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Pro- and antitumor effects of mitochondrial reactive oxygen species.

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  1. Gaude Edoardo, Frezza Christian, Defects in mitochondrial metabolism and cancer, 10.1186/2049-3002-2-10
  2. Sabharwal Simran S., Schumacker Paul T., Mitochondrial ROS in cancer: initiators, amplifiers or an Achilles' heel?, 10.1038/nrc3803
  3. Corbet Cyril, Feron Olivier, Tumour acidosis: from the passenger to the driver's seat, 10.1038/nrc.2017.77
  4. Justus Calvin, Sanderlin Edward, Yang Li, Molecular Connections between Cancer Cell Metabolism and the Tumor Microenvironment, 10.3390/ijms160511055
  5. Corbet Cyril, Pinto Adán, Martherus Ruben, Santiago de Jesus João Pedro, Polet Florence, Feron Olivier, Acidosis Drives the Reprogramming of Fatty Acid Metabolism in Cancer Cells through Changes in Mitochondrial and Histone Acetylation, 10.1016/j.cmet.2016.07.003
  6. Riemann A., Schneider B., Gündel D., Stock C., Gekle M., Thews O., Acidosis Promotes Metastasis Formation by Enhancing Tumor Cell Motility, Advances in Experimental Medicine and Biology (2016) ISBN:9781493930227 p.215-220, 10.1007/978-1-4939-3023-4_27
  7. Gupta Subash C., Singh Ramesh, Pochampally Radhika, Watabe Kounosuke, Mo Yin-Yuan, Acidosis promotes invasiveness of breast cancer cells through ROS-AKT-NF-κB pathway, 10.18632/oncotarget.2514
  8. Murphy Michael P., How mitochondria produce reactive oxygen species, 10.1042/bj20081386
  9. Sena Laura A., Chandel Navdeep S., Physiological Roles of Mitochondrial Reactive Oxygen Species, 10.1016/j.molcel.2012.09.025
  10. Muller Florian L., Liu Yuhong, Van Remmen Holly, Complex III Releases Superoxide to Both Sides of the Inner Mitochondrial Membrane, 10.1074/jbc.m407715200
  11. Wellen Kathryn E., Thompson Craig B., Cellular Metabolic Stress: Considering How Cells Respond to Nutrient Excess, 10.1016/j.molcel.2010.10.004
  12. Khacho Mireille, Tarabay Michelle, Patten David, Khacho Pamela, MacLaurin Jason G., Guadagno Jennifer, Bergeron Richard, Cregan Sean P., Harper Mary-Ellen, Park David S., Slack Ruth S., Acidosis overrides oxygen deprivation to maintain mitochondrial function and cell survival, 10.1038/ncomms4550
  13. Guzy Robert D., Hoyos Beatrice, Robin Emmanuel, Chen Hong, Liu Liping, Mansfield Kyle D., Simon M. Celeste, Hammerling Ulrich, Schumacker Paul T., Mitochondrial complex III is required for hypoxia-induced ROS production and cellular oxygen sensing, 10.1016/j.cmet.2005.05.001
  14. Chandel Navdeep S., McClintock David S., Feliciano Carlos E., Wood Teresa M., Melendez J. Andres, Rodriguez Ana M., Schumacker Paul T., Reactive Oxygen Species Generated at Mitochondrial Complex III Stabilize Hypoxia-inducible Factor-1α during Hypoxia : A MECHANISM OF O2SENSING, 10.1074/jbc.m001914200
  15. Beckman J. S., Koppenol W. H., Nitric oxide, superoxide, and peroxynitrite: the good, the bad, and ugly, 10.1152/ajpcell.1996.271.5.c1424
  16. Winterbourn Christine C., Metodiewa Diana, Reactivity of biologically important thiol compounds with superoxide and hydrogen peroxide, 10.1016/s0891-5849(99)00051-9
  17. Quinlan Casey L., Goncalves Renata L. S., Hey-Mogensen Martin, Yadava Nagendra, Bunik Victoria I., Brand Martin D., The 2-Oxoacid Dehydrogenase Complexes in Mitochondria Can Produce Superoxide/Hydrogen Peroxide at Much Higher Rates Than Complex I, 10.1074/jbc.m113.545301
  18. Goncalves Renata L.S., Bunik Victoria I., Brand Martin D., Production of superoxide/hydrogen peroxide by the mitochondrial 2-oxoadipate dehydrogenase complex, 10.1016/j.freeradbiomed.2015.12.020
  19. Marí Montserrat, Morales Albert, Colell Anna, García-Ruiz Carmen, Fernández-Checa José C., Mitochondrial Glutathione, a Key Survival Antioxidant, 10.1089/ars.2009.2695
  20. Chung W. J., Inhibition of Cystine Uptake Disrupts the Growth of Primary Brain Tumors, 10.1523/jneurosci.5258-04.2005
  21. Zhang Wan, Trachootham Dunyaporn, Liu Jinyun, Chen Gang, Pelicano Helene, Garcia-Prieto Celia, Lu Weiqin, Burger Jan A., Croce Carlo M., Plunkett William, Keating Michael J., Huang Peng, Stromal control of cystine metabolism promotes cancer cell survival in chronic lymphocytic leukaemia, 10.1038/ncb2432
  22. Cramer Shira L, Saha Achinto, Liu Jinyun, Tadi Surendar, Tiziani Stefano, Yan Wupeng, Triplett Kendra, Lamb Candice, Alters Susan E, Rowlinson Scott, Zhang Yan Jessie, Keating Michael J, Huang Peng, DiGiovanni John, Georgiou George, Stone Everett, Systemic depletion of L-cyst(e)ine with cyst(e)inase increases reactive oxygen species and suppresses tumor growth, 10.1038/nm.4232
  23. Maddocks Oliver D. K., Berkers Celia R., Mason Susan M., Zheng Liang, Blyth Karen, Gottlieb Eyal, Vousden Karen H., Serine starvation induces stress and p53-dependent metabolic remodelling in cancer cells, 10.1038/nature11743
  24. Ma Qiang, Role of Nrf2 in Oxidative Stress and Toxicity, 10.1146/annurev-pharmtox-011112-140320
  25. Szatrowski, T. P., & Nathan, C. F. (1991). Production of large amounts of hydrogen peroxide by human tumor cells. Cancer Research, 51(3), 794–798.
  26. Assi Mohamad, Rébillard Amélie, The Janus-Faced Role of Antioxidants in Cancer Cachexia: New Insights on the Established Concepts, 10.1155/2016/9579868
  27. Govindarajan Baskaran, Sligh James E., Vincent Bethaney J., Li Meiling, Canter Jeffrey A., Nickoloff Brian J., Rodenburg Richard J., Smeitink Jan A., Oberley Larry, Zhang Yuping, Slingerland Joyce, Arnold Rebecca S., Lambeth J. David, Cohen Cynthia, Hilenski Lu, Griendling Kathy, Martínez-Diez Marta, Cuezva José M., Arbiser Jack L., Overexpression of Akt converts radial growth melanoma to vertical growth melanoma, 10.1172/jci30102
  28. Ferraro D, Corso S, Fasano E, Panieri E, Santangelo R, Borrello S, Giordano S, Pani G, Galeotti T, Pro-metastatic signaling by c-Met through RAC-1 and reactive oxygen species (ROS), 10.1038/sj.onc.1209409
  29. Radisky Derek C., Levy Dinah D., Littlepage Laurie E., Liu Hong, Nelson Celeste M., Fata Jimmie E., Leake Devin, Godden Elizabeth L., Albertson Donna G., Angela Nieto M., Werb Zena, Bissell Mina J., Rac1b and reactive oxygen species mediate MMP-3-induced EMT and genomic instability, 10.1038/nature03688
  30. Girnun Geoffrey D., The diverse role of the PPARγ coactivator 1 family of transcriptional coactivators in cancer, 10.1016/j.semcdb.2012.01.007
  31. LeBleu Valerie S., O’Connell Joyce T., Gonzalez Herrera Karina N., Wikman Harriet, Pantel Klaus, Haigis Marcia C., de Carvalho Fernanda Machado, Damascena Aline, Domingos Chinen Ludmilla Thome, Rocha Rafael M., Asara John M., Kalluri Raghu, PGC-1α mediates mitochondrial biogenesis and oxidative phosphorylation in cancer cells to promote metastasis, 10.1038/ncb3039
  32. Chen E. I., Hewel J., Krueger J. S., Tiraby C., Weber M. R., Kralli A., Becker K., Yates J. R., Felding-Habermann B., Adaptation of Energy Metabolism in Breast Cancer Brain Metastases, 10.1158/0008-5472.can-06-3137
  33. Torrano Veronica, Valcarcel-Jimenez Lorea, Cortazar Ana Rosa, Liu Xiaojing, Urosevic Jelena, Castillo-Martin Mireia, Fernández-Ruiz Sonia, Morciano Giampaolo, Caro-Maldonado Alfredo, Guiu Marc, Zúñiga-García Patricia, Graupera Mariona, Bellmunt Anna, Pandya Pahini, Lorente Mar, Martín-Martín Natalia, Sutherland James David, Sanchez-Mosquera Pilar, Bozal-Basterra Laura, Zabala-Letona Amaia, Arruabarrena-Aristorena Amaia, Berenguer Antonio, Embade Nieves, Ugalde-Olano Aitziber, Lacasa-Viscasillas Isabel, Loizaga-Iriarte Ana, Unda-Urzaiz Miguel, Schultz Nikolaus, Aransay Ana Maria, Sanz-Moreno Victoria, Barrio Rosa, Velasco Guillermo, Pinton Paolo, Cordon-Cardo Carlos, Locasale Jason W., Gomis Roger R., Carracedo Arkaitz, The metabolic co-regulator PGC1α suppresses prostate cancer metastasis, 10.1038/ncb3357
  34. Luo Chi, Lim Ji-Hong, Lee Yoonjin, Granter Scott R., Thomas Ajith, Vazquez Francisca, Widlund Hans R., Puigserver Pere, A PGC1α-mediated transcriptional axis suppresses melanoma metastasis, 10.1038/nature19347
  35. St-Pierre Julie, Drori Stavit, Uldry Marc, Silvaggi Jessica M., Rhee James, Jäger Sibylle, Handschin Christoph, Zheng Kangni, Lin Jiandie, Yang Wenli, Simon David K., Bachoo Robert, Spiegelman Bruce M., Suppression of Reactive Oxygen Species and Neurodegeneration by the PGC-1 Transcriptional Coactivators, 10.1016/j.cell.2006.09.024
  36. Ruas Jorge L., White James P., Rao Rajesh R., Kleiner Sandra, Brannan Kevin T., Harrison Brooke C., Greene Nicholas P., Wu Jun, Estall Jennifer L., Irving Brian A., Lanza Ian R., Rasbach Kyle A., Okutsu Mitsuharu, Nair K. Sreekumaran, Yan Zhen, Leinwand Leslie A., Spiegelman Bruce M., A PGC-1α Isoform Induced by Resistance Training Regulates Skeletal Muscle Hypertrophy, 10.1016/j.cell.2012.10.050
  37. Esparza-Moltó Pau B., Cuezva José M., The Role of Mitochondrial H+-ATP Synthase in Cancer, 10.3389/fonc.2018.00053
  38. Santacatterina Fulvio, Sánchez-Cenizo Laura, Formentini Laura, Mobasher Maysa A., Casas Estela, Rueda Carlos B., Martínez-Reyes Inmaculada, de Arenas Cristina Núñez, García-Bermúdez Javier, Zapata Juan M., Sánchez-Aragó María, Satrústegui Jorgina, Valverde Ángela M., Cuezva José M., Down-regulation of oxidative phosphorylation in the liver by expression of the ATPase inhibitory factor 1 induces a tumor-promoter metabolic state, 10.18632/oncotarget.6357
  39. Alexeyev M., Shokolenko I., Wilson G., LeDoux S., The Maintenance of Mitochondrial DNA Integrity--Critical Analysis and Update, 10.1101/cshperspect.a012641
  40. Canter Jeffrey A., Kallianpur Asha R., Parl Fritz F., Millikan Robert C., Mitochondrial DNA G10398A Polymorphism and Invasive Breast Cancer in African-American Women, 10.1158/0008-5472.can-05-1428
  41. Darvishi Katayoon, Sharma Swarkar, Bhat Audesh K., Rai Ekta, Bamezai R.N.K., Mitochondrial DNA G10398A polymorphism imparts maternal Haplogroup N a risk for breast and esophageal cancer, 10.1016/j.canlet.2006.09.005
  42. Ebner Sabine, Lang Roland, Mueller Edith E., Eder Waltraud, Oeller Michaela, Moser Alexandra, Koller Josef, Paulweber Bernhard, Mayr Johannes A., Sperl Wolfgang, Kofler Barbara, Mitochondrial Haplogroups, Control Region Polymorphisms and Malignant Melanoma: A Study in Middle European Caucasians, 10.1371/journal.pone.0027192
  43. Polyak Kornelia, Li Yunbo, Zhu Hong, Lengauer Christoph, Willson James K.V., Markowitz Sanford D., Trush Michael A., Kinzler Kenneth W., Vogelstein Bert, Somatic mutations of the mitochondrial genome in human colorectal tumours, 10.1038/3108
  44. Ishikawa K., Takenaga K., Akimoto M., Koshikawa N., Yamaguchi A., Imanishi H., Nakada K., Honma Y., Hayashi J.-I., ROS-Generating Mitochondrial DNA Mutations Can Regulate Tumor Cell Metastasis, 10.1126/science.1156906
  45. Ishikawa Kaori, Hashizume Osamu, Koshikawa Nobuko, Fukuda Sayaka, Nakada Kazuto, Takenaga Keizo, Hayashi Jun-Ichi, Enhanced glycolysis induced by mtDNA mutations does not regulate metastasis, 10.1016/j.febslet.2008.09.024
  46. Petros J. A., Baumann A. K., Ruiz-Pesini E., Amin M. B., Sun C. Q., Hall J., Lim S., Issa M. M., Flanders W. D., Hosseini S. H., Marshall F. F., Wallace D. C., mtDNA mutations increase tumorigenicity in prostate cancer, 10.1073/pnas.0408894102
  47. Singh Rajnish Kumar, Srivastava Archita, Kalaiarasan Ponnusamy, Manvati Siddharth, Chopra Rupali, Bamezai Rameshwar N. K., mtDNA germ line variation mediated ROS generates retrograde signaling and induces pro-cancerous metabolic features, 10.1038/srep06571
  48. Dasgupta S., Hoque M. O., Upadhyay S., Sidransky D., Mitochondrial Cytochrome B Gene Mutation Promotes Tumor Growth in Bladder Cancer, 10.1158/0008-5472.can-07-5532
  49. Morais, R., Zinkewich-Peotti, K., Parent, M., Wang, H., Babai, F., & Zollinger, M. (1994). Tumor-forming ability in athymic nude mice of human cell lines devoid of mitochondrial DNA. Cancer Research, 54(14), 3889–3896.
  50. Cavalli, L. R., Varella-Garcia, M., & Liang, B. C. (1997). Diminished tumorigenic phenotype after depletion of mitochondrial DNA. Cell Growth & Differentiation, 8(11), 1189–1198.
  51. Gasparre Giuseppe, Hervouet Eric, de Laplanche Elodie, Demont Jocelyne, Pennisi Lucia Fiammetta, Colombel Marc, Mège-Lechevallier Florence, Scoazec Jean-Yves, Bonora Elena, Smeets Roel, Smeitink Jan, Lazar Vladimir, Lespinasse James, Giraud Sophie, Godinot Catherine, Romeo Giovanni, Simonnet Hélène, Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in the benign renal oncocytoma, 10.1093/hmg/ddm371
  52. Gasparre Giuseppe, Romeo Giovanni, Rugolo Michela, Porcelli Anna Maria, Learning from oncocytic tumors: Why choose inefficient mitochondria?, 10.1016/j.bbabio.2010.08.006
  53. Mayr J. A., Meierhofer D., Zimmermann F., Feichtinger R., Kogler C., Ratschek M., Schmeller N., Sperl W., Kofler B., Loss of Complex I due to Mitochondrial DNA Mutations in Renal Oncocytoma, 10.1158/1078-0432.ccr-07-4131
  54. Tallini Giovanni, Oncocytic tumours, 10.1007/s004280050209
  55. Gasparre G., Kurelac I., Capristo M., Iommarini L., Ghelli A., Ceccarelli C., Nicoletti G., Nanni P., De Giovanni C., Scotlandi K., Betts C. M., Carelli V., Lollini P. L., Romeo G., Rugolo M., Porcelli A. M., A Mutation Threshold Distinguishes the Antitumorigenic Effects of the Mitochondrial Gene MTND1, an Oncojanus Function, 10.1158/0008-5472.can-11-1042
  56. Oliva Claudia R., Nozell Susan E., Diers Anne, McClugage Samuel G., Sarkaria Jann N., Markert James M., Darley-Usmar Victor M., Bailey Shannon M., Gillespie G. Yancey, Landar Aimee, Griguer Corinne E., Acquisition of Temozolomide Chemoresistance in Gliomas Leads to Remodeling of Mitochondrial Electron Transport Chain, 10.1074/jbc.m110.147504
  57. Griguer Corinne E., Cantor Alan B., Fathallah-Shaykh Hassan M., Gillespie G. Yancey, Gordon Amber S., Markert James M., Radovanovic Ivan, Clement-Schatlo Virginie, Shannon Chevis N., Oliva Claudia R., Prognostic Relevance of Cytochrome c Oxidase in Primary Glioblastoma Multiforme, 10.1371/journal.pone.0061035
  58. Oliva Claudia R., Moellering Douglas R., Gillespie G. Yancey, Griguer Corinne E., Acquisition of Chemoresistance in Gliomas Is Associated with Increased Mitochondrial Coupling and Decreased ROS Production, 10.1371/journal.pone.0024665
  59. Bell Eric L., Klimova Tatyana A., Eisenbart James, Moraes Carlos T., Murphy Michael P., Budinger G.R. Scott, Chandel Navdeep S., The Qosite of the mitochondrial complex III is required for the transduction of hypoxic signaling via reactive oxygen species production, 10.1083/jcb.200609074
  60. Brunelle Joslyn K., Bell Eric L., Quesada Nancy M., Vercauteren Kristel, Tiranti Valeria, Zeviani Massimo, Scarpulla Richard C., Chandel Navdeep S., Oxygen sensing requires mitochondrial ROS but not oxidative phosphorylation, 10.1016/j.cmet.2005.05.002
  61. Mansfield Kyle D., Guzy Robert D., Pan Yi, Young Regina M., Cash Timothy P., Schumacker Paul T., Simon M. Celeste, Mitochondrial dysfunction resulting from loss of cytochrome c impairs cellular oxygen sensing and hypoxic HIF-α activation, 10.1016/j.cmet.2005.05.003
  62. De Saedeleer C J, Porporato P E, Copetti T, Pérez-Escuredo J, Payen V L, Brisson L, Feron O, Sonveaux P, Glucose deprivation increases monocarboxylate transporter 1 (MCT1) expression and MCT1-dependent tumor cell migration, 10.1038/onc.2013.454
  63. Graham Nicholas A, Tahmasian Martik, Kohli Bitika, Komisopoulou Evangelia, Zhu Maggie, Vivanco Igor, Teitell Michael A, Wu Hong, Ribas Antoni, Lo Roger S, Mellinghoff Ingo K, Mischel Paul S, Graeber Thomas G, Glucose deprivation activates a metabolic and signaling amplification loop leading to cell death, 10.1038/msb.2012.20
  64. Nazarewicz Rafal R., Dikalova Anna E., Bikineyeva Alfiya, Dikalov Sergey I., Nox2 as a potential target of mitochondrial superoxide and its role in endothelial oxidative stress, 10.1152/ajpheart.00063.2013
  65. Dikalova Anna E., Bikineyeva Alfiya T., Budzyn Klaudia, Nazarewicz Rafal R., McCann Louise, Lewis William, Harrison David G., Dikalov Sergey I., Therapeutic Targeting of Mitochondrial Superoxide in Hypertension, 10.1161/circresaha.109.214601
  66. Molognoni Fernanda, de Melo Fabiana Henriques Machado, da Silva Camila Tainah, Jasiulionis Miriam Galvonas, Ras and Rac1, Frequently Mutated in Melanomas, Are Activated by Superoxide Anion, Modulate Dnmt1 Level and Are Causally Related to Melanocyte Malignant Transformation, 10.1371/journal.pone.0081937
  67. Imhoff Barry R., Hansen Jason M., Extracellular redox status regulates Nrf2 activation through mitochondrial reactive oxygen species, 10.1042/bj20091286
  68. Korshunov Sergey S., Skulachev Vladimir P., Starkov Anatoly A., High protonic potential actuates a mechanism of production of reactive oxygen species in mitochondria, 10.1016/s0014-5793(97)01159-9
  69. Skulachev Vladimir P, Uncoupling: new approaches to an old problem of bioenergetics, 10.1016/s0005-2728(97)00091-1
  70. Checchetto Vanessa, Azzolini Michele, Peruzzo Roberta, Capitanio Paola, Leanza Luigi, Mitochondrial potassium channels in cell death, 10.1016/j.bbrc.2017.06.095
  71. Malinska Dominika, Mirandola Sandra R., Kunz Wolfram S., Mitochondrial potassium channels and reactive oxygen species, 10.1016/j.febslet.2010.01.013
  72. Lluis J. M., Buricchi F., Chiarugi P., Morales A., Fernandez-Checa J. C., Dual Role of Mitochondrial Reactive Oxygen Species in Hypoxia Signaling: Activation of Nuclear Factor- B via c-SRC and Oxidant-Dependent Cell Death, 10.1158/0008-5472.can-07-0515
  73. DeNicola Gina M., Karreth Florian A., Humpton Timothy J., Gopinathan Aarthi, Wei Cong, Frese Kristopher, Mangal Dipti, Yu Kenneth H., Yeo Charles J., Calhoun Eric S., Scrimieri Francesca, Winter Jordan M., Hruban Ralph H., Iacobuzio-Donahue Christine, Kern Scott E., Blair Ian A., Tuveson David A., Oncogene-induced Nrf2 transcription promotes ROS detoxification and tumorigenesis, 10.1038/nature10189
  74. Weinberg F., Hamanaka R., Wheaton W. W., Weinberg S., Joseph J., Lopez M., Kalyanaraman B., Mutlu G. M., Budinger G. R. S., Chandel N. S., Mitochondrial metabolism and ROS generation are essential for Kras-mediated tumorigenicity, 10.1073/pnas.1003428107
  75. Anastasiou D., Poulogiannis G., Asara J. M., Boxer M. B., Jiang J.-k., Shen M., Bellinger G., Sasaki A. T., Locasale J. W., Auld D. S., Thomas C. J., Vander Heiden M. G., Cantley L. C., Inhibition of Pyruvate Kinase M2 by Reactive Oxygen Species Contributes to Cellular Antioxidant Responses, 10.1126/science.1211485
  76. Kong Hyewon, Chandel Navdeep S., Regulation of redox balance in cancer and T cells, 10.1074/jbc.tm117.000257
  77. Di Marcantonio Daniela, Martinez Esteban, Sidoli Simone, Vadaketh Jessica, Nieborowska-Skorska Margaret, Gupta Anushk, Meadows Jake M., Ferraro Francesca, Masselli Elena, Challen Grant A., Milsom Michael D., Scholl Claudia, Fröhling Stefan, Balachandran Siddharth, Skorski Tomasz, Garcia Benjamin A., Mirandola Prisco, Gobbi Giuliana, Garzon Ramiro, Vitale Marco, Sykes Stephen M., Protein Kinase C Epsilon Is a Key Regulator of Mitochondrial Redox Homeostasis in Acute Myeloid Leukemia, 10.1158/1078-0432.ccr-17-2684
  78. Karnati Srikanth, Lüers Georg, Pfreimer Susanna, Baumgart-Vogt Eveline, Mammalian SOD2 is exclusively located in mitochondria and not present in peroxisomes, 10.1007/s00418-013-1099-4
  79. Sreevalsan Sandeep, Safe Stephen, Reactive Oxygen Species and Colorectal Cancer, 10.1007/s11888-013-0190-5
  80. Assi Mohamad, The differential role of reactive oxygen species in early and late stages of cancer, 10.1152/ajpregu.00247.2017
  81. Chen Pinjia, Luo Xiaoyong, Nie Peipei, Wu Baoyan, Xu Wei, Shi Xinpeng, Chang Haocai, Li Bing, Yu Xiurong, Zou Zhengzhi, CQ synergistically sensitizes human colorectal cancer cells to SN-38/CPT-11 through lysosomal and mitochondrial apoptotic pathway via p53-ROS cross-talk, 10.1016/j.freeradbiomed.2017.01.033
  82. Kang Kyoung Ah, Zhang Rui, Kim Gi Young, Bae Suk Chul, Hyun Jin Won, Epigenetic changes induced by oxidative stress in colorectal cancer cells: methylation of tumor suppressor RUNX3, 10.1007/s13277-012-0322-6
  83. Ott M., Robertson J. D., Gogvadze V., Zhivotovsky B., Orrenius S., Cytochrome c release from mitochondria proceeds by a two-step process, 10.1073/pnas.241655498
  84. Zamzami N., Sequential reduction of mitochondrial transmembrane potential and generation of reactive oxygen species in early programmed cell death, 10.1084/jem.182.2.367
  85. Thorpe Geoffrey W., Reodica Mayfebelle, Davies Michael J., Heeren Gino, Jarolim Stefanie, Pillay Bethany, Breitenbach Michael, Higgins Vincent J., Dawes Ian W., Superoxide radicals have a protective role during H2O2 stress, 10.1091/mbc.e13-01-0052
  86. De Haes W., Frooninckx L., Van Assche R., Smolders A., Depuydt G., Billen J., Braeckman B. P., Schoofs L., Temmerman L., Metformin promotes lifespan through mitohormesis via the peroxiredoxin PRDX-2, 10.1073/pnas.1321776111
  87. Zarse Kim, Schmeisser Sebastian, Groth Marco, Priebe Steffen, Beuster Gregor, Kuhlow Doreen, Guthke Reinhard, Platzer Matthias, Kahn C. Ronald, Ristow Michael, Impaired Insulin/IGF1 Signaling Extends Life Span by Promoting Mitochondrial L-Proline Catabolism to Induce a Transient ROS Signal, 10.1016/j.cmet.2012.02.013
  88. Dewaele Michael, Maes Hannelore, Agostinis Patrizia, ROS-mediated mechanisms of autophagy stimulation and their relevance in cancer therapy, 10.4161/auto.6.7.12113
  89. White Eileen, Deconvoluting the context-dependent role for autophagy in cancer, 10.1038/nrc3262
  90. Chandel N. S., Maltepe E., Goldwasser E., Mathieu C. E., Simon M. C., Schumacker P. T., Mitochondrial reactive oxygen species trigger hypoxia-induced transcription, 10.1073/pnas.95.20.11715
  91. Chang Junghwa, Jung Hye Jin, Jeong Seung Hun, Kim Hyoung Kyu, Han Jin, Kwon Ho Jeong, A mutation in the mitochondrial protein UQCRB promotes angiogenesis through the generation of mitochondrial reactive oxygen species, 10.1016/j.bbrc.2014.11.005
  92. Masson Norma, Singleton Rachelle S, Sekirnik Rok, Trudgian David C, Ambrose Lucy J, Miranda Melroy X, Tian Ya-Min, Kessler Benedikt M, Schofield Christopher J, Ratcliffe Peter J, The FIH hydroxylase is a cellular peroxide sensor that modulates HIF transcriptional activity, 10.1038/embor.2012.9
  93. Fukuda Ryo, Zhang Huafeng, Kim Jung-whan, Shimoda Larissa, Dang Chi V., Semenza Gregg L., HIF-1 Regulates Cytochrome Oxidase Subunits to Optimize Efficiency of Respiration in Hypoxic Cells, 10.1016/j.cell.2007.01.047
  94. Kim Jung-whan, Tchernyshyov Irina, Semenza Gregg L., Dang Chi V., HIF-1-mediated expression of pyruvate dehydrogenase kinase: A metabolic switch required for cellular adaptation to hypoxia, 10.1016/j.cmet.2006.02.002
  95. Semenza, G. L., Roth, P. H., Fang, H. M., & Wang, G. L. (1994). Transcriptional regulation of genes encoding glycolytic enzymes by hypoxia-inducible factor 1. The Journal of Biological Chemistry, 269(38), 23757–23763.
  96. Jurica Melissa S, Mesecar Andrew, Heath Patrick J, Shi Wuxian, Nowak Thomas, Stoddard Barry L, The allosteric regulation of pyruvate kinase by fructose-1,6-bisphosphate, 10.1016/s0969-2126(98)00021-5
  97. Dombrauckas Jill D., Santarsiero Bernard D., Mesecar Andrew D., Structural Basis for Tumor Pyruvate Kinase M2 Allosteric Regulation and Catalysis†,‡, 10.1021/bi0474923
  98. Bellot G., Garcia-Medina R., Gounon P., Chiche J., Roux D., Pouyssegur J., Mazure N. M., Hypoxia-Induced Autophagy Is Mediated through Hypoxia-Inducible Factor Induction of BNIP3 and BNIP3L via Their BH3 Domains, 10.1128/mcb.00166-09
  99. Zhang Huafeng, Bosch-Marce Marta, Shimoda Larissa A., Tan Yee Sun, Baek Jin Hyen, Wesley Jacob B., Gonzalez Frank J., Semenza Gregg L., Mitochondrial Autophagy Is an HIF-1-dependent Adaptive Metabolic Response to Hypoxia, 10.1074/jbc.m800102200
  100. Keith Brian, Johnson Randall S., Simon M. Celeste, HIF1α and HIF2α: sibling rivalry in hypoxic tumour growth and progression, 10.1038/nrc3183
  101. Wen Jianfei, Wang Yao, Gao Cheng, Zhang Guoxin, You Qiang, Zhang Weiming, Zhang Zhihong, Wang Shoulin, Peng Guangyong, Shen Lizong, Helicobacter pylori infection promotes Aquaporin 3 expression via the ROS–HIF-1α–AQP3–ROS loop in stomach mucosa: a potential novel mechanism for cancer pathogenesis, 10.1038/s41388-018-0208-1
  102. Zhao Xian-Li, Yu Chun-Zhi, Vosaroxin induces mitochondrial dysfunction and apoptosis in cervical cancer HeLa cells: Involvement of AMPK/Sirt3/HIF-1 pathway, 10.1016/j.cbi.2018.05.011
  103. Moeller Benjamin J., Richardson Rachel A., Dewhirst Mark W., Hypoxia and radiotherapy: opportunities for improved outcomes in cancer treatment, 10.1007/s10555-007-9056-0
  104. Rohwer Nadine, Cramer Thorsten, Hypoxia-mediated drug resistance: Novel insights on the functional interaction of HIFs and cell death pathways, 10.1016/j.drup.2011.03.001
  105. Semenza Gregg L., Hypoxia-inducible factors: mediators of cancer progression and targets for cancer therapy, 10.1016/j.tips.2012.01.005
  106. Yu Tianchi, Tang Bo, Sun Xueying, Development of Inhibitors Targeting Hypoxia-Inducible Factor 1 and 2 for Cancer Therapy, 10.3349/ymj.2017.58.3.489
  107. Fiaschi T., Marini A., Giannoni E., Taddei M. L., Gandellini P., De Donatis A., Lanciotti M., Serni S., Cirri P., Chiarugi P., Reciprocal Metabolic Reprogramming through Lactate Shuttle Coordinately Influences Tumor-Stroma Interplay, 10.1158/0008-5472.can-12-1949
  108. Sanità Patrizia, Capulli Mattia, Teti Anna, Galatioto Giuseppe Paradiso, Vicentini Carlo, Chiarugi Paola, Bologna Mauro, Angelucci Adriano, Tumor-stroma metabolic relationship based on lactate shuttle can sustain prostate cancer progression, 10.1186/1471-2407-14-154
  109. Morselli Eugenia, Galluzzi Lorenzo, Kepp Oliver, Vicencio José-Miguel, Criollo Alfredo, Maiuri Maria Chiara, Kroemer Guido, Anti- and pro-tumor functions of autophagy, 10.1016/j.bbamcr.2009.01.006
  110. Scherz-Shouval Ruth, Shvets Elena, Fass Ephraim, Shorer Hagai, Gil Lidor, Elazar Zvulun, Reactive oxygen species are essential for autophagy and specifically regulate the activity of Atg4, 10.1038/sj.emboj.7601623
  111. Poillet-Perez Laura, Despouy Gilles, Delage-Mourroux Régis, Boyer-Guittaut Michaël, Interplay between ROS and autophagy in cancer cells, from tumor initiation to cancer therapy, 10.1016/j.redox.2014.12.003
  112. Tan An S., Baty James W., Dong Lan-Feng, Bezawork-Geleta Ayenachew, Endaya Berwini, Goodwin Jacob, Bajzikova Martina, Kovarova Jaromira, Peterka Martin, Yan Bing, Pesdar Elham Alizadeh, Sobol Margarita, Filimonenko Anatolyj, Stuart Shani, Vondrusova Magdalena, Kluckova Katarina, Sachaphibulkij Karishma, Rohlena Jakub, Hozak Pavel, Truksa Jaroslav, Eccles David, Haupt Larisa M., Griffiths Lyn R., Neuzil Jiri, Berridge Michael V., Mitochondrial Genome Acquisition Restores Respiratory Function and Tumorigenic Potential of Cancer Cells without Mitochondrial DNA, 10.1016/j.cmet.2014.12.003
  113. He Xuelian, Zhou Aifen, Lu Hao, Chen Yong, Huang Guochang, Yue Xin, Zhao Peiwei, Wu Yanxiang, Suppression of Mitochondrial Complex I Influences Cell Metastatic Properties, 10.1371/journal.pone.0061677
  114. Comito Giuseppina, Calvani Maura, Giannoni Elisa, Bianchini Francesca, Calorini Lido, Torre Eugenio, Migliore Cristina, Giordano Silvia, Chiarugi Paola, HIF-1α stabilization by mitochondrial ROS promotes Met-dependent invasive growth and vasculogenic mimicry in melanoma cells, 10.1016/j.freeradbiomed.2011.05.042
  115. Arnold Rebecca S., Sun Carrie Q., Richards Jendai C., Grigoriev Galina, Coleman Ilsa M., Nelson Peter S., Hsieh Chia-Ling, Lee Jae K., Xu Zhiheng, Rogatko Andre, Osunkoya Adeboye O., Zayzafoon Majd, Chung Leland, Petros John A., Mitochondrial DNA mutation stimulates prostate cancer growth in bone stromal environment, 10.1002/pros.20854
  116. Porporato Paolo E., Payen Valéry L., Pérez-Escuredo Jhudit, De Saedeleer Christophe J., Danhier Pierre, Copetti Tamara, Dhup Suveera, Tardy Morgane, Vazeille Thibaut, Bouzin Caroline, Feron Olivier, Michiels Carine, Gallez Bernard, Sonveaux Pierre, A Mitochondrial Switch Promotes Tumor Metastasis, 10.1016/j.celrep.2014.06.043
  117. Riemann Anne, Schneider Bettina, Gündel Daniel, Stock Christian, Thews Oliver, Gekle Michael, Acidic priming enhances metastatic potential of cancer cells, 10.1007/s00424-014-1458-6
  118. Paoli Paolo, Giannoni Elisa, Chiarugi Paola, Anoikis molecular pathways and its role in cancer progression, 10.1016/j.bbamcr.2013.06.026
  119. Piskounova Elena, Agathocleous Michalis, Murphy Malea M., Hu Zeping, Huddlestun Sara E., Zhao Zhiyu, Leitch A. Marilyn, Johnson Timothy M., DeBerardinis Ralph J., Morrison Sean J., Oxidative stress inhibits distant metastasis by human melanoma cells, 10.1038/nature15726
  120. Kamarajugadda S, Cai Q, Chen H, Nayak S, Zhu J, He M, Jin Y, Zhang Y, Ai L, Martin S S, Tan M, Lu J, Manganese superoxide dismutase promotes anoikis resistance and tumor metastasis, 10.1038/cddis.2013.20
  121. Lu Xin, Bennet Bryson, Mu Euphemia, Rabinowitz Joshua, Kang Yibin, Metabolomic Changes Accompanying Transformation and Acquisition of Metastatic Potential in a Syngeneic Mouse Mammary Tumor Model, 10.1074/jbc.c110.104448
  122. Le Gal Kristell, Ibrahim Mohamed X., Wiel Clotilde, Sayin Volkan I., Akula Murali K., Karlsson Christin, Dalin Martin G., Akyürek Levent M., Lindahl Per, Nilsson Jonas, Bergo Martin O., Antioxidants can increase melanoma metastasis in mice, 10.1126/scitranslmed.aad3740
  123. Sayin V. I., Ibrahim M. X., Larsson E., Nilsson J. A., Lindahl P., Bergo M. O., Antioxidants Accelerate Lung Cancer Progression in Mice, 10.1126/scitranslmed.3007653
  124. Gao Ping, Zhang Huafeng, Dinavahi Ramani, Li Feng, Xiang Yan, Raman Venu, Bhujwalla Zaver M., Felsher Dean W., Cheng Linzhao, Pevsner Jonathan, Lee Linda A., Semenza Gregg L., Dang Chi V., HIF-Dependent Antitumorigenic Effect of Antioxidants In Vivo, 10.1016/j.ccr.2007.08.004
  125. Klein Eric A., Thompson Ian M., Tangen Catherine M., Crowley John J., Lucia M. Scott, Goodman Phyllis J., Minasian Lori M., Ford Leslie G., Parnes Howard L., Gaziano J. Michael, Karp Daniel D., Lieber Michael M., Walther Philip J., Klotz Laurence, Parsons J. Kellogg, Chin Joseph L., Darke Amy K., Lippman Scott M., Goodman Gary E., Meyskens Frank L., Baker Laurence H., Vitamin E and the Risk of Prostate Cancer : The Selenium and Vitamin E Cancer Prevention Trial (SELECT), 10.1001/jama.2011.1437
  126. Hercberg Serge, Galan Pilar, Preziosi Paul, Bertrais Sandrine, Mennen Louise, Malvy Denis, Roussel Anne-Marie, Favier Alain, Briançon Serge, The SU.VI.MAX Study : A Randomized, Placebo-Controlled Trial of the Health Effects of Antioxidant Vitamins and Minerals, 10.1001/archinte.164.21.2335
  127. Jacobs C., Hutton B., Ng T., Shorr R., Clemons M., Is There a Role for Oral or Intravenous Ascorbate (Vitamin C) in Treating Patients With Cancer? A Systematic Review, 10.1634/theoncologist.2014-0381
  128. Bairati Isabelle, Meyer François, Gélinas Michel, Fortin André, Nabid Abdenour, Brochet François, Mercier Jean-Philippe, Têtu Bernard, Harel François, Abdous Belkacem, Vigneault Éric, Vass Sylvie, del Vecchio Pierre, Roy Jean, Randomized Trial of Antioxidant Vitamins to Prevent Acute Adverse Effects of Radiation Therapy in Head and Neck Cancer Patients, 10.1200/jco.2005.05.514
  129. Lawenda B. D., Kelly K. M., Ladas E. J., Sagar S. M., Vickers A., Blumberg J. B., Should Supplemental Antioxidant Administration Be Avoided During Chemotherapy and Radiation Therapy?, 10.1093/jnci/djn148
  130. Ozben Tomris, Antioxidant Supplementation on Cancer Risk and During Cancer Therapy: An Update, 10.2174/1568026615666141209160918
  131. Bonner Michael Y, Arbiser Jack L, The antioxidant paradox: what are antioxidants and how should they be used in a therapeutic context for cancer, 10.4155/fmc.14.86
  132. Jin Huajun, Kanthasamy Arthi, Ghosh Anamitra, Anantharam Vellareddy, Kalyanaraman Balaraman, Kanthasamy Anumantha G., Mitochondria-targeted antioxidants for treatment of Parkinson's disease: Preclinical and clinical outcomes, 10.1016/j.bbadis.2013.09.007
  133. Chandel Navdeep S., Tuveson David A., The Promise and Perils of Antioxidants for Cancer Patients, 10.1056/nejmcibr1405701
  134. Nazarewicz Rafal R., Dikalova Anna, Bikineyeva Alfiya, Ivanov Sergey, Kirilyuk Igor A., Grigor'ev Igor A., Dikalov Sergey I., Does Scavenging of Mitochondrial Superoxide Attenuate Cancer Prosurvival Signaling Pathways?, 10.1089/ars.2013.5185
  135. Cheriyath Venugopalan, Kaur Jaspreet, Davenport Anne, Khalel Ashjan, Chowdhury Nobel, Gaddipati Lalitha, G1P3 (IFI6), a mitochondrial localised antiapoptotic protein, promotes metastatic potential of breast cancer cells through mtROS, 10.1038/s41416-018-0137-3
  136. Wang Bibo, Fu Jing, Yu Ting, Xu An, Qin Wenhao, Yang Zhishi, Chen Yao, Wang Hongyang, Contradictory effects of mitochondria- and non-mitochondria-targeted antioxidants on hepatocarcinogenesis by altering DNA repair in mice : Wang, Fu, et al., 10.1002/hep.29518
  137. Titova Ekaterina, Shagieva Galina, Ivanova Olga, Domnina Lidiya, Domninskaya Maria, Strelkova Olga, Khromova Natalya, Kopnin Pavel, Chernyak Boris, Skulachev Vladimir, Dugina Vera, Mitochondria-targeted antioxidant SkQ1 suppresses fibrosarcoma and rhabdomyosarcoma tumour cell growth, 10.1080/15384101.2018.1496748
  138. Aceto Nicola, Bardia Aditya, Miyamoto David T., Donaldson Maria C., Wittner Ben S., Spencer Joel A., Yu Min, Pely Adam, Engstrom Amanda, Zhu Huili, Brannigan Brian W., Kapur Ravi, Stott Shannon L., Shioda Toshi, Ramaswamy Sridhar, Ting David T., Lin Charles P., Toner Mehmet, Haber Daniel A., Maheswaran Shyamala, Circulating Tumor Cell Clusters Are Oligoclonal Precursors of Breast Cancer Metastasis, 10.1016/j.cell.2014.07.013
  139. Verrax Julien, Cadrobbi Julie, Marques Carole, Taper Henryk, Habraken Yvette, Piette Jacques, Calderon Pedro Buc, Ascorbate potentiates the cytotoxicity of menadione leading to an oxidative stress that kills cancer cells by a non-apoptotic caspase-3 independent form of cell death, 10.1023/b:appt.0000018804.26026.1a
  140. Verrax Julien, Delvaux Marianne, Beghein Nelson, Taper Henryk, Gallez Bernard, Buc Calderon Pedro, Enhancement of quinone redox cycling by ascorbate induces a caspase-3 independent cell death in human leukaemia cells. Anin vitrocomparative study, 10.1080/10715760500097906
  141. Verrax Julien, Stockis Julie, Tison Aurélie, Taper Henryk S., Calderon Pedro Buc, Oxidative stress by ascorbate/menadione association kills K562 human chronic myelogenous leukaemia cells and inhibits its tumour growth in nude mice, 10.1016/j.bcp.2006.05.025
  142. Trachootham Dunyaporn, Zhou Yan, Zhang Hui, Demizu Yusuke, Chen Zhao, Pelicano Helene, Chiao Paul J., Achanta Geetha, Arlinghaus Ralph B., Liu Jinsong, Huang Peng, Selective killing of oncogenically transformed cells through a ROS-mediated mechanism by β-phenylethyl isothiocyanate, 10.1016/j.ccr.2006.08.009
  143. Stacpoole Peter W, Therapeutic Targeting of the Pyruvate Dehydrogenase Complex/Pyruvate Dehydrogenase Kinase (PDC/PDK) Axis in Cancer, 10.1093/jnci/djx071
  144. Shaw A. T., Winslow M. M., Magendantz M., Ouyang C., Dowdle J., Subramanian A., Lewis T. A., Maglathin R. L., Tolliday N., Jacks T., Selective killing of K-ras mutant cancer cells by small molecule inducers of oxidative stress, 10.1073/pnas.1105941108
  145. Yagoda Nicholas, von Rechenberg Moritz, Zaganjor Elma, Bauer Andras J., Yang Wan Seok, Fridman Daniel J., Wolpaw Adam J., Smukste Inese, Peltier John M., Boniface J. Jay, Smith Richard, Lessnick Stephen L., Sahasrabudhe Sudhir, Stockwell Brent R., RAS–RAF–MEK-dependent oxidative cell death involving voltage-dependent anion channels, 10.1038/nature05859
  146. Hou Xiao-Shuang, Wang Huai-Song, Mugaka Benson Peter, Yang Gong-Jun, Ding Ya, Mitochondria: promising organelle targets for cancer diagnosis and treatment, 10.1039/c8bm00673c
  147. Basit Farhan, van Oppen Lisanne MPE, Schöckel Laura, Bossenbroek Hasse M, van Emst-de Vries Sjenet E, Hermeling Johannes CW, Grefte Sander, Kopitz Charlotte, Heroult Melanie, HGM Willems Peter, Koopman Werner JH, Mitochondrial complex I inhibition triggers a mitophagy-dependent ROS increase leading to necroptosis and ferroptosis in melanoma cells, 10.1038/cddis.2017.133
  148. Hammerová Jindřiška, Uldrijan Stjepan, Táborská Eva, Vaculová Alena Hyršlová, Slaninová Iva, Necroptosis modulated by autophagy is a predominant form of melanoma cell death induced by sanguilutine, 10.1515/hsz-2011-0279
  149. Sonkusre Praveen, Cameotra Swaranjit Singh, Biogenic selenium nanoparticles induce ROS-mediated necroptosis in PC-3 cancer cells through TNF activation, 10.1186/s12951-017-0276-3
  150. Jung Hyo Sung, Lee Jae-Hong, Kim Kyutae, Koo Seyoung, Verwilst Peter, Sessler Jonathan L., Kang Chulhun, Kim Jong Seung, A Mitochondria-Targeted Cryptocyanine-Based Photothermogenic Photosensitizer, 10.1021/jacs.7b04263
  151. Jung Hyo Sung, Han Jiyou, Lee Jae-Hong, Lee Ji Ha, Choi Jong-Min, Kweon Hee-Seok, Han Ji Hye, Kim Jong-Hoon, Byun Kyung Min, Jung Jong Hwa, Kang Chulhun, Kim Jong Seung, Enhanced NIR Radiation-Triggered Hyperthermia by Mitochondrial Targeting, 10.1021/ja5122809
  152. Chakrabortty Sabyasachi, Agrawalla Bikram Keshari, Stumper Anne, Vegi Naidu M, Fischer Stephan, Reichardt Christian, Kögler Michael, Dietzek Benjamin, Feuring-Buske Michaela, Buske Christian, Rau Sven, Weil Tanja, Mitochondria Targeted Protein-Ruthenium Photosensitizer for Efficient Photodynamic Applications, 10.1021/jacs.6b13399
  153. Guo Ranran, Peng Haibao, Tian Ye, Shen Shun, Yang Wuli, Mitochondria-Targeting Magnetic Composite Nanoparticles for Enhanced Phototherapy of Cancer, 10.1002/smll.201601094
  154. Stolik S, Delgado J.A, Pérez A, Anasagasti L, Measurement of the penetration depths of red and near infrared light in human “ex vivo” tissues, 10.1016/s1011-1344(00)00082-8
Bibliographic reference Payen, Valéry L ; Zampieri, Luca ; Porporato, Paolo E ; Sonveaux, Pierre. Pro- and antitumor effects of mitochondrial reactive oxygen species.. In: Cancer metastasis reviews, Vol. 38, no. 1-2, p. 189-203 (2019)
Permanent URL http://hdl.handle.net/2078.1/214400