Breaking the mold: 3D cell cultures reshaping the future of cancer research

被引:1
作者
Cordeiro, Sandra [1 ,2 ]
Oliveira, Beatriz B. [1 ,2 ]
Valente, Ruben [1 ,2 ]
Ferreira, Daniela [1 ,2 ]
Luz, Andre [1 ,2 ]
Baptista, Pedro V. [1 ,2 ]
Fernandes, Alexandra R. [1 ,2 ]
机构
[1] Univ Nova Lisboa, Fac Ciencias & Tecnol, Dept Ciencias Vida, UCIBIO, Caparica, Portugal
[2] Univ Nova Lisboa, Inst Hlth & Bioecon, Fac Ciencias & Tecnol, Associate Lab,i4HB, Caparica, Portugal
来源
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY | 2024年 / 12卷
关键词
3D models; spheroids; patient-derived organoids (PDOs); chips; drug screening; personalized medicine; PLURIPOTENT STEM-CELLS; ON-A-CHIP; PATIENT-DERIVED ORGANOIDS; CIRCULATING TUMOR-CELLS; IN-VITRO; BREAST-CANCER; MICROFLUIDIC PLATFORM; RECENT PROGRESS; BLADDER-CANCER; DRUG;
D O I
10.3389/fcell.2024.1507388
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Despite extensive efforts to unravel tumor behavior and develop anticancer therapies, most treatments fail when advanced to clinical trials. The main challenge in cancer research has been the absence of predictive cancer models, accurately mimicking the tumoral processes and response to treatments. The tumor microenvironment (TME) shows several human-specific physical and chemical properties, which cannot be fully recapitulated by the conventional 2D cell cultures or the in vivo animal models. These limitations have driven the development of novel in vitro cancer models, that get one step closer to the typical features of in vivo systems while showing better species relevance. This review introduces the main considerations required for developing and exploiting tumor spheroids and organoids as cancer models. We also detailed their applications in drug screening and personalized medicine. Further, we show the transition of these models into novel microfluidic platforms, for improved control over physiological parameters and high-throughput screening. 3D culture models have provided key insights into tumor biology, more closely resembling the in vivo TME and tumor characteristics, while enabling the development of more reliable and precise anticancer therapies.
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页数:23
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共 175 条
  • [1] Abdulla A., Liu W., Gholamipour-Shirazi A., Sun J., Ding X., High-throughput isolation of circulating tumor cells using cascaded inertial focusing microfluidic channel, Anal. Chem, 90, pp. 4397-4405, (2018)
  • [2] Abuwatfa W.H., Pitt W.G., Husseini G.A., Scaffold-based 3D cell culture models in cancer research, J. Biomed. Sci, 31, (2024)
  • [3] Acosta M.A., Jiang X., Huang P.-K., Cutler K.B., Grant C.S., Walker G.M., Et al., A microfluidic device to study cancer metastasis under chronic and intermittent hypoxia, Biomicrofluidics, 8, (2014)
  • [4] Ahvaraki A., Gheytanchi E., Behroodi E., Latifi H., Vakhshiteh F., Bagheri Z., Et al., Advanced co-culture 3D breast cancer model to study cell death and nanodrug sensitivity of tumor spheroids, Biochem. Eng. J, 209, (2024)
  • [5] Al-Hamaly M.A., Turner L.T., Rivera-Martinez A., Rodriguez A., Blackburn J.S., Zebrafish cancer avatars: a translational platform for analyzing tumor heterogeneity and predicting patient outcomes, Int. J. Mol. Sci, 24, (2023)
  • [6] Alix-Panabieres C., Perspective: the future of liquid biopsy, Nature, 579, (2020)
  • [7] Alix-Panabieres C., Pantel K., Liquid biopsy: from discovery to clinical application, Cancer Discov, 11, pp. 858-873, (2021)
  • [8] Altmann B., Steinberg T., Giselbrecht S., Gottwald E., Tomakidi P., Bachle-Haas M., Et al., Promotion of osteoblast differentiation in 3D biomaterial micro-chip arrays comprising fibronectin-coated poly(methyl methacrylate) polycarbonate, Biomaterials, 32, pp. 8947-8956, (2011)
  • [9] Amin N.D., Pasca S.P., Building models of brain disorders with three-dimensional organoids, Neuron, 100, pp. 389-405, (2018)
  • [10] Antoine E.E., Vlachos P.P., Rylander M.N., Tunable collagen I hydrogels for engineered physiological tissue micro-environments, PLoS One, 10, (2015)