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Erschienen in: Cancer and Metastasis Reviews 1/2023

25.01.2023

The role of cancer cell bioenergetics in dormancy and drug resistance

verfasst von: Steven Tau, Todd W. Miller

Erschienen in: Cancer and Metastasis Reviews | Ausgabe 1/2023

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Abstract

While anti-cancer drug treatments are often effective for the clinical management of cancer, these treatments frequently leave behind drug-tolerant persister cancer cells that can ultimately give rise to recurrent disease. Such persistent cancer cells can lie dormant for extended periods of time, going undetected by conventional clinical means. Understanding the mechanisms that such dormant cancer cells use to survive, and the mechanisms that drive emergence from dormancy, is critical to the development of improved therapeutic strategies to prevent and manage disease recurrence. Cancer cells often exhibit metabolic alterations compared to their non-transformed counterparts. An emerging body of evidence supports the notion that dormant cancer cells also have unique metabolic adaptations that may offer therapeutically targetable vulnerabilities. Herein, we review mechanisms through which cancer cells metabolically adapt to persist during drug treatments and develop drug resistance. We also highlight emerging therapeutic strategies to target dormant cancer cells via their metabolic features.
Literatur
4.
Zurück zum Zitat Roesch, A., Vultur, A., Bogeski, I., Wang, H., Zimmermann, K. M., Speicher, D., Körbel, C., Laschke, M. W., Gimotty, P. A., Philipp, S. E., et al. (2013). Overcoming intrinsic multidrug resistance in melanoma by blocking the mitochondrial respiratory chain of slow-cycling JARID1B(high) cells. Cancer Cell, 23(6), 811–825. https://doi.org/10.1016/j.ccr.2013.05.003CrossRefPubMed Roesch, A., Vultur, A., Bogeski, I., Wang, H., Zimmermann, K. M., Speicher, D., Körbel, C., Laschke, M. W., Gimotty, P. A., Philipp, S. E., et al. (2013). Overcoming intrinsic multidrug resistance in melanoma by blocking the mitochondrial respiratory chain of slow-cycling JARID1B(high) cells. Cancer Cell, 23(6), 811–825. https://​doi.​org/​10.​1016/​j.​ccr.​2013.​05.​003CrossRefPubMed
14.
Zurück zum Zitat Zaugg, K., Yao, Y., Reilly, P. T., Kannan, K., Kiarash, R., Mason, J., Huang, P., Sawyer, S. K., Fuerth, B., Faubert, B., et al. (2011). Carnitine palmitoyltransferase 1C promotes cell survival and tumor growth under conditions of metabolic stress. Genes & Development, 25(10), 1041–1051. https://doi.org/10.1101/gad.1987211CrossRef Zaugg, K., Yao, Y., Reilly, P. T., Kannan, K., Kiarash, R., Mason, J., Huang, P., Sawyer, S. K., Fuerth, B., Faubert, B., et al. (2011). Carnitine palmitoyltransferase 1C promotes cell survival and tumor growth under conditions of metabolic stress. Genes & Development, 25(10), 1041–1051. https://​doi.​org/​10.​1101/​gad.​1987211CrossRef
15.
Zurück zum Zitat Wang, C., Li, Z., Lu, Y., Du, R., Katiyar, S., Yang, J., Fu, M., Leader, J. E., Quong, A., Novikoff, P. M., et al. (2006). Cyclin D1 repression of nuclear respiratory factor 1 integrates nuclear DNA synthesis and mitochondrial function. Proceedings of the National Academy of Sciences, 103(31), 11567–11572. https://doi.org/10.1073/pnas.0603363103CrossRef Wang, C., Li, Z., Lu, Y., Du, R., Katiyar, S., Yang, J., Fu, M., Leader, J. E., Quong, A., Novikoff, P. M., et al. (2006). Cyclin D1 repression of nuclear respiratory factor 1 integrates nuclear DNA synthesis and mitochondrial function. Proceedings of the National Academy of Sciences, 103(31), 11567–11572. https://​doi.​org/​10.​1073/​pnas.​0603363103CrossRef
19.
Zurück zum Zitat Madak-Erdogan, Z., Band, S., Zhao, Y. C., Smith, B. P., Kulkoyluoglu-Cotul, E., Zuo, Q., Santaliz Casiano, A., Wrobel, K., Rossi, G., Smith, R. L., et al. (2019). Free fatty acids rewire cancer metabolism in obesity-associated breast cancer via estrogen receptor and mTOR signaling. Cancer Research, canres.2849.2018. https://doi.org/10.1158/0008-5472.CAN-18-2849 Madak-Erdogan, Z., Band, S., Zhao, Y. C., Smith, B. P., Kulkoyluoglu-Cotul, E., Zuo, Q., Santaliz Casiano, A., Wrobel, K., Rossi, G., Smith, R. L., et al. (2019). Free fatty acids rewire cancer metabolism in obesity-associated breast cancer via estrogen receptor and mTOR signaling. Cancer Research, canres.2849.2018. https://​doi.​org/​10.​1158/​0008-5472.​CAN-18-2849
26.
Zurück zum Zitat Naik, P. P., Mukhopadhyay, S., Praharaj, P. P., Bhol, C. S., Panigrahi, D. P., Mahapatra, K. K., Patra, S., Saha, S., Panda, A. K., Panda, K., et al. (2021). Secretory clusterin promotes oral cancer cell survival via inhibiting apoptosis by activation of autophagy in AMPK/mTOR/ULK1 dependent pathway. Life Sciences, 264, 118722. https://doi.org/10.1016/j.lfs.2020.118722CrossRefPubMed Naik, P. P., Mukhopadhyay, S., Praharaj, P. P., Bhol, C. S., Panigrahi, D. P., Mahapatra, K. K., Patra, S., Saha, S., Panda, A. K., Panda, K., et al. (2021). Secretory clusterin promotes oral cancer cell survival via inhibiting apoptosis by activation of autophagy in AMPK/mTOR/ULK1 dependent pathway. Life Sciences, 264, 118722. https://​doi.​org/​10.​1016/​j.​lfs.​2020.​118722CrossRefPubMed
29.
Zurück zum Zitat Peart, T., Valdes, Y. R., Correa, R. J. M., Fazio, E., Bertrand, M., McGee, J., Préfontaine, M., Sugimoto, A., DiMattia, G. E., & Shepherd, T. G. (2015). Intact LKB1 activity is required for survival of dormant ovarian cancer spheroids. Oncotarget, 6(26), 22424–22438.CrossRefPubMedPubMedCentral Peart, T., Valdes, Y. R., Correa, R. J. M., Fazio, E., Bertrand, M., McGee, J., Préfontaine, M., Sugimoto, A., DiMattia, G. E., & Shepherd, T. G. (2015). Intact LKB1 activity is required for survival of dormant ovarian cancer spheroids. Oncotarget, 6(26), 22424–22438.CrossRefPubMedPubMedCentral
38.
41.
44.
Zurück zum Zitat Bosc, C., Saland, E., Bousard, A., Gadaud, N., Sabatier, M., Cognet, G., Farge, T., Boet, E., Gotanègre, M., Aroua, N., et al. (2021). Mitochondrial inhibitors circumvent adaptive resistance to venetoclax and cytarabine combination therapy in acute myeloid leukemia. Nature Cancer, 2(11), 1204–1223. https://doi.org/10.1038/s43018-021-00264-yCrossRefPubMed Bosc, C., Saland, E., Bousard, A., Gadaud, N., Sabatier, M., Cognet, G., Farge, T., Boet, E., Gotanègre, M., Aroua, N., et al. (2021). Mitochondrial inhibitors circumvent adaptive resistance to venetoclax and cytarabine combination therapy in acute myeloid leukemia. Nature Cancer, 2(11), 1204–1223. https://​doi.​org/​10.​1038/​s43018-021-00264-yCrossRefPubMed
46.
Zurück zum Zitat Echeverria, G. V., Ge, Z., Seth, S., Zhang, X., Jeter-Jones, S., Zhou, X., Cai, S., Tu, Y., McCoy, A., Peoples, M., et al. (2019). Resistance to neoadjuvant chemotherapy in triple-negative breast cancer mediated by a reversible drug-tolerant state. Science Translational Medicine, 11(488), 936. https://doi.org/10.1126/scitranslmed.aav0936CrossRef Echeverria, G. V., Ge, Z., Seth, S., Zhang, X., Jeter-Jones, S., Zhou, X., Cai, S., Tu, Y., McCoy, A., Peoples, M., et al. (2019). Resistance to neoadjuvant chemotherapy in triple-negative breast cancer mediated by a reversible drug-tolerant state. Science Translational Medicine, 11(488), 936. https://​doi.​org/​10.​1126/​scitranslmed.​aav0936CrossRef
50.
Zurück zum Zitat Kunimasa, K., Nagano, T., Shimono, Y., Dokuni, R., Kiriu, T., Tokunaga, S., Tamura, D., Yamamoto, M., Tachihara, M., Kobayashi, K., et al. (2017). Glucose metabolism-targeted therapy and withaferin A are effective for epidermal growth factor receptor tyrosine kinase inhibitor-induced drug-tolerant persisters. Cancer Science, 108(7), 1368–1377. https://doi.org/10.1111/cas.13266CrossRefPubMedPubMedCentral Kunimasa, K., Nagano, T., Shimono, Y., Dokuni, R., Kiriu, T., Tokunaga, S., Tamura, D., Yamamoto, M., Tachihara, M., Kobayashi, K., et al. (2017). Glucose metabolism-targeted therapy and withaferin A are effective for epidermal growth factor receptor tyrosine kinase inhibitor-induced drug-tolerant persisters. Cancer Science, 108(7), 1368–1377. https://​doi.​org/​10.​1111/​cas.​13266CrossRefPubMedPubMedCentral
51.
56.
Zurück zum Zitat Harper, M.-E., Antoniou, A., Villalobos-Menuey, E., Russo, A., Trauger, R., Vendemelio, M., George, A., Bartholomew, R., Carlo, D., Shaikh, A., et al. (2002). Characterization of a novel metabolic strategy used by drug-resistant tumor cells. The FASEB Journal, 16(12), 1550–1557. https://doi.org/10.1096/fj.02-0541comCrossRefPubMed Harper, M.-E., Antoniou, A., Villalobos-Menuey, E., Russo, A., Trauger, R., Vendemelio, M., George, A., Bartholomew, R., Carlo, D., Shaikh, A., et al. (2002). Characterization of a novel metabolic strategy used by drug-resistant tumor cells. The FASEB Journal, 16(12), 1550–1557. https://​doi.​org/​10.​1096/​fj.​02-0541comCrossRefPubMed
57.
Zurück zum Zitat Oren, Y., Tsabar, M., Cuoco, M. S., Amir-Zilberstein, L., Cabanos, H. F., Hütter, J.-C., Hu, B., Thakore, P. I., Tabaka, M., Fulco, C. P., et al. (2021). Cycling cancer persister cells arise from lineages with distinct programs. Nature, 1–7. https://doi.org/10.1038/s41586-021-03796-6 Oren, Y., Tsabar, M., Cuoco, M. S., Amir-Zilberstein, L., Cabanos, H. F., Hütter, J.-C., Hu, B., Thakore, P. I., Tabaka, M., Fulco, C. P., et al. (2021). Cycling cancer persister cells arise from lineages with distinct programs. Nature, 1–7. https://​doi.​org/​10.​1038/​s41586-021-03796-6
58.
Zurück zum Zitat Pike, L. S., Smift, A. L., Croteau, N. J., Ferrick, D. A., & Wu, M. (2011). Inhibition of fatty acid oxidation by etomoxir impairs NADPH production and increases reactive oxygen species resulting in ATP depletion and cell death in human glioblastoma cells. Biochimica et Biophysica Acta (BBA). Bioenergetics, 1807(6), 726–734. https://doi.org/10.1016/j.bbabio.2010.10.022CrossRef Pike, L. S., Smift, A. L., Croteau, N. J., Ferrick, D. A., & Wu, M. (2011). Inhibition of fatty acid oxidation by etomoxir impairs NADPH production and increases reactive oxygen species resulting in ATP depletion and cell death in human glioblastoma cells. Biochimica et Biophysica Acta (BBA). Bioenergetics, 1807(6), 726–734. https://​doi.​org/​10.​1016/​j.​bbabio.​2010.​10.​022CrossRef
60.
Zurück zum Zitat Kaplan, O., Navon, G., Lyon, R. C., Faustino, P. J., Straka, E. J., & Cohen, J. S. (1990). Effects of 2-deoxyglucose on drug-sensitive and drug-resistant human breast cancer cells: Toxicity and magnetic resonance spectroscopy studies of metabolism. Cancer Research, 50(3), 544–551.PubMed Kaplan, O., Navon, G., Lyon, R. C., Faustino, P. J., Straka, E. J., & Cohen, J. S. (1990). Effects of 2-deoxyglucose on drug-sensitive and drug-resistant human breast cancer cells: Toxicity and magnetic resonance spectroscopy studies of metabolism. Cancer Research, 50(3), 544–551.PubMed
62.
Zurück zum Zitat Morris, V. L., Tuck, A. B., Wilson, S. M., Percy, D., & Chambers, A. F. (1993). Tumor progression and metastasis in murine D2 hyperplastic alveolar nodule mammary tumor cell lines. Clinical & Experimental Metastasis, 11(1), 103–112. https://doi.org/10.1007/BF00880071CrossRef Morris, V. L., Tuck, A. B., Wilson, S. M., Percy, D., & Chambers, A. F. (1993). Tumor progression and metastasis in murine D2 hyperplastic alveolar nodule mammary tumor cell lines. Clinical & Experimental Metastasis, 11(1), 103–112. https://​doi.​org/​10.​1007/​BF00880071CrossRef
70.
Zurück zum Zitat Yap, T. A., Rodon Ahnert, J., Piha-Paul, S. A., Fu, S., Janku, F., Karp, D. D., Naing, A., Ileana Dumbrava, E. E., Pant, S., Subbiah, V., et al. (2019). Phase I trial of IACS-010759 (IACS), a potent, selective inhibitor of complex I of the mitochondrial electron transport chain, in patients (pts) with advanced solid tumors. Journal of Clinical Oncology, 37(15_suppl), 3014–3014. https://doi.org/10.1200/JCO.2019.37.15_suppl.3014CrossRef Yap, T. A., Rodon Ahnert, J., Piha-Paul, S. A., Fu, S., Janku, F., Karp, D. D., Naing, A., Ileana Dumbrava, E. E., Pant, S., Subbiah, V., et al. (2019). Phase I trial of IACS-010759 (IACS), a potent, selective inhibitor of complex I of the mitochondrial electron transport chain, in patients (pts) with advanced solid tumors. Journal of Clinical Oncology, 37(15_suppl), 3014–3014. https://​doi.​org/​10.​1200/​JCO.​2019.​37.​15_​suppl.​3014CrossRef
74.
Zurück zum Zitat Zhang, X., Fryknäs, M., Hernlund, E., Fayad, W., De Milito, A., Olofsson, M. H., Gogvadze, V., Dang, L., Påhlman, S., Schughart, L. A. K., et al. (2014). Induction of mitochondrial dysfunction as a strategy for targeting tumour cells in metabolically compromised microenvironments. Nature Communications, 5(1), 1–14. https://doi.org/10.1038/ncomms4295CrossRef Zhang, X., Fryknäs, M., Hernlund, E., Fayad, W., De Milito, A., Olofsson, M. H., Gogvadze, V., Dang, L., Påhlman, S., Schughart, L. A. K., et al. (2014). Induction of mitochondrial dysfunction as a strategy for targeting tumour cells in metabolically compromised microenvironments. Nature Communications, 5(1), 1–14. https://​doi.​org/​10.​1038/​ncomms4295CrossRef
75.
Zurück zum Zitat Sharon, D., Cathelin, S., Mirali, S., Di Trani, J. M., Yanofsky, D. J., Keon, K. A., Rubinstein, J. L., Schimmer, A. D., Ketela, T., & Chan, S. M. (2019). Inhibition of mitochondrial translation overcomes venetoclax resistance in AML through activation of the integrated stress response. Science Translational Medicine, 11(516), 2863. https://doi.org/10.1126/scitranslmed.aax2863CrossRef Sharon, D., Cathelin, S., Mirali, S., Di Trani, J. M., Yanofsky, D. J., Keon, K. A., Rubinstein, J. L., Schimmer, A. D., Ketela, T., & Chan, S. M. (2019). Inhibition of mitochondrial translation overcomes venetoclax resistance in AML through activation of the integrated stress response. Science Translational Medicine, 11(516), 2863. https://​doi.​org/​10.​1126/​scitranslmed.​aax2863CrossRef
79.
Zurück zum Zitat Samudio, I., Harmancey, R., Fiegl, M., Kantarjian, H., Konopleva, M., Korchin, B., Kaluarachchi, K., Bornmann, W., Duvvuri, S., Taegtmeyer, H., et al. (2010). Pharmacologic inhibition of fatty acid oxidation sensitizes human leukemia cells to apoptosis induction. The Journal of Clinical Investigation, 120(1), 142–156. https://doi.org/10.1172/JCI38942CrossRefPubMed Samudio, I., Harmancey, R., Fiegl, M., Kantarjian, H., Konopleva, M., Korchin, B., Kaluarachchi, K., Bornmann, W., Duvvuri, S., Taegtmeyer, H., et al. (2010). Pharmacologic inhibition of fatty acid oxidation sensitizes human leukemia cells to apoptosis induction. The Journal of Clinical Investigation, 120(1), 142–156. https://​doi.​org/​10.​1172/​JCI38942CrossRefPubMed
82.
Zurück zum Zitat Heuer, T. S., Ventura, R., Mordec, K., Lai, J., Fridlib, M., Buckley, D., & Kemble, G. (2017). FASN inhibition and taxane treatment combine to enhance anti-tumor efficacy in diverse xenograft tumor models through disruption of tubulin palmitoylation and microtubule organization and fasn inhibition-mediated effects on oncogenic signaling and gene expression. EBioMedicine, 16, 51–62. https://doi.org/10.1016/j.ebiom.2016.12.012CrossRefPubMed Heuer, T. S., Ventura, R., Mordec, K., Lai, J., Fridlib, M., Buckley, D., & Kemble, G. (2017). FASN inhibition and taxane treatment combine to enhance anti-tumor efficacy in diverse xenograft tumor models through disruption of tubulin palmitoylation and microtubule organization and fasn inhibition-mediated effects on oncogenic signaling and gene expression. EBioMedicine, 16, 51–62. https://​doi.​org/​10.​1016/​j.​ebiom.​2016.​12.​012CrossRefPubMed
83.
84.
Zurück zum Zitat Falchook, G., Infante, J., Arkenau, H.-T., Patel, M. R., Dean, E., Borazanci, E., Brenner, A., Cook, N., Lopez, J., Pant, S., et al. (2021). First-in-human study of the safety, pharmacokinetics, and pharmacodynamics of first-in-class fatty acid synthase inhibitor TVB-2640 alone and with a taxane in advanced tumors. eClinicalMedicine, 34. https://doi.org/10.1016/j.eclinm.2021.100797CrossRef Falchook, G., Infante, J., Arkenau, H.-T., Patel, M. R., Dean, E., Borazanci, E., Brenner, A., Cook, N., Lopez, J., Pant, S., et al. (2021). First-in-human study of the safety, pharmacokinetics, and pharmacodynamics of first-in-class fatty acid synthase inhibitor TVB-2640 alone and with a taxane in advanced tumors. eClinicalMedicine, 34. https://​doi.​org/​10.​1016/​j.​eclinm.​2021.​100797CrossRef
86.
87.
Zurück zum Zitat Holubarsch, C. J. F., Rohrbach, M., Karrasch, M., Boehm, E., Polonski, L., Ponikowski, P., & Rhein, S. (2007). A double-blind randomized multicentre clinical trial to evaluate the efficacy and safety of two doses of etomoxir in comparison with placebo in patients with moderate congestive heart failure: the ERGO (etomoxir for the recovery of glucose oxidation) study. Clinical Science, 113(4), 205–212. https://doi.org/10.1042/CS20060307CrossRefPubMed Holubarsch, C. J. F., Rohrbach, M., Karrasch, M., Boehm, E., Polonski, L., Ponikowski, P., & Rhein, S. (2007). A double-blind randomized multicentre clinical trial to evaluate the efficacy and safety of two doses of etomoxir in comparison with placebo in patients with moderate congestive heart failure: the ERGO (etomoxir for the recovery of glucose oxidation) study. Clinical Science, 113(4), 205–212. https://​doi.​org/​10.​1042/​CS20060307CrossRefPubMed
88.
Zurück zum Zitat Zachar, Z., Marecek, J., Maturo, C., Gupta, S., Stuart, S. D., Howell, K., Schauble, A., Lem, J., Piramzadian, A., Karnik, S., et al. (2011). Non-redox-active lipoate derivates disrupt cancer cell mitochondrial metabolism and are potent anticancer agents in vivo. Journal of Molecular Medicine, 89(11), 1137. https://doi.org/10.1007/s00109-011-0785-8CrossRefPubMed Zachar, Z., Marecek, J., Maturo, C., Gupta, S., Stuart, S. D., Howell, K., Schauble, A., Lem, J., Piramzadian, A., Karnik, S., et al. (2011). Non-redox-active lipoate derivates disrupt cancer cell mitochondrial metabolism and are potent anticancer agents in vivo. Journal of Molecular Medicine, 89(11), 1137. https://​doi.​org/​10.​1007/​s00109-011-0785-8CrossRefPubMed
89.
Zurück zum Zitat Arnold, C., Demuth, P., Seiwert, N., Wittmann, S., Boengler, K., Rasenberger, B., Christmann, M., Huber, M., Brunner, T., Linnebacher, M., et al. (2022). The mitochondrial disruptor devimistat (CPI-613) synergizes with genotoxic anticancer drugs in colorectal cancer therapy in a Bim-dependent manner. Molecular Cancer Therapeutics, 21(1), 100–112. https://doi.org/10.1158/1535-7163.MCT-21-0393CrossRefPubMed Arnold, C., Demuth, P., Seiwert, N., Wittmann, S., Boengler, K., Rasenberger, B., Christmann, M., Huber, M., Brunner, T., Linnebacher, M., et al. (2022). The mitochondrial disruptor devimistat (CPI-613) synergizes with genotoxic anticancer drugs in colorectal cancer therapy in a Bim-dependent manner. Molecular Cancer Therapeutics, 21(1), 100–112. https://​doi.​org/​10.​1158/​1535-7163.​MCT-21-0393CrossRefPubMed
90.
Zurück zum Zitat Pardee, T. S., Luther, S., Buyse, M., Powell, B. L., & Cortes, J. (2019). Devimistat in combination with high dose cytarabine and mitoxantrone compared with high dose cytarabine and mitoxantrone in older patients with relapsed/refractory acute myeloid leukemia: ARMADA 2000 Phase III study. Future Oncology, 15(28), 3197–3208. https://doi.org/10.2217/fon-2019-0201CrossRefPubMed Pardee, T. S., Luther, S., Buyse, M., Powell, B. L., & Cortes, J. (2019). Devimistat in combination with high dose cytarabine and mitoxantrone compared with high dose cytarabine and mitoxantrone in older patients with relapsed/refractory acute myeloid leukemia: ARMADA 2000 Phase III study. Future Oncology, 15(28), 3197–3208. https://​doi.​org/​10.​2217/​fon-2019-0201CrossRefPubMed
99.
Zurück zum Zitat McGowan, M. M., Eisenberg, B. L., Lewis, L. D., Froehlich, H. M., Wells, W. A., Eastman, A., Kuemmerle, N. B., Rosenkrantz, K. M., Barth, R. J., Schwartz, G. N., et al. (2013). A proof of principle clinical trial to determine whether conjugated linoleic acid modulates the lipogenic pathway in human breast cancer tissue. Breast Cancer Research and Treatment, 138(1), 175–183. https://doi.org/10.1007/s10549-013-2446-9CrossRefPubMedPubMedCentral McGowan, M. M., Eisenberg, B. L., Lewis, L. D., Froehlich, H. M., Wells, W. A., Eastman, A., Kuemmerle, N. B., Rosenkrantz, K. M., Barth, R. J., Schwartz, G. N., et al. (2013). A proof of principle clinical trial to determine whether conjugated linoleic acid modulates the lipogenic pathway in human breast cancer tissue. Breast Cancer Research and Treatment, 138(1), 175–183. https://​doi.​org/​10.​1007/​s10549-013-2446-9CrossRefPubMedPubMedCentral
100.
Zurück zum Zitat Mayer, E. L., Dueck, A. C., Martin, M., Rubovszky, G., Burstein, H. J., Bellet-Ezquerra, M., Miller, K. D., Zdenkowski, N., Winer, E. P., Pfeiler, G., et al. (2021). Palbociclib with adjuvant endocrine therapy in early breast cancer (PALLAS): Interim analysis of a multicentre, open-label, randomised, phase 3 study. The Lancet Oncology, 22(2), 212–222. https://doi.org/10.1016/S1470-2045(20)30642-2CrossRefPubMed Mayer, E. L., Dueck, A. C., Martin, M., Rubovszky, G., Burstein, H. J., Bellet-Ezquerra, M., Miller, K. D., Zdenkowski, N., Winer, E. P., Pfeiler, G., et al. (2021). Palbociclib with adjuvant endocrine therapy in early breast cancer (PALLAS): Interim analysis of a multicentre, open-label, randomised, phase 3 study. The Lancet Oncology, 22(2), 212–222. https://​doi.​org/​10.​1016/​S1470-2045(20)30642-2CrossRefPubMed
101.
Zurück zum Zitat Vansteenkiste, J. F., Cho, B. C., Vanakesa, T., De Pas, T., Zielinski, M., Kim, M. S., Jassem, J., Yoshimura, M., Dahabreh, J., Nakayama, H., et al. (2016). Efficacy of the MAGE-A3 cancer immunotherapeutic as adjuvant therapy in patients with resected MAGE-A3-positive non-small-cell lung cancer (MAGRIT): A randomised, double-blind, placebo-controlled, phase 3 trial. The Lancet. Oncology, 17(6), 822–835. https://doi.org/10.1016/S1470-2045(16)00099-1CrossRefPubMed Vansteenkiste, J. F., Cho, B. C., Vanakesa, T., De Pas, T., Zielinski, M., Kim, M. S., Jassem, J., Yoshimura, M., Dahabreh, J., Nakayama, H., et al. (2016). Efficacy of the MAGE-A3 cancer immunotherapeutic as adjuvant therapy in patients with resected MAGE-A3-positive non-small-cell lung cancer (MAGRIT): A randomised, double-blind, placebo-controlled, phase 3 trial. The Lancet. Oncology, 17(6), 822–835. https://​doi.​org/​10.​1016/​S1470-2045(16)00099-1CrossRefPubMed
102.
Zurück zum Zitat Alberts, S. R., Sargent, D. J., Nair, S., Mahoney, M. R., Mooney, M., Thibodeau, S. N., Smyrk, T. C., Sinicrope, F. A., Chan, E., Gill, S., et al. (2012). Effect of oxaliplatin, fluorouracil, and leucovorin with or without cetuximab on survival among patients with resected stage III colon cancer: A randomized trial. JAMA, 307(13), 1383–1393. https://doi.org/10.1001/jama.2012.385CrossRefPubMedPubMedCentral Alberts, S. R., Sargent, D. J., Nair, S., Mahoney, M. R., Mooney, M., Thibodeau, S. N., Smyrk, T. C., Sinicrope, F. A., Chan, E., Gill, S., et al. (2012). Effect of oxaliplatin, fluorouracil, and leucovorin with or without cetuximab on survival among patients with resected stage III colon cancer: A randomized trial. JAMA, 307(13), 1383–1393. https://​doi.​org/​10.​1001/​jama.​2012.​385CrossRefPubMedPubMedCentral
103.
Zurück zum Zitat Nielsen, T. O., Jensen, M.-B., Burugu, S., Gao, D., Jørgensen, C. L. T., Balslev, E., & Ejlertsen, B. (2017). High-risk premenopausal luminal a breast cancer patients derive no benefit from adjuvant cyclophosphamide-based chemotherapy: Results from the DBCG77B clinical trial. Clinical Cancer Research: An Official Journal of the American Association for Cancer Research, 23(4), 946–953. https://doi.org/10.1158/1078-0432.CCR-16-1278CrossRefPubMed Nielsen, T. O., Jensen, M.-B., Burugu, S., Gao, D., Jørgensen, C. L. T., Balslev, E., & Ejlertsen, B. (2017). High-risk premenopausal luminal a breast cancer patients derive no benefit from adjuvant cyclophosphamide-based chemotherapy: Results from the DBCG77B clinical trial. Clinical Cancer Research: An Official Journal of the American Association for Cancer Research, 23(4), 946–953. https://​doi.​org/​10.​1158/​1078-0432.​CCR-16-1278CrossRefPubMed
104.
Zurück zum Zitat Haas, N. B., Manola, J., Uzzo, R. G., Flaherty, K. T., Wood, C. G., Kane, C., Jewett, M., Dutcher, J. P., Atkins, M. B., Pins, M., et al. (2016). Adjuvant sunitinib or sorafenib for high-risk, non-metastatic renal-cell carcinoma (ECOG-ACRIN E2805): A double-blind, placebo-controlled, randomised, phase 3 trial. Lancet (London, England), 387(10032), 2008–2016. https://doi.org/10.1016/S0140-6736(16)00559-6CrossRefPubMed Haas, N. B., Manola, J., Uzzo, R. G., Flaherty, K. T., Wood, C. G., Kane, C., Jewett, M., Dutcher, J. P., Atkins, M. B., Pins, M., et al. (2016). Adjuvant sunitinib or sorafenib for high-risk, non-metastatic renal-cell carcinoma (ECOG-ACRIN E2805): A double-blind, placebo-controlled, randomised, phase 3 trial. Lancet (London, England), 387(10032), 2008–2016. https://​doi.​org/​10.​1016/​S0140-6736(16)00559-6CrossRefPubMed
105.
Zurück zum Zitat de Gramont, A., Van Cutsem, E., Schmoll, H.-J., Tabernero, J., Clarke, S., Moore, M. J., Cunningham, D., Cartwright, T. H., Hecht, J. R., Rivera, F., et al. (2012). Bevacizumab plus oxaliplatin-based chemotherapy as adjuvant treatment for colon cancer (AVANT): A phase 3 randomised controlled trial. The Lancet Oncology, 13(12), 1225–1233. https://doi.org/10.1016/S1470-2045(12)70509-0CrossRefPubMed de Gramont, A., Van Cutsem, E., Schmoll, H.-J., Tabernero, J., Clarke, S., Moore, M. J., Cunningham, D., Cartwright, T. H., Hecht, J. R., Rivera, F., et al. (2012). Bevacizumab plus oxaliplatin-based chemotherapy as adjuvant treatment for colon cancer (AVANT): A phase 3 randomised controlled trial. The Lancet Oncology, 13(12), 1225–1233. https://​doi.​org/​10.​1016/​S1470-2045(12)70509-0CrossRefPubMed
106.
Zurück zum Zitat Allegra, C. J., Yothers, G., O’Connell, M. J., Sharif, S., Petrelli, N. J., Colangelo, L. H., Atkins, J. N., Seay, T. E., Fehrenbacher, L., Goldberg, R. M., et al. (2011). Phase III trial assessing bevacizumab in stages II and III carcinoma of the colon: Results of NSABP protocol C-08. Journal of Clinical Oncology: Official Journal of the American Society of Clinical Oncology, 29(1), 11–16. https://doi.org/10.1200/JCO.2010.30.0855CrossRefPubMed Allegra, C. J., Yothers, G., O’Connell, M. J., Sharif, S., Petrelli, N. J., Colangelo, L. H., Atkins, J. N., Seay, T. E., Fehrenbacher, L., Goldberg, R. M., et al. (2011). Phase III trial assessing bevacizumab in stages II and III carcinoma of the colon: Results of NSABP protocol C-08. Journal of Clinical Oncology: Official Journal of the American Society of Clinical Oncology, 29(1), 11–16. https://​doi.​org/​10.​1200/​JCO.​2010.​30.​0855CrossRefPubMed
Metadaten
Titel
The role of cancer cell bioenergetics in dormancy and drug resistance
verfasst von
Steven Tau
Todd W. Miller
Publikationsdatum
25.01.2023
Verlag
Springer US
Erschienen in
Cancer and Metastasis Reviews / Ausgabe 1/2023
Print ISSN: 0167-7659
Elektronische ISSN: 1573-7233
DOI
https://doi.org/10.1007/s10555-023-10081-7

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