The hope and the hype of organoid research
Open accessAbstract
The recent increase in organoid research has been met with great enthusiasm, as well as expectation, from the scientific community and the public alike. There is no doubt that this technology opens up a world of possibilities for scientific discovery in developmental biology as well as in translational research, but whether organoids can truly live up to this challenge is, for some, still an open question. In this Spotlight article, Meritxell Huch and Juergen Knoblich begin by discussing the exciting promise of organoid technology and give concrete examples of how this promise is starting to be realised. In the second part, Matthias Lutolf and Alfonso Martinez-Arias offer a careful and considered view of the state of the organoid field and its current limitations, and lay out the approach they feel is necessary to maximise the potential of organoid technology.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Lot-to-lot variations of Matrigel compound the difficulty of identifying the signals necessary for organoid structure and function.
“The undefined nature of Matrigel makes it difficult to identify the signals necessary for organoid structure and function; this difficulty is compounded by lot-to-lot variations of Matrigel45–48.”
From Towards organoid culture without Matrigel (2021) · cites this paper as [48]
Cites
Single Lgr5 stem cells build crypt-villus structures in vitro without a mesenchymal niche
Sato, T., Vries, R. G., Snippert, H. J., van de Wetering, M., Barker, N., Stange, D. E., van Es, J. H., Abo, A., Kujala, P., Peters, P. J., et al. (2009) · Nature · doi:10.1038/nature07935 · Cited by 7,204 · see citing works
Cerebral organoids model human brain development and microcephaly
Lancaster, M. A., Renner, M., Martin, C.-A., Wenzel, D., Bicknell, L. S., Hurles, M. E., Homfray, T., Penninger, J. M., Jackson, A. P., & Knoblich, J. A. (2013) · Nature · doi:10.1038/nature12517 · Cited by 5,372 · see citing works
Self-citationSato, T., Stange, D. E., Ferrante, M., Vries, R. G. J., van Es, J. H., van den Brink, S., van Houdt, W. J., Pronk, A., van Gorp, J., Siersema, P. D., et al. (2011) · Gastroenterology · doi:10.1053/j.gastro.2011.07.050 · Cited by 3,753 · see citing works
Organogenesis in a dish: Modeling development and disease using organoid technologies
Lancaster, M. A., & Knoblich, J. A. (2014) · Science · doi:10.1126/science.1247125 · Cited by 2,931 · see citing works
Self-citationProspective Derivation of a Living Organoid Biobank of Colorectal Cancer Patients
van de Wetering, M., Francies, H. E., Francis, J. M., Bounova, G., Iorio, F., Pronk, A., van Houdt, W., van Gorp, J., Taylor-Weiner, A., Kester, L., et al. (2015) · Cell · doi:10.1016/j.cell.2015.03.053 · Cited by 2,408 · see citing works
Vascularized and functional human liver from an iPSC-derived organ bud transplant
Takebe, T., Sekine, K., Enomura, M., Koike, H., Kimura, M., Ogaeri, T., Zhang, R.-R., Ueno, Y., Zheng, Y.-W., Koike, N., et al. (2013) · Nature · doi:10.1038/nature12271 · Cited by 2,170 · see citing works
Organoid models of human and mouse ductal pancreatic cancer
Boj, S. F., Hwang, C.-I., Baker, L. A., Chio, I. I. C., Engle, D. D., Corbo, V., Jager, M., Ponz-Sarvise, M., Tiriac, H., Spector, M. S., et al. (2015) · Cell · doi:10.1016/j.cell.2014.12.021 · Cited by 2,150 · see citing works
Self-citationBrain-Region-Specific Organoids Using Mini-bioreactors for Modeling ZIKV Exposure
Qian, X., Nguyen, H. N., Song, M. M., Hadiono, C., Ogden, S. C., Hammack, C., Yao, B., Hamersky, G. R., Jacob, F., Zhong, C., et al. (2016) · Cell · doi:10.1016/j.cell.2016.04.032 · Cited by 2,127 · see citing works
Self-organizing optic-cup morphogenesis in three-dimensional culture
Eiraku, M., Takata, N., Ishibashi, H., Kawada, M., Sakakura, E., Okuda, S., Sekiguchi, K., Adachi, T., & Sasai, Y. (2011) · Nature · doi:10.1038/nature09941 · Cited by 2,001 · see citing works
Directed differentiation of human pluripotent stem cells into intestinal tissue in vitro
Spence, J., Mayhew, C., Rankin, S., Kuhar, M., Vallance, J. E., Tolle, K., Hoskins, E. E., Kalinichenko, V., Wells, S., Zorn, A., et al. (2010) · Nature · doi:10.1038/nature09691 · Cited by 1,850 · see citing works
Generation of cerebral organoids from human pluripotent stem cells
Lancaster, M. A., & Knoblich, J. A. (2014) · Nature Protocols · doi:10.1038/nprot.2014.158 · Cited by 1,764 · see citing works
Self-citationLong-Term Culture of Genome-Stable Bipotent Stem Cells from Adult Human Liver
Huch, M., Gehart, H., van Boxtel, R., Hamer, K., Blokzijl, F., Verstegen, M. M. A., Ellis, E., van Wenum, M., Fuchs, S. A., de Ligt, J., et al. (2015) · Cell · doi:10.1016/j.cell.2014.11.050 · Cited by 1,619 · see citing works
Self-citationOrganoid Cultures Derived from Patients with Advanced Prostate Cancer
Gao, D., Vela, I., Sboner, A., Iaquinta, P. J., Karthaus, W. R., Gopalan, A., Dowling, C., Wanjala, J. N., Undvall, E. A., Arora, V. K., et al. (2014) · Cell · doi:10.1016/j.cell.2014.08.016 · Cited by 1,559 · see citing works
In vitro expansion of single Lgr5+ liver stem cells induced by Wnt-driven regeneration
Huch, M., Dorrell, C., Boj, S. F., van Es, J. H., Li, V. S. W., van de Wetering, M., Sato, T., Hamer, K., Sasaki, N., Finegold, M. J., et al. (2013) · Nature · doi:10.1038/nature11826 · Cited by 1,555 · see citing works
Self-citationEiraku, M., Watanabe, K., Matsuo-Takasaki, M., Kawada, M., Yonemura, S., Matsumura, M., Wataya, T., Nishiyama, A., Muguruma, K., & Sasai, Y. (2008) · Cell Stem Cell · doi:10.1016/j.stem.2008.09.002 · Cited by 1,522 · see citing works
Self-formation of optic cups and storable stratified neural retina from human ESCs
Nakano, T., Ando, S., Takata, N., Kawada, M., Muguruma, K., Sekiguchi, K., Saito, K., Yonemura, S., Eiraku, M., & Sasai, Y. (2012) · Cell stem cell · doi:10.1016/j.stem.2012.05.009 · Cited by 1,447 · see citing works
Designer matrices for intestinal stem cell and organoid culture
Gjorevski, N., Sachs, N., Manfrin, A., Giger, S., Bragina, M. E., Ordóñez-Morán, P., Clevers, H., & Lutolf, M. P. (2016) · Nature · doi:10.1038/nature20168 · Cited by 1,426 · see citing works
Schwank, G., Koo, B.-K., Sasselli, V., Dekkers, J. F., Heo, I., Demircan, T., Sasaki, N., Boymans, S., Cuppen, E., van der Ent, C. K., et al. (2013) · Cell Stem Cell · doi:10.1016/j.stem.2013.11.002 · Cited by 1,424 · see citing works
Modelling human development and disease in pluripotent stem-cell-derived gastric organoids
McCracken, K. W., Catá, E. M., Crawford, C. M., Sinagoga, K. L., Schumacher, M., Rockich, B. E., Tsai, Y.-H., Mayhew, C. N., Spence, J. R., Zavros, Y., et al. (2014) · Nature · doi:10.1038/nature13863 · Cited by 980 · see citing works
Preparing for the First Breath: Genetic and Cellular Mechanisms in Lung Development
Morrisey, E. E., & Hogan, B. L. M. (2010) · Developmental Cell · doi:10.1016/j.devcel.2009.12.010 · Cited by 967 · see citing works
Tissue-specific mutation accumulation in human adult stem cells during life
Blokzijl, F., de Ligt, J., Jager, M., Sasselli, V., Roerink, S., Sasaki, N., Huch, M., Boymans, S., Kuijk, E., Prins, P., et al. (2016) · Nature · doi:10.1038/nature19768 · Cited by 935 · see citing works
Self-citationIn vitro generation of human pluripotent stem cell derived lung organoids
Dye, B. R., Hill, D. R., Ferguson, M. A. H., Tsai, Y.-H., Nagy, M. S., Dyal, R., Wells, J. M., Mayhew, C. N., Nattiv, R., Klein, O. D., et al. (2015) · eLife · doi:10.7554/elife.05098 · Cited by 824 · see citing works
Directed differentiation of telencephalic precursors from embryonic stem cells
Watanabe, K., Kamiya, D., Nishiyama, A., Katayama, T., Nozaki, S., Kawasaki, H., Watanabe, Y., Mizuseki, K., & Sasai, Y. (2005) · Nature Neuroscience · doi:10.1038/nn1402 · Cited by 784 · see citing works
Identification of Multipotent Luminal Progenitor Cells in Human Prostate Organoid Cultures
Karthaus, W. R., Iaquinta, P. J., Drost, J., Gracanin, A., van Boxtel, R., Wongvipat, J., Dowling, C., Gao, D., Begthel, H., Sachs, N., et al. (2014) · Cell · doi:10.1016/j.cell.2014.08.017 · Cited by 720 · see citing works
Isolation and in vitro expansion of human colonic stem cells
Jung, P., Sato, T., Merlos-Suárez, A., Barriga, F. M., Iglesias, M., Rossell, D., Auer, H., Gallardo, M., Blasco, M. A., Sancho, E., et al. (2011) · Nature Medicine · doi:10.1038/nm.2470 · Cited by 709 · see citing works
Dekkers, J. F., Berkers, G., Kruisselbrink, E., Vonk, A., de Jonge, H. R., Janssens, H. M., Bronsveld, I., van de Graaf, E. A., Nieuwenhuis, E. E. S., Houwen, R. H. J., et al. (2016) · Science Translational Medicine · doi:10.1126/scitranslmed.aad8278 · Cited by 548 · see citing works
Modeling mouse and human development using organoid cultures
Huch, M., & Koo, B. (2015) · Development · doi:10.1242/dev.118570 · Cited by 543 · see citing works
Self-citationMcCauley, H. A., & Wells, J. M. (2017) · Development · doi:10.1242/dev.140731 · Cited by 322 · see citing works
Using brain organoids to understand Zika virus-induced microcephaly
Qian, X., Nguyen, H. N., Jacob, F., Song, H., & Ming, G. (2017) · Development · doi:10.1242/dev.140707 · Cited by 241 · see citing works
Setting Global Standards for Stem Cell Research and Clinical Translation: The 2016 ISSCR Guidelines
Daley, G. Q., Hyun, I., Apperley, J. F., Barker, R. A., Benvenisty, N., Bredenoord, A. L., Breuer, C. K., Caulfield, T., Cedars, M. I., Frey-Vasconcells, J. L., et al. (2016) · Stem Cell Reports · doi:10.1016/j.stemcr.2016.05.001 · Cited by 223 · see citing works
Wnt/β-catenin promotes gastric fundus specification in mice and humans
McCracken, K. W., Aihara, E., Martin, B., Crawford, C. M., Broda, T. R., Tréguier, J., Zhang, X., Shannon, J. M., Montrose, M. H., & Wells, J. M. (2017) · Nature · doi:10.1038/nature21021 · Cited by 222 · see citing works
Embryology policy: Revisit the 14-day rule
Hyun, I., Wilkerson, A., & Johnston, J. (2016) · Nature · doi:10.1038/533169a · Cited by 212 · see citing works
In vitro organogenesis in three dimensions: self-organising stem cells
Sasai, Y., Eiraku, M., & Suga, H. (2012) · Development · doi:10.1242/dev.079590 · Cited by 201 · see citing works
Translational applications of adult stem cell-derived organoids
Drost, J., & Clevers, H. C. (2017) · Development · doi:10.1242/dev.140566 · Cited by 141 · see citing works
The Neurobiology of Zika Virus
Li, H., Saucedo-Cuevas, L. P., Shresta, S., & Gleeson, J. G. (2016) · Neuron · doi:10.1016/j.neuron.2016.11.031 · Cited by 131 · see citing works
Generation of stomach tissue from mouse embryonic stem cells
Noguchi, T.-A. K., Ninomiya, N., Sekine, M., Komazaki, S., Wang, P.-C., Asashima, M., & Kurisaki, A. (2015) · Nature Cell Biology · doi:10.1038/ncb3200 · Cited by 100 · see citing works
Light sheet-based fluorescence microscopy (LSFM) for the quantitative imaging of cells and tissues
Pampaloni, F., Chang, B.-J., & Stelzer, E. H. K. (2015) · Cell and Tissue Research · doi:10.1007/s00441-015-2144-5 · Cited by 81 · see citing works
History of Developmental Biology
Horder, T. (2010) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0003080.pub2 · Cited by 12 · see citing works
Robertis, E. M. D. (2014) · Developmental Cell · doi:10.1016/j.devcel.2014.08.022 · Cited by 2 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Flow-enhanced vascularization and maturation of kidney organoids in vitro
Homan, K. A., Gupta, N., Kroll, K. T., Kolesky, D. B., Skylar-Scott, M., Miyoshi, T., Mau, D., Valerius, M. T., Ferrante, T., Bonventre, J. V., et al. (2019) · Nature Methods · doi:10.1038/s41592-019-0325-y · Cited by 939 · see citing works
Dysregulation of brain and choroid plexus cell types in severe COVID-19
Yang, A. C., Kern, F., Losada, P. M., Agam, M. R., Maat, C. A., Schmartz, G. P., Fehlmann, T., Stein, J. A., Schaum, N., Lee, D. P., et al. (2021) · Nature · doi:10.1038/s41586-021-03710-0 · Cited by 620 · see citing works
Tissue geometry drives deterministic organoid patterning
Gjorevski, N., Nikolaev, M., Brown, T. E., Mitrofanova, O., Brandenberg, N., DelRio, F. W., Yavitt, F. M., Liberali, P., Anseth, K. S., & Lutolf, M. P. (2022) · Science · doi:10.1126/science.aaw9021 · Cited by 505 · see citing works
Modeling amyloid beta and tau pathology in human cerebral organoids
Gonzalez, C., Armijo, E., Bravo-Alegria, J., Becerra-Calixto, A., Mays, C. E., & Soto, C. (2018) · Molecular Psychiatry · doi:10.1038/s41380-018-0229-8 · Cited by 430 · see citing works
Towards organoid culture without Matrigel
Kozlowski, M. T., Crook, C. J., & Ku, H. T. (2021) · Communications Biology · doi:10.1038/s42003-021-02910-8 · Cited by 409 · see citing works
Mouse embryonic stem cells self-organize into trunk-like structures with neural tube and somites
Veenvliet, J. V., Bolondi, A., Kretzmer, H., Haut, L., Scholze‐Wittler, M., Schifferl, D., Koch, F., Guignard, L., Kumar, A. S., Pustet, M., et al. (2020) · Science · doi:10.1126/science.aba4937 · Cited by 318 · see citing works
In vitro Models of Neurodegenerative Diseases
Slanzi, A., Iannoto, G., Rossi, B., Zenaro, E., & Constantin, G. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00328 · Cited by 293 · see citing works
Wörsdörfer, P., Dalda, N., Kern, A., Krüger, S., Wagner, N., Kwok, C. K., Henke, E., & Ergün, S. (2019) · Scientific Reports · doi:10.1038/s41598-019-52204-7 · Cited by 278 · see citing works
Synthetic dynamic hydrogels promote degradation-independent in vitro organogenesis
Chrisnandy, A., Blondel, D., Rezakhani, S., Broguiere, N., & Lutolf, M. P. (2022) · Nature Materials · doi:10.1038/s41563-021-01136-7 · Cited by 237 · see citing works
Nonadhesive Alginate Hydrogels Support Growth of Pluripotent Stem Cell-Derived Intestinal Organoids
Capeling, M. M., Czerwinski, M., Huang, S., Tsai, Y.-H., Wu, A., Nagy, M. S., Juliar, B., Sundaram, N., Song, Y., Han, W. M., et al. (2019) · Stem Cell Reports · doi:10.1016/j.stemcr.2018.12.001 · Cited by 226 · see citing works
“A pivotal development in the fields of developmental biology and regenerative medicine was the use of human pluripotent stem cells (hPSCs) to generate human cell types, tissues, and organoid model systems in vitro (Huch et al., 2017; Johnston, 2015; Little, 2017).”
MethodMechanisms of human embryo development: from cell fate to tissue shape and back
Shahbazi, M. N. (2020) · Development · doi:10.1242/dev.190629 · Cited by 216 · see citing works
“…during development, future experimental strategies need to: be based on the use of robust, reproducible and relevant stem cell models of the embryo (Huch et al., 2017; Van Den Brink et al., 2020); allow mapping of intrinsic stresses and application of extrinsic forces in a precise manner (Vianello…”
BackgroundSignaling in the stem cell niche: regulating cell fate, function and plasticity
Chacón‐Martínez, C. A., Koester, J., & Wickström, S. A. (2018) · Development · doi:10.1242/dev.165399 · Cited by 193 · see citing works
“These models are rapidly advancing basic and applied research (Huch et al., 2017), and are also being expanded to disease models and predictive tools of drug-treatment outcomes, as exemplified by the recently established human cancer organoid biobanks (Sachs et al.”
Wang, Y., Kim, R., Gunasekara, D. B., Reed, M. I., DiSalvo, M., Nguyen, D. L., Bultman, S. J., Sims, C. E., Magness, S. T., & Allbritton, N. L. (2017) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2017.10.007 · Cited by 184 · see citing works
“These characteristics preclude the use of the organoid system in numerous applications and a true living construct suitable for assay of dietary metabolites, cytokines, microorganisms, and drug interactions has not been available.(23,24)”
BackgroundEthical issues related to brain organoid research
Hyun, I., Scharf-Deering, J. C., & Lunshof, J. E. (2020) · Brain Research · doi:10.1016/j.brainres.2020.146653 · Cited by 186 · see citing works
“…and Renner, 2013; Mansour and Gonçalves, 2018; Editorial, 2018; Kelava and Lancaster, 2016; Buchanan, 2018; Arlotta, 2018; Rossi and Manfrin, 2018; Huch, 2017; Di Lullo and Kriegstein, 2017); and that represent the whole brain or specific regions in 3D (Shuler and Hickman, 2014; Cheah and…”
BackgroundDisease Modeling Using 3D Organoids Derived from Human Induced Pluripotent Stem Cells
Ho, B. X., Pek, N. M. Q., & Soh, B.-S. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19040936 · Cited by 181 · see citing works
“, size and shape), cellular composition, phenotypic and molecular characteristics [60].”
BackgroundEngineered Tissue Folding by Mechanical Compaction of the Mesenchyme
Hughes, A. J., Miyazaki, H., Coyle, M. C., Zhang, J., Laurie, M. T., Chu, D. B., Vavrušová, Z., Schneider, R. A., Klein, O. D., & Gartner, Z. J. (2017) · Developmental Cell · doi:10.1016/j.devcel.2017.12.004 · Cited by 170 · see citing works
“Engineered tissues have applications in basic sciences, drug testing, and regenerative medicine (Bajaj et al., 2014; Clevers, 2016; Huch et al., 2017).”
InfluentialSajjad, H., Imtiaz, S., Noor, T., Siddiqui, Y. H., Sajjad, A., & Zia, M. (2021) · Animal Models and Experimental Medicine · doi:10.1002/ame2.12165 · Cited by 175 · see citing works
Cerebral organoids: ethical issues and consciousness assessment
Lavazza, A., & Massimini, M. (2018) · Journal of Medical Ethics · doi:10.1136/medethics-2017-104555 · Cited by 217 · see citing works
Qu, J., Kalyani, F. S., Liu, L., Cheng, T., & Chen, L. (2021) · 癌症:英文版 · doi:10.1002/cac2.12224 · Cited by 166 · see citing works
“Although organoids have shown strong potential in cancer research and clinical applications, there are still many drawbacks [165,166].”
BackgroundPereira, J. D., DuBreuil, D. M., Devlin, A., Held, A., Sapir, Y., Berezovski, E., Hawrot, J., Dorfman, K., Chander, V., & Wainger, B. J. (2021) · Nature Communications · doi:10.1038/s41467-021-24776-4 · Cited by 155 · see citing works
Human organoids: a new dimension in cell biology
Lehmann, R., Lee, C. M., Shugart, E. C., Benedetti, M., Charo, R. A., Gartner, Z. J., Hogan, B. L. M., Knoblich, J. A., Nelson, C. M., & Wilson, K. (2019) · Molecular Biology of the Cell · doi:10.1091/mbc.e19-03-0135 · Cited by 153 · see citing works
Self-citationThree-dimensional bio-printing of primary human hepatocellular carcinoma for personalized medicine
Xie, F., Sun, L., Pang, Y., Xu, G., Jin, B., Xu, H., Lu, X., Xu, Y., Du, S., Wang, Y., et al. (2021) · Biomaterials · doi:10.1016/j.biomaterials.2020.120416 · Cited by 147 · see citing works
Human Cardiac Organoids for Disease Modeling
Nugraha, B., Buono, M. F., von Boehmer, L., Hoerstrup, S. P., & Emmert, M. Y. (2018) · Clinical Pharmacology & Therapeutics · doi:10.1002/cpt.1286 · Cited by 142 · see citing works
“Recently, so- called 3D organoid cultures have advanced to a level where the re creation of human tissues emulating human physiology and pathophysiology in vitro is now possible.(6) Organoids are 3D tissue mimicries that are composed of different cell types (i.”
BackgroundLarge‐Scale Production of LGR5‐Positive Bipotential Human Liver Stem Cells
Schneeberger, K., Sánchez‐Romero, N., Ye, S., van Steenbeek, F. G., Oosterhoff, L. A., Pla Palacin, I., Chen, C., van Wolferen, M. E., van Tienderen, G., Lieshout, R., et al. (2020) · Hepatology · doi:10.1002/hep.31037 · Cited by 141 · see citing works
“(9,10) Unfortunately, reproducibility and upscaling of current organoid systems remain major bottlenecks in their clinical application.(11) Establishing large numbers of organoids with current protocols is tedious, as organoids are cultured in droplets of Matrigel,(9,10) which hampers clinically relevant production ti…”
BackgroundLiver Organoids: Recent Developments, Limitations and Potential
Harrison, S. P., Baumgarten, S., Verma, R., Lunov, O., Dejneka, A., & Sullivan, G. J. (2021) · Frontiers in Medicine · doi:10.3389/fmed.2021.574047 · Cited by 141 · see citing works
“Organoids are in vitro cellular systems that self-organize through mechanisms similar to in vivo, they recapitulate the structure and in many cases the function of the in vivo tissue in question, ultimately providing utility in both the clinical and basic research arenas (1, 2).”
BackgroundDecarli, M. C., do Amaral, R. L. F., dos Santos, D. P., Tofani, L. B., Katayama, E. T., Rezende, R. A., da Silva, J. V. L., Swiech, K., Suazo, C. A. T., Mota, C., et al. (2021) · Biofabrication · doi:10.1088/1758-5090/abe6f2 · Cited by 132 · see citing works
“…obtained from pancreas cells, derived from stem cells or induced pluripotent stem cells, have emerged as an important tool for the production of β cells for the therapy of type 1 diabetes [274] and as models in gene identification studies associated with pancreatic cancer progression [269].”
Mechanisms of radial glia progenitor cell lineage progression
Beattie, R., & Hippenmeyer, S. (2017) · FEBS Letters · doi:10.1002/1873-3468.12906 · Cited by 127 · see citing works
Engineering induction of singular neural rosette emergence within hPSC-derived tissues
Knight, G. T., Lundin, B. F., Iyer, N. R., Ashton, L., Sethares, W. A., Willett, R. M., & Ashton, R. S. (2018) · eLife · doi:10.7554/elife.37549 · Cited by 129 · see citing works
“DOI: https://doi.org/10.7554/eLife.37549 1 of 23 for example N-cadherin, and tight junction proteins towards an apical lumen while depositing extracellular matrix (ECM) proteins at their basal surface (Eiraku et al., 2008; Lancaster et al., 2013; Gilbert, 2006).”
BackgroundInfluentialExperimental models and tools to tackle glioblastoma
Robertson, F., Marqués‐Torrejón, M. Á., Morrison, G. M., & Pollard, S. M. (2019) · Disease Models & Mechanisms · doi:10.1242/dmm.040386 · Cited by 121 · see citing works
“These have been termed ‘ organoids ’ to highlight their similarities to existing organoid systems defined for endodermal stem cell cultures, like the use of Matrigel in suspension (Huch et al., 2017; Tuveson and Clevers, 2019).”
Organoid systems to study the human female reproductive tract and pregnancy
Alzamil, L., Νικολακοπούλου, Κ., & Turco, M. Y. (2020) · Cell Death and Differentiation · doi:10.1038/s41418-020-0565-5 · Cited by 121 · see citing works
“Efforts are now being made to define the common issues affecting all organoids systems such as reproducibility, standardization, and diligence validation [141].”
BackgroundTargeting the “hallmarks of aging” to slow aging and treat age-related disease: fact or fiction?
Keshavarz, M., Xie, K., Schaaf, K., Bano, D., & Ehninger, D. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01680-x · Cited by 122 · see citing works
“Another disadvantage is the lack of complete vascularization, which precludes the modelling of key aspects of brain physiology [157].”
BackgroundStatistical mechanics meets single-cell biology
Teschendorff, A. E., & Feinberg, A. P. (2021) · Nature Reviews Genetics · doi:10.1038/s41576-021-00341-z · Cited by 117 · see citing works
Human biomimetic liver microphysiology systems in drug development and precision medicine
Gough, A., Soto-Gutierrez, A., Vernetti, L., Ebrahimkhani, M. R., Stern, A. M., & Taylor, D. L. (2021) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-020-00386-1 · Cited by 117 · see citing works
Logan, S., Arzua, T., Canfield, S. G., Seminary, E. R., Sison, S. L., Ebert, A. D., & Bai, X. (2019) · Comprehensive physiology · doi:10.1002/cphy.c180025 · Cited by 139 · see citing works
VanDussen, K. L., Sonnek, N. M., & Stappenbeck, T. S. (2019) · Stem Cell Research · doi:10.1016/j.scr.2019.101430 · Cited by 117 · see citing works
“The basic and translational research applications for primary gastrointestinal epithelial cells will continue to rapidly expand as more and more laboratories adopt these culture platforms for their research (Clevers, 2016; Nakamura and Sato, 2018; Huch et al., 2017).”
BackgroundSilva, L. B. A. R., Castro, N., Novaes, G. M., Pascoal, G. D. F. L., & Ong, T. P. (2019) · Food Research International · doi:10.1016/j.foodres.2019.108646 · Cited by 116 · see citing works
MOrgAna: accessible quantitative analysis of organoids with machine learning
Gritti, N., Lim, J. L., Anlaş, K., Pandya, M., Aalderink, G., Martínez-Ara, G., & Trivedi, V. (2021) · Development · doi:10.1242/dev.199611 · Cited by 111 · see citing works
“Organoids are cell aggregates capable of generating complex structures, thereby mimicking fully grown organs in vitro (Huch et al., 2017; Lancaster and Knoblich, 2014; Kretzschmar and Clevers, 2016).”
BackgroundModeling and Targeting Alzheimer’s Disease With Organoids
Papaspyropoulos, A., Tsolaki, M., Foroglou, N., & Pantazaki, Α. A. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.00396 · Cited by 107 · see citing works
Intestinal organoids: A new paradigm for engineering intestinal epithelium in vitro
Rahmani, S., Breyner, N. M., Su, H.-M., Verdu, E. F., & Didar, T. F. (2019) · Biomaterials · doi:10.1016/j.biomaterials.2018.12.006 · Cited by 98 · see citing works
A Novel Microplate 3D Bioprinting Platform for the Engineering of Muscle and Tendon Tissues
Laternser, S., Keller, H., Leupin, O., Rausch, M., Graf‐Hausner, U., & Rimann, M. (2018) · SLAS TECHNOLOGY · doi:10.1177/2472630318776594 · Cited by 102 · see citing works
“The formation of spheroids and organoids has allowed the establishment of mouse and human 3D tissue equivalents that demonstrate at least some organ functionality and application as in vitro disease models, particularly in tumor biology.(10,11) While cardiac and smooth muscle cells are able to form spheroids, offering…”
BackgroundAnimal and Organoid Models of Liver Fibrosis
Bao, Y., Wang, L., Pan, H., Zhang, T.-R., Chen, Y., Xu, S.-J., Mao, X., & Li, S.-W. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.666138 · Cited by 101 · see citing works
Organoids in image-based phenotypic chemical screens
Lukonin, I., Zinner, M., & Liberali, P. (2021) · Experimental & Molecular Medicine · doi:10.1038/s12276-021-00641-8 · Cited by 99 · see citing works
Testicular organoids: a new model to study the testicular microenvironment in vitro?
Alves-Lopes, J. P., & Stukenborg, J. (2017) · Human Reproduction Update · doi:10.1093/humupd/dmx036 · Cited by 99 · see citing works
“Organoids can be originated by differentiation of pluripotent embryonic stem (ES) cells, induced pluripotent stem (iPS) cells or adult stem cells from adult tissues cultured in a supportive extracellular matrix (ECM) (usually Matrigel) which, together with morphogenic and differentiation factors in the culture medium,…”
BackgroundOrganoids as hybrids: ethical implications for the exchange of human tissues
Boers, S. N., van Delden, J. J. M., & Bredenoord, A. L. (2018) · Journal of Medical Ethics · doi:10.1136/medethics-2018-104846 · Cited by 99 · see citing works
Organoids: a novel modality in disease modeling
Heydari, Z., Moeinvaziri, F., Agarwal, T., Pooyan, P., Shpichka, A. I., Maiti, T. K., Timashev, P. S., Baharvand, H., & Vosough, M. (2021) · Bio-Design and Manufacturing · doi:10.1007/s42242-021-00150-7 · Cited by 100 · see citing works
“The latter add significant value while presenting many challenges, including high time and monetary costs, ethical concerns, and most importantly, they fail to accurately predict the clinical efficacy of therapeutics due to different pharmacokinetics, pharmacodynamics, and interspecific genetic or metabolic variations…”
BackgroundBMP4 patterns Smad activity and generates stereotyped cell fate organization in spinal organoids
Duval, N., Vaslin, C., Barata, T. C., Frarma, Y., Contremoulins, V., Baudin, X., Nedelec, S., & Ribes, V. C. (2019) · Development · doi:10.1242/dev.175430 · Cited by 93 · see citing works
“…stem cells (PSC) derived organoids, containing multiple cellular subtypes arrayed in three dimensions (3D) structures, has opened new avenues to decipher the developmental principles underlying the emergence of patterns of cellular differentiation (Huch et al., 2017; Trujillo and Muotri, 2018).”
BackgroundEngineered Matrices Enable the Culture of Human Patient‐Derived Intestinal Organoids
Hunt, D. R., Klett, K. C., Mascharak, S., Wang, H., Gong, D. N., Lou, J., Li, X., Cai, P. C., Suhar, R. A., Co, J. Y., et al. (2021) · Advanced Science · doi:10.1002/advs.202004705 · Cited by 96 · see citing works
Hof, L., Moreth, T., Koch, M., Liebisch, T., Kurtz, M., Tarnick, J., Lissek, S. M., Verstegen, M. M. A., van der Laan, L. J. W., Huch, M., et al. (2021) · BMC Biology · doi:10.1186/s12915-021-00958-w · Cited by 95 · see citing works
Self-citationBiologically inspired approaches to enhance human organoid complexity
Holloway, E. M., Capeling, M. M., & Spence, J. R. (2019) · Development · doi:10.1242/dev.166173 · Cited by 96 · see citing works
“Bioengineering 3D environments to increase reproducibility and clinical use of organoid technology One of the major challenges facing organoid research is reproducibility and limited control over the 3D self-organization process (Huch et al., 2017; Spence, 2018).”
BackgroundOrganoids of the female reproductive tract
Chumduri, C., & Turco, M. Y. (2021) · Journal of Molecular Medicine · doi:10.1007/s00109-020-02028-0 · Cited by 98 · see citing works
Yavitt, F. M., Kirkpatrick, B. E., Blatchley, M. R., Speckl, K. F., Mohagheghian, E., Moldovan, R., Wang, N., Dempsey, P. J., & Anseth, K. S. (2023) · Science Advances · doi:10.1126/sciadv.add5668 · Cited by 96 · see citing works
Patient-derived cell line, xenograft and organoid models in lung cancer therapy
Huo, K.-G., D’Arcangelo, E., & Tsao, M. (2020) · Translational Lung Cancer Research · doi:10.21037/tlcr-20-154 · Cited by 93 · see citing works
“Further, culture scalability represents a major bottleneck, especially for high-throughput drug screening applications, as LCOs vary wildly in growth dynamics (149).”
BackgroundTowards a better understanding of diabetes mellitus using organoid models
Beydag-Tasöz, B. S., Yennek, S., & Grapin‐Botton, A. (2023) · Nature Reviews Endocrinology · doi:10.1038/s41574-022-00797-x · Cited by 83 · see citing works
Dissecting the stem cell niche with organoid models: an engineering-based approach
Murrow, L. M., Weber, R. J., & Gartner, Z. J. (2017) · Development · doi:10.1242/dev.140905 · Cited by 81 · see citing works
“This is crucial if we are to be able to use organoids in any meaningful way to address fundamental questions in developmental and regenerative biology (Huch et al., 2017).”
BackgroundStandardization of organoid culture in cancer research
Zhou, C., Wu, Y., Wang, Z., Liu, Y., Yu, J., Wang, W., Chen, S., Wu, W., Wang, J., Qian, G., et al. (2023) · Cancer Medicine · doi:10.1002/cam4.5943 · Cited by 84 · see citing works
Understanding the Mechanobiology of Early Mammalian Development through Bioengineered Models
Vianello, S., & Lütolf, M. P. (2019) · Developmental Cell · doi:10.1016/j.devcel.2019.02.024 · Cited by 79 · see citing works
Stem cell-derived intestinal organoids: a novel modality for IBD
Tian, C., Yang, M., Xu, H., Zhu, M., Yue, N.-N., Zhang, Y., Shi, R., Yao, J., Wang, L., Liang, Y.-J., et al. (2023) · Cell Death Discovery · doi:10.1038/s41420-023-01556-1 · Cited by 85 · see citing works
Advances in development and application of human organoids
Shankaran, A., Prasad, K., Chaudhari, S., Brand, A. M., & Satyamoorthy, K. (2021) · 3 Biotech · doi:10.1007/s13205-021-02815-7 · Cited by 74 · see citing works
Organoid technology for tissue engineering
He, J., Zhang, X., Xia, X., Han, M., Li, F., Li, C., Li, Y., & Gao, D. (2020) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjaa012 · Cited by 77 · see citing works
Towards manufacturing of human organoids
Ashok, A., Choudhury, D., Fang, Y., & Hunziker, W. (2019) · Biotechnology Advances · doi:10.1016/j.biotechadv.2019.107460 · Cited by 71 · see citing works
Exploring single cells in space and time during tissue development, homeostasis and regeneration
Mayr, U., Serra, D., & Liberali, P. (2019) · Development · doi:10.1242/dev.176727 · Cited by 63 · see citing works
Hydrogels for bone organoid construction: From a materiobiological perspective
Wu, S., Wu, X., Wang, X., & Su, J. (2022) · Journal of Material Science and Technology · doi:10.1016/j.jmst.2022.07.008 · Cited by 72 · see citing works
Organoids and Colorectal Cancer
Barbáchano, A., Fernández‐Barral, A., Bustamante‐Madrid, P., Prieto, I., Rodrı́guez-Salas, N., Larriba, M. J., & Múñoz, A. (2021) · Cancers · doi:10.3390/cancers13112657 · Cited by 68 · see citing works
“Definitions of the term organoid have been provided by several key researchers in the field [3,5,6].”
BackgroundBioinspired Hydrogels for 3D Organoid Culture
Blondel, D., & Lütolf, M. P. (2019) · CHIMIA International Journal for Chemistry · doi:10.2533/chimia.2019.81 · Cited by 65 · see citing works
Microstructured Hydrogels to Guide Self‐Assembly and Function of Lung Alveolospheres
Loebel, C., Weiner, A. I., Eiken, M. K., Katzen, J. B., Morley, M. P., Bala, V., Cardenas‐Diaz, F. L., Davidson, M. D., Shiraishi, K., Basil, M. C., et al. (2022) · Advanced Materials · doi:10.1002/adma.202202992 · Cited by 64 · see citing works
Biomaterials Regulate Mechanosensors YAP/TAZ in Stem Cell Growth and Differentiation
Virdi, J. K., & Pethe, P. S. (2020) · Tissue Engineering and Regenerative Medicine · doi:10.1007/s13770-020-00301-4 · Cited by 63 · see citing works
Defining the Teratoma as a Model for Multi-lineage Human Development
McDonald, D., Wu, Y., Dailamy, A., Tat, J., Parekh, U., Zhao, D., Hu, M. Y., Tipps, A. M. P., Zhang, K., & Mali, P. (2020) · Cell · doi:10.1016/j.cell.2020.10.018 · Cited by 58 · see citing works
“Organoids are 3D ‘‘mini-organs’’ derived from hPSCs in which the cells spontaneously selfassemble into differentiated, functional cell types that structurally and functionally mimic their in vivo counterparts (Huch and Koo, 2015; Clevers, 2016; Yin et al., 2016; Dutta et al., 2017; Huch et al., 2017; Fligor et al., 20…”
BackgroundThree-Dimensional 3D Culture Models in Gynecological and Breast Cancer Research
Salinas-Vera, Y. M., Valdés, J., Pérez‐Navarro, Y., Mandujano-Lázaro, G., Marchat, L. A., Ramos‐Payán, R., Núñez-Olvera, S. I., Pérez‐Plasencia, C., & López‐Camarillo, C. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.826113 · Cited by 64 · see citing works
Do not keep it simple: recent advances in the generation of complex organoids
Wörsdörfer, P., Ito, T., Asahina, I., Sumita, Y., & Ergün, S. (2020) · Journal of Neural Transmission · doi:10.1007/s00702-020-02198-8 · Cited by 61 · see citing works
An update on animal models of liver fibrosis
Wu, S., Wang, X., Xing, W., Li, F., Liang, M., Li, K., He, Y., & Wang, J. (2023) · Frontiers in Medicine · doi:10.3389/fmed.2023.1160053 · Cited by 71 · see citing works
Advances in human organoids-on-chips in biomedical research
Wang, Y., & Qin, J. (2023) · Life Medicine · doi:10.1093/lifemedi/lnad007 · Cited by 56 · see citing works
Electro-metabolic coupling in multi-chambered vascularized human cardiac organoids
Ghosheh, M., Ehrlich, A., Ioannidis, K., Ayyash, M., Goldfracht, I., Cohen, M., Fischer, A., Mintz, Y., Gepstein, L., & Nahmias, Y. (2023) · Nature Biomedical Engineering · doi:10.1038/s41551-023-01071-9 · Cited by 57 · see citing works
“Recent studies have led to a growing appreciation for the contribution of cardiomyocyte metabolism to disease progression 4,5 , showing metabolic changes occurring during heart failure 6–8 and arrhythmogen-esis 9 .”
BackgroundOral Organoids: Progress and Challenges
Gao, X., Wu, Y., Liao, L., & Tian, W. (2021) · Journal of Dental Research · doi:10.1177/0022034520983808 · Cited by 56 · see citing works
“Although autologous iPSCs are used as the potential cell source to construct oral organoids in the future, the efficiency, stability, and reproductivity of the organoid culture system to generate specific cell types still need to be improved (Huch et al. 2017).”
BackgroundMoving from in vitro to in vivo CRISPR screens
Kuhn, M., Santinha, A. J., & Platt, R. J. (2021) · Gene and Genome Editing · doi:10.1016/j.ggedit.2021.100008 · Cited by 53 · see citing works
Human Pluripotent Stem Cell-Derived Engineered Tissues: Clinical Considerations
Stevens, K. R., & Murry, C. E. (2018) · Cell stem cell · doi:10.1016/j.stem.2018.01.015 · Cited by 51 · see citing works
“…to fabrication of hPSC-derived tissues may include cellular “self-assembly” processes, which rely on intrinsic cell-cell and cellmatrix receptor-ligand interactions to drive morphogenesis and create architectural relationships found in native tissue (Hayashi et al., 2016; Huch et al., 2017).”
BackgroundEngineering the 3D structure of organoids
Moss, S. P., Bakırcı, E., & Feinberg, A. W. (2024) · Stem Cell Reports · doi:10.1016/j.stemcr.2024.11.009 · Cited by 51 · see citing works
Pinto, S. F. T., Hosseini, M., Buckley, S. T., Yin, W., Garousi, J., Gräslund, T., van IJzendoorn, S., Santos, H. A., & Sarmento, B. F. C. C. (2024) · Journal of Controlled Release · doi:10.1016/j.jconrel.2024.01.015 · Cited by 48 · see citing works
In Vitro Models for Studying Transport Across Epithelial Tissue Barriers
Arumugasaamy, N., Navarro, J., Leach, J. K., Kim, P. C. W., & Fisher, J. P. (2018) · Annals of Biomedical Engineering · doi:10.1007/s10439-018-02124-w · Cited by 47 · see citing works
Layer-By-Layer: The Case for 3D Bioprinting Neurons to Create Patient-Specific Epilepsy Models
Antill‐O'Brien, N., Bourke, J., & O’Connell, C. D. (2019) · Materials · doi:10.3390/ma12193218 · Cited by 47 · see citing works
“Organoids are restricted to a small size (maximum of several millimeters), due to the lack of nutritional supply to deeper regions [23,24,31,41].”
BackgroundRenner, H., Schöler, H. R., & Bruder, J. M. (2021) · Movement Disorders · doi:10.1002/mds.28775 · Cited by 47 · see citing works
“smNPCs are stable and easily expandable cells that can help limit the inherently higher stochastic biological noise of PSC-derived organoids.(126) Although smNPCs can still yield all neural cell types and form self-organized 3D microtissues, their ectodermrestricted developmental potential compared to PSCs results in…”
BackgroundProgramming Morphogenesis through Systems and Synthetic Biology
Velazquez, J. J., Su, E. Y., Cahan, P., & Ebrahimkhani, M. R. (2017) · Trends in biotechnology · doi:10.1016/j.tibtech.2017.11.003 · Cited by 44 · see citing works
“Current in vitro morphogenesis models frequently lack spatiotemporal control, robustness, and reproducibility that are exhibited in vivo by natural biological systems such as developing organs [10].”
Advancement of Organoid Technology in Regenerative Medicine
Arjmand, B., Rabbani, Z. H., Soveyzi, F., Tayanloo-Beik, A., Rezaei–Tavirani, M., Biglar, M., Adibi, H., & Larijani, B. A. (2022) · Regenerative Engineering and Translational Medicine · doi:10.1007/s40883-022-00271-0 · Cited by 45 · see citing works
“Organoid models of patient-derived induced pluripotent stem cells (iPSC) can be used in the field of personalized medicine [9, 12, 13].”
BackgroundInfluentialIntestinal Organoid Culture in Polymer Film‐Based Microwell Arrays
Kakni, P., Hueber, R., Knoops, K., López‐Iglesias, C., Truckenmüller, R. K., Habibović, P., & Giselbrecht, S. (2020) · Advanced Biosystems · doi:10.1002/adbi.202000126 · Cited by 45 · see citing works
Lensink, M. A., Boers, S. N., Jongsma, K. R., Carter, S. E., van der Ent, C. K., & Bredenoord, A. L. (2020) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2020.11.015 · Cited by 46 · see citing works
“Organoids are emerging as valuable tools in biomedical research, including drug development, disease modeling, and ultimately even clinical transplantation [2–4] .”
BackgroundMethodTissue mechanics regulates form, function, and dysfunction
Anlaş, A. A., & Nelson, C. M. (2018) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2018.05.012 · Cited by 44 · see citing works
“However, organoids are not perfect in the sense that they can only recapitulate certain stages of development and are often difficult toreproduce[60].”
High-Resolution Imaging of Tumor Spheroids and Organoids Enabled by Expansion Microscopy
Edwards, S. J., Carannante, V., Kuhnigk, K., Ring, H., Tararuk, T., Hallböök, F., Blom, H., Önfelt, B., & Brismar, H. (2020) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2020.00208 · Cited by 44 · see citing works
“Whilst sharing some of the advantages of tumor spheroids, the possibility of organoid production from human stem cells permits translational research and the study of developmental biology whilst reducing the ethical concerns and practical limitations associated with the study of explant tissue (Huch et al., 2017; Mun…”
BackgroundDistler, T., Lauria, I., Detsch, R., Sauter, C. M., Bendt, F., Kapr, J., Rütten, S., Boccaccini, A. R., & Fritsche, E. (2021) · Biomedicines · doi:10.3390/biomedicines9030261 · Cited by 44 · see citing works
“While conventional 3D in vitro models might capture the structural and cytoarchitectural aspects of the human brain, they are also prone to variability [10,11].”
BackgroundChambers, B. E., Weaver, N. E., & Wingert, R. A. (2023) · Cells · doi:10.3390/cells12040549 · Cited by 43 · see citing works
“The ability to recapitulate aspects of human development in vitro marks a major milestone, as nearly all of our current understanding of embryogenesis has been drawn from landmark studies conducted in animal models [3].”
BackgroundCurrent challenges and future directions of ATMPs in regenerative medicine
Kakroodi, F. A., Khodadoust, E., Alizadeh, M., Tehrani, R. S. H., Sarabi, P. A., Rahmanian, M., & Vosough, M. (2025) · Regenerative Therapy · doi:10.1016/j.reth.2025.06.017 · Cited by 42 · see citing works
“Notably, these cells have the potential to develop into brain components in an in vitro setting, a process that occurs independently of the natural evolutionary cycle [74,76].”
In Vitro Models of the Liver: Disease Modeling, Drug Discovery and Clinical Applications
Collins, S. D., Yuen, G., Tu, T., Budzinska, M. A., Spring, K. J., Bryant, K., & Shackel, N. A. (2019) · Codon Publications eBooks · doi:10.15586/hepatocellularcarcinoma.2019.ch3 · Cited by 41 · see citing works
“Further heterogeneity between organoid cultures can cause inconsistency in reproducing phenotypic traits such as size, shape, cellular composition, and 3D architecture (95, 96).”
BackgroundBioengineering tissue morphogenesis and function in human neural organoids
Fedorchak, N. J., Iyer, N. R., & Ashton, R. S. (2020) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2020.05.025 · Cited by 41 · see citing works
“and others, organoids are derived from hPSCs or organ progenitors and form tissues that self-organize through cell sorting and spatially restricted lineage commitment in a biomimetic manner [17, 18, 19].”
BackgroundActive morphogenesis of patterned epithelial shells
Khoromskaia, D., & Salbreux, G. (2022) · eLife · doi:10.7554/elife.75878 · Cited by 42 · see citing works
“[7] Meritxell Huch, Juergen A Knoblich, Matthias P Lutolf, and Alfonso Martinez-Arias.”
Lawrence, M. L., Elhendawi, M., Morlock, M., Liu, W. Y., Liu, S., Palakkan, A. A., Seidl, L. F., Hohenstein, P., Sjogren, A.-K. M., & Davies, J. A. (2022) · iScience · doi:10.1016/j.isci.2022.103884 · Cited by 41 · see citing works
“Testing the response of these organoids to nephrotoxicants has provided pilot data suggesting renal organoids have potential as an assay system (Xinaris et al., 2015; Huch et al., 2017; Davies and Lawrence, 2018).”
BackgroundVivarelli, S., Candido, S., Caruso, G., Falzone, L., & Libra, M. (2020) · Cancers · doi:10.3390/cancers12123636 · Cited by 41 · see citing works
“For example, PDTOs can be: Genetically edited, co-cultured with immune cells, stromal cells, microinjected with mic obes [68].”
BackgroundInfluentialBrain organoids: A promising model to assess oxidative stress‐induced central nervous system damage
Oyefeso, F. A., Muotri, A. R., Wilson, C. G., & Pecaut, M. J. (2021) · Developmental Neurobiology · doi:10.1002/dneu.22828 · Cited by 44 · see citing works
Biomedical and societal impacts of in vitro embryo models of mammalian development
Moris, N., Alev, C., Pera, M. F., & Arias, A. M. (2021) · Stem Cell Reports · doi:10.1016/j.stemcr.2021.03.023 · Cited by 40 · see citing works
3D bioprinted liver tissue and disease models: Current advances and future perspectives
Sun, L., Wang, Y., Zhang, S., Yang, H., & Mao, Y. (2023) · Biomaterials Advances · doi:10.1016/j.bioadv.2023.213499 · Cited by 39 · see citing works
Serafini, M. M., Sepehri, S., Midali, M., Stinckens, M., Biesiekierska, M., Wolniakowska, A., Gatzios, A., Rundén‐Pran, E., Reszka, E., Marinovich, M., et al. (2024) · Archives of Toxicology · doi:10.1007/s00204-024-03703-8 · Cited by 41 · see citing works
“An organoid is defined as “A 3D structure derived from pluripotent stem cells […] in which cells spontaneously self-organize into properly differentiated functional cell types and which recapitulates at least some functions of the organ” (Huch et al. 2017).”
BackgroundMa, P., Chen, Y., Lai, X., Zheng, J., Ye, E., Loh, X. J., Zhao, Y., Parikh, B. H., Su, X., You, M., et al. (2021) · Macromolecular Bioscience · doi:10.1002/mabi.202100191 · Cited by 39 · see citing works
Left–right symmetry of zebrafish embryos requires somite surface tension
Naganathan, S. R., Popovic, M. A., & Oates, A. C. (2022) · Nature · doi:10.1038/s41586-022-04646-9 · Cited by 38 · see citing works
- Authors
- Huch, M., Knoblich, J. A., Lutolf, M. P., & Martinez-Arias, A.
- Affiliations
- Wellcome/MRC Cambridge Stem Cell Institute (GB)
- Institute of Molecular Biotechnology (AT)
- Venue
- Development
- Publisher
- The Company of Biologists
- Published
- 2017-03-14
- Volume
- 144
- Issue
- 6
- Pages
- 938-941
- ISSN
- 0950-1991 (ISSN-L)
- 1477-9129
- OpenAlex
- W2597311576
- Cited by
- 409
- References
- 39
- Citations by year
- 2026: 36 · 2025: 30 · 2024: 42 · 2023: 36 · 2022: 50 · 2021: 85 · 2020: 54 · 2019: 38 · 2018: 24 · 2017: 14
- FWCI
- 2.86
- Type
- journal article
- Language
- en
- Open access
- green
- infoscience.epfl.ch
- Locations
- Development (publishedVersion)
- PubMed (publishedVersion)
- Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion)
- Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion, cc-by-nc-nd)
- HighWire Press Open Archive (submittedVersion)
- Funders
- Wellcome Trust
- Royal Society (104151/Z/14/Z)
- Horizon 2020 (LSFM4LIFE)
- Austrian Academy of Sciences
- Austrian Science Fund (I_1281-B19, Z_153_B09)
- European Research Council
- École Polytechnique Fédérale de Lausanne
- Seventh Framework Programme
- Novartis Foundation
- Biotechnology and Biological Sciences Research Council
- Isaac Newton Trust
- Topics
- Physical Sciences › Engineering › Biomedical Engineering › 3D Printing in Biomedical Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Pluripotent Stem Cells Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- organoids, organoid technology, translational research, developmental biology, research limitations
- MeSH terms
- Humans, Organoids, Tissue Engineering, Growth and Development, Translational Research, Biomedical
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review