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Mitochondrial metabolism and ROS generation are essential for Kras-mediated tumorigenicity
Open accessAbstract
Otto Warburg's theory on the origins of cancer postulates that tumor cells have defects in mitochondrial oxidative phosphorylation and therefore rely on high levels of aerobic glycolysis as the major source of ATP to fuel cellular proliferation (the Warburg effect). This is in contrast to normal cells, which primarily utilize oxidative phosphorylation for growth and survival. Here we report that the major function of glucose metabolism for Kras-induced anchorage-independent growth, a hallmark of transformed cells, is to support the pentose phosphate pathway. The major function of glycolytic ATP is to support growth under hypoxic conditions. Glutamine conversion into the tricarboxylic acid cycle intermediate alpha-ketoglutarate through glutaminase and alanine aminotransferase is essential for Kras-induced anchorage-independent growth. Mitochondrial metabolism allows for the generation of reactive oxygen species (ROS) which are required for Kras-induced anchorage-independent growth through regulation of the ERK MAPK signaling pathway. We show that the major source of ROS generation required for anchorage-independent growth is the Q o site of mitochondrial complex III. Furthermore, disruption of mitochondrial function by loss of the mitochondrial transcription factor A (TFAM) gene reduced tumorigenesis in an oncogenic Kras-driven mouse model of lung cancer. These results demonstrate that mitochondrial metabolism and mitochondrial ROS generation are essential for Kras-induced cell proliferation and tumorigenesis.
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“Providing cells with αKG, oxaloacetate, or pyruvate is sufficient to rescue cancer cell proliferation in conditions of glutamine starvation, confirming that glutamine supports proliferation by replenishing depleted TCA cycle intermediates, a process termed anaplerosis (Altman et al., 2016; Weinberg et al., 2010; Yuneva et al., 2007).”
From Targeting Metabolism for Cancer Therapy (2017) · cites this paper as Weinberg et al., 2010
In the citing paper
“However, KRAS has also been shown to promote cancer cell growth by stimulating alanine aminotransferase activity, leading to high levels of α-ketoglutarate for the TCA cycle and mitochondrial ROS generation, which was required for mutant KRAS-driven tumorigenesis in a mouse model of lung cancer64.”
From The metabolic landscape of RAS-driven cancers from biology to therapy (2021) · cites this paper as [64]
In the citing paper
“A low level of reactive oxygen species (ROS) activates tumorigenic growth signaling; however, when the level exceeds the cellular redox capacity, ROS can damage macromolecules such as proteins, lipids and nucleotides55.”
From Glutamine reliance in cell metabolism (2020) · cites this paper as [55]
In the citing paper
“Correspondingly, in K-Ras mutant cells, the oxygen consumption rate and ATP generation are enhanced by glutamine, contributing to tumorigenesis55.”
From Glutamine reliance in cell metabolism (2020) · cites this paper as [55]
In the citing paper
“Notably, alanine levels were significantly decreased in Mpc knockdown cells, highlighting a role for mitochondrial pyruvate and mitochondrial alanine aminotransferase (ALT2) in mediating glutamine anaplerosis which was previously described in cancer cells (Weinberg et al., 2010).”
From Regulation of Substrate Utilization by the Mitochondrial Pyruvate Carrier (2014) · cites this paper as Weinberg et al., 2010
In the citing paper
“Another study reported that mitochondrial ROS are necessary for the KRAS (Kirsten rat sarcoma virus)—induced anchored-independent growth of lung cancer.”
From Reactive Oxygen Species, Toxicity, Oxidative Stress, and Antioxidants: Chronic Diseases and Aging (2023) · cites this paper as Weinberg et al. 2010
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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
Warburg, O. (1956) · Science · doi:10.1126/science.123.3191.309 · Cited by 13,425
The Biology of Cancer: Metabolic Reprogramming Fuels Cell Growth and Proliferation
DeBerardinis, R. J., Lum, J. J., Hatzivassiliou, G., & Thompson, C. B. (2008) · Cell Metabolism · doi:10.1016/j.cmet.2007.10.002 · Cited by 4,088
On Respiratory Impairment in Cancer Cells
Warburg, O. H. (1956) · Science · doi:10.1126/science.124.3215.269 · Cited by 3,472
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
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
Hypoxia, HIF1 and glucose metabolism in the solid tumour
Denko, N. C. (2008) · Nature Reviews Cancer · doi:10.1038/nrc2468 · Cited by 1,707
Fantin, V. R., St-Pierre, J., & Leder, P. (2006) · Cancer Cell · doi:10.1016/j.ccr.2006.04.023 · Cited by 1,635
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Cellular metabolism in pancreatic cancer as a tool for prognosis and treatment (Review)
Zuzčák, M., & Trnka, J. (2022) · International Journal of Oncology · doi:10.3892/ijo.2022.5383 · Cited by 33
Xu, J., Zhu, K., Wang, Y., & Chen, J. (2022) · Journal of Cancer Research and Clinical Oncology · doi:10.1007/s00432-022-04447-7 · Cited by 32
Mitochondrial genome instability in colorectal adenoma and adenocarcinoma
de Araújo, L. F., Fonseca, A. S., Muys, B. R., Plaça, J. R., Bueno, R. D. B. E. L., Lorenzi, J. C. C., dos Santos, A. R. D., de Molfetta, G. A., Zanette, D. L., de Souza, J. E. S., et al. (2015) · Tumor Biology · doi:10.1007/s13277-015-3640-7 · Cited by 32
Jeong, S. H., Song, I. S., Kim, H. K., Lee, S. R., Song, S., Suh, H., Yoon, Y. G., Yoo, Y. H., Kim, N., Rhee, B. D., et al. (2012) · Molecules and Cells · doi:10.1007/s10059-012-0081-7 · Cited by 32
Tang, S., Yang, L., Tang, X., & Liu, M. (2014) · Cancer Letters · doi:10.1016/j.canlet.2014.07.028 · Cited by 33
Oxidative Stress Response Biomarkers of Ovarian Cancer Based on Single-Cell and Bulk RNA Sequencing
Zheng, M., Hu, Y., Liu, O., Li, S., Wang, Y., Li, X., Liu, J., Yang, Q. F., Li, X., & Lin, B. (2023) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2023/1261039 · Cited by 31
How the Disruption of Mitochondrial Redox Signalling Contributes to Ageing
Castejón‐Vega, B., Cordero, M. D., & Sanz, A. (2023) · Antioxidants · doi:10.3390/antiox12040831 · Cited by 32
Skildum, A. J., Dornfeld, K. J., & Wallace, K. B. (2010) · Breast Cancer Research and Treatment · doi:10.1007/s10549-010-1268-2 · Cited by 32
Glutamine, Glucose and other Fuels for Cancer
Ruiz-Pérez, M. V., Sánchez‐Jiménez, F., Alonso, F. J., Segura, J., Márquez, J., & Medina, M. Á. (2014) · Current Pharmaceutical Design · doi:10.2174/13816128113199990482 · Cited by 31
Toxico‐Metabolomics of Engineered Nanomaterials: Progress and Challenges
Ahmad, F., Wang, X., & Li, W. (2019) · Advanced Functional Materials · doi:10.1002/adfm.201904268 · Cited by 31
Kalyanaraman, B. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101665 · Cited by 31
Self-citationZheng, B., Wu, L., Ma, L., Liu, S., Li, L., Xie, W., & Li, X. (2013) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b13-00058 · Cited by 31
Reactive Oxygen Species and Oncoprotein Signaling-A Dangerous Liaison
Chong, S. J. F., Lai, J. X. H., Eu, J. Q., Bellot, G. L., & Pervaiz, S. (2017) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7441 · Cited by 30
Anderson, R. G., Pladna, K. M., Schramm, N. J., Wheeler, F. B., Kridel, S. J., & Pardee, T. S. (2023) · Cancers · doi:10.3390/cancers15020484 · Cited by 29
Beyond cell cycle regulation: The pleiotropic function of CDK4 in cancer
Ziegler, D. V., Parashar, K., & Fajas, L. (2023) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2023.12.002 · Cited by 32
Lee, H. M., Muhammad, N., Lieu, E. L., Cai, F., Mu, J., Ha, Y., Cao, G., Suchors, C., Joves, K., Chronis, C., et al. (2024) · Nature Metabolism · doi:10.1038/s42255-024-01066-z · Cited by 33
CRISPR-StAR enables high-resolution genetic screening in complex in vivo models
Uijttewaal, E. C. H., Lee, J., Sell, A. C., Botay, N., Vainorius, G., Novatchkova, M., Baar, J. C., Yang, J., Potzler, T., Leij, S., et al. (2024) · Nature Biotechnology · doi:10.1038/s41587-024-02512-9 · Cited by 35
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Brisudová, P., Stojanovic, D., Novák, J., Nahácka, Z., Oliveira, G. L., Vaňátko, O., Dvorakova, S., Endaya, B., Truksa, J., Kubiskova, M., et al. (2025) · Oncogene · doi:10.1038/s41388-025-03429-6 · Cited by 29
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Kwon, H. N., Oh, S., Jin, X., An, Y., & Park, S. (2015) · Archives of Pharmacal Research · doi:10.1007/s12272-015-0552-4 · Cited by 32
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Bettoun, A., Joffre, C., Zago, G., Surdez, D., Vallerand, D., Gündoğdu, R., Sharif, A. A. D., Gómez-Ferrer, M., Cascone, I., Meunier, B., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.9875 · Cited by 31
Pseudo‑Ginsenoside Rh2 induces A549 cells apoptosis via the Ras/Raf/ERK/p53 pathway
Wang, Y., Xu, H., Lu, Z., Yu, X., Lv, C., Tian, Y., & Sui, D. (2018) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2018.6067 · Cited by 30
Shang, Y., Zhang, F., Li, D., Li, C., Li, H., Jiang, Y., & Zhang, D. (2018) · Pathology - Research and Practice · doi:10.1016/j.prp.2018.08.012 · Cited by 30
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Tripodi, F., Castoldi, A., Nicastro, R., Reghellin, V., Lombardi, L., Airoldi, C., Falletta, E., Maffioli, E., Scarcia, P., Palmieri, L., et al. (2018) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2018.09.007 · Cited by 31
Aberrant mitochondrial function in ageing and cancer
Whitehall, J. C., & Greaves, L. C. (2019) · Biogerontology · doi:10.1007/s10522-019-09853-y · Cited by 34
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Kafkova, A., & Trnka, J. (2020) · Neoplasma · doi:10.4149/neo_2020_190725n671 · Cited by 30
Protective effects of curcumin on chemical and drug-induced cardiotoxicity: a review
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Pal, D., Rai, A., Checker, R., Patwardhan, R. S., Singh, B., Sharma, D., & Sandur, S. K. (2021) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2021.108890 · Cited by 29
Daraei, H., Toolabian, K., Thompson, I. P., & Qiu, G. (2021) · Frontiers of Environmental Science & Engineering · doi:10.1007/s11783-021-1453-z · Cited by 30
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Ahn, J. S., Li, J., Chen, E., Kent, D. G., Park, H. J., & Green, A. R. (2015) · Oncogene · doi:10.1038/onc.2015.285 · Cited by 31
Wang, S., Wu, X., Bi, W., Xu, J., Hou, L., Li, G., Pan, Y., Zhang, H., Li, M., Du, S., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-56444-2 · Cited by 29
Dai, H., Zhao, K., Zhao, Y., Jiang, K., Hang, Z., Huang, X., Luo, W., Nie, J., Qin, C., & Zhou, W. (2025) · BMC Urology · doi:10.1186/s12894-025-01914-4 · Cited by 29
Zhang, S., Yang, C., Yang, Z., Zhang, D., Ma, X., Mills, G. B., & Liu, Z. (2015) · Europe PMC (PubMed Central) · Cited by 29
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Han, Y., Cho, U., Kim, S., Park, I. S., Cho, J., Dhanasekaran, D. N., & Song, Y. S. (2018) · Free Radical Research · doi:10.1080/10715762.2018.1459594 · Cited by 28
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Huang, C., Huang, C., Pai, Y.-C., Lin, B., Lee, T., Liang, P., & Yu, L. C. (2019) · Frontiers in Oncology · doi:10.3389/fonc.2019.01282 · Cited by 29
Cheng, G., Hardy, M., Zielonka, J., Weh, K. M., Zielonka, M., Boyle, K. A., AbuEid, M., McAllister, D. M., Bennett, B., Kresty, L. A., et al. (2020) · Cancer Treatment and Research Communications · doi:10.1016/j.ctarc.2020.100210 · Cited by 29
Self-citationAlrumaihi, F., Khan, M. A., Allemailem, K. S., Alsahli, M. A., Almatroudi, A., Younus, H., Alsuhaibani, S. A., Algahtani, M., & Khan, A. (2021) · Journal of Inflammation Research · doi:10.2147/jir.s300025 · Cited by 33
Ge, C., Wang, Y., Feng, Y., Wang, S., Zhang, K., Xu, X., Zhang, Z., Zhao, Y., Wang, Y., Gao, L., et al. (2021) · Cancer Letters · doi:10.1016/j.canlet.2021.06.015 · Cited by 29
Ravera, S., Bertola, N., Pasquale, C., Bruno, S., Benedicenti, S., Ferrando, S., Zekiy, A. O., Arany, P. R., & Amaroli, A. (2021) · Biomedicines · doi:10.3390/biomedicines9111717 · Cited by 29
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Chen, N., Zhou, Y.-S., Wang, L.-C., & Huang, J. (2022) · Oncology Reports · doi:10.3892/or.2022.8266 · Cited by 29
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Ghosh, J. C., Perego, M., Agarwal, E., Bertolini, I., Wang, Y., Goldman, A. R., Tang, H., Kossenkov, A. V., Landis, C. J., Languino, L. R., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2115624119 · Cited by 29
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Noè, R., Inglese, N., Romani, P., Serafini, T., Paoli, C., Calciolari, B., Fantuz, M., Zamborlin, A., Surdo, N. C., Spada, V., et al. (2023) · Redox Biology · doi:10.1016/j.redox.2023.102962 · Cited by 30
Liu, Z., Liu, J., Li, L., Nie, D., Tao, Q., Wu, J., Fan, J., Lin, C., Zhao, S., & Ju, D. (2015) · PLoS ONE · doi:10.1371/journal.pone.0135236 · Cited by 29
Li, W., Li, X., Wang, W., Yi, M., Zhou, Y., Zheng, P., Xiong, W., Yang, J., Peng, S., McCarthy, J. B., et al. (2013) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2013.06.020 · Cited by 29
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Dickerson, T., Jauregui, C. E., & Teng, Y. (2017) · Future Medicinal Chemistry · doi:10.4155/fmc-2017-0110 · Cited by 28
Chen, D., Sun, X., Zhang, X., & Cao, J. (2018) · Journal of Biochemical and Molecular Toxicology · doi:10.1002/jbt.22195 · Cited by 29
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Cordero, C., Mehta, K. P. M., Weaver, T., Ling, J. A., Freudenthal, B., Cortez, D., & Roberts, S. A. (2024) · Nature Communications · doi:10.1038/s41467-024-55497-z · Cited by 36
Shi, Y.-L., Feng, S., Chen, W., Hua, Z.-C., Bian, J.-J., & Yin, W. (2014) · Cell Death and Disease · doi:10.1038/cddis.2014.547 · Cited by 28
Identification of a redox-modulatory interaction between selenoprotein W and 14-3-3 protein
Jeon, Y. H., Ko, K. Y., Lee, J. H., Park, K., Jang, J. K., & Kim, I. Y. (2015) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2015.10.006 · Cited by 28
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Kamino, H., Nakamura, Y., Tsuneki, M., Sano, H., Miyamoto, Y., Kitamura, N., Futamura, M., Kanai, Y., Taniguchi, H., Shida, D., et al. (2016) · Oncogenesis · doi:10.1038/oncsis.2015.43 · Cited by 30
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Cruz‐Bermúdez, A., Vicente-Blanco, R. J., González‐Vioque, E., Provencio, M., Fernández‐Moreno, M. Á., & Garesse, R. (2016) · Clinical & Translational Oncology · doi:10.1007/s12094-016-1561-6 · Cited by 29
Zhou, W.-X., Chen, C., Liu, X., Li, Y., Lin, Y., Wu, X.-T., Kong, L., & Luo, J. (2020) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2020.112980 · Cited by 28
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Bustos, G., Ahumada-Castro, U., Silva-Pavez, E., Puebla, A., Lovy, A., & Cárdenas, C. (2021) · International review of cytology · doi:10.1016/bs.ircmb.2021.03.006 · Cited by 28
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Wang, S., Kang, Y., Wang, R., Deng, J., Yu, Y., Yu, J. J., & Wang, J. (2022) · Molecules · doi:10.3390/molecules27248754 · Cited by 28
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Wang, X., & Xiong, X. (2025) · International Journal of Nanomedicine · doi:10.2147/ijn.s510972 · Cited by 28
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Subramanian, V., Rodemoyer, B., Shastri, V. M., Rasmussen, L. J., Desler, C., & Schmidt, K. H. (2021) · Scientific Reports · doi:10.1038/s41598-021-81075-0 · Cited by 26
Gal, K. L., Wiel, C., Ibrahim, M. X., Henricsson, M., Sayin, V. I., & Bergö, M. O. (2021) · Antioxidants · doi:10.3390/antiox10020163 · Cited by 26
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Cáceres-Gutiérrez, R. E., Alfaro‐Mora, Y., Andonegui, M. A., Díaz‐Chávez, J., & Herrera, L. A. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.751367 · Cited by 28
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Nair, R., Gupta, P., & Shanmugam, M. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.1000106 · Cited by 29
Hu, P., Song, W., Shan, Y., Du, M., Huang, M., Song, C., & Zhang, L. (2015) · Food & Function · doi:10.1039/c5fo00248f · Cited by 27
Somers, K., Wen, V. W., Middlemiss, S., Osborne, B., Forgham, H., Jung, M., Karsa, M., Clifton, M., Bongers, A., Gao, J., et al. (2019) · Oncogene · doi:10.1038/s41388-018-0666-5 · Cited by 28
Tian, J., Luo, J., Zeng, X., Ke, C., Wang, Y., Liu, Z., Li, L., Zhang, Y., Hu, Z., & Yang, C. (2024) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2023-008226 · Cited by 28
Puurand, M., Peet, N., Piirsoo, A., Peetsalu, M., Soplepmann, J., Sirotkina, M., Peetsalu, A., Hemminki, A., & Seppet, E. K. (2012) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-012-1399-3 · Cited by 26
Yi, M., Yang, J., Li, W., Li, X., Xiong, W., McCarthy, J. B., Li, G., & Xiang, B. (2017) · Journal of Cancer · doi:10.7150/jca.17579 · Cited by 26
Chong, S. J. F., Lai, J. X. H., Qu, J., Hirpara, J. L., Kang, J., Swaminathan, K., Loh, T. K. S., Kumar, A., Vali, S., Abbasi, T., et al. (2019) · Cancer Letters · doi:10.1016/j.canlet.2019.05.009 · Cited by 26
Mitochondrial NOS1 suppresses apoptosis in colon cancer cells through increasing SIRT3 activity
Wang, Q., Ye, S., Chen, X., Xu, P., Li, K., Zeng, S., Huang, M., Gao, W., Chen, J., Zhang, Q., et al. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.05.114 · Cited by 26
Peroxynitrite promotes serine-62 phosphorylation-dependent stabilization of the oncoprotein c-Myc
Raman, D., Chong, S. J. F., Iskandar, K. B., Hirpara, J. L., & Pervaiz, S. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101587 · Cited by 25
DRP1 promotes lactate utilization in KRAS‐mutant non‐small‐cell lung cancer cells
Hu, M., Zhao, Y. C., Cao, Y., Tang, Q., Feng, Z., Ni, J., & Zhou, X. (2020) · Cancer Science · doi:10.1111/cas.14603 · Cited by 27
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Zhang, Y., Liang, S., Zhao, L., Yang, H., Marti, T. M., Hegedűs, B., Gao, Y., Zheng, B., Chen, C., Wang, W., et al. (2022) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-022-02240-5 · Cited by 28
Li, R., Tao, M., Xu, T., Huang, Y., Zogona, D., Pan, S., Wu, T., & Xu, X. (2022) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.11808 · Cited by 25
Zhao, Y., Wang, Y., Miao, Z., Liu, Y., & Yang, Q. (2023) · Molecular Biology Reports · doi:10.1007/s11033-023-08495-1 · Cited by 26
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Porporato, P. E., & Sonveaux, P. (2014) · Molecular & Cellular Oncology · doi:10.4161/23723548.2014.968043 · Cited by 26
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Zeng, T., Li, B., Shu, X., Pang, J., Wang, H., Cai, X., Liao, Y., Xiao, X., Chong, Y., Gong, J., et al. (2023) · Frontiers in Oncology · doi:10.3389/fonc.2023.1183474 · Cited by 25
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Metadata
- Authors
- 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.
- Affiliations
- Northwestern University (US)
- Division of Pulmonary and Critical Care, Department of Medicine,
- Medical College of Wisconsin (US)
- Department of Biophysics and Free Radical Research Center, Medical College of Wisconsin, Milwaukee, WI 53226
- ORCID
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2010-04-26
- Volume
- 107
- Issue
- 19
- Pages
- 8788-8793
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC2889315
- OpenAlex
- W1982330633
- Cited by
- 1,742
- References
- 29
- Citations by year
- 2026: 63 · 2025: 100 · 2024: 124 · 2023: 122 · 2022: 149 · 2021: 154 · 2020: 137 · 2019: 138 · 2018: 111 · 2017: 108 · 2016: 100 · 2015: 113 · 2014: 89 · 2013: 77 · 2012: 77
- FWCI
- 23.58
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- U.S. Department of Veterans Affairs (I01 BX000201)
- LUNGevity Foundation
- Respiratory Health Association of Metropolitan Chicago
- Respiratory Health Association
- National Institutes of Health
- National Heart, Lung, and Blood Institute (P01HL071643)
- National Cancer Institute (R01CA125112, R01CA152810, R01CA123067, CA125112, P30CA060553, T32CA070085, T32CA009560)
- National Institute of Environmental Health Sciences (ES 013995, ES015024, R01ES013995, R01ES015024)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Hypoxia, and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- KRAS, mitochondrial metabolism, reactive oxygen species, pentose phosphate pathway, aerobic glycolysis, Warburg effect, anchorage-independent growth, glutaminase, alpha-ketoglutarate, TCA cycle, ERK signaling, mitochondrial complex III, TFAM, lung cancer, carcinogenesis, hypoxia
- MeSH terms
- Aerobiosis, Animals, Cell Adhesion, Cell Transformation, Neoplastic, Glutamine, Glycolysis, Humans, Lung Neoplasms, Mitochondria, Oxidative Phosphorylation, Pentose Phosphate Pathway, Electron Transport Complex III, Proto-Oncogene Proteins p21(ras), Reactive Oxygen Species, HCT116 Cells, Extracellular Signal-Regulated MAP Kinases, Cell Proliferation, Mice
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