Regulation of cancer cell metabolism by hypoxia-inducible factor 1

Targeting HIF-1 for cancer therapy

Semenza, G. L. (2003) · Nature Reviews Cancer · doi:10.1038/nrc1187 · Cited by 6,717

Hypoxia-inducible factor 1 is a basic-helix-loop-helix-PAS heterodimer regulated by cellular O2 tension.

Wang, G. L., Jiang, B. H., Rue, E. A., & Semenza, G. L. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.12.5510 · Cited by 6,212

Targeting of HIF-α to the von Hippel-Lindau Ubiquitylation Complex by O 2 -Regulated Prolyl Hydroxylation

Jaakkola, P., Mole, D. R., Tian, Y.-M., Wilson, M. I., Gielbert, J., Gaskell, S. J., Kriegsheim, A. V., Hebestreit, H. F., Mukherji, M., Schofield, C. J., et al. (2001) · Science · doi:10.1126/science.1059796 · Cited by 5,535

The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysis

Maxwell, P. H., Wiesener, M. S., Chang, G.-W., Clifford, S. C., Vaux, E. C., Cockman, M. E., Wykoff, C. C., Pugh, C. W., Maher, E. R., & Ratcliffe, P. J. (1999) · Nature · doi:10.1038/20459 · Cited by 5,180

HIFα Targeted for VHL-Mediated Destruction by Proline Hydroxylation: Implications for O 2 Sensing

Ivan, M., Kondo, K., Yang, H., Kim, W., Valiando, J., Ohh, M., Salic, A., Asara, J. M., Lane, W. S., & Kaelin Jr., W. G. (2001) · Science · doi:10.1126/science.1059817 · Cited by 4,735

HIF-1-mediated expression of pyruvate dehydrogenase kinase: A metabolic switch required for cellular adaptation to hypoxia

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

C. elegans EGL-9 and mammalian homologs define a family of dioxygenases that regulate HIF by prolyl hydroxylation

Epstein, A. C. R., Gleadle, J. M., McNeill, L. A., Hewitson, K. S., O'Rourke, J., Mole, D. R., Mukherji, M., Metzen, E., Wilson, M. I., Dhanda, A., et al. (2001) · Cell · doi:10.1016/s0092-8674(01)00507-4 · Cited by 3,333

Discovery and development of bevacizumab, an anti-VEGF antibody for treating cancer

Ferrara, N., Hillan, K. J., Gerber, H.-P., & Novotny, W. (2004) · Nature Reviews Drug Discovery · doi:10.1038/nrd1381 · Cited by 2,625

Cellular and developmental control of O 2 homeostasis by hypoxia-inducible factor 1α

Iyer, N. V., Kotch, L. E., Agani, F., Leung, S. W., Laughner, E., Wenger, R. H., Gassmann, M., Gearhart, J. D., Lawler, A. M., Yu, A. Y., et al. (1998) · Genes & Development · doi:10.1101/gad.12.2.149 · Cited by 2,476

Pulmonary Hypertension as a Metabolic Disease

Fessel, J. P., & Oldham, W. M. (2015) · Springer eBooks · doi:10.1007/978-3-319-23594-3_8 · Cited by 1

Colorectal Cancer Risk in Relation to Hypoxia Inducible Factor-1α (Hif-1 α) and Von Hippel-Lindau (Vhl) Gene Polymorphisms.

Demirel, S. (2017) · International Journal of Hematology and Oncology · doi:10.4999/uhod.171674 · Cited by 1

Les nouvelles cibles thérapeutiques dans le cancer du rein

Méric, J., Billemont, B., & Rixe, O. (2010) · Bulletin du Cancer · doi:10.1684/bdc.2010.1070 · Cited by 1

The Association between the C1772T Genetic Polymorphism in Human HIF-1α Gene and Breast Cancer Risk: A Meta-analysis

Cheng, K., Yuan, Y., Liu, J., Wang, V. S., Hua, Y. I., Zm, J., Han, Y., Hg, S., & Zl, Y. (2017) · Chemotherapy Open access · doi:10.4172/2167-7700.1000243 · Cited by 1

Biological Imaging and Radiobiological Modeling for Treatment Planning and Response Assessment in Radiation Therapy

Moiseenko, V., Bowen, S. R., Kirkpatrick, J. P., Jeraj, R., & Marks, L. B. (2018) · CRC Press eBooks · doi:10.1201/9780429508141-3 · Cited by 1

HIF-опосредованные механизмы взаимосвязи устойчивости к гипоксии и опухолевого роста

Dzhalilova, D. S., & Makarova, O. V. (2021) · Biochemistry (Moscow) · doi:10.31857/s0320972521100018 · Cited by 1

The Effect of Lactic Acid on Mast Cell Function

Spence, A. (2014) · VCU Scholars Compass (Virginia Commonwealth University) · doi:10.25772/kndf-gy69 · Cited by 1

Hypoxia, Anerobic Metabolism, and Interstitial Hypertension

Milosevic, M. (2010) · Wiley eBooks · doi:10.1002/9780470669891.ch9 · Cited by 1

Novel bioresponsive drug eluting microspheres to enhance chemoembolisation therapy

Ashrafi, K. (2014) · University of Brighton Repository (University of Brighton) · Cited by 1

The role of hypoxia-inducible factor-1 in hyperthermia-induced tumor reoxygenation and therapy resistance

Moon, E. J. (2010) · DukeSpace (Duke University) · Cited by 1

Exploiting the Bioenergetics of Disease-Causing Lymphocytes for Selective Immunomodulation.

Wahl, D. R. (2012) · Deep Blue (University of Michigan)

Elucidating the role of Cdc25A in hypoxia-mediated cell cycle arrest

de Oliveira, Q., & Pierre, E. (2009) · D-Scholarship@Pitt (University of Pittsburgh)

A systems biology approach to target identification using three-dimensional multi-cellular tumour spheroids (MCTS). Regio-specific molecular dissection of gene expression, protein expression and functional activity in 3D MCTS.

McMahon, K. M. (2011) · Bradford Scholars (University of Bradford)

The relationship between HIF-1α and autophagy activity in the hypoxic environment of breast cancer

Mills, J. (2013) · SUNScholar (Stellenbosch University)

Regulated Extracellular Nucleotide Metabolism and Function at the Mucosa

MacManus, C. F., Eltzschig, H. K., & Colgan, S. P. (2010) · Springer eBooks · doi:10.1007/978-90-481-3435-9_8

The Leukemic Bone Marrow Microenvironment: Targeting Hypoxia with Hypoxia-Activated Prodrugs

Benito, J., Konopleva, M. Y., & Wilson, W. R. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1393-0_35

The Role of the Transcription Factor atF4iin Tumor Progression Under Nutrient Deprivation and Hypoxia

Ye, J. (2010) · ScholarlyCommons (University of Pennsylvania)

factor-2 in clear cell renal carcinoma

Kong, H., Lee, S., Beebe, K. E., Scroggins, B. T., Gupta, G. N., Jung, Y., Trepel, J. B., & Neckers, L. Μ. (2010)

Research approach identifies the hypoxia gene signature as a predictor of the outcome of neuroblastoma patients

Fardin, P., Barla, A., Mosci, S., Rosasco, L., Verri, A., Versteeg, R., Caron, H. N., Molenaar, J. J., Øra, I., Eva, A., et al. (2010)

EVOLUTION OF CYTOCHROME C OXIDASE SUBUNIT 4 IN RELATION TO HYPOXIA

Kocha, K. M. (2012) · QSpace (Queen's University Library)

Roll-on scaffolds

DelNero, P. F., & Fischbach, C. (2016) · Nature Materials · doi:10.1038/nmat4549

Residual breast cancer metabolic phenotype after docetaxel treatment

Volpari, T. (2016) · University of Birmingham Institutional Research Archive (University of Birmingham)

Interplay Between Metabolism and Oncogenic Process: Role of microRNAs

Ambedkar, B. R. (2015)

Proteomics of Sub-cellular Protein Distribution in Oestrogen and Tamoxifen Stimulated MCF-7 Breast Cancer Cells

Alkhanjaf, A. A. M. (2016) · UCL Discovery (University College London)

The ketogenic diet in the treatment of malignant glioma: mechanistic effects on hypoxia and angiogenesis

Woolf, E. C. (2014)

Review Role of angiogenesis on bone formation

Portal‐Núñez, S., Lozano, D., & Esbrit, P. (2012)

Metabolic Reprogramming and Hyaluronan Production in Cancer Stem Cells

Izumikawa, T., & Itano, N. (2018) · Trends in Glycoscience and Glycotechnology · doi:10.4052/tigg.1713.1e

Investigating the role of the apelinergic system in glioblastoma

Venkatesh, V. S. (2018) · Open Access Victoria University of Wellington | Te Herenga Waka (Figshare) · doi:10.26686/wgtn.17134046

Role of Selected Transcription Factors in Pancreatic and Colorectal Cancer Growth and Metastasis

Peela, S., Dariya, B., & Nagaraju, G. P. (2020) · Diagnostics and therapeutic advances in GI malignancies · doi:10.1007/978-981-15-5471-1_12

Tear hypoxia-inducible factor-1α expression, lactate dehydrogenase, and malate dehydrogenase activity changes in soft contact lens wear

Rahayu, T. S. M., Gondhowiardjo, T. D., Artini, W., & Wanandi, S. I. (2020) · Medical Journal of Indonesia · doi:10.13181/mji.oa.203405

The expression of neuroglobin in astrocytoma

Zhang, H. Q. G., ZhangMingyuan, L., & Guan, L. (2012)

The Effects of Modified Ketogenic Diet on Blood Parameters of Patients with Glioblastoma: A Retrospective Study

Dinç, S., Kılıç, O. N., Kırnap, E., Mavcioğlu, İ., Saraç, N., Sefer, S., Şenyuva, M. A., Al-Beyati, E. S. M., Doğan, Ö., Hayme, S., et al. (2022) · Journal of Ankara University Faculty of Medicine · doi:10.4274/atfm.galenos.2021.97659

Bioimaging of Fluorescence-Labeled Mitochondria in Subcutaneously Grafted Murine Melanoma Cells by the “In Vivo Cryotechnique”

Ohno, N., Lei, T., Huang, Z., Sakoh, T., Saitoh, Y., & Ohno, S. (2015) · Springer eBooks · doi:10.1007/978-4-431-55723-4_52

Investigating the role of the apelinergic system in glioblastoma

Venkatesh, V. S. (2018) · doi:10.26686/wgtn.17134046.v1

Hemangioblastoma

Singh, J. C., & Zagzag, D. (2014) · Molecular pathology library · doi:10.1007/978-1-4939-1830-0_14

Data from β2-Microglobulin Induces Epithelial to Mesenchymal Transition and Confers Cancer Lethality and Bone Metastasis in Human Cancer Cells

Josson, S., Nomura, T., Lin, J., Huang, W., Wu, D., Zhau, H. E., Zayzafoon, M., Weizmann, M. N., Gururajan, M., & Chung, L. W. K. (2023) · doi:10.1158/0008-5472.c.6502796.v1

Data from MTAP Deficiency–Induced Metabolic Reprogramming Creates a Vulnerability to Cotargeting De Novo Purine Synthesis and Glycolysis in Pancreatic Cancer

Hu, Q., Qin, Y., Ji, S., Shi, X., Dai, W., Fan, G., Li, S., Xu, W., Liu, W., Liu, M., et al. (2023) · doi:10.1158/0008-5472.c.6513193.v1

Data from Transplanting Normal Vascular Proangiogenic Cells to Tumor-Bearing Mice Triggers Vascular Remodeling and Reduces Hypoxia in Tumors

Sasajima, J., Mizukami, Y., Sugiyama, Y., Nakamura, K., Kawamoto, T., Koizumi, K., Fujii, R., Motomura, W., Sato, K., Suzuki, Y., et al. (2023) · doi:10.1158/0008-5472.c.6499997.v1

Hallmarks of an Aging and Malignant Tumor Microenvironment and the Rise of Resilient Cell Subpopulations

Peña, C. M., Lee, A. H., Frare, M. F., Ghosh, D., & Dawson, M. (2023) · Current cancer research · doi:10.1007/978-3-031-22802-5_4

Metabolite profiling of human renal cell carcinoma reveals tissue-origin dominance in nutrient availabilityPreprint

Abbott, K. L., Ali, A., Reinfeld, B. I., Deik, A., Subudhi, S., Landis, M. D., Hongo, R. A., Young, K. L., Kunchok, T., Nabel, C. S., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.12.24.573250

Metabolite profiling of human renal cell carcinoma reveals tissue-origin dominance in nutrient availabilityPreprint

Abbott, K. L., Ali, A., Reinfeld, B. I., Deik, A., Subudhi, S., Landis, M. D., Hongo, R. A., Young, K. L., Kunchok, T., Nabel, C. S., et al. (2024) · eLife · doi:10.7554/elife.95652.1

Avaliação imuno-histoquímica das expressões de LOX, LOXL2 e HIF1A em tumores mamários caninos

Daniel, J. M. (2023) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.74.2023.tde-23022024-085638

Additional file 1 of MiR-103a-3p promotes tumour glycolysis in colorectal cancer via hippo/YAP1/HIF1A axis

Sun, Z., Zhang, Q., Yuan, W., Li, X., Chen, C., Guo, Y., Shao, B., Dang, Q., Zhou, Q., Wang, Q., et al. (2020) · Figshare · doi:10.6084/m9.figshare.13269900

Metabolite profiling of human renal cell carcinoma reveals tissue-origin dominance in nutrient availabilityPreprint

Abbott, K. L., Ali, A., Reinfeld, B. I., Deik, A., Subudhi, S., Landis, M. D., Hongo, R. A., Young, K. L., Kunchok, T., Nabel, C. S., et al. (2024) · eLife · doi:10.7554/elife.95652.2

Metabolic Reprogramming of Clear Cell Renal Cell Carcinoma and Its Clinical Significance

周, 文. (2024) · Advances in Clinical Medicine · doi:10.12677/acm.2024.1451486

BCKDK, A Novel Hypoxia-Responsive Kinase That Exacerbates Cerebral Ischemia Injury

Liao, B., Zhang, F., Han, C., Yi, X., Zhang, Z., Jin, L., Geng, L., Wong, S. S. C., Hoo, R. L. C., Geng, L., et al. (2026) · Stroke · doi:10.1161/strokeaha.125.053856

Angiogenesis and the Tumor Microenvironment

Murphy, J. F. (2025) · Springer eBooks · doi:10.1007/978-3-032-00761-2_87

Oncostatin M induces epigenetic reprogramming in renal cell carcinoma-associated endothelial cells

Nguyen-Tran, H.-H., Nguyen, T.-N., & Hsu, T. (2025) · Communications Biology · doi:10.1038/s42003-025-08907-x

Taming Bacterial Toxins into an Anticancer Platform

Yang, C., & Chen, C. (2025) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2025.152976

Additional file 3 of Extracellular lipid loading augments hypoxic paracrine signaling and promotes glioma angiogenesis and macrophage infiltration

Offer, S., Menard, J. A., Pérez, J. E., de Oliveira, K. G., Indira Chandran, V., Johansson, M. C., Bång-Rudenstam, A., Siesjö, P., Ebbesson, A., Hedenfalk, I. A., et al. (2019) · Figshare · doi:10.6084/m9.figshare.8245394

Additional file of The prolyl hydroxylase enzymes are positively associated with hypoxia-inducible factor-1α and vascular endothelial growth factor in human breast cancer and alter in response to primary systemic treatment with epirubicin and tamoxifen

Fox, S. B., Generali, D., Berruti, A., Brizzi, M. P., Campo, L., Bonardi, S., Bersiga, A., Allevi, G., Milani, M., Aguggini, S., et al. (2020) · Figshare · doi:10.6084/m9.figshare.12879662

Additional file 1 of Extracellular lipid loading augments hypoxic paracrine signaling and promotes glioma angiogenesis and macrophage infiltration

Offer, S., Menard, J. A., Pérez, J. E., de Oliveira, K. G., Indira Chandran, V., Johansson, M. C., Bång-Rudenstam, A., Siesjö, P., Ebbesson, A., Hedenfalk, I. A., et al. (2019) · Figshare · doi:10.6084/m9.figshare.8245379

Additional file 1 of The prolyl hydroxylase enzymes are positively associated with hypoxia-inducible factor-1α and vascular endothelial growth factor in human breast cancer and alter in response to primary systemic treatment with epirubicin and tamoxifen

Fox, S. B., Generali, D., Berruti, A., Brizzi, M. P., Campo, L., Bonardi, S., Bersiga, A., Allevi, G., Milani, M., Aguggini, S., et al. (2020) · Figshare · doi:10.6084/m9.figshare.12879665

Additional file 5 of Extracellular lipid loading augments hypoxic paracrine signaling and promotes glioma angiogenesis and macrophage infiltration

Offer, S., Menard, J. A., Pérez, J. E., de Oliveira, K. G., Indira Chandran, V., Johansson, M. C., Bång-Rudenstam, A., Siesjö, P., Ebbesson, A., Hedenfalk, I. A., et al. (2019) · Figshare · doi:10.6084/m9.figshare.8245412

Additional file 4 of Extracellular lipid loading augments hypoxic paracrine signaling and promotes glioma angiogenesis and macrophage infiltration

Offer, S., Menard, J. A., Pérez, J. E., de Oliveira, K. G., Indira Chandran, V., Johansson, M. C., Bång-Rudenstam, A., Siesjö, P., Ebbesson, A., Hedenfalk, I. A., et al. (2019) · Figshare · doi:10.6084/m9.figshare.8245403

Additional file 2 of Extracellular lipid loading augments hypoxic paracrine signaling and promotes glioma angiogenesis and macrophage infiltration

Offer, S., Menard, J. A., Pérez, J. E., de Oliveira, K. G., Indira Chandran, V., Johansson, M. C., Bång-Rudenstam, A., Siesjö, P., Ebbesson, A., Hedenfalk, I. A., et al. (2019) · Figshare · doi:10.6084/m9.figshare.8245388

Combined therapies of antithrombotics and antioxidants delay in silico brain tumor progressionPreprint

Mart\'inez-Gonz\'alez, A., Durán‐Prado, M., Calvo, G. F., Alcain, F. J., P\'erez-Romasanta, L. A., & Pérez‐García, V. M. (2014) · arXiv (Cornell University) · doi:10.48550/arxiv.1401.2397

Zebrafish pkm activates the Hif-1α signaling pathway and promotes metabolic reprogramming

Zhang, W., Liu, D., Zhou, J., Zu, C., Li, Y., Liu, C., Sun, X., Lu, L., & Liu, Y. (2026) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2026.153543

Recent advances in purpose-built 3D bioprinted cancer models for drug development

Ramos, L., Robinson, M., Lallous, N., Flannigan, R. K., & Daugaard, M. (2026) · Expert Opinion on Drug Discovery · doi:10.1080/17460441.2026.2642320 · Cited by 1

Synthèse de prodrogues bispécifiques activables en milieu hypoxique : application au traitement du chondrosarcome et nouvelles perspectives dans le cadre du cancer de la prostate

Gérard, Y. (2018) · theses.fr (ABES) · doi:10.70675/90d554f3z247fz414fzb972z3e282901963f

Hétérogénéité métabolique des gliomes : apport de la spectroscopie RMN HRMAS

Bund, C. (2020) · theses.fr (ABES) · doi:10.70675/2f880f7az9a01z463fz9f4az0dcaad5fcf59

Long-term regulation of colorectal cancer cells under mechanical stress

Mouelhi, M. (2023) · theses.fr (ABES) · doi:10.70675/c4c32dd5zfd5ez4187za887z25dd0c7e3452

AGAP1 and noncanonical GDP binding regulate triple-negative breast cancer development

Zhang, Y., Zhang, S., Deng, X., Cheng, N., Wang, J., Huang, H., Zhuo, Z., Ye, S., Yu, X., Li, Z., et al. (2026) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-026-06196-z

Hydroxysafflor yellow A alleviates high fat diet induced hyperlipidemia and improves host intestinal environment via hepatic signaling regulation

Xu, C., Ji, K., Li, H., Zhang, J. Y., Wu, M., Chen, C., Niu, R., Sun, Y., & Liu, C. (2026) · Scientific Reports · doi:10.21203/rs.3.rs-9650845/v1

Hydrostatic pressure activates HIF ‐1α via β‐catenin to promote stemness in breast cancer cells

Zhai, D., Xu, Y., Ma, J., Duangrat, R., Yan, C., Liang, J., Wei, H., Jiang, B., & Li, T. (2026) · FEBS Open Bio · doi:10.1002/2211-5463.70267

DNA methylation and chromatin modifications-updates based on chromatin modifiers

Sepehri, Z., Beacon, T. H., Osman, F. D. S., Jahan, S., & Davie, J. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-15572-7.00002-4

Immunometabolic Stress and Immune Suppression in Clear-Cell Renal Cell Carcinoma: Perspectives in Therapeutic Strategy

Nguyen, T. V., & Hsu, T. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27136021 · Cited by 1

HOXC9 promotes gastric cancer cell proliferation, invasion, and migration via regulating HIF-1 pathway

何光洲, Zhang, N., Xun, D., He, N., Chen, X., & Yang, X. (2026) · Gene · doi:10.1016/j.gene.2026.150476

Beyond hypoxia and ccRCC: the expanding universe of VHL novel targets and next-generation therapeutics

Deng, R., Wang, B., Zou, M., Mao, K., Shang, J., Qiu, J., Zhou, J., Xu, H., Ma, X., Wang, Y., et al. (2026) · Biomarker Research · doi:10.1186/s40364-026-00986-0

Metabolic Dysfunction and T-Cell Exhaustion in Colorectal Cancer: Mechanisms, Microenvironment Remodeling, and Therapeutic Opportunities

Jeon, J., Baek, H. S., Park, K., Park, M., Heo, N. H., Cheon, S., Kim, G., & Kim, S. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27209134

BindingDB Entry 50003085: 4-Hydroxy-3-nitro-5-ureido-benzenesulfonamides Selectively Target the Tumor-Associated Carbonic Anhydrase Isoforms IX and XII Showing Hypoxia-Enhanced Antiproliferative Profiles.

BindingDB (2020) · UC San Diego · doi:10.7270/q2db84jn

BindingDB Entry 50020451: Reprogramming Energy Metabolism with Synthesized PDK Inhibitors Based on Dichloroacetate Derivatives and Targeted Delivery Systems for Enhanced Cancer Therapy.

BindingDB (2024) · UC San Diego · doi:10.7270/q2m049w3

BindingDB Entry 22: A systematic quantitative approach to rational drug design and discovery of novel human carbonic anhydrase IX inhibitors.

BindingDB (2018) · UC San Diego · doi:10.7270/q2nc5zcq

Metabolic–Epigenetic Crosstalk Between Cancer Cells and Tumor-Associated Macrophages: The Lactate–Histone Lactylation Feedback Axis

Singh, D. D., Yadav, D. K., & Shin, D. (2026) · Antioxidants · doi:10.3390/antiox15111414

Role of p53 in Adaptation to the Tumor Microenvironment

Mendoza, E. E. (2010) · UA Campus Repository (The University of Arizona)

HIF-1 mediates metabolic responses to intratumoral hypoxia and oncogenic mutations

Semenza, G. L. (2013) · Journal of Clinical Investigation · doi:10.1172/jci67230 · Cited by 1,335

Therapeutic Targeting Hypoxia-Inducible Factor (HIF-1) in Cancer: Cutting Gordian Knot of Cancer Cell Metabolism

Sharma, A., Sinha, S., & Shrivastava, N. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.849040 · Cited by 85

Regulation of Hypoxia Dependent Reprogramming of Cancer Metabolism: Role of HIF-1 and Its Potential Therapeutic Implications in Leukemia

Pandey, S., Singh, R., Habib, N., Tripathi, R., Kushwaha, R., & Mahdi, A. A. (2024) · Asian Pacific Journal of Cancer Prevention · doi:10.31557/apjcp.2024.25.4.1121 · Cited by 11

HIF-1-regulated glucose metabolism in the control of apoptosis signaling

Fulda, S. (2008) · Expert Review of Endocrinology & Metabolism · doi:10.1586/17446651.3.3.303 · Cited by 3

HIF-1: upstream and downstream of cancer metabolism

Semenza, G. L. (2009) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2009.10.009 · Cited by 1,431