Cancer tissue of origin constrains the growth and metabolism of metastases.
Journal
Nature metabolism
ISSN: 2522-5812
Titre abrégé: Nat Metab
Pays: Germany
ID NLM: 101736592
Informations de publication
Date de publication:
19 Aug 2024
19 Aug 2024
Historique:
received:
31
05
2024
accepted:
09
07
2024
medline:
20
8
2024
pubmed:
20
8
2024
entrez:
19
8
2024
Statut:
aheadofprint
Résumé
Metastases arise from subsets of cancer cells that disseminate from the primary tumour
Identifiants
pubmed: 39160333
doi: 10.1038/s42255-024-01105-9
pii: 10.1038/s42255-024-01105-9
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI)
ID : R35CA242379
Organisme : U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI)
ID : P30CA14051
Organisme : U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI)
ID : R01CA201276
Informations de copyright
© 2024. The Author(s), under exclusive licence to Springer Nature Limited.
Références
Yang, D. et al. Lineage tracing reveals the phylodynamics, plasticity, and paths of tumor evolution. Cell 185, 1905–1923 (2022).
pubmed: 35523183
pmcid: 9452598
doi: 10.1016/j.cell.2022.04.015
Celià-Terrassa, T. & Kang, Y. Distinctive properties of metastasis-initiating cells. Genes Dev. 30, 892–908 (2016).
pubmed: 27083997
pmcid: 4840296
doi: 10.1101/gad.277681.116
Boutin, A. T. et al. Oncogenic Kras drives invasion and maintains metastases in colorectal cancer. Genes Dev. 31, 370–382 (2017).
pubmed: 28289141
pmcid: 5358757
doi: 10.1101/gad.293449.116
Makohon-Moore, A. P. et al. Limited heterogeneity of known driver gene mutations among the metastases of individual patients with pancreatic cancer. Nat. Genet. 49, 358–366 (2017).
pubmed: 28092682
pmcid: 5663439
doi: 10.1038/ng.3764
Muir, A. & Vander Heiden, M. G. The nutrient environment affects therapy. Science 360, 962–963 (2018).
pubmed: 29853672
pmcid: 6368963
doi: 10.1126/science.aar5986
Abbott, K. L. et al. Screening in serum-derived medium reveals differential response to compounds targeting metabolism. Cell Chem. Biol. 30, 1156–1168 (2023).
pubmed: 37689063
doi: 10.1016/j.chembiol.2023.08.007
Altea‐Manzano, P., Cuadros, A. M., Broadfield, L. A. & Fendt, S. Nutrient metabolism and cancer in the in vivo context: a metabolic game of give and take. EMBO Rep. 21, e50635 (2020).
pubmed: 32964587
pmcid: 7534637
doi: 10.15252/embr.202050635
Mayers, J. R. et al. Tissue of origin dictates branched-chain amino acid metabolism in mutant Kras-driven cancers. Science 353, 1161–1165 (2016).
pubmed: 27609895
pmcid: 5245791
doi: 10.1126/science.aaf5171
Yuneva, M. O. et al. The metabolic profile of tumors depends on both the responsible genetic lesion and tissue type. Cell Metab. 15, 157–170 (2012).
pubmed: 22326218
pmcid: 3282107
doi: 10.1016/j.cmet.2011.12.015
Sullivan, M. R. et al. Quantification of microenvironmental metabolites in murine cancers reveals determinants of tumor nutrient availability. Elife 8, e44235 (2019).
pubmed: 30990168
pmcid: 6510537
doi: 10.7554/eLife.44235
Reinfeld, B. I. et al. Cell-programmed nutrient partitioning in the tumour microenvironment. Nature 593, 282–288 (2021).
pubmed: 33828302
pmcid: 8122068
doi: 10.1038/s41586-021-03442-1
Ferraro, G. B. et al. Fatty acid synthesis is required for breast cancer brain metastasis. Nat. Cancer 2, 414–428 (2021).
pubmed: 34179825
pmcid: 8223728
doi: 10.1038/s43018-021-00183-y
Schild, T., Low, V., Blenis, J. & Gomes, A. P. Unique metabolic adaptations dictate distal organ-specific metastatic colonization. Cancer Cell 33, 347–354 (2018).
pubmed: 29533780
pmcid: 5889305
doi: 10.1016/j.ccell.2018.02.001
Lehúede, C., Dupuy, F., Rabinovitch, R., Jones, R. G. & Siegel, P. M. Metabolic plasticity as a determinant of tumor growth and metastasis. Cancer Res. 76, 5201–5208 (2016).
pubmed: 27587539
doi: 10.1158/0008-5472.CAN-16-0266
Bartman, C. R. et al. Slow TCA flux and ATP production in primary solid tumours but not metastases. Nature 614, 349–357 (2023).
pubmed: 36725930
pmcid: 10288502
doi: 10.1038/s41586-022-05661-6
Basnet, H. et al. Flura-seq identifies organ-specific metabolic adaptations during early metastatic colonization. Elife 8, e43627 (2019).
pubmed: 30912515
pmcid: 6440742
doi: 10.7554/eLife.43627
Piskounova, E. et al. Oxidative stress inhibits distant metastasis by human melanoma cells. Nature 527, 186–191 (2015).
pubmed: 26466563
pmcid: 4644103
doi: 10.1038/nature15726
Gaude, E. & Frezza, C. Tissue-specific and convergent metabolic transformation of cancer correlates with metastatic potential and patient survival. Nat. Commun. 7, 13041 (2016).
pubmed: 27721378
pmcid: 5062467
doi: 10.1038/ncomms13041
Hu, J. et al. Heterogeneity of tumor-induced gene expression changes in the human metabolic network. Nat. Biotechnol. 31, 522–529 (2013).
pubmed: 23604282
pmcid: 3681899
doi: 10.1038/nbt.2530
Fidler, I. J. The pathogenesis of cancer metastasis: The ‘seed and soil’ hypothesis revisited. Nat. Rev. Cancer 3, 453–458 (2003).
pubmed: 12778135
doi: 10.1038/nrc1098
Hingorani, S. R. et al. Trp53R172H and KrasG12D cooperate to promote chromosomal instability and widely metastatic pancreatic ductal adenocarcinoma in mice. Cancer Cell 7, 469–483 (2005).
pubmed: 15894267
doi: 10.1016/j.ccr.2005.04.023
Kim, M. Y. et al. Tumor self-seeding by circulating cancer cells. Cell 139, 1315–1326 (2009).
pubmed: 20064377
pmcid: 2810531
doi: 10.1016/j.cell.2009.11.025
Gejman, R. S. et al. Rejection of immunogenic tumor clones is limited by clonal fraction. Elife 7, e41090 (2018).
pubmed: 30499773
pmcid: 6269121
doi: 10.7554/eLife.41090
Obenauf, A. C. & Massagué, J. Surviving at a distance: organ-specific metastasis. Trends Cancer 1, 76–91 (2015).
pubmed: 28741564
pmcid: 4673677
doi: 10.1016/j.trecan.2015.07.009
Maddipati, R. & Stanger, B. Z. Pancreatic cancer metastases harbor evidence of polyclonality. Cancer Discov. 5, 1086–1097 (2015).
pubmed: 26209539
pmcid: 4657730
doi: 10.1158/2159-8290.CD-15-0120
Lambert, A. W., Pattabiraman, D. R. & Weinberg, R. A. Emerging biological principles of metastasis. Cell 168, 670–691 (2017).
pubmed: 28187288
pmcid: 5308465
doi: 10.1016/j.cell.2016.11.037
Simeonov, K. P. et al. Single-cell lineage tracing of metastatic cancer reveals selection of hybrid EMT states. Cancer Cell 39, 1150–1162 (2021).
pubmed: 34115987
pmcid: 8782207
doi: 10.1016/j.ccell.2021.05.005
Elia, I., Doglioni, G. & Fendt, S. M. Metabolic hallmarks of metastasis formation. Trends Cell Biol. 28, 673–684 (2018).
pubmed: 29747903
doi: 10.1016/j.tcb.2018.04.002
Lau, A. N. et al. Dissecting cell-type-specific metabolism in pancreatic ductal adenocarcinoma. Elife 9, e56782 (2020).
pubmed: 32648540
pmcid: 7406355
doi: 10.7554/eLife.56782
Ariston Gabriel, A. N. et al. Differences between KC and KPC pancreatic ductal adenocarcinoma mice models, in terms of their modeling biology and their clinical relevance. Pancreatology 20, 79–88 (2020).
pubmed: 31780287
doi: 10.1016/j.pan.2019.11.006
Pérez-Mancera, P. A., Guerra, C., Barbacid, M. & Tuveson, D. A. What we have learned about pancreatic cancer from mouse models. Gastroenterology 142, 1079–1092 (2012).
pubmed: 22406637
doi: 10.1053/j.gastro.2012.03.002
Faubert, B., Solmonson, A. & DeBerardinis, R. J. Metabolic reprogramming and cancer progression. Science 368, eaaw5473 (2020).
pubmed: 32273439
pmcid: 7227780
doi: 10.1126/science.aaw5473
Yamaguchi, N. et al. PCK1 and DHODH drive colorectal cancer liver metastatic colonization and hypoxic growth by promoting nucleotide synthesis. Elife 8, e52135 (2019).
pubmed: 31841108
pmcid: 7299340
doi: 10.7554/eLife.52135
Minn, A. J. et al. Genes that mediate breast cancer metastasis to lung. Nature 436, 518–524 (2005).
pubmed: 16049480
pmcid: 1283098
doi: 10.1038/nature03799
Bos, P. D. et al. Genes that mediate breast cancer metastasis to the brain. Nature 459, 1005–1009 (2009).
pubmed: 19421193
pmcid: 2698953
doi: 10.1038/nature08021
DuPage, M., Dooley, A. L. & Jacks, T. Conditional mouse lung cancer models using adenoviral or lentiviral delivery of Cre recombinase. Nat. Protoc. 4, 1064–1072 (2009).
pubmed: 19561589
pmcid: 2757265
doi: 10.1038/nprot.2009.95
Kapanadze, T. et al. Regulation of accumulation and function of myeloid derived suppressor cells in different murine models of hepatocellular carcinoma. J. Hepatol. 59, 1007–1013 (2013).
pubmed: 23796475
pmcid: 3805787
doi: 10.1016/j.jhep.2013.06.010
Zender, L. et al. Generation and analysis of genetically defined liver carcinomas derived from bipotential liver progenitors. Cold Spring Harb. Symp. Quant. Biol. 70, 251–261 (2005).
pubmed: 16869761
pmcid: 4595853
doi: 10.1101/sqb.2005.70.059
Raphael, B. J. et al. Integrated genomic characterization of pancreatic ductal adenocarcinoma. Cancer Cell 32, 185–203 (2017).
doi: 10.1016/j.ccell.2017.07.007
Aguirre, A. J. et al. Real-time genomic characterization of advanced pancreatic cancer to enable precision medicine. Cancer Discov. 8, 1096–1111 (2018).
pubmed: 29903880
pmcid: 6192263
doi: 10.1158/2159-8290.CD-18-0275
Schug, Z. T. et al. Acetyl-CoA synthetase 2 promotes acetate utilization and maintains cancer cell growth under metabolic stress. Cancer Cell 27, 57–71 (2015).
pubmed: 25584894
pmcid: 4297291
doi: 10.1016/j.ccell.2014.12.002
Elia, I. et al. Breast cancer cells rely on environmental pyruvate to shape the metastatic niche. Nature 568, 117–121 (2019).
pubmed: 30814728
pmcid: 6451642
doi: 10.1038/s41586-019-0977-x
Rinaldi, G. et al. In Vivo evidence for serine biosynthesis-defined sensitivity of lung metastasis, but not of primary breast tumors, to mTORC1 inhibition. Mol. Cell 81, 386–397 (2021).
pubmed: 33340488
doi: 10.1016/j.molcel.2020.11.027
Elia, I. et al. Proline metabolism supports metastasis formation and could be inhibited to selectively target metastasizing cancer cells. Nat. Commun. 8, 15267 (2017).
pubmed: 28492237
pmcid: 5437289
doi: 10.1038/ncomms15267
Chi, Y. et al. Cancer cells deploy lipocalin-2 to collect limiting iron in leptomeningeal metastasis. Science 369, 276–282 (2020).
pubmed: 32675368
pmcid: 7816199
doi: 10.1126/science.aaz2193
Klein, C. A. Parallel progression of primary tumours and metastases. Nat. Rev. Cancer 9, 302–312 (2009).
pubmed: 19308069
doi: 10.1038/nrc2627
Oda, T. et al. Growth rates of primary and metastatic lesions of renal cell carcinoma. Int. J. Urol. 8, 473–477 (2001).
pubmed: 11683965
doi: 10.1046/j.1442-2042.2001.00353.x
Boj, S. F. et al. Organoid models of human and mouse ductal pancreatic cancer. Cell 160, 324–338 (2015).
pubmed: 25557080
doi: 10.1016/j.cell.2014.12.021
Gocheva, V. et al. Quantitative proteomics identify Tenascin-C as a promoter of lung cancer progression and contributor to a signature prognostic of patient survival. Proc. Natl Acad. Sci. USA 114, E5625–E5634 (2017).
pubmed: 28652369
pmcid: 5514763
doi: 10.1073/pnas.1707054114
Davidson, S. M. et al. Environment impacts the metabolic dependencies of ras-driven non-small cell lung cancer. Cell Metab. 23, 517–528 (2016).
pubmed: 26853747
pmcid: 4785096
doi: 10.1016/j.cmet.2016.01.007