The warburg effect in leukemia-stroma cocultures is mediated by mitochondrial uncoupling associated with uncoupling protein 2 activation
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Abstract
In 1956, Otto Warburg proposed that the origin of cancer cells was closely linked to a permanent respiratory defect that bypassed the Pasteur effect (i.e., the inhibition of anaerobic fermentation by oxygen). Since then, permanent defects in oxygen consumption that could explain the dependence of cancer cells on aerobic glycolysis have not been identified. Here, we show that under normoxic conditions exposure of leukemia cells to bone marrow-derived mesenchymal stromal cells (MSC) promotes accumulation of lactate in the culture medium and reduces mitochondrial membrane potential (DeltaPsiM) in both cell types. Notably, the consumption of glucose was not altered in cocultures, suggesting that the accumulation of lactate was the result of reduced pyruvate metabolism. Interestingly, the decrease in DeltaPsiM was mediated by mitochondrial uncoupling in leukemia cells and was accompanied by increased expression of uncoupling protein 2 (UCP2). HL60 cells fail to increase UCP2 expression, are not uncoupled after coculture, and do not exhibit increased aerobic glycolysis, whereas small interfering RNA-mediated suppression of UCP2 in OCI-AML3 cells reversed mitochondrial uncoupling and aerobic glycolysis elicited by MSC. Taken together, these data suggest that microenvironment activation of highly conserved mammalian UCPs may facilitate the Warburg effect in the absence of permanent respiratory impairment.
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The critical role of UCP2 in promoting aerobic glycolysis and inhibiting oxidative phosphorylation has been established from multiple experimental models.
“the critical role of UCP2 (uncoupling protein 2) in promoting aerobic glycolysis and inhibiting oxidative phosphorylation has been established from multiple experimental models (Pecqueur et al., 2008; Samudio et al., 2008; Bouillaud, 2009; Zhang et al., 2011).”
From Metabolic reprogramming during neuronal differentiation from aerobic glycolysis to neuronal oxidative phosphorylation (2016) · cites this paper as Samudio et al., 2008
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Cites
Warburg, O. (1956) · Science · doi:10.1126/science.123.3191.309 · Cited by 13,425 · see citing works
Cossarizza, A., Baccarani-Contri, M., Kalashnikova, G., & Franceschi, C. (1993) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1993.2438 · Cited by 1,031 · see citing works
Konopleva, M. Y., Contractor, R., Tsao, T., Samudio, I. J., Ruvolo, P. P., Kitada, S., Deng, X., Zhai, D., Shi, Y.-X., Sneed, T. B., et al. (2006) · Cancer Cell · doi:10.1016/j.ccr.2006.10.006 · Cited by 1,020 · see citing works
Self-citationThe uncoupling protein homologues: UCP1, UCP2, UCP3, StUCP and AtUCP
Ricquier, D., & Bouillaud, F. (2000) · Biochemical Journal · doi:10.1042/bj3450161 · Cited by 806 · see citing works
Physiological functions of the mitochondrial uncoupling proteins UCP2 and UCP3
Brand, M. D., & Esteves, T. C. (2005) · Cell Metabolism · doi:10.1016/j.cmet.2005.06.002 · Cited by 785 · see citing works
Mitochondrial remodeling in adipose tissue associated with obesity and treatment with rosiglitazone.
Wilson-Fritch, L., Nicoloro, S., Chouinard, M., Lazar, M. A., Chui, P. C., Leszyk, J., Straubhaar, J., Czech, M. P., & Corvera, S. (2004) · Journal of Clinical Investigation · doi:10.1172/jci21752 · Cited by 616 · see citing works
A signalling role for 4‐hydroxy‐2‐nonenal in regulation of mitochondrial uncoupling
Echtay, K. S., Esteves, T. C., Pakay, J. L., Jekabsons, M. B., Lambert, A. J., Portero‐Otín, M., Pamplona, R., Vidal‐Puig, A. J., Wang, S., Roebuck, S. J., et al. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg412 · Cited by 597 · see citing works
Excess Lipid Availability Increases Mitochondrial Fatty Acid Oxidative Capacity in Muscle
Turner, N., Bruce, C. R., Beale, S. M., Hoehn, K. L., So, T., Rolph, M. S., & Cooney, G. J. (2007) · Diabetes · doi:10.2337/db07-0093 · Cited by 520 · see citing works
Mattiasson, G., Shamloo, M., Gido, G., Mathi, K., Tomasevic, G., Yi, S., Warden, C. H., Castilho, R. F., Melcher, T., Gonzalez-Zulueta, M., et al. (2003) · Nature Medicine · doi:10.1038/nm903 · Cited by 515 · see citing works
Budd, S. L., & Nicholls, D. G. (1996) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1996.67062282.x · Cited by 435 · see citing works
Lum, J. J., Bui, T., Gruber, M., Gordan, J. D., DeBerardinis, R. J., Covello, K. L., Simon, M. C., & Thompson, C. B. (2007) · Genes & Development · doi:10.1101/gad.1529107 · Cited by 429 · see citing works
Stromal cells prevent apoptosis of AML cells by up-regulation of anti-apoptotic proteins
Konopleva, M. Y., Konoplev, S. N., Hu, W., Zaritskey, A. Y., Afanasyev, B. V., & Andreeff, M. (2002) · Leukemia · doi:10.1038/sj.leu.2402608 · Cited by 389 · see citing works
Self-citationSuperoxide Activates Mitochondrial Uncoupling Protein 2 from the Matrix Side
Echtay, K. S., Murphy, M. P., Smith, R. A. J., Talbot, D. A., & Brand, M. D. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m208262200 · Cited by 388 · see citing works
Transport function and regulation of mitochondrial uncoupling proteins 2 and 3
Jabůrek, M., Vařecha, M., Gimeno, R. E., Dembski, M., Ježek, P., Zhang, M., Burn, P., Tartaglia, L. A., & Garlid, K. D. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.37.26003 · Cited by 321 · see citing works
The glycolytic phenotype in carcinogenesis and tumor invasion: insights through mathematical models.
Gatenby, R. A., & Gawlinski, E. T. (2003) · PubMed · Cited by 314 · see citing works
HIF-1 mediates the Warburg effect in clear cell renal carcinoma
Semenza, G. L. (2007) · Journal of Bioenergetics and Biomembranes · doi:10.1007/s10863-007-9081-2 · Cited by 281 · see citing works
Adipocyte-Derived Hormones, Cytokines, and Mediators
Rondinone, C. M. (2006) · Endocrine · doi:10.1385/endo:29:1:81 · Cited by 246 · see citing works
Bouillaud, F., Ricquier, D., Thibault, J., & Weissenbach, J. (1985) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.82.2.445 · Cited by 244 · see citing works
Pecqueur, C., Bui, T., Gelly, C., Hauchard, J., Barbot, C., Bouillaud, F., Ricquier, D., Miroux, B., & Thompson, C. B. (2008) · The FASEB Journal · doi:10.1096/fj.07-8945com · Cited by 209 · see citing works
Konopleva, M. Y., Mikhail, A. A., Estrov, Z. E., Zhao, S., Harris, D., Sanchez‐Williams, G., Kornblau, S. M., Dong, J., Kliche, K. O., Jiang, S., et al. (1999) · Blood · doi:10.1182/blood.v93.5.1668 · Cited by 187 · see citing works
Self-citationA predictive model for the selective accumulation of chemicals in tumor cells
Trapp, S., & Horobin, R. W. (2005) · European Biophysics Journal · doi:10.1007/s00249-005-0472-1 · Cited by 180 · see citing works
The Emerging Functions of UCP2 in Health, Disease, and Therapeutics
Mattiasson, G., & Sullivan, P. G. (2006) · Antioxidants and Redox Signaling · doi:10.1089/ars.2006.8.1 · Cited by 176 · see citing works
Characterization of a novel metabolic strategy used by drug‐resistant tumor cells
Harper, M., Antoniou, A., Villalobos‐Menuey, E., Russo, A., Trauger, R. J., Vendemelio, M., George, A., Bartholomew, R. M., Carlo, D. J., Shaikh, A., et al. (2002) · The FASEB Journal · doi:10.1096/fj.02-0541com · Cited by 172 · see citing works
Mitochondrial UCPs: New insights into regulation and impact
Sluse, F. E., Jarmuszkiewicz, W., Navet, R., Douette, P., Mathy, G., & Sluse‐Goffart, C. M. (2006) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2006.02.004 · Cited by 144 · see citing works
Bouillaud, F., Ricquier, D., Mory, G., & Thibault, J. (1984) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)90902-6 · Cited by 142 · see citing works
The Oligomycin Axis of Mitochondrial ATP Synthase: OSCP and the Proton Channel
Devenish, R. J., Prescott, M., Boyle, G. M., & Nagley, P. (2000) · Journal of Bioenergetics and Biomembranes · doi:10.1023/a:1005621125812 · Cited by 119 · see citing works
Tabe, Y., Konopleva, M., Munsell, M. F., Marini, F. C., Zompetta, C., McQueen, T., Tsao, T., Zhao, S., Pierce, S., Igari, J., et al. (2004) · Blood · doi:10.1182/blood-2003-03-0802 · Cited by 93 · see citing works
Self-citationUCP2, UCP3 and leptin gene expression: modulation by food restriction and leptin
Scarpace, P., Nicolson, M. A., & Matheny, M. E. (1998) · Journal of Endocrinology · doi:10.1677/joe.0.1590349 · Cited by 92 · see citing works
Qian, H., Hausman, G., Compton, M. M., Azain, M. J., Hartzell, D. L., & Baile, C. A. (1998) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1998.8680 · Cited by 84 · see citing works
Konopleva, M. Y., Mikhail, A. A., Estrov, Z. E., et al. (1999) · Blood · doi:10.1182/blood.v93.5.1668.405a15_1668_1676 · Cited by 78 · see citing works
The stem cell niche in health and leukemic disease
Scadden, D. T. (2007) · Best Practice & Research Clinical Haematology · doi:10.1016/j.beha.2006.11.001 · Cited by 77 · see citing works
Die Rolle der Phosphors�ure bei Dehydrierungsvorg�ngen und ihre biologische Bedeutung
Lynen, F. (1942) · Die Naturwissenschaften · doi:10.1007/bf01475305 · Cited by 71 · see citing works
Desquiret‐Dumas, V., Loiseau, D., Jacques, C., Douay, O., Malthièry, Y., Ritz, P., & Roussel, D. (2005) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2005.11.005 · Cited by 69 · see citing works
Wang, L., O’Leary, H. A., Fortney, J. E., & Gibson, L. F. (2007) · Blood · doi:10.1182/blood-2007-01-068122 · Cited by 65 · see citing works
Samudio, I., Konopleva, M., Pelicano, H., Huang, P., Frolova, O., Bornmann, W., Ying, Y., Evans, R., Contractor, R., & Andreeff, M. (2006) · Molecular Pharmacology · doi:10.1124/mol.105.018051 · Cited by 58 · see citing works
Self-citationTHE EFFECT OF DINITROPHENOL ON THE METABOLISM OF FROG MUSCLE
Ronzoni, E., & Ehrenfest, E. (1936) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)74713-3 · Cited by 55 · see citing works
Targeting the Leukemia Microenvironment
Konopleva, M. Y., & Andreeff, M. (2007) · Current Drug Targets · doi:10.2174/138945007780830827 · Cited by 53 · see citing works
Self-citationUncoupling protein 2 protects testicular germ cells from hyperthermia-induced apoptosis
Zhang, K., Shang, Y., Liao, S., Zhang, W., Nian, H., Liu, Y., Chen, Q., & Han, C. (2007) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2007.06.071 · Cited by 36 · see citing works
Oncogene-dependent engraftment of human myeloid leukemia cells in immunosuppressed mice
Kiser, M. N., McCubrey, J. A., Steelman, L., Shelton, J. G., Ramage, J. G., ALEXANDER, R. L., Kucera, G. L., Pettenati, M. J., Willingham, M. C., Miller, M., et al. (2001) · Leukemia · doi:10.1038/sj.leu.2402084 · Cited by 23 · see citing works
Boyle, G. M., Roucou, X., Nagley, P., Devenish, R. J., & Prescott, M. (2000) · Journal of Bioenergetics and Biomembranes · doi:10.1023/a:1005674628249 · Cited by 11 · see citing works
Tabe, Y., Konopleva, M. Y., Igari, J., & Andreeff, M. (2004) · PubMed · Cited by 9 · see citing works
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Flagged first, then by citations
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Cancer metabolism: fatty acid oxidation in the limelight
Carracedo, A., Cantley, L. C., & Pandolfi, P. P. (2013) · Nature reviews. Cancer · doi:10.1038/nrc3483 · Cited by 1,316 · see citing works
Samudio, I. J., Harmancey, R., Fiegl, M., Kantarjian, H. M., Konopleva, M. Y., Korchin, B., Kaluarachchi, K. K., Bornmann, W. G., Duvvuri, S. R., Taegtmeyer, H., et al. (2009) · Journal of Clinical Investigation · doi:10.1172/jci38942 · Cited by 710 · see citing works
Self-citationZheng, X., Boyer, L., Jin, M., Mertens, J., Kim, Y., Ma, L., Ma, L., Hamm, M., Gage, F. H., & Hunter, T. (2016) · eLife · doi:10.7554/elife.13374 · Cited by 671 · see citing works
“In addition to the conventional regulators of glycolysis, TCA and oxidative phosphorylation, the critical role of UCP2 (uncoupling protein 2) in promoting aerobic glycolysis and inhibiting oxidative phosphorylation has been established from multiple experimental models (Pecqueur et al., 2008; Samudio et al., 2008; Bou…”
MethodUCP2 regulates energy metabolism and differentiation potential of human pluripotent stem cells
Zhang, J., Khvorostov, I., Hong, J. S., Oktay, Y., Vergnes, L., Nuebel, E., Wahjudi, P. N., Setoguchi, K., Wang, G., Do, A., et al. (2011) · The EMBO Journal · doi:10.1038/emboj.2011.401 · Cited by 499 · see citing works
Phan, L. M., Yeung, S. J., & Lee, M. H. (2014) · Europe PMC (PubMed Central) · doi:10.7497/j.issn.2095-3941.2014.01.001 · Cited by 500 · see citing works
Moschoi, R., Imbert, V., Nebout, M., Chiche, J., Mary, D. A. S. G., Prébet, T., Saland, E., Castellano, R., Pouyet, L., Collette, Y., et al. (2016) · Blood · doi:10.1182/blood-2015-07-655860 · Cited by 467 · see citing works
UCP2 transports C4 metabolites out of mitochondria, regulating glucose and glutamine oxidation
Vozza, A., Parisi, G., De Leonardis, F., Lasorsa, F. M., Castegna, A., Amorese, D., Marmo, R., Calcagnile, V. M., Palmieri, L., Ricquier, D., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1317400111 · Cited by 407 · see citing works
The PI3K-Akt-mTOR Signaling Pathway in Human Acute Myeloid Leukemia (AML) Cells
Nepstad, I., Hatfield, K. J., Grønningsæter, I. S., & Reikvam, H. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21082907 · Cited by 350 · see citing works
The metabolism of human mesenchymal stem cells during proliferation and differentiation
Pattappa, G., Heywood, H. K., de Bruijn, J. D., & Lee, D. A. (2010) · Journal of Cellular Physiology · doi:10.1002/jcp.22605 · Cited by 336 · see citing works
Mitochondrial Channels: Ion Fluxes and More
Szabó, I., & Zoratti, M. (2014) · Physiological Reviews · doi:10.1152/physrev.00021.2013 · Cited by 321 · see citing works
Samudio, I. J., Fiegl, M., & Andreeff, M. (2009) · Cancer Research · doi:10.1158/0008-5472.can-08-3722 · Cited by 309 · see citing works
Self-citationThe Warburg effect: Insights from the past decade
Upadhyay, M., Samal, J., Kandpal, M., Singh, O. V., & Vivekanandan, P. (2012) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2012.11.003 · Cited by 245 · see citing works
UCP2-induced fatty acid synthase promotes NLRP3 inflammasome activation during sepsis
Moon, J.-S., Lee, S., Park, M.-A., Siempos, I. I., Haslip, M., Lee, P. J., Yun, M., Kim, C. K., Howrylak, J., Ryter, S. W., et al. (2015) · Journal of Clinical Investigation · doi:10.1172/jci78253 · Cited by 238 · see citing works
RetractedGlut 1 in Cancer Cells and the Inhibitory Action of Resveratrol as A Potential Therapeutic Strategy
Zambrano, Á., Molt, M., Uribe, E. A., & Salas, M. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20133374 · Cited by 212 · see citing works
Rattigan, Y. I., Patel, B. B., Ackerstaff, E., Sukenick, G., Koutcher, J. A., Glod, J. W., & Banerjee, D. (2012) · Experimental Cell Research · doi:10.1016/j.yexcr.2011.11.014 · Cited by 196 · see citing works
Inhibiting glutaminase in acute myeloid leukemia: metabolic dependency of selected AML subtypes
Matre, P., Velez, J., Jacamo, R., Qi, Y., Su, X., Cai, T., Chan, S. M., Lodi, A., Sweeney, S. R., Ma, H., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.12944 · Cited by 185 · see citing works
Self-citationMetabolic Plasticity in Chemotherapy Resistance
Desbats, M. A., Giacomini, I., Prayer‐Galetti, T., & Montopoli, M. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.00281 · Cited by 180 · see citing works
Mesenchymal Stem Cells: Flip Side of the Coin
Mishra, P. J., Mishra, P. J., Glod, J. W., & Banerjee, D. (2009) · Cancer Research · doi:10.1158/0008-5472.can-08-3562 · Cited by 181 · see citing works
Martinez‐Outschoorn, U., Goldberg, A. F., Zhao, L., Ko, Y., Flomenberg, N., Wang, C., Pavlides, S., Pestell, R. G., Howell, A., Sotgia, F., et al. (2011) · Cancer Biology & Therapy · doi:10.4161/cbt.12.10.17780 · Cited by 175 · see citing works
Mitochondrial Transfer and Regulators of Mesenchymal Stromal Cell Function and Therapeutic Efficacy
Mohammadalipour, A., Dumbali, S. P., & Wenzel, P. L. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.603292 · Cited by 176 · see citing works
UCP2, a mitochondrial protein regulated at multiple levels
Donadelli, M., Dando, I., Fiorini, C., & Palmieri, M. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1407-0 · Cited by 176 · see citing works
Myeloid malignancies and the microenvironment
Korn, C., & Méndez‐Ferrer, S. (2016) · Blood · doi:10.1182/blood-2016-09-670224 · Cited by 169 · see citing works
Vanniarajan, A., Owens, K. M., Desouki, M. M., Liang, P., Bakin, A. V., Kumarasamy Thangaraj, K., Buchsbaum, D. J., LoBuglio, A. F., & Singh, K. K. (2011) · PLoS ONE · doi:10.1371/journal.pone.0024792 · Cited by 148 · see citing works
Bouillaud, F. (2009) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2009.01.003 · Cited by 146 · see citing works
Mitochondrial VDAC1: Function in Cell Life and Death and a Target for Cancer Therapy
Shoshan‐Barmatz, V., & Golan, M. (2012) · Current Medicinal Chemistry · doi:10.2174/092986712798992110 · Cited by 139 · see citing works
Hao, W., Chang, C.-P. B., Tsao, C.-C., & Xu, J. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.084194 · Cited by 138 · see citing works
Potential role of genipin in cancer therapy
Shanmugam, M. K., Shen, H., Tang, F. R., Arfuso, F., Rajesh, M., Wang, L., Kumar, A. P., Bian, J., Goh, B. C., Bishayee, A., et al. (2018) · Pharmacological Research · doi:10.1016/j.phrs.2018.05.007 · Cited by 138 · see citing works
Liao, Z., Li, S., Lu, S., Liu, H., Li, G., Ma, L., Luo, R., Ke, W., Wang, B., Xiang, Q., et al. (2021) · Biomaterials · doi:10.1016/j.biomaterials.2021.120850 · Cited by 135 · see citing works
Scotland, S., Saland, E., Skuli, N., de Toni, F., Boutzen, H., Micklow, E., Sénégas, I., Peyraud, R., Peyriga, L., Théodoro, F., et al. (2013) · Leukemia · doi:10.1038/leu.2013.107 · Cited by 131 · see citing works
Intracellular ion channels and cancer
Leanza, L., Biasutto, L., Managò, A., Gulbins, E., Zoratti, M., & Szabó, I. (2013) · Frontiers in Physiology · doi:10.3389/fphys.2013.00227 · Cited by 128 · see citing works
Ohkouchi, S., Block, G. J., Katsha, A. M., Kanehira, M., Ebina, M., Kikuchi, T., Saijo, Y., Nukiwa, T., & Prockop, D. J. (2011) · Molecular Therapy · doi:10.1038/mt.2011.259 · Cited by 121 · see citing works
Uncoupling protein-2 and cancer
Baffy, G. (2009) · Mitochondrion · doi:10.1016/j.mito.2009.12.143 · Cited by 119 · see citing works
Sun, W., Liu, Y., Glazer, C. A., Shao, C., Bhan, S., Demokan, S., Zhao, M., Rudek, M. A., Ha, P. K., & Califano, J. A. (2010) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-09-2604 · Cited by 119 · see citing works
Cai, J., Wang, J., Huang, Y., Wu, H., Xia, T., Xiao, J., Chen, X., Li, H., Qiu, Y., Wang, Y., et al. (2016) · Cell Death and Disease · doi:10.1038/cddis.2016.370 · Cited by 116 · see citing works
Inhibition of Fatty Acid Metabolism Reduces Human Myeloma Cells Proliferation
Tirado-Vélez, J. M., Joumady, I., Sáez-Benito, A., Cózar‐Castellano, I., & Perdomo, G. (2012) · PLoS ONE · doi:10.1371/journal.pone.0046484 · Cited by 113 · see citing works
Ono, M., Ohkouchi, S., Kanehira, M., Tode, N., Kobayashi, M., Ebina, M., Nukiwa, T., Irokawa, T., Ogawa, H., Akaike, T., et al. (2014) · Molecular Therapy · doi:10.1038/mt.2014.217 · Cited by 111 · see citing works
Oxidative stress and hypoxia in normal and leukemic stem cells
Testa, U., Labbaye, C., Castelli, G., & Pelosi, E. (2016) · Experimental Hematology · doi:10.1016/j.exphem.2016.04.012 · Cited by 112 · see citing works
Mitochondria in cancer: in the aspects of tumorigenesis and targeted therapy
Badrinath, N., & Yoo, S. Y. (2018) · Carcinogenesis · doi:10.1093/carcin/bgy148 · Cited by 108 · see citing works
Mesenchymal stem cell signaling in cancer progression
Torsvik, A., & Bjerkvig, R. (2013) · Cancer Treatment Reviews · doi:10.1016/j.ctrv.2012.03.005 · Cited by 100 · see citing works
Resveratrol induces mitochondrial respiration and apoptosis in SW620 colon cancer cells
Blanquer-Rosselló, M. D. M., Hernández‐López, R., Roca, P., Oliver, J., & Valle, A. (2016) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2016.10.009 · Cited by 93 · see citing works
Metabolic features of macrophages in inflammatory diseases and cancer
Na, Y. R., Je, S., & Seok, S. H. (2017) · Cancer Letters · doi:10.1016/j.canlet.2017.10.044 · Cited by 95 · see citing works
Mitochondrial ion channels as oncological targets
Leanza, L., Zoratti, M., Gulbins, E., & Szabó, I. (2014) · Oncogene · doi:10.1038/onc.2013.578 · Cited by 90 · see citing works
UCP2, a metabolic sensor coupling glucose oxidation to mitochondrial metabolism?
Pecqueur, C., Alves‐Guerra, M., Ricquier, D., & Bouillaud, F. (2009) · IUBMB Life · doi:10.1002/iub.188 · Cited by 89 · see citing works
Mitochondrial recoupling: a novel therapeutic strategy for cancer
Baffy, G., Derdak, Z., & Robson, S. C. (2011) · British Journal of Cancer · doi:10.1038/bjc.2011.245 · Cited by 88 · see citing works
“A better understanding of the molecular mechanisms that facilitate cancer cell survival should help guide novel therapeutic strategies.”
BackgroundLuo, Z., Yao, J., Wang, Z., & Xu, J. (2023) · Journal of Translational Medicine · doi:10.1186/s12967-023-04286-1 · Cited by 87 · see citing works
Non-glucose metabolism in cancer cells—is it all in the fat?
Biswas, S., Lunec, J., & Bartlett, K. (2012) · Cancer and Metastasis Reviews · doi:10.1007/s10555-012-9384-6 · Cited by 86 · see citing works
Estèves, P., Pecqueur, C., Ransy, C., Esnous, C., Lenoir, V., Bouillaud, F., Bulteau, A., Lombès, A., Prip‐Buus, C., Ricquier, D., et al. (2014) · Cancer Research · doi:10.1158/0008-5472.can-13-3383 · Cited by 86 · see citing works
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Can, M. M., Kaymaz, C., Tanboğa, İ. H., Tokgöz, H. C., Canpolat, N., Türkyılmaz, E., Sönmez, K., & Özdemir, N. (2011) · Clinical Nuclear Medicine · doi:10.1097/rlu.0b013e3182177389 · Cited by 85 · see citing works
Uncoupling protein 2 and metabolic diseases
Sreedhar, A., & Zhao, Y. (2017) · Mitochondrion · doi:10.1016/j.mito.2017.03.005 · Cited by 82 · see citing works
Hypoxia-Activated Prodrug TH-302 Targets Hypoxic Bone Marrow Niches in Preclinical Leukemia Models
Benito, J., Ramirez, M. S., Zacharias, N. M., Vélez, J., Harutyunyan, K. G., Lu, H., Shi, Y.-X., Matre, P. R., Jacamo, R. O., Ma, H., et al. (2015) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-14-3378 · Cited by 75 · see citing works
Self-citationIL-8 as mediator in the microenvironment-leukaemia network in acute myeloid leukaemia
Kütt, A., Rieger, C. T., Perathoner, D., Herold, T., Wagner, M. M., Sironi, S., Sotlar, K., Horny, H., Deniffel, C., Drolle, H., et al. (2015) · Scientific Reports · doi:10.1038/srep18411 · Cited by 72 · see citing works
Self-citationForrest, M. (2015) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/025197 · Cited by 71 · see citing works
Brandi, J., Cecconi, D., Cordani, M., Torrens‐Mas, M., Pacchiana, R., Pozza, E. D., Butera, G., Manfredi, M., Marengo, E., Oliver, J., et al. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.10.499 · Cited by 71 · see citing works
Balancing biosynthesis and bioenergetics: metabolic programs in oncogenesis
Barger, J. F., & Plas, D. R. (2010) · Endocrine Related Cancer · doi:10.1677/erc-10-0106 · Cited by 65 · see citing works
Enzymatic features of the glucose metabolism in tumor cells
Herling, A., König, M., Bulik, S., & Holzhütter, H. (2011) · FEBS Journal · doi:10.1111/j.1742-4658.2011.08174.x · Cited by 67 · see citing works
Cancer Stem Cell Theory and the Warburg Effect, Two Sides of the Same Coin?
Pacini, N., & Borziani, F. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms15058893 · Cited by 67 · see citing works
Ionizing radiation, ion transports, and radioresistance of cancer cells
Huber, S. M., Butz, L., Stegen, B., Klumpp, D., Braun, N., Ruth, P., & Eckert, F. (2013) · Frontiers in Physiology · doi:10.3389/fphys.2013.00212 · Cited by 67 · see citing works
Role of Uncoupling Proteins in Cancer
Valle, A., Oliver, J., & Roca, P. (2010) · Cancers · doi:10.3390/cancers2020567 · Cited by 67 · see citing works
Metabolic flexibility and cell hierarchy in metastatic cancer
Berridge, M. V., Herst, P. M., & Tan, A. S. (2010) · Mitochondrion · doi:10.1016/j.mito.2010.08.002 · Cited by 66 · see citing works
Metformin: A metabolic disruptor and anti-diabetic drug to target human leukemia
Rosilio, C., Ben‐Sahra, I., Bost, F., & Peyron, J. (2014) · Cancer Letters · doi:10.1016/j.canlet.2014.01.006 · Cited by 59 · see citing works
Amano, Y., Mandai, M., Yamaguchi, K. D., Matsumura, N., Kharma, B., Baba, T., Abiko, K., Hamanishi, J., Yoshioka, Y., & Konishi, I. (2015) · Oncotarget · doi:10.18632/oncotarget.4692 · Cited by 58 · see citing works
Targeting the Warburg effect in hematological malignancies: from PET to therapy
Shanmugam, M., McBrayer, S. K., & Rosen, S. T. (2009) · Current Opinion in Oncology · doi:10.1097/cco.0b013e32832f57ec · Cited by 56 · see citing works
Ke, Q., Yuan, Q., Qin, N., Shi, C., Luo, J., Fang, Y., Xu, L., Sun, Q., Zen, K., Jiang, L., et al. (2020) · Cell Death and Disease · doi:10.1038/s41419-019-2219-4 · Cited by 56 · see citing works
The Role of Tumor-Associated Macrophages in Hematologic Malignancies
Cencini, E., Fabbri, A., Sicuranza, A., Gozzetti, A., & Bocchia, M. (2021) · Cancers · doi:10.3390/cancers13143597 · Cited by 55 · see citing works
Li, W., Nichols, K., Nathan, C. O., & Zhao, Y. (2013) · Cancer Biomarkers · doi:10.3233/cbm-130369 · Cited by 52 · see citing works
Nadal‐Serrano, M., Sastre‐Serra, J., Pons, D. G., Miró, A. M., Oliver, J., & Roca, P. (2012) · Journal of Cellular Biochemistry · doi:10.1002/jcb.24192 · Cited by 52 · see citing works
Impact of intracellular ion channels on cancer development and progression
Peruzzo, R., Biasutto, L., Szabó, I., & Leanza, L. (2016) · European Biophysics Journal · doi:10.1007/s00249-016-1143-0 · Cited by 49 · see citing works
Tesfai, Y., Ford, J., Carter, K. W., Firth, M. J., O’Leary, R. A., Gottardo, N. G., Cole, C., & Kees, U. R. (2011) · Leukemia Research · doi:10.1016/j.leukres.2011.08.001 · Cited by 48 · see citing works
Manganese superoxide dismutase deficiency triggers mitochondrial uncoupling and the Warburg effect
Xu, Y., Miriyala, S., Fang, F., Bakthavatchalu, V., Noel, T. J., Schell, D. M., Wang, C., Clair, W. H. S., & Clair, D. K. S. (2014) · Oncogene · doi:10.1038/onc.2014.355 · Cited by 48 · see citing works
Pizzuto, R., Paventi, G., Porcile, C., Sarnataro, D., Daniele, A., & Passarella, S. (2012) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2012.05.010 · Cited by 48 · see citing works
β3‐Adrenoreceptors Control Mitochondrial Dormancy in Melanoma and Embryonic Stem Cells
Calvani, M., Cavallini, L., Tondo, A., Spinelli, V., Ricci, L., Pasha, A., Bruno, G., Buonvicino, D., Bigagli, E., Vignoli, M., et al. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/6816508 · Cited by 48 · see citing works
Loussouarn, C., Pers, Y., Bony, C., Jørgensen, C., & Noël, D. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.623973 · Cited by 46 · see citing works
Kouzi, F., Zibara, K., Bourgeais, J., Picou, F., Gallay, N., Brossaud, J., Dakik, H., Roux, B., Hamard, S., Nail, L. L., et al. (2019) · Oncogene · doi:10.1038/s41388-019-1069-y · Cited by 47 · see citing works
Su, W.-P., Lo, Y.-C., Yan, J., Liao, I., Tsai, P.-J., Wang, H., Yeh, H.-H., Lin, C., Chen, H. H. W., Lai, W., et al. (2012) · Carcinogenesis · doi:10.1093/carcin/bgs253 · Cited by 45 · see citing works
Mitochondrial Uncoupling and the Reprograming of Intermediary Metabolism in Leukemia Cells
Vélez, J., Hail, N., Konopleva, M. Y., Zeng, Z., Kojima, K., Samudio, I. J., & Andreeff, M. (2013) · Frontiers in Oncology · doi:10.3389/fonc.2013.00067 · Cited by 45 · see citing works
Self-citationCiciarello, M., Corradi, G., Loscocco, F., Visani, G., Monaco, F., Cavo, M., Curti, A., & Isidori, A. (2019) · Frontiers in Oncology · doi:10.3389/fonc.2019.01135 · Cited by 44 · see citing works
Ciciarello, M., Corradi, G., Forte, D., Cavo, M., & Curti, A. (2021) · Cancers · doi:10.3390/cancers13215319 · Cited by 39 · see citing works
Vélez, J., Pan, R. A., Lee, J. T. C., Enciso, L. J., Suarez, M., Duque, J. E., Jaramillo, D., López, C., Morales, L., Bornmann, W. G., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.9843 · Cited by 41 · see citing works
Self-citationMitochondria as emerging targets for therapies against T cell acute lymphoblastic leukemia
Olivas-Aguirre, M., Pottosin, I. I., & Dobrovinskaya, O. R. (2019) · Journal of Leukocyte Biology · doi:10.1002/jlb.5vmr0818-330rr · Cited by 42 · see citing works
The role of glycolysis in tumorigenesis: From biological aspects to therapeutic opportunities
Cordani, M., Michetti, F., Zarrabi, A., Zarepour, A., Rumio, C., Strippoli, R., & Marcucci, F. (2024) · Neoplasia · doi:10.1016/j.neo.2024.101076 · Cited by 40 · see citing works
Targeting the Akt, GSK-3, Bcl-2 axis in acute myeloid leukemia
Ricciardi, M. R., Mirabilii, S., Licchetta, R., Piedimonte, M., & Tafuri, A. (2017) · Advances in Biological Regulation · doi:10.1016/j.jbior.2017.05.002 · Cited by 40 · see citing works
Singh, A. K., & Cancelas, J. A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21030796 · Cited by 39 · see citing works
Rupprecht, A., Sittner, D., Тихоновна, С. А., Hilse, K. E., Goyn, J., Moldzio, R., Seiler, A. E. M., Bräuer, A. U., & Pohl, E. E. (2014) · PLoS ONE · doi:10.1371/journal.pone.0088474 · Cited by 40 · see citing works
CXCL12 promotes glycolytic reprogramming in acute myeloid leukemia cells via the CXCR4/mTOR axis
Braun, M., Qorraj, M., Büttner, M., Klein, F. A., Saul, D., Aigner, M., Huber, W. K., Mackensen, A., Jitschin, R., & Mougiakakos, D. (2016) · Leukemia · doi:10.1038/leu.2016.58 · Cited by 39 · see citing works
Shimasaki, Y., Pan, N., Messina, L. M., Li, C., Chen, K., Liu, L., Cooper, M. P., Vita, J. A., & Keaney, J. F. (2013) · Circulation Research · doi:10.1161/circresaha.113.301319 · Cited by 38 · see citing works
Epigenetic-Transcriptional Regulation of Fatty Acid Metabolism and Its Alterations in Leukaemia
Maher, M., Diesch, J., Casquero, R., & Buschbeck, M. (2018) · Frontiers in Genetics · doi:10.3389/fgene.2018.00405 · Cited by 39 · see citing works
Nagler, C., Hardt, C., Zänker, K. S., & Dittmar, T. (2011) · Cancer Cell International · doi:10.1186/1475-2867-11-21 · Cited by 37 · see citing works
Vélez, J., Enciso, L. J., Suarez, M., Fiegl, M., Grismaldo, A., López, C., Barreto, A., Cardozo, C., Palacios, P., Morales, L., et al. (2014) · Cancer Microenvironment · doi:10.1007/s12307-014-0149-3 · Cited by 36 · see citing works
Self-citationCheng, Y., Diao, D., Zhang, H., Guo, Q., Wu, X., Song, Y., & Dang, C. (2013) · Biomedical Reports · doi:10.3892/br.2013.211 · Cited by 36 · see citing works
Allende-Vega, N., Krzywińska, E., Orecchioni, S., López-Royuela, N., Reggiani, F., Talarico, G., Rossi, J., Rossignol, R., Hicheri, Y., Cartron, G., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.4653 · Cited by 36 · see citing works
Chen, B., Cai, T., Huang, C., Zang, X., Sun, L., Guo, S., Wang, Q., Chen, Z., Zhao, Y., Han, Z., et al. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.648706 · Cited by 34 · see citing works
Immunometabolism modulation, a new trick of edible and medicinal plants in cancer treatment
Tan, W., Pan, T., Wang, S., Li, P., Men, Y., Tan, R., Zhong, Z., & Wang, Y. (2021) · Food Chemistry · doi:10.1016/j.foodchem.2021.131860 · Cited by 35 · see citing works
Pardee, T. S., Luther, S., Buyse, M. E., Powell, B. L., & Cortes, J. E. (2019) · Future Oncology · doi:10.2217/fon-2019-0201 · Cited by 32 · see citing works
Tang, S., Yang, L., Tang, X., & Liu, M. (2014) · Cancer Letters · doi:10.1016/j.canlet.2014.07.028 · Cited by 32 · see citing works
Vasold, J., Wagner, M. M., Drolle, H., Deniffel, C., Kütt, A., Oostendorp, R. A. J., Sironi, S., Rieger, C. T., & Fiegl, M. (2014) · Leukemia Research · doi:10.1016/j.leukres.2014.12.001 · Cited by 31 · see citing works
Self-citationMetabolic Remodeling Induced by Adipocytes: A New Achilles' Heel in Invasive Breast Cancer?
Attané, C., Milhas, D., Hoy, A. J., & Muller, C. (2018) · Current Medicinal Chemistry · doi:10.2174/0929867325666180426165001 · Cited by 31 · see citing works
Rupprecht, A., Moldzio, R., Mödl, B., & Pohl, E. E. (2019) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2019.03.006 · Cited by 31 · see citing works
Catalano, G., Zaza, A., Banella, C., Pelosi, E., Castelli, G., Marinis, E. D., Smigliani, A., Travaglini, S., Ottone, T., Divona, M., et al. (2023) · Leukemia · doi:10.1038/s41375-023-01946-5 · Cited by 30 · see citing works
From gametogenesis and stem cells to cancer: common metabolic themes
Pereira, S. L., Rodrigues, A. S., Sousa, M. I., Correia, M., Perestrelo, T., & Ramalho‐Santos, J. (2014) · Human Reproduction Update · doi:10.1093/humupd/dmu034 · Cited by 29 · see citing works
BH3 Mimetics in AML Therapy: Death and Beyond?
Cerella, C., Dicato, M. A., & Diederich, M. F. (2020) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2020.09.004 · Cited by 29 · see citing works
- Authors
- Samudio, I., Fiegl, M., McQueen, T., Clise-Dwyer, K., & Andreeff, M.
- Affiliations
- 1Section of Molecular Hematology and Therapy, Department of Stem Cell Transplantation and Cellular Therapy, and
- The University of Texas MD Anderson Cancer Center (US)
- Venue
- Cancer Research
- Published
- 2008-07-01
- Volume
- 68
- Issue
- 13
- Pages
- 5198-5205
- ISSN
- 0008-5472 (ISSN-L)
- 1538-7445
- PMC
- PMC2562568
- OpenAlex
- W2032999577
- Cited by
- 168
- References
- 40
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 3 · 2023: 5 · 2022: 4 · 2021: 17 · 2020: 9 · 2019: 7 · 2018: 8 · 2017: 5 · 2016: 14 · 2015: 10 · 2014: 20 · 2013: 14 · 2012: 12
- FWCI
- 4.09
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Cancer Research (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Cancer Institute (P01 CA-55164, P01CA055164)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Hypoxia, and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Keywords
- Warburg effect, leukemia, mesenchymal stem cells, mitochondrial uncoupling, UCP2, aerobic glycolysis, mitochondrial membrane potential, lactate accumulation, pyruvate metabolism, bone marrow microenvironment, HL-60 cells, OCI-AML3 cells, oxygen consumption
- MeSH terms
- Uncoupling Protein 2, Aerobiosis, Bone Marrow Cells, Cells, Cultured, Glycolysis, Humans, Ion Channels, Leukemia, Mitochondria, Uncoupling Agents, Culture Media, Conditioned, Stromal Cells, Coculture Techniques, HL-60 Cells, Mitochondrial Proteins, Membrane Potential, Mitochondrial, Mesenchymal Stem Cells
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