The DOI matches its Crossref record; 58 of the 58 references it cites were found in a registry or an index.
Lactate promotes glutamine uptake and metabolism in oxidative cancer cells
Open accessAbstract
Oxygenated cancer cells have a high metabolic plasticity as they can use glucose, glutamine and lactate as main substrates to support their bioenergetic and biosynthetic activities. Metabolic optimization requires integration. While glycolysis and glutaminolysis can cooperate to support cellular proliferation, oxidative lactate metabolism opposes glycolysis in oxidative cancer cells engaged in a symbiotic relation with their hypoxic/glycolytic neighbors. However, little is known concerning the relationship between oxidative lactate metabolism and glutamine metabolism. Using SiHa and HeLa human cancer cells, this study reports that intracellular lactate signaling promotes glutamine uptake and metabolism in oxidative cancer cells. It depends on the uptake of extracellular lactate by monocarboxylate transporter 1 (MCT1). Lactate first stabilizes hypoxia-inducible factor-2α (HIF-2α), and HIF-2α then transactivates c-Myc in a pathway that mimics a response to hypoxia. Consequently, lactate-induced c-Myc activation triggers the expression of glutamine transporter ASCT2 and of glutaminase 1 (GLS1), resulting in improved glutamine uptake and catabolism. Elucidation of this metabolic dependence could be of therapeutic interest. First, inhibitors of lactate uptake targeting MCT1 are currently entering clinical trials. They have the potential to indirectly repress glutaminolysis. Second, in oxidative cancer cells, resistance to glutaminolysis inhibition could arise from compensation by oxidative lactate metabolism and increased lactate signaling.
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?
The cited source says what the claim attributes to it.
In the citing paper
“It has long been established that Myc activation upregulates glutamine metabolism [79,80], increasing glutamine flux by upregulating the glutamine transporter (ASCT2) and glutaminase-1, thus increasing glutamine conversion to glutamate [81].”
From HIF-1-Independent Mechanisms Regulating Metabolic Adaptation in Hypoxic Cancer Cells (2021) · cites this paper as [81]
In the citing paper
“In addition, extracellular lactate stabilizes HIF-2α, and HIF-2α then transactivates MYC, increasing the levels of glutamine transporters and GLS1, in turn resulting in increased glutamine catabolism72.”
From Glutamine reliance in cell metabolism (2020) · cites this paper as [72]
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
Understanding the Warburg Effect: The Metabolic Requirements of Cell Proliferation
Vander Heiden, M. G., Cantley, L. C., & Thompson, C. B. (2009) · Science · doi:10.1126/science.1160809 · Cited by 16,197
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
Metabolic Reprogramming: A Cancer Hallmark Even Warburg Did Not Anticipate
Ward, P. S., & Thompson, C. B. (2012) · Cancer Cell · doi:10.1016/j.ccr.2012.02.014 · Cited by 3,233
The M2 splice isoform of pyruvate kinase is important for cancer metabolism and tumour growth
Christofk, H. R., Vander Heiden, M. G., Harris, M. H., Ramanathan, A., Gerszten, R. E., Wei, R., Fleming, M. D., Schreiber, S. L., & Cantley, L. C. (2008) · Nature · doi:10.1038/nature06734 · Cited by 2,820
DeBerardinis, R. J., Mancuso, A., Daikhin, E., Nissim, I., Yudkoff, M., Wehrli, S., & Thompson, C. B. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0709747104 · Cited by 2,622
Direct observation of individual endogenous protein complexes in situ by proximity ligation
Söderberg, O., Gullberg, M., Jarvius, M., Ridderstråle, K., Leuchowius, K.-J., Jarvius, J., Wester, K., Hydbring, P., Bahram, F., Larsson, L.-G., et al. (2006) · Nature Methods · doi:10.1038/nmeth947 · Cited by 2,419
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
Gao, P., Tchernyshyov, I., Chang, T.-C., Lee, Y.-S., Kita, K., Ochi, T., Zeller, K. I., De Marzo, A. M., Van Eyk, J. E., Mendell, J. T., et al. (2009) · Nature · doi:10.1038/nature07823 · Cited by 2,124
Wise, D. R., DeBerardinis, R. J., Mancuso, A., Sayed, N., Zhang, X.-Y., Pfeiffer, H. K., Nissim, I., Daikhin, E., Yudkoff, M., McMahon, S. B., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0810199105 · Cited by 2,001
Targeting lactate-fueled respiration selectively kills hypoxic tumor cells in mice
Sonveaux, P., Végran, F., Schroeder, T., Wergin, M., Verrax, J., Rabbani, Z. N., Saedeleer, C. J. D., Kennedy, K. M., Diepart, C., Jordan, B. F., et al. (2008) · Journal of Clinical Investigation · doi:10.1172/jci36843 · Cited by 1,635
Self-citation
Research works printed but not linked: 2
- Sowter HM, 2003, Cancer Res, 63, 6130
- Russell RR, 1991, Am J Physiol, 261, H1756
Cited by
Sorted by citations
Items 101–200 of 231
Yoshida, G. J. (2021) · Metabolites · doi:10.3390/metabo11010027 · Cited by 32
Hée, V. F. V., Labar, D., Dehon, G., Grasso, D., Grégoire, V., Muccioli, G. G., Frédérick, R., & Sonveaux, P. (2017) · Oncotarget · doi:10.18632/oncotarget.14705 · Cited by 34
Self-citationMetabolomics-Driven Biomarker Discovery for Breast Cancer Prognosis and Diagnosis
Kaur, R., Gupta, S. K., Kulshrestha, S., Khandelwal, V., Pandey, S., Kumar, A., Sharma, G., Kumar, U., Parashar, D., & Das, K. (2024) · Cells · doi:10.3390/cells14010005 · Cited by 34
A GSTP1-mediated lactic acid signaling promotes tumorigenesis through the PPP oxidative branch
Sun, Y., He, Q., Li, J., Yang, Z., Ahmad, M., Lin, Y., Wu, D., Zheng, L., Li, J., Wang, B., et al. (2023) · Cell Death and Disease · doi:10.1038/s41419-023-05998-4 · Cited by 26
Metabolic and oncogenic adaptations to pyruvate dehydrogenase inactivation in fibroblasts
Wang, H., Lu, J. L., Kulkarni, S., Zhang, W., Gorka, J. E., Mandel, J. A., Goetzman, E. S., & Prochownik, E. V. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.005200 · Cited by 29
Causes and Consequences of A Glutamine Induced Normoxic HIF1 Activity for the Tumor Metabolism
Kappler, M., Pabst, U., Weinholdt, C., Taubert, H. W., Rot, S., Kaune, T., Kotrba, J., Porsch, M., Güttler, A., Bache, M., et al. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20194742 · Cited by 29
GLUT1 production in cancer cells: a tragedy of the commons
Bukkuri, A., Gatenby, R. A., & Brown, J. S. (2022) · npj Systems Biology and Applications · doi:10.1038/s41540-022-00229-6 · Cited by 28
Yang, S., Tan, H.-X., Lai, Z., Peng, H., Yang, H., Fu, Q., Wang, H., Li, D., & Li, M. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-022-04639-x · Cited by 33
Zeng, Y., Huang, Y., Tan, Q., Peng, L., Wang, J., Tong, F., & Dong, X. (2024) · Molecular Medicine Reports · doi:10.3892/mmr.2024.13413 · Cited by 31
Metabolic and Amino Acid Alterations of the Tumor Microenvironment
Štěpka, P., Všianský, V., Raudenská, M., Gumulec, J., Adam, V., & Masařík, M. (2020) · Current Medicinal Chemistry · doi:10.2174/0929867327666200207114658 · Cited by 28
Impact of Medium pH on DOX Toxicity toward HeLa and A498 Cell Lines
Trębińska-Stryjewska, A., Święch, O., Opuchlik, L. J., Grzybowska, E. A., & Bilewicz, R. (2020) · ACS Omega · doi:10.1021/acsomega.9b04479 · Cited by 27
Metabolic Signaling in the Tumor Microenvironment
Clay, R., Li, K., & Jin, L. (2025) · Cancers · doi:10.3390/cancers17010155 · Cited by 31
Gao, J., Guo, Z., Cheng, J., Sun, B. H., Yang, J., Li, H., Wu, S., Dong, F., & Yan, X. (2020) · Scientific Reports · doi:10.1038/s41598-020-78955-2 · Cited by 29
Autophagy preserves hematopoietic stem cells by restraining MTORC1-mediated cellular anabolism
Borsa, M., Obba, S., Richter, F. C., Zhang, H., Riffelmacher, T., Carrelha, J., Alsaleh, G., Jacobsen, S. E. W., & Simon, A. K. (2023) · Autophagy · doi:10.1080/15548627.2023.2247310 · Cited by 27
Oxidative and Glycolytic Metabolism: Their Reciprocal Regulation and Dysregulation in Cancer
Cordani, M., Rumio, C., Bontempi, G., Strippoli, R., & Marcucci, F. (2025) · Cells · doi:10.3390/cells14151177 · Cited by 28
A Scaffold-Free 3-D Co-Culture Mimics the Major Features of the Reverse Warburg Effect In Vitro
Keller, F., Bruch, R., Schneider, R., Meier-Hubberten, J. C., Hafner, M., & Rudolf, R. (2020) · Cells · doi:10.3390/cells9081900 · Cited by 24
MCT4/Lactate Promotes PD-L1 Glycosylation in Triple-Negative Breast Cancer Cells
Duan, X., Xie, Y., Yu, J., Hu, X., Liu, Z., Li, N., Qin, J., Lan, L., Yuan, M., Pan, Z., et al. (2022) · Journal of Oncology · doi:10.1155/2022/3659714 · Cited by 25
The emerging potential role of p62 in cancer treatment by regulating metabolism
Zhang, X., Dai, M., Li, S., Li, M., Cheng, B., Ma, T., & Zhou, Z. G. (2023) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2023.05.004 · Cited by 30
Metabolic Escape Routes of Cancer Stem Cells and Therapeutic Opportunities
Turdo, A., Porcelli, G., D’Accardo, C., Franco, S. D., Verona, F., Forte, S., Giuffrida, D., Memeo, L., Todaro, M., & Stassi, G. (2020) · Cancers · doi:10.3390/cancers12061436 · Cited by 27
Yan, R., Cai, H., Zhou, X., Bao, G., Bai, Z., & Ge, R. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2024.1344971 · Cited by 28
Zhao, X., Li, K., Chen, M., & Liu, L. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.114601 · Cited by 23
Role and therapeutic targeting of glutamine metabolism in non‑small cell lung cancer (Review)
Zhou, L., Zhang, Q., Zhu, Q., Zhan, Y., Li, Y., & Huang, X. (2023) · Oncology Letters · doi:10.3892/ol.2023.13745 · Cited by 23
Dietary approaches for exploiting metabolic vulnerabilities in cancer
Menyhárt, O., & Győrffy, B. (2023) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2023.189062 · Cited by 23
Bernier, M., Catazaro, J., Singh, N., Wnorowski, A., Boguszewska‐Czubara, A., Jóźwiak, K., Powers, R., & Wainer, I. W. (2017) · International Journal of Cancer · doi:10.1002/ijc.30904 · Cited by 21
Acidity induces durable enhancement of Treg cell suppressive functions for tumor immune evasion
Mani, N. L., Weinberg, S. E., Chaudhuri, S. M., Montauti, E. I., Tang, A. Y., Iyer, R., & Fang, D. (2024) · Molecular Immunology · doi:10.1016/j.molimm.2024.08.004 · Cited by 23
Revisiting lactate dynamics in cancer—a metabolic expertise or an alternative attempt to survive?
Mendes, C., & Serpa, J. (2020) · Journal of Molecular Medicine · doi:10.1007/s00109-020-01965-0 · Cited by 20
SIPA1 Enhances Aerobic Glycolysis Through HIF-2α Pathway to Promote Breast Cancer Metastasis
Yao, C., Weng, J., Feng, L., Zhang, W., Xu, Y. K., Zhang, P., Tanaka, Y., & Su, L. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.779169 · Cited by 20
Role of monocarboxylate transporters in head and neck squamous cell carcinoma
Chandel, V., Maru, S., Kumar, A. J., Kumar, A., Sharma, A. K., Rathi, B., & Kumar, D. (2021) · Life Sciences · doi:10.1016/j.lfs.2021.119709 · Cited by 20
Review of cancer cell volatile organic compounds: their metabolism and evolution
Furuhashi, T., Toda, K., & Weckwerth, W. (2025) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2024.1499104 · Cited by 20
Wu, P., Zhang, J., Jiang, Z., Liu, X., Jiang, N., Zou, J., Chen, X., Wu, D., & Li, Y. (2026) · Biomarker Research · doi:10.1186/s40364-026-00898-z · Cited by 21
Li, K., Cao, J., Zhang, Z., Chen, K., Ma, T., Yang, W., Yang, S., Rao, J., & Zhang, K. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.598256 · Cited by 19
Role of monocarboxylate transporters in cancer immunology and their therapeutic potential
Faghihkhorasani, F., Moosavi, M., Abdulwahid, A. R. R., Kavei, M., Karimi, S., Karimi, M. S., Vezvaei, P., Varkiani, M. M., Aref, A. R., & Ebrahimi, N. (2025) · British Journal of Pharmacology · doi:10.1111/bph.70110 · Cited by 24
Perspective on the dynamics of cancer
Derbal, Y. (2017) · Theoretical Biology and Medical Modelling · doi:10.1186/s12976-017-0066-5 · Cited by 18
Fernandez‐Martell, A., Johari, Y. B., & James, D. C. (2017) · Biotechnology and Bioengineering · doi:10.1002/bit.26485 · Cited by 17
Zhou, S., Xie, J., Yu, C., Feng, Z., Cheng, K., Ma, J., Wang, Y., Duan, C., Zhang, Y., Jin, B., et al. (2021) · The FASEB Journal · doi:10.1096/fj.202101134r · Cited by 17
Afonso, J., Barbosa-Matos, C., Silvestre, R., Pereira-Vieira, J., Gonçalves, S. M., Mendes-Alves, C., Parpot, P., Pinto, J., Carapito, Â., de Pinho, P. G., et al. (2024) · Cancers · doi:10.3390/cancers16071418 · Cited by 17
Metabolism of Immune Cells in the Tumor Microenvironment
Jung, J. G., & Le, A. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-65768-0_13 · Cited by 16
Crosstalk between colorectal tumor metabolism and immune cells in the tumor microenvironment
Li, P., Zhang, Y., Huang, C., & Wang, G. (2025) · Oncology and Translational Medicine · doi:10.1097/ot9.0000000000000083 · Cited by 15
Zhang, Q., & Li, W. (2022) · World Journal of Stem Cells · doi:10.4252/wjsc.v14.i4.267 · Cited by 16
Li, L., Lei, Q., Zhen, Y., Cao, L., Dong, Y., Liu, X., & Wang, M. (2024) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.4c08211 · Cited by 15
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
A preclinical model of cutaneous melanoma based on reconstructed human epidermis
Leikeim, A., Wußmann, M., Schmidt, F. F., Neto, N. G. B., Benz, F., Tiltmann, K., Junger, C., Monaghan, M. G., Schilling, B., & Groeber-Becker, F. K. (2022) · Scientific Reports · doi:10.1038/s41598-022-19307-0 · Cited by 17
Shi, W., Xu, X., Yan, F., Wang, B., Zhao, H., Chan, A., Ren, Z., Ma, Y., Wang, F., & Yuan, J. (2017) · Oncology Letters · doi:10.3892/ol.2017.7024 · Cited by 15
Metabolic reprogramming of drug resistance in pancreatic cancer: mechanisms and effects
Zhang, J., Kong, X., Zhou, B., Li, R., Yu, Z., Zhu, J., Xi, Q., Li, Y., Zhao, Z., & Zhang, R. (2025) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2025.101368 · Cited by 15
Min, K., Yenilmez, B., Kelly, M., Echeverria, D., Elleby, M., Lifshitz, L. M., Raymond, N., Tsagkaraki, E., Harney, S. M., DiMarzio, C., et al. (2023) · eLife · doi:10.7554/elife.89136 · Cited by 21
Purba, T. S., Berriche, L., & Paus, R. (2021) · Experimental Dermatology · doi:10.1111/exd.14300 · Cited by 14
Zhou, J., Zhang, J., Ma, W., Zhang, W., Ke, Z., & Ling-guo, M. (2018) · RSC Advances · doi:10.1039/c8ra04514c · Cited by 14
Why and how citrate may sensitize malignant tumors to immunotherapy
Icard, P., Prieto, M., Coquerel, A., Fournel, L., Gligorov, J., Noel, J., Mouren, A., Dohan, A. J. J., Alifano, M., & Simula, L. (2024) · Drug Resistance Updates · doi:10.1016/j.drup.2024.101177 · Cited by 14
Koncošová, M., Vrzáčková, N., Křížová, I., Tomášová, P., Rimpelová, S., Dvořák, A., Vı́tek, L., Rumlová, M., Ruml, T., & Zelenka, J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221910790 · Cited by 13
Elingaard-Larsen, L. O., Rolver, M. G., Sørensen, E. E., & Pedersen, S. F. (2020) · Reviews of physiology, biochemistry and pharmacology · doi:10.1007/112_2020_23 · Cited by 14
Moreira, R., Martins, A. D., Ferreira, R. M., Alves, M. G., Pereira, M. D. L., & Oliveira, P. F. (2023) · Antioxidants · doi:10.3390/antiox13010040 · Cited by 14
1H NMR-based metabolomics of skin squamous cell carcinoma and peri-tumoral region tissues
Mei, L., Li, Y., Wang, H., Xu, G., Ye, X.-G., & Yang, G. (2022) · Journal of Pharmaceutical and Biomedical Analysis · doi:10.1016/j.jpba.2022.114643 · Cited by 12
Metabolism in the tumor microenvironment: implications for pathogenesis and therapeutics
Wik, J. A., Berge, E. R., Stromsnes, K., & Skålhegg, B. S. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1610255 · Cited by 13
Vadlakonda, L., Indracanti, M., Kalangi, S. K., Gayatri, B. M., Gajula, N. N., & Reddy, A. B. M. (2020) · Journal of Diabetes & Metabolic Disorders · doi:10.1007/s40200-020-00566-5 · Cited by 11
Peltanová, B., Polanska, H. H., Raudenská, M., Balvan, J., Navrátil, J., Vičar, T., Gumulec, J., Čechová, B., Kräter, M., Guck, J. R., et al. (2022) · Cancers · doi:10.3390/cancers14092286 · Cited by 11
Neto, N. G. B., Suku, M., Hoey, D. A., & Monaghan, M. G. (2023) · Stem Cell Research & Therapy · doi:10.1186/s13287-023-03606-y · Cited by 10
Vera, M. J., Ponce, I., Almarza, C., Ramirez, G., Guajardo, F., Dubois‐Camacho, K., Tobar, N., Urra, F. A., & Martínez, J. (2024) · Antioxidants · doi:10.3390/antiox13070801 · Cited by 10
On mitochondrial metabolism in tumor biology
Shoshan, M. C. (2016) · Current Opinion in Oncology · doi:10.1097/cco.0000000000000336 · Cited by 10
Tripathi, V., Jaiswal, P., Sahu, K., Majumder, S. K., Kashyap, D., Jha, H. C., Dixit, A. K., & Parmar, H. S. (2022) · Advances in Cancer Biology - Metastasis · doi:10.1016/j.adcanc.2022.100065 · Cited by 9
Ginsenoside compound K restrains hepatic fibrotic response by dual-inhibition of GLS1 and LDHA
Wu, W., Yang, Y., Wang, T., Sun, X., Wei, M., Zhou, X.-Y., Zhu, L.-Z., Ma, G., Liu, B., Qi, L., et al. (2024) · Phytomedicine · doi:10.1016/j.phymed.2024.156223 · Cited by 9
Metabolic Reprogramming and Adaption in Breast Cancer Progression and Metastasis
Zuo, Q., & Kang, Y. (2025) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-70875-6_17 · Cited by 9
Long noncoding RNAs regulating enzymatic reactions in cancer
Shin, C. H., Kim, K., Ho, C. W., Lee, J. W., Jo, M. J., Min, K., & Yoon, J. (2025) · Experimental & Molecular Medicine · doi:10.1038/s12276-025-01464-7 · Cited by 12
Kerslake, R., Panfilov, S., Mustafa, N., Hall, M., Kyrou, I., Randeva, H. S., Karteris, E., & Godfrey, R. (2022) · Journal of Clinical Medicine · doi:10.3390/jcm12010217 · Cited by 9
METTL3-mediated m6A methylation of SLC38A1 stimulates cervical cancer growth
Liu, H., Zhao, Y., Wang, H., & Liu, Q. (2024) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2024.150039 · Cited by 9
Monocarboxylate Transporter 1 in Brain Diseases and Cancers
Sun, Y., Sun, J., He, Z., Wang, G., Wang, Y., Zhao, D., Wang, Z., Luo, C., Tian, C., & Jiang, Q. (2019) · Current Drug Metabolism · doi:10.2174/1389200220666191021103018 · Cited by 9
Hints for a kidney lactate shuttle and lactomone
Sheikh‐Hamad, D. (2021) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00160.2021 · Cited by 9
Basheer, H. A., Elsalem, L., Salem, A., Tailor, A., Hunter, K. D., & Afarinkia, K. (2021) · Current Cancer Drug Targets · doi:10.2174/1568009622666211224111425 · Cited by 8
Icard, P., Teboul, B., & Baze, P. E. (2017) · Anticancer Research · doi:10.21873/anticanres.12069 · Cited by 8
Wang, T., Wang, X., Zheng, X., Guo, Z., Mohsin, A., Zhuang, Y., & Wang, G. (2024) · Biotechnology Journal · doi:10.1002/biot.202400163 · Cited by 7
Prolyl Hydroxylase 3 Knockdown Accelerates VHL-Mutant Kidney Cancer Growth In Vivo
Zacharias, N. M., Wang, L., Maity, T., Li, L., Millward, S. W., Karam, J. A., Wood, C. G., & Navai, N. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22062849 · Cited by 7
Hou, K.-L., Lin, S.-K., Kok, S.-H., Wang, H.-W., Lai, E. H.-H., Hong, C.-Y., Yang, H., Wang, J.-S., Lin, L.-D., & Chang, J. Z.-C. (2017) · Journal of Endodontics · doi:10.1016/j.joen.2016.11.005 · Cited by 7
Glutaminase 1 inhibitors: Therapeutic potential, mechanisms of action, and clinical perspectives
Wang, H., Li, X., Hu, H., & Gao, Z. (2025) · Biochemical Pharmacology · doi:10.1016/j.bcp.2025.117275 · Cited by 10
Zhang, J., Gao, T., Chen, S., Wu, S., Mao, Y., Cai, D., & Lu, T. (2025) · Annals of Hematology · doi:10.1007/s00277-025-06321-1 · Cited by 6
Ma, Y., Ling, S., Li, Y., Hu, M., Kong, B., Huang, P., & Liu, H. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23126697 · Cited by 6
Delineating cell behavior and metabolism of non-melanoma skin cancer in vitro
Mendez, T., Saffari, S., Cowan, J. M., Laver, N., Baleja, J., & Alt‐Holland, A. (2020) · In Vitro Cellular & Developmental Biology - Animal · doi:10.1007/s11626-019-00416-6 · Cited by 6
Bellal, S., Rolley, C., Richard, J., Bounaix, N., Corre, V. L., Copin, M., Blanchet, O., Bigot, P., Procaccio, V., & Bris, C. (2025) · Pathology & Oncology Research · doi:10.3389/pore.2025.1612172 · Cited by 8
Min, K., Yenilmez, B., Kelly, M., Echeverria, D., Elleby, M., Lifshitz, L. M., Raymond, N., Tsagkaraki, E., Harney, S. M., DiMarzio, C., et al. (2024) · eLife · doi:10.7554/elife.89136.3 · Cited by 5
Yan, L., Sundaram, S., RUST, B. M., Picklo, M. J., & Bukowski, M. R. (2020) · Anticancer Research · doi:10.21873/anticanres.14358 · Cited by 4
Glucose and glutamine metabolism-related protein expression in breast ductal carcinoma in situ
Ryu, H. J., & Koo, J. S. (2022) · Neoplasma · doi:10.4149/neo_2022_220103n3 · Cited by 4
Onyango, C., Anyona, S. B., Hurwitz, I., Raballah, E., Wasena, S. A., Osata, S. W., Seidenberg, P., McMahon, B. H., Lambert, C. G., Schneider, K. A., et al. (2024) · Pathogens · doi:10.3390/pathogens13100867 · Cited by 3
Li, J., Qiu, Z., Xie, R., Ma, L., Tang, L., Yao, M., Zhang, Z., Chen, L., & Zhang, L. (2025) · Thrombosis and Haemostasis · doi:10.1055/a-2600-6318 · Cited by 3
Untargeted Metabolomic Identifies Potential Seasonal Biomarkers of Semen Quality in Duroc Boars
Dlamini, N. H., Kameni, S. L. L., & Feugang, J. M. (2025) · Biology · doi:10.3390/biology14080995 · Cited by 3
Huang, R., Han, B. R., Zhang, Y., Yang, J., Wang, K., Liu, X., & Wang, Z. (2024) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.18208 · Cited by 2
Chegodaev, D., & Pavlova, P. (2024) · Frontiers in Neurology · doi:10.3389/fneur.2024.1393274 · Cited by 3
Min, K., Yenilmez, B., Kelly, M., Echeverria, D., Elleby, M., Lifshitz, L. M., Raymond, N., Tsagkaraki, E., Harney, S. M., DiMarzio, C., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.03.539244 · Cited by 3
Tsingas, M., Tsingas, K., Zhang, W., Goldman, A. R., & Risbud, M. V. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.24.640004 · Cited by 3
Drug Repurposing: A Conduit to Unravelling Metabolic Reprogramming for Cancer Treatment
Chaudhary, S., Rana, A., & Bhatnagar, S. (2025) · Mini-Reviews in Medicinal Chemistry · doi:10.2174/0113895575339660250106093738 · Cited by 3
Oxidative stress and cancer metabolism: From pathogenesis to therapeutic opportunities
Agnihotri, T. G., Gomte, S. S., Rout, B., Peddinti, V., Maharana, S. K., Yallappa, D., & Jain, A. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-33459-7.00006-5 · Cited by 3
Nutritional modulation of metabolic signaling within the tumor microenvironment for cancer therapy
Aghdam, M. M., Rezagholizadeh, L., Fazaeli, A., Moradi, A., & Ojarudi, M. (2026) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-025-05462-1 · Cited by 3
Lactate Facilitates the Survival and Invasion of Pancreatic Cancer Cells Under Glucose Deprivation
Wang, F., Hu, P., Han, S., Zhang, Y., Li, Y., Zhuo, W., Zhao, Y. B., Huang, Y., Lv, G., Wang, H., et al. (2026) · The FASEB Journal · doi:10.1096/fj.202503162rr · Cited by 2
Global translational and metabolic remodeling during iron deprivation in Toxoplasma gondii
Hanna, J. C., Shikha, S., Sloan, M. A., & Harding, C. R. (2026) · mBio · doi:10.1128/mbio.03788-25 · Cited by 2
Lactate and lactylation: metabolic architects of tumor progression and metastasis
Ma, H., Gu, Z., & Wang, Z. (2026) · Cellular Oncology · doi:10.1007/s13402-026-01182-w · Cited by 4
PCK2-Mediated PQBP1 Lactylation Promotes Asthmatic Inflammation through PRMT5 Inhibition
Bai, Q., Ding, N., Feng, R., Shang, F., Wang, Z., Li, L., Wang, Z., Piao, Y., Wang, C., Song, Y., et al. (2026) · Research · doi:10.34133/research.1321 · Cited by 2
Wu, Y., Chen, X.-D., Chen, Z., Sun, R., Zhang, Q., Zengin, G., & Li, M. (2026) · BioFactors · doi:10.1002/biof.70126 · Cited by 2
Hsu, T., Wang, W., Chen, H., Wang, T.-H., Su, C.-M., Liao, P., Chen, A., Tsai, K., Kokotos, G., Kuo, C.-C., et al. (2025) · Cancer & Metabolism · doi:10.1186/s40170-025-00377-3 · Cited by 2
Cancer-associated transporters: Molecular drivers and drug delivery gateways
Khan, A. A., Biswas, S., Garg, M., & Sengupta, S. (2025) · Biochemical Pharmacology · doi:10.1016/j.bcp.2025.117376 · Cited by 2
Zhao, L., Deng, H., Zhang, J., Zamboni, N., Geest, G. A., Yang, H., Zhang, Y., Gao, Y., Xu, D., Zhong, H., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.02.12.525859 · Cited by 2
Dou, Y. (2025) · New cell · doi:10.61958/ncjt1177 · Cited by 1
CircRBM33 facilitates colorectal cancer progression by regulating the miR-512–5p/SLC1A5 axis
Zhang, J., Zhang, L., Tanaka, K., Shi, F., She, J., & He, S. (2025) · Pathology - Research and Practice · doi:10.1016/j.prp.2025.156248 · Cited by 1
The role of glutamine/Nrf2-enhanced PHGDH in Cadmium-induced lactate utilization
Pang, Y., Li, S., Zhang, Q., Liu, Y., Kong, Y., & Cao, J. (2025) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2025.12.015 · Cited by 1
Metadata
- Authors
- Pérez-Escuredo, J., Dadhich, R. K., Dhup, S., Cacace, A., Van Hée, V. F., De Saedeleer, C. J., Sboarina, M., Rodriguez, F., Fontenille, M.-J., Brisson, L., Porporato, P. E., & Sonveaux, P.
- Affiliations
- From the Pole of Pharmacology, Institute of Experimental and Clinical Research (IREC), Université catholique de Louvain (UCL) Medical School, Brussels, Belgium
- UCLouvain (BE)
- Corresponding author
- Sonveaux, Pierre
- Venue
- Cell Cycle
- Publisher
- Informa UK Limited
- Published
- 2016-01-02
- Volume
- 15
- Issue
- 1
- Pages
- 72-83
- ISSN
- 1538-4101 (ISSN-L)
- 1551-4005
- PMC
- PMC4825768
- OpenAlex
- W2184384535
- Cited by
- 231
- References
- 56
- Citations by year
- 2026: 15 · 2025: 26 · 2024: 27 · 2023: 24 · 2022: 22 · 2021: 27 · 2020: 29 · 2019: 19 · 2018: 11 · 2017: 22 · 2016: 9
- FWCI
- 4.63
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Cell Cycle (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Digital Access to Libraries (submittedVersion)
- Institutional Research Information System University of Turin (University of Turin) (submittedVersion)
- Funders
- Fonds De La Recherche Scientifique - FNRS
- Belgian Federal Science Policy Office (UP7-03)
- Fonds Joseph Maisin
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Hypoxia, and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Amino Acid Enzymes and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- lactate metabolism, glutamine uptake, glutaminolysis, MCT1, HIF-2α, c-Myc, ASCT2, GLS1, cancer metabolism, metabolic plasticity, lactate signaling, glycolysis
- MeSH terms
- Endothelial PAS Domain-Containing Protein 1, Monocarboxylate Transport Protein 1, Animals, Glutaminase, Glutamine, HeLa Cells, Humans, Male, Mice, Inbred BALB C, Mice, Nude, Neoplasms, Oxidation-Reduction, Lactic Acid, Monocarboxylic Acid Transporters, Symporters, Mice, Basic Helix-Loop-Helix Proteins
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