Circulating tumor cell-derived preclinical models: current status and future perspectives
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články, přehledy, práce podpořená grantem
PubMed
37591867
PubMed Central
PMC10435501
DOI
10.1038/s41419-023-06059-6
PII: 10.1038/s41419-023-06059-6
Knihovny.cz E-zdroje
- MeSH
- buněčné kultury MeSH
- heterografty MeSH
- individualizovaná medicína MeSH
- lidé MeSH
- nádorové cirkulující buňky * MeSH
- transplantace heterologní MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- přehledy MeSH
Despite the advancements made in the diagnosis and treatment of cancer, the stages associated with metastasis remain largely incurable and represent the primary cause of cancer-related deaths. The dissemination of cancer is facilitated by circulating tumor cells (CTCs), which originate from the primary tumor or metastatic sites and enter the bloodstream, subsequently spreading to distant parts of the body. CTCs have garnered significant attention in research due to their accessibility in peripheral blood, despite their low abundance. They are being extensively studied to gain a deeper understanding of the mechanisms underlying cancer dissemination and to identify effective therapeutic strategies for advanced stages of the disease. Therefore, substantial efforts have been directed towards establishing and characterizing relevant experimental models derived from CTCs, aiming to provide relevant tools for research. In this review, we provide an overview of recent progress in the establishment of preclinical CTC-derived models, such as CTC-derived xenografts (CDX) and cell cultures, which show promise for the study of CTCs. We discuss the advantages and limitations of these models and conclude by summarizing the potential future use of CTCs and CTC-derived models in cancer treatment decisions and their utility as precision medicine tools.
Department of Comprehensive Cancer Care Masaryk Memorial Cancer Institute 656 53 Brno Czech Republic
Department of Experimental Biology Faculty of Science Masaryk University 625 00 Brno Czech Republic
Department of Molecular Oncology H Lee Moffitt Cancer Center and Research Institute Tampa FL USA
International Clinical Research Center St Anne's University Hospital 602 00 Brno Czech Republic
Zobrazit více v PubMed
Kim MY, Oskarsson T, Acharyya S, Nguyen DX, Zhang XH, Norton L, et al. Tumor self-seeding by circulating cancer cells. Cell. 2009;139:1315–26. doi: 10.1016/j.cell.2009.11.025. PubMed DOI PMC
Cameron MD, Schmidt EE, Kerkvliet N, Nadkarni KV, Morris VL, Groom AC, et al. Temporal progression of metastasis in lung: cell survival, dormancy, and location dependence of metastatic inefficiency. Cancer Res. 2000;60:2541–6. PubMed
Lambert AW, Pattabiraman DR, Weinberg RA. Emerging biological principles of metastasis. Cell. 2017;168:670–91.. doi: 10.1016/j.cell.2016.11.037. PubMed DOI PMC
Luzzi KJ, MacDonald IC, Schmidt EE, Kerkvliet N, Morris VL, Chambers AF, et al. Multistep nature of metastatic inefficiency: dormancy of solitary cells after successful extravasation and limited survival of early micrometastases. Am J Pathol. 1998;153:865–73. doi: 10.1016/S0002-9440(10)65628-3. PubMed DOI PMC
Massagué J, Obenauf AC. Metastatic colonization by circulating tumour cells. Nature. 2016;529:298–306. doi: 10.1038/nature17038. PubMed DOI PMC
Chiang AC, Massague J. Molecular basis of metastasis. N Engl J Med. 2008;359:2814–23. doi: 10.1056/NEJMra0805239. PubMed DOI PMC
Hu Z, Curtis C. Looking backward in time to define the chronology of metastasis. Nat Commun. 2020;11:3213. doi: 10.1038/s41467-020-16995-y. PubMed DOI PMC
Hosseini H, Obradović MMS, Hoffmann M, Harper KL, Sosa MS, Werner-Klein M, et al. Early dissemination seeds metastasis in breast cancer. Nature. 2016;540:552–8. doi: 10.1038/nature20785. PubMed DOI PMC
Klein CA. Parallel progression of primary tumours and metastases. Nat Rev Cancer. 2009;9:302–12. doi: 10.1038/nrc2627. PubMed DOI
Klein CA, Blankenstein TJ, Schmidt-Kittler O, Petronio M, Polzer B, Stoecklein NH, et al. Genetic heterogeneity of single disseminated tumour cells in minimal residual cancer. Lancet. 2002;360:683–9. doi: 10.1016/S0140-6736(02)09838-0. PubMed DOI
Schmidt-Kittler O, Ragg T, Daskalakis A, Granzow M, Ahr A, Blankenstein TJ, et al. From latent disseminated cells to overt metastasis: genetic analysis of systemic breast cancer progression. Proc Natl Acad Sci USA. 2003;100:7737–42. doi: 10.1073/pnas.1331931100. PubMed DOI PMC
Rhim AD, Mirek ET, Aiello NM, Maitra A, Bailey JM, McAllister F, et al. EMT and dissemination precede pancreatic tumor formation. Cell. 2012;148:349–61. doi: 10.1016/j.cell.2011.11.025. PubMed DOI PMC
Engel J, Eckel R, Kerr J, Schmidt M, Fürstenberger G, Richter R, et al. The process of metastasisation for breast cancer. Eur J Cancer. 2003;39:1794–806. doi: 10.1016/S0959-8049(03)00422-2. PubMed DOI
Haerinck J, Goossens S, Berx G. The epithelial-mesenchymal plasticity landscape: principles of design and mechanisms of regulation. Nat Rev Genet. 2023;24:590–609. doi: 10.1038/s41576-023-00601-0. PubMed DOI
Lüönd F, Tiede S, Christofori G. Breast cancer as an example of tumour heterogeneity and tumour cell plasticity during malignant progression. Br J Cancer. 2021;125:164–75.. doi: 10.1038/s41416-021-01328-7. PubMed DOI PMC
Pinto CA, Widodo E, Waltham M, Thompson EW. Breast cancer stem cells and epithelial mesenchymal plasticity - Implications for chemoresistance. Cancer Lett. 2013;341:56–62. doi: 10.1016/j.canlet.2013.06.003. PubMed DOI
Brabletz S, Schuhwerk H, Brabletz T, Stemmler MP. Dynamic EMT: a multi-tool for tumor progression. EMBO J. 2021;40:e108647. doi: 10.15252/embj.2021108647. PubMed DOI PMC
Jolly MK, Boareto M, Huang B, Jia D, Lu M, Ben-Jacob E, et al. Implications of the hybrid epithelial/mesenchymal phenotype in metastasis. Front Oncol. 2015;5:155. doi: 10.3389/fonc.2015.00155. PubMed DOI PMC
Jolly MK, Somarelli JA, Sheth M, Biddle A, Tripathi SC, Armstrong AJ, et al. Hybrid epithelial/mesenchymal phenotypes promote metastasis and therapy resistance across carcinomas. Pharmacol Ther. 2019;194:161–84.. doi: 10.1016/j.pharmthera.2018.09.007. PubMed DOI
Dongre A, Weinberg RA. New insights into the mechanisms of epithelial-mesenchymal transition and implications for cancer. Nat Rev Mol Cell Biol. 2019;20:69–84. doi: 10.1038/s41580-018-0080-4. PubMed DOI
Mani SA, Guo W, Liao MJ, Eaton EN, Ayyanan A, Zhou AY, et al. The epithelial-mesenchymal transition generates cells with properties of stem cells. Cell. 2008;133:704–15. doi: 10.1016/j.cell.2008.03.027. PubMed DOI PMC
Celia-Terrassa T, Jolly MK. Cancer stem cells and epithelial-to-mesenchymal transition in cancer metastasis. Cold Spring Harb Perspect Med. 2020;10:a036905. doi: 10.1101/cshperspect.a036905. PubMed DOI PMC
Genna A, Vanwynsberghe AM, Villard AV, Pottier C, Ancel J, Polette M, et al. EMT-associated heterogeneity in circulating tumor cells: sticky friends on the road to metastasis. Cancers. 2020;12:1632. doi: 10.3390/cancers12061632. PubMed DOI PMC
Yu M, Bardia A, Wittner BS, Stott SL, Smas ME, Ting DT, et al. Circulating breast tumor cells exhibit dynamic changes in epithelial and mesenchymal composition. Science. 2013;339:580–4. doi: 10.1126/science.1228522. PubMed DOI PMC
Allard WJ, Matera J, Miller MC, Repollet M, Connelly MC, Rao C, et al. Tumor cells circulate in the peripheral blood of all major carcinomas but not in healthy subjects or patients with nonmalignant diseases. Clin Cancer Res. 2004;10:6897–904. doi: 10.1158/1078-0432.CCR-04-0378. PubMed DOI
Olmos D, Baird RD, Yap TA, Massard C, Pope L, Sandhu SK, et al. Baseline circulating tumor cell counts significantly enhance a prognostic score for patients participating in phase I oncology trials. Clin Cancer Res. 2011;17:5188–96. doi: 10.1158/1078-0432.CCR-10-3019. PubMed DOI
Vetter M, Landin J, Szczerba BM, Castro-Giner F, Gkountela S, Donato C, et al. Denosumab treatment is associated with the absence of circulating tumor cells in patients with breast cancer. Breast Cancer Res. 2018;20:141. doi: 10.1186/s13058-018-1067-y. PubMed DOI PMC
Diamantopoulou Z, Castro-Giner F, Schwab FD, Foerster C, Saini M, Budinjas S, et al. The metastatic spread of breast cancer accelerates during sleep. Nature. 2022;607:156–62.. doi: 10.1038/s41586-022-04875-y. PubMed DOI
Terai M, Mu Z, Eschelman DJ, Gonsalves CF, Kageyama K, Chervoneva I, et al. Arterial blood, rather than venous blood, is a better source for circulating melanoma cells. EBioMedicine. 2015;2:1821–6. doi: 10.1016/j.ebiom.2015.09.019. PubMed DOI PMC
Reddy RM, Murlidhar V, Zhao L, Grabauskiene S, Zhang Z, Ramnath N, et al. Pulmonary venous blood sampling significantly increases the yield of circulating tumor cells in early-stage lung cancer. J Thorac Cardiovasc Surg. 2016;151:852–8. doi: 10.1016/j.jtcvs.2015.09.126. PubMed DOI
Crosbie PA, Shah R, Krysiak P, Zhou C, Morris K, Tugwood J, et al. Circulating tumor cells detected in the tumor-draining pulmonary vein are associated with disease recurrence after surgical resection of NSCLC. J Thorac Oncol. 2016;11:1793–7. doi: 10.1016/j.jtho.2016.06.017. PubMed DOI PMC
Andree KC, van Dalum G, Terstappen LW. Challenges in circulating tumor cell detection by the CellSearch system. Mol Oncol. 2016;10:395–407. doi: 10.1016/j.molonc.2015.12.002. PubMed DOI PMC
Cristofanilli M, Budd GT, Ellis MJ, Stopeck A, Matera J, Miller MC, et al. Circulating tumor cells, disease progression, and survival in metastatic breast cancer. N Engl J Med. 2004;351:781–91. doi: 10.1056/NEJMoa040766. PubMed DOI
Cristofanilli M, Hayes DF, Budd GT, Ellis MJ, Stopeck A, Reuben JM, et al. Circulating tumor cells: a novel prognostic factor for newly diagnosed metastatic breast cancer. J Clin Oncol. 2005;23:1420–30. doi: 10.1200/JCO.2005.08.140. PubMed DOI
Hayes DF, Cristofanilli M, Budd GT, Ellis MJ, Stopeck A, Miller MC, et al. Circulating tumor cells at each follow-up time point during therapy of metastatic breast cancer patients predict progression-free and overall survival. Clin Cancer Res. 2006;12:4218–24. doi: 10.1158/1078-0432.CCR-05-2821. PubMed DOI
Riethdorf S, Fritsche H, Muller V, Rau T, Schindlbeck C, Rack B, et al. Detection of circulating tumor cells in peripheral blood of patients with metastatic breast cancer: a validation study of the CellSearch system. Clin Cancer Res. 2007;13:920–8. doi: 10.1158/1078-0432.CCR-06-1695. PubMed DOI
de Bono JS, Scher HI, Montgomery RB, Parker C, Miller MC, Tissing H, et al. Circulating tumor cells predict survival benefit from treatment in metastatic castration-resistant prostate cancer. Clin Cancer Res. 2008;14:6302–9. doi: 10.1158/1078-0432.CCR-08-0872. PubMed DOI
Cohen SJ, Punt CJ, Iannotti N, Saidman BH, Sabbath KD, Gabrail NY, et al. Relationship of circulating tumor cells to tumor response, progression-free survival, and overall survival in patients with metastatic colorectal cancer. J Clin Oncol. 2008;26:3213–21. doi: 10.1200/JCO.2007.15.8923. PubMed DOI
Negin BP, Cohen SJ. Circulating tumor cells in colorectal cancer: past, present, and future challenges. Curr Treat Options Oncol. 2010;11:1–13. doi: 10.1007/s11864-010-0115-3. PubMed DOI
Morrow CJ, Trapani F, Metcalf RL, Bertolini G, Hodgkinson CL, Khandelwal G, et al. Tumourigenic non-small-cell lung cancer mesenchymal circulating tumour cells: a clinical case study. Ann Oncol. 2016;27:1155–60.. doi: 10.1093/annonc/mdw122. PubMed DOI PMC
Miller MC, Robinson PS, Wagner C, O’Shannessy DJ. The Parsortix cell separation system-a versatile liquid biopsy platform. Cytom A. 2018;93:1234–9. doi: 10.1002/cyto.a.23571. PubMed DOI PMC
Banko P, Lee SY, Nagygyorgy V, Zrinyi M, Chae CH, Cho DH, et al. Technologies for circulating tumor cell separation from whole blood. J Hematol Oncol. 2019;12:48. doi: 10.1186/s13045-019-0735-4. PubMed DOI PMC
Rushton AJ, Nteliopoulos G, Shaw JA, Coombes RC. A review of circulating tumour cell enrichment technologies. Cancers. 2021;13:970. doi: 10.3390/cancers13050970. PubMed DOI PMC
Eslami SZ, Cortes-Hernandez LE, Thomas F, Pantel K, Alix-Panabieres C. Functional analysis of circulating tumour cells: the KEY to understand the biology of the metastatic cascade. Br J Cancer. 2022;127:800–10. doi: 10.1038/s41416-022-01819-1. PubMed DOI PMC
Joosse SA, Gorges TM, Pantel K. Biology, detection, and clinical implications of circulating tumor cells. EMBO Mol Med. 2015;7:1–11. doi: 10.15252/emmm.201303698. PubMed DOI PMC
Habli Z, AlChamaa W, Saab R, Kadara H, Khraiche ML. Circulating tumor cell detection technologies and clinical utility: challenges and opportunities. Cancers. 2020;12:1930. doi: 10.3390/cancers12071930. PubMed DOI PMC
Ju S, Chen C, Zhang J, Xu L, Zhang X, Li Z, et al. Detection of circulating tumor cells: opportunities and challenges. Biomark Res. 2022;10:58. doi: 10.1186/s40364-022-00403-2. PubMed DOI PMC
Chelakkot C, Yang H, Shin YK. Relevance of circulating tumor cells as predictive markers for cancer incidence and relapse. Pharmaceuticals. 2022;15:75. doi: 10.3390/ph15010075. PubMed DOI PMC
Baccelli I, Schneeweiss A, Riethdorf S, Stenzinger A, Schillert A, Vogel V, et al. Identification of a population of blood circulating tumor cells from breast cancer patients that initiates metastasis in a xenograft assay. Nat Biotechnol. 2013;31:539–44. doi: 10.1038/nbt.2576. PubMed DOI
Pereira-Veiga T, Abreu M, Robledo D, Matias-Guiu X, Santacana M, Sánchez L, et al. CTCs-derived xenograft development in a triple negative breast cancer case. Int J Cancer. 2019;144:2254–65.. doi: 10.1002/ijc.32001. PubMed DOI
Vishnoi M, Liu NH, Yin W, Boral D, Scamardo A, Hong D, et al. The identification of a TNBC liver metastasis gene signature by sequential CTC-xenograft modeling. Mol Oncol. 2019;13:1913–26.. doi: 10.1002/1878-0261.12533. PubMed DOI PMC
Klotz R, Thomas A, Teng T, Han SM, Iriondo O, Li L, et al. Circulating tumor cells exhibit metastatic tropism and reveal brain metastasis drivers. Cancer Discov. 2020;10:86–103. doi: 10.1158/2159-8290.CD-19-0384. PubMed DOI PMC
Faugeroux V, Pailler E, Oulhen M, Deas O, Brulle-Soumare L, Hervieu C, et al. Genetic characterization of a unique neuroendocrine transdifferentiation prostate circulating tumor cell-derived eXplant model. Nat Commun. 2020;11:1884. doi: 10.1038/s41467-020-15426-2. PubMed DOI PMC
Foy V, Fernandez-Gutierrez F, Faivre-Finn C, Dive C, Blackhall F. The clinical utility of circulating tumour cells in patients with small cell lung cancer. Transl Lung Cancer Res. 2017;6:409–17.. doi: 10.21037/tlcr.2017.07.05. PubMed DOI PMC
Hodgkinson CL, Morrow CJ, Li Y, Metcalf RL, Rothwell DG, Trapani F, et al. Tumorigenicity and genetic profiling of circulating tumor cells in small-cell lung cancer. Nat Med. 2014;20:897–903. doi: 10.1038/nm.3600. PubMed DOI
Lallo A, Gulati S, Schenk MW, Khandelwal G, Berglund UW, Pateras IS, et al. Ex vivo culture of cells derived from circulating tumour cell xenograft to support small cell lung cancer research and experimental therapeutics. Br J Pharmacol. 2019;176:436–50.. doi: 10.1111/bph.14542. PubMed DOI PMC
Drapkin BJ, George J, Christensen CL, Mino-Kenudson M, Dries R, Sundaresan T, et al. Genomic and functional fidelity of small cell lung cancer patient-derived xenografts. Cancer Discov. 2018;8:600–15.. doi: 10.1158/2159-8290.CD-17-0935. PubMed DOI PMC
Simpson KL, Stoney R, Frese KK, Simms N, Rowe W, Pearce SP, et al. A biobank of small cell lung cancer CDX models elucidates inter- and intratumoral phenotypic heterogeneity. Nat Cancer. 2020;1:437–51.. doi: 10.1038/s43018-020-0046-2. PubMed DOI
Stewart CA, Gay CM, Xi Y, Sivajothi S, Sivakamasundari V, Fujimoto J, et al. Single-cell analyses reveal increased intratumoral heterogeneity after the onset of therapy resistance in small-cell lung cancer. Nat Cancer. 2020;1:423–36.. doi: 10.1038/s43018-019-0020-z. PubMed DOI PMC
Tayoun T, Faugeroux V, Oulhen M, Deas O, Michels J, Brulle-Soumare L, et al. Targeting genome integrity dysfunctions impedes metastatic potency in non-small cell lung cancer circulating tumor cell-derived explants. JCI Insight. 2022;7:e155804. doi: 10.1172/jci.insight.155804. PubMed DOI PMC
Girotti MR, Gremel G, Lee R, Galvani E, Rothwell D, Viros A, et al. Application of sequencing, liquid biopsies, and patient-derived xenografts for personalized medicine in melanoma. Cancer Discov. 2016;6:286–99. doi: 10.1158/2159-8290.CD-15-1336. PubMed DOI
Vishnoi M, Boral D, Liu H, Sprouse ML, Yin W, Goswami-Sewell D, et al. Targeting USP7 identifies a metastasis-competent state within bone marrow-resident melanoma CTCs. Cancer Res. 2018;78:5349–62.. doi: 10.1158/0008-5472.CAN-18-0644. PubMed DOI PMC
Scheidmann MC, Castro-Giner F, Strittmatter K, Krol I, Paasinen-Sohns A, Scherrer R, et al. An in vivo CRISPR screen identifies stepwise genetic dependencies of metastatic progression. Cancer Res. 2022;82:681–94.. doi: 10.1158/0008-5472.CAN-21-3908. PubMed DOI PMC
Lambros MB, Seed G, Sumanasuriya S, Gil V, Crespo M, Fontes M, et al. Single-cell analyses of prostate cancer liquid biopsies acquired by apheresis. Clin Cancer Res. 2018;24:5635–44.. doi: 10.1158/1078-0432.CCR-18-0862. PubMed DOI
Andree KC, Mentink A, Zeune LL, Terstappen L, Stoecklein NH, Neves RP, et al. Toward a real liquid biopsy in metastatic breast and prostate cancer: diagnostic LeukApheresis increases CTC yields in a European prospective multicenter study (CTCTrap) Int J Cancer. 2018;143:2584–91.. doi: 10.1002/ijc.31752. PubMed DOI PMC
Gorges TM, Tinhofer I, Drosch M, Rose L, Zollner TM, Krahn T, et al. Circulating tumour cells escape from EpCAM-based detection due to epithelial-to-mesenchymal transition. BMC Cancer. 2012;12:178. doi: 10.1186/1471-2407-12-178. PubMed DOI PMC
Dasgupta A, Lim AR, Ghajar CM. Circulating and disseminated tumor cells: harbingers or initiators of metastasis? Mol Oncol. 2017;11:40–61. doi: 10.1002/1878-0261.12022. PubMed DOI PMC
Kuchimaru T, Kataoka N, Nakagawa K, Isozaki T, Miyabara H, Minegishi M, et al. A reliable murine model of bone metastasis by injecting cancer cells through caudal arteries. Nat Commun. 2018;9:2981. doi: 10.1038/s41467-018-05366-3. PubMed DOI PMC
Zhang L, Ridgway LD, Wetzel MD, Ngo J, Yin W, Kumar D, et al. The identification and characterization of breast cancer CTCs competent for brain metastasis. Sci Transl Med. 2013;5:180ra48. doi: 10.1126/scitranslmed.3005109. PubMed DOI PMC
Yu M, Bardia A, Aceto N, Bersani F, Madden MW, Donaldson MC, et al. Cancer therapy. Ex vivo culture of circulating breast tumor cells for individualized testing of drug susceptibility. Science. 2014;345:216–20. doi: 10.1126/science.1253533. PubMed DOI PMC
Koch C, Kuske A, Joosse SA, Yigit G, Sflomos G, Thaler S, et al. Characterization of circulating breast cancer cells with tumorigenic and metastatic capacity. EMBO Mol Med. 2020;12:e11908. doi: 10.15252/emmm.201911908. PubMed DOI PMC
Xiao J, McGill JR, Stanton K, Kassner JD, Choudhury S, Schlegel R, et al. Efficient propagation of circulating tumor cells: a first step for probing tumor metastasis. Cancers. 2020;12:2784. doi: 10.3390/cancers12102784. PubMed DOI PMC
Xiao J, Sharma U, Arab A, Miglani S, Bhalla S, Suguru S, et al. Propagated circulating tumor cells uncover the potential role of NFkappaB, EMT, and TGFbeta signaling pathways and COP1 in metastasis. Cancers. 2023;15:1831. doi: 10.3390/cancers15061831. PubMed DOI PMC
Zhao P, Zhou W, Liu C, Zhang H, Cheng Z, Wu W, et al. Establishment and characterization of a CTC cell line from peripheral blood of breast cancer patient. J Cancer. 2019;10:6095–104.. doi: 10.7150/jca.33157. PubMed DOI PMC
Khoo BL, Grenci G, Lim YB, Lee SC, Han J, Lim CT. Expansion of patient-derived circulating tumor cells from liquid biopsies using a CTC microfluidic culture device. Nat Protoc. 2018;13:34–58. doi: 10.1038/nprot.2017.125. PubMed DOI
Carmona-Ule N, Abuín-Redondo C, Costa C, Piñeiro R, Pereira-Veiga T, Martínez-Pena I, et al. Nanoemulsions to support ex vivo cell culture of breast cancer circulating tumor cells. Mater Today Chem. 2020;16:100265. doi: 10.1016/j.mtchem.2020.100265. DOI
Gao D, Vela I, Sboner A, Iaquinta PJ, Karthaus WR, Gopalan A, et al. Organoid cultures derived from patients with advanced prostate cancer. Cell. 2014;159:176–87.. doi: 10.1016/j.cell.2014.08.016. PubMed DOI PMC
Mout L, van Dessel LF, Kraan J, de Jong AC, Neves RPL, Erkens-Schulze S, et al. Generating human prostate cancer organoids from leukapheresis enriched circulating tumour cells. Eur J Cancer. 2021;150:179–89.. doi: 10.1016/j.ejca.2021.03.023. PubMed DOI
Hamilton G, Burghuber O, Zeillinger R. Circulating tumor cells in small cell lung cancer: ex vivo expansion. Lung. 2015;193:451–2. doi: 10.1007/s00408-015-9725-7. PubMed DOI
Hamilton G, Rath B, Holzer S, Hochmair M. Second-line therapy for small cell lung cancer: exploring the potential role of circulating tumor cells. Transl Lung Cancer Res. 2016;5:71–7. PubMed PMC
Lee HL, Chiou JF, Wang PY, Lu LS, Shen CN, Hsu HL, et al. Ex vivo expansion and drug sensitivity profiling of circulating tumor cells from patients with small cell lung cancer. Cancers. 2020;12:3394. doi: 10.3390/cancers12113394. PubMed DOI PMC
Que Z, Luo B, Zhou Z, Dong C, Jiang Y, Wang L, et al. Establishment and characterization of a patient-derived circulating lung tumor cell line in vitro and in vivo. Cancer Cell Int. 2019;19:21. doi: 10.1186/s12935-019-0735-z. PubMed DOI PMC
Wang Z, Wu W, Wang Z, Tang Y, Deng Y, Xu L, et al. Ex vivo expansion of circulating lung tumor cells based on one-step microfluidics-based immunomagnetic isolation. Analyst. 2016;141:3621–5. doi: 10.1039/C5AN02554K. PubMed DOI
Zhang Z, Shiratsuchi H, Lin J, Chen G, Reddy RM, Azizi E, et al. Expansion of CTCs from early stage lung cancer patients using a microfluidic co-culture model. Oncotarget. 2014;5:12383–97. doi: 10.18632/oncotarget.2592. PubMed DOI PMC
Dizdar L, Fluegen G, van Dalum G, Honisch E, Neves RP, Niederacher D, et al. Detection of circulating tumor cells in colorectal cancer patients using the GILUPI CellCollector: results from a prospective, single-center study. Mol Oncol. 2019;13:1548–58.. doi: 10.1002/1878-0261.12507. PubMed DOI PMC
Cayrefourcq L, Mazard T, Joosse S, Solassol J, Ramos J, Assenat E, et al. Establishment and characterization of a cell line from human circulating colon cancer cells. Cancer Res. 2015;75:892–901. doi: 10.1158/0008-5472.CAN-14-2613. PubMed DOI
Soler A, Cayrefourcq L, Mazard T, Babayan A, Lamy PJ, Assou S, et al. Autologous cell lines from circulating colon cancer cells captured from sequential liquid biopsies as model to study therapy-driven tumor changes. Sci Rep. 2018;8:15931. doi: 10.1038/s41598-018-34365-z. PubMed DOI PMC
Grillet F, Bayet E, Villeronce O, Zappia L, Lagerqvist EL, Lunke S, et al. Circulating tumour cells from patients with colorectal cancer have cancer stem cell hallmarks in ex vivo culture. Gut. 2017;66:1802–10.. doi: 10.1136/gutjnl-2016-311447. PubMed DOI PMC
Arnoletti JP, Fanaian N, Reza J, Sause R, Almodovar AJ, Srivastava M, et al. Pancreatic and bile duct cancer circulating tumor cells (CTC) form immune-resistant multi-cell type clusters in the portal venous circulation. Cancer Biol Ther. 2018;19:887–97.. doi: 10.1080/15384047.2018.1480292. PubMed DOI PMC
Rivera-Baez L, Lohse I, Lin E, Raghavan S, Owen S, Harouaka R, et al. Expansion of circulating tumor cells from patients with locally advanced pancreatic cancer enable patient derived xenografts and functional studies for personalized medicine. Cancers. 2020;12:1011. doi: 10.3390/cancers12041011. PubMed DOI PMC
Wu YH, Hung YP, Chiu NC, Lee RC, Li CP, Chao Y, et al. Correlation between drug sensitivity profiles of circulating tumour cell-derived organoids and clinical treatment response in patients with pancreatic ductal adenocarcinoma. Eur J Cancer. 2022;166:208–18.. doi: 10.1016/j.ejca.2022.01.030. PubMed DOI
Shimada Y, Sudo T, Akamatsu S, Sunada T, Myomoto A, Okano K, et al. Cell lines of circulating tumor cells: what is known and what needs to be resolved. J Pers Med. 2022;12:666. doi: 10.3390/jpm12050666. PubMed DOI PMC
Rankin EB, Giaccia AJ. Hypoxic control of metastasis. Science. 2016;352:175–80. doi: 10.1126/science.aaf4405. PubMed DOI PMC
Ameri K, Luong R, Zhang H, Powell AA, Montgomery KD, Espinosa I, et al. Circulating tumour cells demonstrate an altered response to hypoxia and an aggressive phenotype. Br J Cancer. 2010;102:561–9. doi: 10.1038/sj.bjc.6605491. PubMed DOI PMC
Donato C, Kunz L, Castro-Giner F, Paasinen-Sohns A, Strittmatter K, Szczerba BM, et al. Hypoxia triggers the intravasation of clustered circulating tumor cells. Cell Rep. 2020;32:108105. doi: 10.1016/j.celrep.2020.108105. PubMed DOI PMC
Otero-Albiol D, Carnero A. Cellular senescence or stemness: hypoxia flips the coin. J Exp Clin Cancer Res. 2021;40:243. doi: 10.1186/s13046-021-02035-0. PubMed DOI PMC
Carmona-Ule N, Gonzalez-Conde M, Abuin C, Cueva JF, Palacios P, Lopez-Lopez R, et al. Short-term ex vivo culture of CTCs from advance breast cancer patients: clinical implications. Cancers. 2021;13:2668. doi: 10.3390/cancers13112668. PubMed DOI PMC
Kapeleris J, Kulasinghe A, Warkiani ME, Oleary C, Vela I, Leo P, et al. Ex vivo culture of circulating tumour cells derived from non-small cell lung cancer. Transl Lung Cancer Res. 2020;9:1795–809.. doi: 10.21037/tlcr-20-521. PubMed DOI PMC
Guillen KP, Fujita M, Butterfield AJ, Scherer SD, Bailey MH, Chu Z, et al. A human breast cancer-derived xenograft and organoid platform for drug discovery and precision oncology. Nat Cancer. 2022;3:232–50.. doi: 10.1038/s43018-022-00337-6. PubMed DOI PMC
Hwang E, Uh JH, Lee HS, Lee CH, Lee SJ, Ahn SH, et al. Cancer gene panel analysis of cultured circulating tumor cells and primary tumor tissue from patients with breast cancer. Oncol Lett. 2017;13:4627–32.. doi: 10.3892/ol.2017.6077. PubMed DOI PMC
Miebach L, Berner J, Bekeschus S. In ovo model in cancer research and tumor immunology. Front Immunol. 2022;13:1006064. doi: 10.3389/fimmu.2022.1006064. PubMed DOI PMC
Pizon M, Schott D, Pachmann U, Schobert R, Pizon M, Wozniak M, et al. Chick chorioallantoic membrane (CAM) assays as a model of patient-derived xenografts from circulating cancer stem cells (cCSCs) in breast cancer patients. Cancers. 2022;14:1476. doi: 10.3390/cancers14061476. PubMed DOI PMC
Rousset X, Maillet D, Grolleau E, Barthelemy D, Calattini S, Brevet M, et al. Embryonated chicken tumor xenografts derived from circulating tumor cells as a relevant model to study metastatic dissemination: a proof of concept. Cancers. 2022;14:4085. doi: 10.3390/cancers14174085. PubMed DOI PMC
Fischer D, Fluegen G, Garcia P, Ghaffari-Tabrizi-Wizsy N, Gribaldo L, Huang RY, et al. The CAM model-Q&A with experts. Cancers. 2022;15:191. doi: 10.3390/cancers15010191. PubMed DOI PMC
Vasseur A, Kiavue N, Bidard FC, Pierga JY, Cabel L. Clinical utility of circulating tumor cells: an update. Mol Oncol. 2021;15:1647–66. doi: 10.1002/1878-0261.12869. PubMed DOI PMC
Franken A, Behrens B, Reinhardt F, Yang L, Rivandi M, Marass F, et al. Multiparametric circulating tumor cell analysis to select targeted therapies for breast cancer patients. Cancers. 2021;13:6004. doi: 10.3390/cancers13236004. PubMed DOI PMC
Theil G, Boehm C, Fischer K, Bialek J, Hoda R, Weber E, et al. In vivo isolation of circulating tumor cells in patients with different stages of prostate cancer. Oncol Lett. 2021;21:357. doi: 10.3892/ol.2021.12618. PubMed DOI PMC
Xing L, Wan X, Yu MT, He YJ, Wang Y, Zhou TJ, et al. A novel whole blood purifier for efficient capture and separation of circulating tumor cells. Biosens Bioelectron. 2023;232:115292. doi: 10.1016/j.bios.2023.115292. PubMed DOI
Williams ES, Rodriguez-Bravo V, Chippada-Venkata U, De Ia Iglesia-Vicente J, Gong Y, Galsky M, et al. Generation of prostate cancer patient derived xenograft models from circulating tumor cells. J Vis Exp. 2015;104:e53182. PubMed PMC
De Angelis ML, Francescangeli F, Nicolazzo C, Signore M, Giuliani A, Colace L, et al. An organoid model of colorectal circulating tumor cells with stem cell features, hybrid EMT state and distinctive therapy response profile. J Exp Clin Cancer Res. 2022;41:86. doi: 10.1186/s13046-022-02263-y. PubMed DOI PMC
Kolostova K, Broul M, Schraml J, Cegan M, Matkowski R, Fiutowski M, et al. Circulating tumor cells in localized prostate cancer: isolation, cultivation in vitro and relationship to T-stage and Gleason score. Anticancer Res. 2014;34:3641–6. PubMed
Kolostova K, Matkowski R, Gurlich R, Grabowski K, Soter K, Lischke R, et al. Detection and cultivation of circulating tumor cells in gastric cancer. Cytotechnology. 2016;68:1095–102. doi: 10.1007/s10616-015-9866-9. PubMed DOI PMC
Kolostova K, Matkowski R, Jedryka M, Soter K, Cegan M, Pinkas M, et al. The added value of circulating tumor cells examination in ovarian cancer staging. Am J Cancer Res. 2015;5:3363–75. PubMed PMC
Kiss I, Kolostova K, Matkowski R, Jedryka M, Czekanski A, Pavlasek J, et al. Correlation between disease stage and the presence of viable circulating tumor cells in endometrial cancer. Anticancer Res. 2018;38:2983–7. PubMed
Brungs D, Minaei E, Piper A-K, Perry J, Splitt A, Carolan M, et al. Establishment of novel long-term cultures from EpCAM positive and negative circulating tumour cells from patients with metastatic gastroesophageal cancer. Sci Rep. 2020;10:539. doi: 10.1038/s41598-019-57164-6. PubMed DOI PMC