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Targeting amino acid metabolism for cancer therapy
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“Glycine was employed as a source of amino groups that require for cancer growth [33].”
From Targeted Nano-Drug Delivery of Colchicine against Colon Cancer Cells by Means of Mesoporous Silica Nanoparticles (2020) · cites this paper as [33]
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The emerging hallmarks of cancer metabolism
Pavlova, N. N., & Thompson, C. B. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2015.12.006 · Cited by 5,926 · cited 2×
“Indeed, glucose and then glutamine are the most rapidly consumed nutrients by many cultured cancer cell lines [4,5], although altered metabolism of fatty acids, acetate, nucleotides, folate, proteins and several amino acids besides glutamine has also been reported [1].”
BackgroundGlutamine supports pancreatic cancer growth through a KRAS-regulated metabolic pathway
Son, J., Lyssiotis, C. A., Ying, H., Wang, X., Hua, S., Ligorio, M., Perera, R. M., Ferrone, C. R., Mullarky, E., Shyh-Chang, N., et al. (2013) · Nature · doi:10.1038/nature12040 · Cited by 1,990
Functional genomics reveal that the serine synthesis pathway is essential in breast cancer
Possemato, R., Marks, K. M., Shaul, Y. D., Pacold, M. E., Kim, D., Birsoy, K., Sethumadhavan, S., Woo, H.-K., Jang, H. G., Jha, A. K., et al. (2011) · Nature · doi:10.1038/nature10350 · Cited by 1,683
Zhang, W. C., Shyh-Chang, N., Yang, H., Rai, A., Umashankar, S., Ma, S., Soh, B. S., Sun, L. L., Tai, B. C., Nga, M. E., et al. (2012) · Cell · doi:10.1016/j.cell.2011.11.050 · Cited by 660
The metabolic profile of tumors depends on both the responsible genetic lesion and tissue type
Yuneva, M. O., Fan, T. W. M., Allen, T. D., Higashi, R. M., Ferraris, D. V., Tsukamoto, T., Matés, J. M., Alonso, F. J., Wang, C., Seo, Y., et al. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2011.12.015 · Cited by 639
Reductive carboxylation supports redox homeostasis during anchorage-independent growth
Jiang, L., Shestov, A. A., Swain, P., Yang, C., Parker, S. J., Wang, Q. A., Terada, L. S., Adams, N. D., McCabe, M. T., Pietrak, B., et al. (2016) · Nature · doi:10.1038/nature17393 · Cited by 582
Timmerman, L. A., Holton, T., Yuneva, M., Louie, R. J., Padró, M., Daemen, A., Hu, M., Chan, D. A., Ethier, S. P., van ‘t Veer, L. J., et al. (2013) · Cancer Cell · doi:10.1016/j.ccr.2013.08.020 · Cited by 573
Tardito, S., Oudin, A., Ahmed, S. U., Fack, F., Keunen, O., Zheng, L., Miletic, H., Sakariassen, P. Ø., Weinstock, A., Wagner, A., et al. (2015) · Nature Cell Biology · doi:10.1038/ncb3272 · Cited by 557
Absolute quantification of matrix metabolites reveals the dynamics of mitochondrial metabolism
Chen, W. W., Freinkman, E., Wang, T., Birsoy, K., & Sabatini, D. M. (2016) · Cell · doi:10.1016/j.cell.2016.07.040 · Cited by 500
BCAT1 promotes cell proliferation through amino acid catabolism in gliomas carrying wild-type IDH1
Tönjes, M., Barbus, S., Park, Y. J., Wang, W., Schlotter, M., Lindroth, A. M., Pleier, S. V., Bai, A. H. C., Karra, D., Piro, R. M., et al. (2013) · Nature Medicine · doi:10.1038/nm.3217 · Cited by 486
Flagged first, then by citations
Research works printed but not linked: 47
- Warburg, 1927, The metabolism of tumors in the body, J. Gen. Physiol., 8, 519, 10.1085/jgp.8.6.519 · DOI · Paper page
- Eagle, 1955, Nutrition needs of mammalian cells in tissue culture, Science, 122, 501, 10.1126/science.122.3168.501 · DOI · Paper page
- Jain, 2012, Metabolite profiling identifies a key role for glycine in rapid cancer cell proliferation, Science, 336, 1040, 10.1126/science.1218595 · DOI · Paper page
- Hosios, 2016, Amino acids rather than glucose account for the majority of cell mass in proliferating mammalian cells, Dev. Cell, 36, 540, 10.1016/j.devcel.2016.02.012 · DOI · Paper page
- Yang, 2016, Serine and one-carbon metabolism in cancer, Nat. Rev. Cancer, 16, 650, 10.1038/nrc.2016.81 · DOI · Paper page
- Altman, 2016, From Krebs to clinic: glutamine metabolism to cancer therapy, Nat. Rev. Cancer, 16, 619, 10.1038/nrc.2016.71 · DOI · Paper page
- Challapalli, 2016, Positron emission tomography imaging of tumor cell metabolism and application to therapy response monitoring, Front. Oncol., 6, 44, 10.3389/fonc.2016.00044 · DOI
- Covini, 2012, Expanding targets for a metabolic therapy of cancer: l-asparaginase, Recent Pat. Anticancer. Drug Discov., 7, 4, 10.2174/157489212798358001 · DOI
- Qiu, 2015, Targeting arginine metabolism pathway to treat arginine-dependent cancers, Cancer Lett., 364, 1, 10.1016/j.canlet.2015.04.020 · DOI
- Lukey, 2016, The oncogenic transcription factor c-Jun regulates glutaminase expression and sensitizes cells to glutaminase-targeted therapy, Nat. Commun., 7, 11321, 10.1038/ncomms11321 · DOI
- Bhutia, 2015, Amino acid transporters in cancer and their relevance to glutamine addiction: novel targets for the design of a new class of anticancer drugs, Cancer Res., 75, 1782, 10.1158/0008-5472.CAN-14-3745 · DOI
- Elgadi, 1999, Cloning and analysis of unique human glutaminase isoforms generated by tissue-specific alternative splicing, Physiol. Genomics, 1, 51, 10.1152/physiolgenomics.1999.1.2.51 · DOI
- Zhang, 2013, Epigenetic silencing of glutaminase 2 in human liver and colon cancers, BMC Cancer, 13, 601, 10.1186/1471-2407-13-601 · DOI
- Giacobbe, 2013, p63 regulates glutaminase 2 expression, Cell Cycle, 12, 1395, 10.4161/cc.24478 · DOI
- Lukey, 2013, Therapeutic strategies impacting cancer cell glutamine metabolism, Future Med. Chem., 5, 1685, 10.4155/fmc.13.130 · DOI
- Katt, 2014, Glutaminase regulation in cancer cells: a druggable chain of events, Drug Discov. Today, 19, 450, 10.1016/j.drudis.2013.10.008 · DOI
- Le, 2012, Glucose-independent glutamine metabolism via TCA cycling for proliferation and survival in B cells, Cell Metab., 15, 110, 10.1016/j.cmet.2011.12.009 · DOI · Paper page
- Wang, 2010, Targeting mitochondrial glutaminase activity inhibits oncogenic transformation, Cancer Cell, 18, 207, 10.1016/j.ccr.2010.08.009 · DOI · Paper page
- Gross, 2014, Antitumor activity of the glutaminase inhibitor CB-839 in triple-negative breast cancer, Mol. Cancer Ther., 13, 890, 10.1158/1535-7163.MCT-13-0870 · DOI · Paper page
- Bromley-Dulfano, 2013, Antitumor activity of the glutaminase inhibitor CB-839 in hematological malignances, Blood, 122, 4226, 10.1182/blood.V122.21.4226.4226 · DOI
- Garber, 2016, Cancer anabolic metabolism inhibitors move into clinic, Nat. Biotechnol., 34, 794, 10.1038/nbt0816-794 · DOI
- Mullard, 2016, Cancer metabolism pipeline breaks new ground, Nat. Rev. Drug Discov., 15, 735, 10.1038/nrd.2016.223 · DOI
- Davidson, 2016, Environment impacts the metabolic dependencies of ras-driven non-small cell lung cancer, Cell Metab., 23, 517, 10.1016/j.cmet.2016.01.007 · DOI · Paper page
- Zhang, 2014, Asparagine plays a critical role in regulating cellular adaptation to glutamine depletion, Mol. Cell, 56, 205, 10.1016/j.molcel.2014.08.018 · DOI · Paper page
- Hettmer, 2015, Functional genomic screening reveals asparagine dependence as a metabolic vulnerability in sarcoma, Elife, 4, e09436, 10.7554/eLife.09436 · DOI
- Dixon, 2014, Pharmacological inhibition of cystine-glutamate exchange induces endoplasmic reticulum stress and ferroptosis, Elife, 3, e02523, 10.7554/eLife.02523 · DOI · Paper page
- Coloff, 2016, Differential glutamate metabolism in proliferating and quiescent mammary epithelial cells, Cell Metab., 23, 867, 10.1016/j.cmet.2016.03.016 · DOI · Paper page
- Hao, 2016, Oncogenic PIK3CA mutations reprogram glutamine metabolism in colorectal cancer, Nat. Commun., 7, 11971, 10.1038/ncomms11971 · DOI · Paper page
- Smith, 2016, Addiction to coupling of the Warburg effect with glutamine catabolism in cancer cells, Cell Rep., 17, 821, 10.1016/j.celrep.2016.09.045 · DOI
- Jin, 2015, Glutamate dehydrogenase 1 signals through antioxidant glutathione peroxidase 1 to regulate redox homeostasis and tumor growth, Cancer Cell, 27, 257, 10.1016/j.ccell.2014.12.006 · DOI
- Mayers, 2016, Tissue of origin dictates branched-chain amino acid metabolism in mutant Kras-driven cancers, Science, 353, 1161, 10.1126/science.aaf5171 · DOI · Paper page
- Mattaini, 2016, The importance of serine metabolism in cancer, J. Cell Biol., 214, 249, 10.1083/jcb.201604085 · DOI
- Locasale, 2011, Phosphoglycerate dehydrogenase diverts glycolytic flux and contributes to oncogenesis, Nat. Genet., 43, 869, 10.1038/ng.890 · DOI · Paper page
- Maddocks, 2013, Serine starvation induces stress and p53-dependent metabolic remodelling in cancer cells, Nature, 493, 542, 10.1038/nature11743 · DOI · Paper page
- Nilsson, 2014, Metabolic enzyme expression highlights a key role for MTHFD2 and the mitochondrial folate pathway in cancer, Nat. Commun., 5, 3128, 10.1038/ncomms4128 · DOI · Paper page
- Pacold, 2016, A PHGDH inhibitor reveals coordination of serine synthesis and one-carbon unit fate, Nat. Chem. Biol., 12, 452, 10.1038/nchembio.2070 · DOI · Paper page
- Mullarky, 2016, Identification of a small molecule inhibitor of 3-phosphoglycerate dehydrogenase to target serine biosynthesis in cancers, Proc. Natl. Acad. Sci. U. S. A., 113, 1778, 10.1073/pnas.1521548113 · DOI · Paper page
- Liu, 2012, Reprogramming of proline and glutamine metabolism contributes to the proliferative and metabolic responses regulated by oncogenic transcription factor c-MYC, Proc. Natl. Acad. Sci. U. S. A., 109, 8983, 10.1073/pnas.1203244109 · DOI · Paper page
- Loayza-Puch, 2016, Tumour-specific proline vulnerability uncovered by differential ribosome codon reading, Nature, 530, 490, 10.1038/nature16982 · DOI
- Prendergast, 2008, Immune escape as a fundamental trait of cancer: focus on IDO, Oncogene, 27, 3889, 10.1038/onc.2008.35 · DOI
- Vacchelli, 2014, Trial watch: IDO inhibitors in cancer therapy, Oncoimmunology, 3, e957994, 10.4161/21624011.2014.957994 · DOI
- Pilotte, 2012, Reversal of tumoral immune resistance by inhibition of tryptophan 2,3-dioxygenase, Proc. Natl. Acad. Sci. U. S. A., 109, 2497, 10.1073/pnas.1113873109 · DOI
- Marin-Valencia, 2012, Analysis of tumor metabolism reveals mitochondrial glucose oxidation in genetically diverse human glioblastomas in the mouse brain in vivo, Cell Metab., 15, 827, 10.1016/j.cmet.2012.05.001 · DOI · Paper page
- Zhao, 2016, Tumor microenvironment derived exosomes pleiotropically modulate cancer cell metabolism, Elife, 5, e10250, 10.7554/eLife.10250 · DOI · Paper page
- Yang, 2016, Targeting stromal glutamine synthetase in tumors disrupts tumor microenvironment-regulated cancer cell growth, Cell Metab., 24, 685, 10.1016/j.cmet.2016.10.011 · DOI
- Souba, 1993, Glutamine and cancer, Ann. Surg., 218, 715, 10.1097/00000658-199312000-00004 · DOI
- Basun, 1990, Amino acid concentrations in cerebrospinal fluid and plasma in Alzheimer's disease and healthy control subjects, J. Neural Transm. Park Dis. Dement. Sect., 2, 295, 10.1007/BF02252924 · DOI
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Leone, R. D., & Powell, J. D. (2020) · Nature Reviews Cancer · doi:10.1038/s41568-020-0273-y · Cited by 877
AbouAitah, K., Hassan, H. A., Swiderska-Sroda, A., Gohar, L., Shaker, O. G., Wojnarowicz, J., Opalinska, A., Smalc-Koziorowska, J., Gierlotka, S., & Lojkowski, W. (2020) · Cancers · doi:10.3390/cancers12010144 · Cited by 105
Epigenome modifiers and metabolic rewiring: New frontiers in therapeutics
Ferrari, A., Longo, R., Silva, R., Mitro, N., Caruso, D., De Fabiani, E., & Crestani, M. (2019) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2018.08.008 · Cited by 19
Metadata
- Authors
- Lukey, M. J., Katt, W. P., & Cerione, R. A.
- Venue
- Drug Discovery Today
- Publisher
- Elsevier BV
- Published
- 2017-05
- Volume
- 22
- Issue
- 5
- Pages
- 796-804
- ISSN
- 1359-6446
- PMC
- PMC5429979
- Cited by
- 293
- References
- 17
- Language
- en
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