 genes) or low oxygen (109 genes), most without known connection to HIF or ROS. Knockouts of many mitochondrial pathways thought to be essential, including complex I and enzymes in Fe-S biosynthesis, grow relatively well at low oxygen and thus are buffered by hypoxia. In contrast, in certain cell types, knockout of lipid biosynthetic and peroxisomal genes causes fitness defects only in low oxygen. Our resource nominates genetic diseases whose severity may be modulated by oxygen and links hundreds of genes to oxygen homeostasis.
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
“Many autophagy-related genes were also common hits in the two screens (Fig. 2 d,e), such as WIPI2, ATG9A, ATG13, ATG14, and BECN1, suggesting an important role of autophagy in maintaining redox homeostasis in cells, as reported in previous studies31–33.”
From Genome-wide CRISPRi/a screens in human neurons link lysosomal failure to ferroptosis (2021) · cites this paper as [33]
In the citing paper
“Many autophagy-related genes were also common hits in the two screens (Fig. 2 d,e), such as WIPI2, ATG9A, ATG13, ATG14, and BECN1, suggesting an important role of autophagy in maintaining redox homeostasis in cells, as reported in previous studies31–33.”
From Genome-wide CRISPRi/a screens in human neurons link lysosomal failure to ferroptosis (2021) · cites this paper as [33]
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
Subramanian, A., Tamayo, P., Mootha, V. K., Mukherjee, S., Ebert, B. L., Gillette, M. A., Paulovich, A., Pomeroy, S. L., Golub, T. R., Lander, E. S., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0506580102 · Cited by 53,625
Self-citationTrapnell, C., Roberts, A., Goff, L. A., Pertea, G. M., Kim, D., Kelley, D. R., Pimentel, H., Salzberg, S. L., Rinn, J. L., & Pachter, L. S. (2012) · Nature Protocols · doi:10.1038/nprot.2012.016 · Cited by 12,145
KEGG as a reference resource for gene and protein annotation
Kanehisa, M., Sato, Y., Kawashima, M., Furumichi, M., & Tanabe, M. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkv1070 · Cited by 7,387
Full-length RNA-seq from single cells using Smart-seq2
Picelli, S., Faridani, O. R., Björklund, Å. K., Winberg, G., Sagasser, S., & Sandberg, R. (2014) · Nature Protocols · doi:10.1038/nprot.2014.006 · Cited by 4,137
Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders
Hamosh, A. (2004) · Nucleic Acids Research · doi:10.1093/nar/gki033 · Cited by 3,443
Defining a Cancer Dependency Map
Tsherniak, A., Vazquez, F., Montgomery, P. G., Weir, B. A., Kryukov, G., Cowley, G. S., Gill, S., Harrington, W. F., Pantel, S., Krill-Burger, J. M., et al. (2017) · Cell · doi:10.1016/j.cell.2017.06.010 · Cited by 3,276
Li, W., Xu, H., Xiao, T., Cong, L., Love, M. I., Zhang, F., Irizarry, R. A., Liu, J. S., Brown, M., & Liu, X. S. (2014) · Genome Biology · doi:10.1186/s13059-014-0554-4 · Cited by 2,684
Meyers, R. M., Bryan, J. G., McFarland, J. M., Weir, B. A., Sizemore, A. E., Xu, H., Dharia, N. V., Montgomery, P. G., Cowley, G. S., Pantel, S., et al. (2017) · Nature Genetics · doi:10.1038/ng.3984 · Cited by 1,952
Mi, H., Muruganujan, A., & Thomas, P. D. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks1118 · Cited by 1,739
Sequencing of 50 Human Exomes Reveals Adaptation to High Altitude
Yi, X., Liang, Y., Huerta-Sanchez, E., Jin, X., Cuo, Z. X. P., Pool, J. E., Xu, X., Jiang, H., Vinckenbosch, N., Korneliussen, T. S., et al. (2010) · Science · doi:10.1126/science.1190371 · Cited by 1,611 · cited 1×
“These studies have identified polymorphisms in the canonical vHL-PHD-HIF O2 sensing pathways (Beall et al., 2010; Peng et al., 2011; Simonson et al., 2010; Xu et al., 2011; Yang et al., 2017; Yi et al., 2010), representing the most rapid known example of recent natural selection.”
Cited by
Sorted by citations
Oughtred, R., Rust, J., Chang, C., Breitkreutz, B., Stark, C., Willems, A., Boucher, L., Leung, G., Kolas, N., Zhang, F., et al. (2021) · Protein Science · doi:10.1002/pro.3978 · Cited by 1,858
Metabolic determinants of cancer cell sensitivity to canonical ferroptosis inducers
Soula, M., Weber, R. A., Zilka, O., Alwaseem, H., La, K., Yen, F. S., Molina, H., García‐Bermúdez, J., Pratt, D. A., & Birsoy, K. (2020) · Nature Chemical Biology · doi:10.1038/s41589-020-0613-y · Cited by 774
Bock, C., Datlinger, P., Chardon, F. M., Coelho, M. A., Dong, M. B., Lawson, K. A., Lu, T., Maroc, L., Norman, T. M., Song, B., et al. (2022) · Nature Reviews Methods Primers · doi:10.1038/s43586-021-00093-4 · Cited by 641
Therapeutic targeting of the hypoxic tumour microenvironment
Singleton, D. C., Macann, A., & Wilson, W. R. (2021) · Nature Reviews Clinical Oncology · doi:10.1038/s41571-021-00539-4 · Cited by 507
Genome-wide CRISPRi/a screens in human neurons link lysosomal failure to ferroptosis
Tian, R., Abarientos, A., Hong, J., Hashemi, S. H., Yan, R., Dräger, N., Leng, K., Nalls, M. A., Singleton, A. B., Xu, K., et al. (2021) · Nature Neuroscience · doi:10.1038/s41593-021-00862-0 · Cited by 414
Mechanisms of mitochondrial respiratory adaptation
Bennett, C. F., Latorre‐Muro, P., & Puigserver, P. (2022) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-022-00506-6 · Cited by 322
Bock, C., Datlinger, P., Chardon, F. M., Coelho, M. A., Dong, M. B., Lawson, K. A., Lu, T., Maroc, L., Norman, T. M., Song, B., et al. (2022) · Nature Reviews Methods Primers · doi:10.1038/s43586-022-00098-7 · Cited by 264
Seo, J., Jeong, D., Park, J., Lee, K., Fukuda, J., & Chun, Y. (2020) · Communications Biology · doi:10.1038/s42003-020-01367-5 · Cited by 237
Fumarate is a terminal electron acceptor in the mammalian electron transport chain
Spinelli, J. B., Rosen, P. C., Sprenger, H.-G., Puszynska, A. M., Mann, J. L., Roessler, J. M., Cangelosi, A. L., Henne, A., Condon, K. J., Zhang, T., et al. (2021) · Science · doi:10.1126/science.abi7495 · Cited by 221
Peroxisomes as cellular adaptors to metabolic and environmental stress
He, A., Dean, J. M., & Lodhi, I. J. (2021) · Trends in Cell Biology · doi:10.1016/j.tcb.2021.02.005 · Cited by 188
Fatty acid metabolism reprogramming in ccRCC: mechanisms and potential targets
Tan, S. K., Hougen, H. Y., Merchan, J. R., Gonzalgo, M. L., & Welford, S. M. (2022) · Nature Reviews Urology · doi:10.1038/s41585-022-00654-6 · Cited by 181
Hypoxia and HIF-1 as key regulators of gut microbiota and host interactions
Pral, L. P., Fachi, J. L., Corrêa, R. O., Colonna, M., & Vinolo, M. A. R. (2021) · Trends in Immunology · doi:10.1016/j.it.2021.05.004 · Cited by 174
Jing, X., Hu, H., Sun, Y., Yu, B., Cong, H., & Shen, Y. (2022) · Small Methods · doi:10.1002/smtd.202101437 · Cited by 148
CRISPR screens in physiologic medium reveal conditionally essential genes in human cells
Rossiter, N. J., Huggler, K. S., Adelmann, C. H., Keys, H. R., Soens, R. W., Sabatini, D. M., & Cantor, J. R. (2021) · Cell Metabolism · doi:10.1016/j.cmet.2021.02.005 · Cited by 138
Han, R., Liang, J., & Zhou, B. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22115887 · Cited by 125
Peroxisome Metabolism in Cancer
Kim, J. (2020) · Cells · doi:10.3390/cells9071692 · Cited by 129
Epigenetic crosstalk between hypoxia and tumor driven by HIF regulation
Li, T., Mao, C., Wang, X., Shi, Y., & Tao, Y. (2020) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-020-01733-5 · Cited by 125
Niu, Y., Lin, Z., Wan, A., Sun, L., Yan, S., Liang, H., Zhan, S., Chen, D., Bu, X., Liu, P., et al. (2021) · Hepatology · doi:10.1002/hep.31846 · Cited by 115
How protons pave the way to aggressive cancers
Swietach, P., Boedtkjer, E., & Pedersen, S. F. (2023) · Nature reviews. Cancer · doi:10.1038/s41568-023-00628-9 · Cited by 118
Metabolic adaptation supports enhanced macrophage efferocytosis in limited-oxygen environments
Wang, Y., Trzeciak, A. J., Rojas, W. S., Saavedra, P. H. V., Chen, Y., Chirayil, R., Etchegaray, J. I., Lucas, C. D., Puleston, D. J., Keshari, K. R., et al. (2022) · Cell Metabolism · doi:10.1016/j.cmet.2022.12.005 · Cited by 110
First we eat, then we do everything else: The dynamic metabolic regulation of efferocytosis
Trzeciak, A. J., Wang, Y., & Perry, J. S. A. (2021) · Cell Metabolism · doi:10.1016/j.cmet.2021.08.001 · Cited by 109
Targeting ACSS2 with a Transition-State Mimetic Inhibits Triple-Negative Breast Cancer Growth
Miller, K. D., Pniewski, K. A., Perry, C. E., Papp, S. B., Shaffer, J. D., Velasco‐Silva, J. N., Casciano, J. C., Aramburu, T. M., Srikanth, Y. V. V., Cassel, J. A., et al. (2021) · Cancer Research · doi:10.1158/0008-5472.can-20-1847 · Cited by 103
Mitochondrial DNA mutations in ageing and cancer
Smith, A. L. M., Whitehall, J. C., & Greaves, L. C. (2022) · Molecular Oncology · doi:10.1002/1878-0261.13291 · Cited by 105
Wedan, R. J., Longenecker, J. Z., & Nowinski, S. M. (2023) · Cell Metabolism · doi:10.1016/j.cmet.2023.11.017 · Cited by 98
Dietary nutrition for neurological disease therapy: Current status and future directions
Mao, X., Yin, X., Guan, Q.-W., Xia, Q., Yang, N., Zhou, H., Liu, Z., & Jin, W. (2021) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2021.107861 · Cited by 85
Cancer cells depend on environmental lipids for proliferation when electron acceptors are limited
Li, Z., Ji, B. W., Dixit, P. D., Tchourine, K., Lien, E. C., Hosios, A. M., Abbott, K. L., Rutter, J. C., Westermark, A. M., Gorodetsky, E. F., et al. (2022) · Nature Metabolism · doi:10.1038/s42255-022-00588-8 · Cited by 81
Glycerolipid Synthesis and Lipid Droplet Formation in the Endoplasmic ReticulumPreprint
Farese, R. V., & Walther, T. C. (2022) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a041246 · Cited by 76
Turning the Oxygen Dial: Balancing the Highs and Lows
Baik, A. H., & Jain, I. H. (2020) · Trends in Cell Biology · doi:10.1016/j.tcb.2020.04.005 · Cited by 70
Self-citationTumor microenvironmental nutrients, cellular responses, and cancer
Lobel, G. P., Jiang, Y., & Simon, M. C. (2023) · Cell chemical biology · doi:10.1016/j.chembiol.2023.08.011 · Cited by 78
Hypoxia enhances ILC3 responses through HIF-1α-dependent mechanism
Fachi, J. L., Pral, L. P., dos Santos, J. A. C., Codo, A. C., de Oliveira, S., Felipe, J. S., Zambom, F. F. F., Câmara, N. O. S., Moraes‐Vieira, P. M., Colonna, M., et al. (2021) · Mucosal Immunology · doi:10.1038/s41385-020-00371-6 · Cited by 75
Ruiz, M., Ståhlman, M., Borén, J., & Pilon, M. (2019) · Journal of Lipid Research · doi:10.1194/jlr.m092494 · Cited by 69
Single-cell analysis reveals context-dependent, cell-level selection of mtDNA
Kotrys, A. V., Durham, T., Guo, X. A., Vantaku, V. R., Parangi, S., & Mootha, V. K. (2024) · Nature · doi:10.1038/s41586-024-07332-0 · Cited by 75
Self-citationGao, L., Zhang, C., Zheng, Y., Wu, D., Chen, X., Lan, H., Zheng, X., Wu, H., & Li, S. (2022) · Journal of Animal Science · doi:10.1093/jas/skac425 · Cited by 66
PEX13 prevents pexophagy by regulating ubiquitinated PEX5 and peroxisomal ROS
Demers, N. D., Riccio, V., Jo, D. S., Bhandari, S., Law, K. B., Liao, W., Kim, C., McQuibban, G. A., Choe, S., Cho, D., et al. (2022) · Autophagy · doi:10.1080/15548627.2022.2160566 · Cited by 65
Oxidative Stress and Reprogramming of Lipid Metabolism in Cancers
Li, S., Yuan, H., Li, L., Li, Q., Lin, P., & Li, K. (2025) · Antioxidants · doi:10.3390/antiox14020201 · Cited by 75
Adiponectin and Adiponectin Receptors in Atherosclerosis
Gianopoulos, I., Mantzoros, C. S., & Daskalopoulou, S. S. (2024) · Endocrine Reviews · doi:10.1210/endrev/bnae021 · Cited by 76
Limited oxygen in standard cell culture alters metabolism and function of differentiated cells
Tan, J., Virtue, S., Norris, D. M., Conway, O. J., Yang, M. H., Bidault, G., Gribben, C., Lugtu, F., Kamzolas, I., Krycer, J. R., et al. (2024) · The EMBO Journal · doi:10.1038/s44318-024-00084-7 · Cited by 72
Michl, J., Wang, Y., Monterisi, S., Błaszczak, W., Beveridge, R. D. D., Bridges, E., Koth, J., Bodmer, W. F., & Swietach, P. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110493 · Cited by 56
NADH reductive stress drives metabolic reprogramming
Yang, R., Guo, Z., & Li, B. (2025) · Trends in Cell Biology · doi:10.1016/j.tcb.2025.07.005 · Cited by 61
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
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 56
Self-citationMühlenhoff, U., Braymer, J. J., Christ, S., Rietzschel, N., Uzarska, M. A., Weiler, B. D., & Lill, R. (2020) · Biological Chemistry · doi:10.1515/hsz-2020-0237 · Cited by 52
Acidosis orchestrates adaptations of energy metabolism in tumors
Groessl, S., Kalis, R., Snaebjornsson, M. T., Wambach, L., Haider, J., Andersch, F., Schulze, A., Palm, W., & Zuber, J. A. (2025) · Science · doi:10.1126/science.adp7603 · Cited by 58
SUMOylation-Mediated Response to Mitochondrial Stress
He, J., Cheng, J., & Wang, T. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21165657 · Cited by 56
Peroxisomal-derived ether phospholipids link nucleotides to respirasome assembly
Bennett, C. F., O’Malley, K. E., Perry, E. A., Balsa, E., Latorre‐Muro, P., Riley, C. L., Luo, C., Jedrychowski, M. P., Gygi, S. P., & Puigserver, P. (2021) · Nature Chemical Biology · doi:10.1038/s41589-021-00772-z · Cited by 49
Ether phospholipids are required for mitochondrial reactive oxygen species homeostasis
Chen, Z., Ho, I.-L., Soeung, M., Yen, E.-Y., Liu, J., Liang, Y., Rose, J. L., Srinivasan, S., Jiang, S., Chang, Q., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-37924-9 · Cited by 52
Wang, J., Wu, Q., Wang, X., Liu, H., Chen, M., Xu, L. N., Zhang, Z., Li, K., Li, W., & Zhong, J. (2024) · Current Atherosclerosis Reports · doi:10.1007/s11883-024-01229-z · Cited by 55
Molecular insights into peroxisome homeostasis and peroxisome biogenesis disorders
Fujiki, Y., Okumoto, K., Honsho, M., & Abe, Y. (2022) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2022.119330 · Cited by 47
Genome-wide CRISPRi/a screens in human neurons link lysosomal failure to ferroptosis
Tian, R., Abarientos, A., Hong, J., Hashemi, S. H., Yan, R., Dräger, N., Leng, K., Nalls, M. A., Singleton, A. B., Xu, K., et al. (2020) · doi:10.1101/2020.06.27.175679 · Cited by 414
Lipoylation is dependent on the ferredoxin FDX1 and dispensable under hypoxia in human cells
Joshi, P. R., Sadre, S., Guo, X. A., McCoy, J. G., & Mootha, V. K. (2023) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2023.105075 · Cited by 41
Self-citationXiao, C., Wang, R., Fu, R., Yu, P., Guo, J., Li, G., Wang, Z., Wang, H., Nie, J., Liu, W., et al. (2024) · Bioactive Materials · doi:10.1016/j.bioactmat.2024.01.003 · Cited by 42
Yao, X., Lu, S., Feng, C., Suo, R., Li, H., Zhang, Y., Chen, Q., Lü, J., Wu, B., & Guo, J. (2022) · Biomaterials · doi:10.1016/j.biomaterials.2022.121801 · Cited by 39
Engineered stem cells by emerging biomedical stratagems
Wang, J., Zhang, X., Chen, H., Ren, H., Zhou, M., & Zhao, Y. (2024) · Science Bulletin · doi:10.1016/j.scib.2023.12.006 · Cited by 37
Hypoxia and intra-complex genetic suppressors rescue complex I mutants by a shared mechanism
Meisel, J. D., Miranda, M., Skinner, O. S., Wiesenthal, P. P., Wellner, S. M., Jourdain, A. A., Ruvkun, G., & Mootha, V. K. (2024) · Cell · doi:10.1016/j.cell.2023.12.010 · Cited by 38
Self-citationHIF signaling: A new propellant in bone regeneration
Bai, H., Wang, Y., Zhao, Y. D., Chen, X., Xiao, Y. M., & Bao, C. (2022) · Biomaterials Advances · doi:10.1016/j.bioadv.2022.212874 · Cited by 37
Rewiring cell signalling pathways in pathogenic mtDNA mutations
Chung, C.-Y., Valdebenito, G. E., Chacko, A. R., & Duchen, M. R. (2021) · Trends in Cell Biology · doi:10.1016/j.tcb.2021.10.005 · Cited by 37
Genomic structural variation is associated with hypoxia adaptation in high-altitude zokors
An, X., Mao, L., Wang, Y., Xu, Q., Liu, X., Zhang, S., Qiao, Z., Li, B., Li, F., Kuang, Z., et al. (2024) · Nature Ecology & Evolution · doi:10.1038/s41559-023-02275-7 · Cited by 34
Pilon, M. (2021) · Lipids in Health and Disease · doi:10.1186/s12944-021-01468-y · Cited by 34
Mitochondria and CancerPreprint
Kenny, T. C., & Birsoy, K. (2024) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a041534 · Cited by 40
Hypoxia-Induced Signaling in Gut and Liver Pathobiology
Solanki, S. A., & Shah, Y. M. (2023) · Annual Review of Pathology Mechanisms of Disease · doi:10.1146/annurev-pathmechdis-051122-094743 · Cited by 34
Multiplexed Imaging Mass Cytometry Analysis Characterizes the Vascular Niche in Pancreatic Cancer
Sussman, J., Kim, N., Kemp, S. B., Traum, D., Katsuda, T., Kahn, B., Xu, J., Kim, I., Eskandarian, C., Delman, D., et al. (2024) · Cancer Research · doi:10.1158/0008-5472.can-23-2352 · Cited by 32
Renal Lipid Metabolism Abnormalities in Obesity and Clear Cell Renal Cell Carcinoma
Bobulescu, I. A., Pop, L. M., Mani, C., Turner, K., Rivera, C., Khatoon, S., Kairamkonda, S., Hannan, R., & Palle, K. (2021) · Metabolites · doi:10.3390/metabo11090608 · Cited by 32
The Peroxisome-Autophagy Redox Connection: A Double-Edged Sword?
Li, H., Lismont, C., Revenco, I., Hussein, M. A. F., Costa, C. F., & Fransen, M. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.814047 · Cited by 37
A functional analysis of 180 cancer cell lines reveals conserved intrinsic metabolic programs
Cherkaoui, S., Durot, S., Bradley, J., Critchlow, S. E., Dubuis, S., Masiero, M. M., Wegmann, R., Snijder, B., Othman, A., Bendtsen, C., et al. (2022) · Molecular Systems Biology · doi:10.15252/msb.202211033 · Cited by 32
Hypoxic adaptation of mitochondria and its impact on tumor cell function
Benej, M., Papandreou, I., & Denko, N. C. (2024) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2024.03.004 · Cited by 33
Thomas, L. W., Esposito, C., Morgan, R., Price, S., Young, J., Williams, S. P., Maddalena, L. A., McDermott, U., & Ashcroft, M. A. (2021) · Communications Biology · doi:10.1038/s42003-021-02098-x · Cited by 31
Trabecular Meshwork Mitochondrial Function and Oxidative Stress
Wu, H., Shui, Y., Liu, Y., Liu, X., & Siegfried, C. J. (2021) · Ophthalmology Science · doi:10.1016/j.xops.2021.100107 · Cited by 31
Bennett, N. K., Lee, M., Orr, A. L., & Nakamura, K. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2307904121 · Cited by 32
Peroxisomes and PPARs: Emerging role as master regulators of cancer metabolism
Pratama, A. M., Sharma, M., Naidu, S., Bömmel, H. M., Prabhuswamimath, S. C., Madhusudhan, T., Wihadmadyatami, H., Bachhuka, A., & Karnati, S. (2024) · Molecular Metabolism · doi:10.1016/j.molmet.2024.102044 · Cited by 31
HypoxyStat, a small-molecule form of hypoxia therapy that increases oxygen-hemoglobin affinity
Blume, S. Y., Garg, A., Martí-Mateos, Y., Midha, A. D., Chew, B. T. L., Lin, B., Yu, C., Dick, R. A., Lee, P. S., Situ, E., et al. (2025) · Cell · doi:10.1016/j.cell.2025.01.029 · Cited by 29
Self-citationLin, D., Zhang, L., Huang, C., & Shao, W. (2026) · iScience · doi:10.1016/j.isci.2026.115024 · Cited by 35
Rogers, R. S., & Mootha, V. K. (2025) · Science Translational Medicine · doi:10.1126/scitranslmed.adr4049 · Cited by 31
Self-citationSela, Y., Li, J., Maheswaran, S., Norgard, R. J., Yuan, S., Hubbi, M. E., Doepner, M., Xu, J. P., Ho, E. S., Mesaros, C., et al. (2022) · Cancer Research · doi:10.1158/0008-5472.can-22-0431 · Cited by 27
Regulation of membrane fluidity by RNF145‐triggered degradation of the lipid hydrolase ADIPOR2
Volkmar, N., Gawden‐Bone, C. M., Williamson, J. C., Nixon‐Abell, J., West, J. A., George‐Hyslop, P. S., Kaser, A., & Lehner, P. J. (2022) · The EMBO Journal · doi:10.15252/embj.2022110777 · Cited by 27
Sphingolipids and impaired hypoxic stress responses in Huntington disease
Burtscher, J., Pepe, G., Maharjan, N., Riguet, N., Pardo, A. D., Maglione, V., & Millet, G. P. (2023) · Progress in Lipid Research · doi:10.1016/j.plipres.2023.101224 · Cited by 27
Molecular Regulation of the Response of Brain Pericytes to Hypoxia
Carlsson, R., Enström, A., & Paul, G. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24065671 · Cited by 26
Tumor-intrinsic FABP5 is a novel driver for colon cancer cell growth via the HIF-1 signaling pathway
Seo, J., Yun, J.-E., Fukuda, J., & Chun, Y. (2021) · Cancer Genetics · doi:10.1016/j.cancergen.2021.11.001 · Cited by 25
Ehrenreich, H., Garcia‐Agudo, L. F., Steixner-Kumar, A. A., Wilke, J. B. H., & Butt, U. J. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01551-5 · Cited by 23
Induction of DEPP1 by HIF Mediates Multiple Hallmarks of Ischemic Cardiomyopathy
Wyant, G. A., Jiang, Q., Singh, M., Qayyum, S., Levrero, C., Maron, B. A., & Kaelin, W. G. (2024) · Circulation · doi:10.1161/circulationaha.123.066628 · Cited by 24
Padmanabhan, S., Monera-Girona, A. J., Pérez‐Castaño, R., Bastida‐Martínez, E., Pajares-Martínez, E., Bernal‐Bernal, D., Galbis-Martínez, M., Polanco, M. C., Iniesta, A. A., Fontes, M., et al. (2021) · Microorganisms · doi:10.3390/microorganisms9051067 · Cited by 23
Ruiz, M., Palmgren, H., Henricsson, M., Devkota, R., Jaiswal, H., Maresca, M., Bohlooly‐Y, M., Peng, X., Borén, J., & Pilon, M. (2021) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2021.158884 · Cited by 23
Zhao, L., Liao, L., Yan, H., Tang, X. H., He, K., Liu, Q., Luo, J., Du, Z. J., Chen, S. Y., Zhang, X., et al. (2023) · Aquatic Toxicology · doi:10.1016/j.aquatox.2023.106436 · Cited by 21
Li, Q., Xia, Z., Wu, Y., Ma, Y., Zhang, D., Wang, S., Fan, J., Xu, P., Li, X., Bai, L., et al. (2024) · FEBS Journal · doi:10.1111/febs.17132 · Cited by 20
Devkota, R., Henricsson, M., Borén, J., & Pilon, M. (2021) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2021.158883 · Cited by 20
Ehrenreich, H., Gassmann, M., Poustka, L., Burtscher, M., Hammermann, P., Sirén, A., Nave, K., & Miskowiak, K. W. (2023) · Neuroprotection/Neuroprotection (Chichester, England. Print) · doi:10.1002/nep3.15 · Cited by 19
Padmanabhan, S., Monera-Girona, A. J., Pajares-Martínez, E., Bastida‐Martínez, E., Navalón, I. D. R., Pérez‐Castaño, R., Galbis-Martínez, M., Fontes, M., & Arnanz, M. E. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.884689 · Cited by 19
Michl, J., White, B., Monterisi, S., Bodmer, W. F., & Swietach, P. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2319055121 · Cited by 19
Xie, Y., Lv, Z., Li, W., Lin, J., Sun, W. Y., Guo, H., Jin, X., Liu, Y., Jiang, R., Fei, Y., et al. (2025) · Journal of Orthopaedic Translation · doi:10.1016/j.jot.2025.01.001 · Cited by 18
Proteolysis-targeting chimeras in biotherapeutics: Current trends and future applications
Li, Q., Zhou, L., Qin, S., Huang, Z., Li, B., Li, B., Yang, M., Nice, E. C., Zhu, H., & Huang, C. (2023) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2023.115447 · Cited by 17
Physiology: New Insights into Central Oxygen Sensing
SheikhBahaei, S. (2020) · Current Biology · doi:10.1016/j.cub.2020.06.101 · Cited by 17
Han, X., Long, Y., Duan, X., Liu, Z., Hu, X., Zhou, J., Li, N., Wang, Y., & Qin, J. (2022) · Experimental Cell Research · doi:10.1016/j.yexcr.2022.113044 · Cited by 17
Chen, K.-J., Zhang, Y., Zhu, X.-Y., Yu, S., Xie, Y., Jin, C. W., Shen, Y., Zhou, S.-Y., Dai, X.-C., Su, S., et al. (2025) · Military Medical Research · doi:10.1186/s40779-025-00610-6 · Cited by 17
Rogers, Z. J., Colombani, T., Khan, S., Bhatt, K., Nukovic, A., Zhou, G., Woolston, B. M., Taylor, C. T., Gilkes, D. M., Slavov, N., et al. (2024) · Advanced Science · doi:10.1002/advs.202402557 · Cited by 20
d-cysteine impairs tumour growth by inhibiting cysteine desulfurase NFS1
Zangari, J., Stehling, O., Freibert, S., Bhattacharya, K., Rouaud, F., Serre‐Beinier, V., Maundrell, K., Montessuit, S., Ferré, S., Vartholomaiou, E., et al. (2025) · Nature Metabolism · doi:10.1038/s42255-025-01339-1 · Cited by 22
Saldana-Caboverde, A., Nissanka, N., García, S., Lombès, A., & Díaz, F. (2020) · Cells · doi:10.3390/cells9102197 · Cited by 17
Structural Variations Associated with Adaptation and Coat Color in Qinghai-Tibetan Plateau Cattle
Xia, X., Wang, F., Luo, X., Li, S., Lyu, Y., Zheng, Y., Ma, Z., Qu, K., Song, R., Liu, J., et al. (2025) · Advanced Science · doi:10.1002/advs.202503258 · Cited by 14
Cracking the membrane lipid code
Melero, A., & Jiménez‐Rojo, N. (2023) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2023.102203 · Cited by 14
Micro-/nanomotors as platforms for gas therapy
Sun, S., Liu, Y., Wang, S., Gui, Q., Liu, W., & Long, W. (2025) · Biomaterials · doi:10.1016/j.biomaterials.2025.123492 · Cited by 16
Peroxisomal membrane protein PMP70 confers drug resistance in colorectal cancer
Yin, J., Shao, Y., Huang, F., Hong, Y., Wei, W., Jiang, C., Zhao, Q., & Liu, L. (2025) · Cell Death and Disease · doi:10.1038/s41419-025-07572-6 · Cited by 13
MYC overrides HIF-1α to regulate proliferating primary cell metabolism in hypoxia
Copeland, C. A., Olenchock, B. A., Ziehr, D. R., McGarrity, S., Leahy, K., Young, J. D., Loscalzo, J., & Oldham, W. M. (2023) · eLife · doi:10.7554/elife.82597 · Cited by 12
Metadata
- Authors
- Jain, I. H., Calvo, S. E., Markhard, A. L., Skinner, O. S., To, T.-L., Ast, T., & Mootha, V. K.
- Affiliations
- Broad Institute (US)
- Corresponding author
- Mootha, Vamsi K.
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2020-04
- Volume
- 181
- Issue
- 3
- Pages
- 716-727.e11
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC7293541
- OpenAlex
- W3014660178
- Semantic Scholar
- f5cf6ffc17c0afcf964c1821338eea659750c183
- Cited by
- 224
- References
- 71
- Citations by year
- 2026: 30 · 2025: 42 · 2024: 33 · 2023: 37 · 2022: 30 · 2021: 37 · 2020: 14
- FWCI
- 10.09
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information) (submittedVersion)
- Funders
- National Institutes of Health (1F32GM133047-01)
- J. Willard and Alice S. Marriott Foundation
- U.S. Department of Energy
- Howard Hughes Medical Institute
- 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 › Mitochondrial Function and Pathology
- Keywords
- oxygen homeostasis, hypoxia, cell fitness, genome-wide CRISPR screen, mitochondrial metabolism, lipid metabolism, complex I, peroxisomes, lipogenesis, hypoxia-inducible factor, reactive oxygen species
- MeSH terms
- Hypoxia, Genetic Testing, Humans, Lipids, Mitochondria, Oxygen, Signal Transduction, Cell Hypoxia, Reactive Oxygen Species, K562 Cells, Lipid Metabolism, Genome-Wide Association Study, HEK293 Cells, Transcriptome
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