The DOI matches its Crossref record; 63 of the 64 references it cites were found in a registry or an index.
Prospective Derivation of a Living Organoid Biobank of Colorectal Cancer Patients
Open accessAbstract
In Rspondin-based 3D cultures, Lgr5 stem cells from multiple organs form ever-expanding epithelial organoids that retain their tissue identity. We report the establishment of tumor organoid cultures from 20 consecutive colorectal carcinoma (CRC) patients. For most, organoids were also generated from adjacent normal tissue. Organoids closely recapitulate several properties of the original tumor. The spectrum of genetic changes within the "living biobank" agrees well with previous large-scale mutational analyses of CRC. Gene expression analysis indicates that the major CRC molecular subtypes are represented. Tumor organoids are amenable to high-throughput drug screens allowing detection of gene-drug associations. As an example, a single organoid culture was exquisitely sensitive to Wnt secretion (porcupine) inhibitors and carried a mutation in the negative Wnt feedback regulator RNF43, rather than in APC. Organoid technology may fill the gap between cancer genetics and patient trials, complement cell-line- and xenograft-based drug studies, and allow personalized therapy design. PAPERCLIP.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“‘living biobanks’ can provide access to patient-derived cells and organoids from large patient cohorts, and have already been established for different cancers124,151,176–178, genetic diseases such as cystic fibrosis, infectious diseases, chronic obstructive pulmonary disease and inflammatory bowel diseases179”
From Human disease models in drug development (2023) · cites this paper as [151]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Organoids are ideally suited for FPM due to their ease of establishment, similarity with the tissue of origin and tractability158,167 and have been deployed to identify therapeutic leads in a number of tumors168, including rare cancers that tend to be understudied and poorly characterized at the molecular level16,151,169,170.”
From Organoids (2022) · cites this paper as [169]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Recent studies using in vitro organoids grown from different intestinal tumors [33, 34] showed a strong correlation, functionally and molecularly with their primary tissue counterparts, providing a strong argument in favor of the potential for in vitro systems to model intestinal disease.”
From Modeling APC mutagenesis and familial adenomatous polyposis using human iPS cells (2018) · cites this paper as [34]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In short, the wild-type human colon organoid line P26n, as previously described in Van De Wetering et al. (2015) was cultured in domes of Cultrex Pathclear Reduced Growth Factor Basement Membrane Extract (BME) (3533-001; Amsbio).”
From One-step generation of tumor models by base editor multiplexing in adult stem cell-derived organoids (2023) · cites this paper as Van De Wetering et al. (2015)
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“broad clinical implementation of patient-specific disease models, such as PDOs, is currently hindered by low efficiencies in PDO establishment (60–70% success rate on average although, for some tissues, up to 90% have been reported for intestinal organoids151) as well as lengthy generation times and expansion procedures”
From Human disease models in drug development (2023) · cites this paper as [151]
The cited source says what the claim attributes to it.
In the citing paper
“Patient-derived tumor organoid (a.k.a. tumoroid) biobanks can be established from biopsies, surgical resections2,3, and even from Pap brushes4.”
From One-step generation of tumor models by base editor multiplexing in adult stem cell-derived organoids (2023) · cites this paper as [3]
In the citing paper
“The reconstituted TME model recapitulates not only the genetic and phenotypic features of a tumor but also models the functional response of a patient to therapeutic agents [389, 390].”
From Tumor microenvironment signaling and therapeutics in cancer progression (2023) · cites this paper as [389]
In the citing paper
“3D patient-derived tumor models of CRC (i.e., organoid and spheroid cultures) allow maintenance and expansion of functionally relevant cell subfractions and harbor the patients' individual genetic lesions (Ishiguro et al., 2017;van de Wetering et al., 2015).”
From Degradation of CCNK/CDK12 is a druggable vulnerability of colorectal cancer (2021) · cites this paper as van de Wetering et al., 2015
In the citing paper
“Furthermore, with recent technological advancements (e.g. organoid models and conditionally reprogrammed cell lines), a new generation of cancer cell models is being derived to allow full representation of the histopathological and molecular diversity of tumours (37–42).”
From Cell Model Passports-a hub for clinical, genetic and functional datasets of preclinical cancer models (2019) · cites this paper as [37]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Fast and accurate short read alignment with Burrows-Wheeler transform
Li, H., & Durbin, R. (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp324 · Cited by 58,607
Robinson, J. T., Thorvaldsdóttir, H., Winckler, W., Guttman, M., Lander, E. S., Getz, G., & Mesirov, J. P. (2011) · Nature Biotechnology · doi:10.1038/nbt.1754 · Cited by 15,390
Self-citationA genetic model for colorectal tumorigenesis
Fearon, E. R., & Vogelstein, B. (1990) · Cell · doi:10.1016/0092-8674(90)90186-i · Cited by 12,132
Fast and accurate long-read alignment with Burrows-Wheeler transform.
Li, H., & Durbin, R. (2010) · Bioinformatics · doi:10.1093/bioinformatics/btp698 · Cited by 12,063
A framework for variation discovery and genotyping using next-generation DNA sequencing data
DePristo, M. A., Banks, E., Poplin, R. E., Garimella, K. V., Maguire, J., Hartl, C., Philippakis, A., del Angel, G., Rivas, M. A., Hanna, M., et al. (2011) · Nature Genetics · doi:10.1038/ng.806 · Cited by 11,457
Self-citationAdjusting batch effects in microarray expression data using empirical Bayes methods
Johnson, W. E., Li, C., & Rabinovic, A. (2007) · Biostatistics · doi:10.1093/biostatistics/kxj037 · Cited by 8,658
Comprehensive molecular characterization of human colon and rectal cancer
The Cancer Genome Atlas Network (2012) · Nature · doi:10.1038/nature11252 · Cited by 8,499
The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity
Barretina, J., Caponigro, G., Stransky, N., Venkatesan, K., Margolin, A. A., Kim, S., Wilson, C. J., Lehár, J., Kryukov, G. V., Sonkin, D., et al. (2012) · Nature · doi:10.1038/nature11003 · Cited by 7,950
Self-citationVogelstein, B., Papadopoulos, N., Velculescu, V. E., Zhou, S., Diaz, L. A., & Kinzler, K. W. (2013) · Science · doi:10.1126/science.1235122 · Cited by 7,863
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
Self-citation
Cited by
Sorted by citations
Items 801–900 of 1,001
Mascolo, D. D., Varesano, S., Benelli, R., Mollica, H., Salis, A., Zocchi, M. R., Decuzzi, P., & Poggi, A. D. (2019) · Cancers · doi:10.3390/cancers12010104 · Cited by 39
Josenhans, C., Müthing, J., Elling, L., Bartfeld, S., & Schmidt, H. (2020) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2020.151392 · Cited by 40
Self-citationBreast cancer organoids from a patient with giant papillary carcinoma as a high-fidelity model
Li, X., Pan, B., Song, X., Li, N., Zhao, D., Li, M., & Zhao, Z. (2020) · Cancer Cell International · doi:10.1186/s12935-020-01171-5 · Cited by 39
3D organoids derived from the small intestine: An emerging tool for drug transport research
Zhang, Y., Huang, S., Zhong, W., Chen, W., Yao, B., & Wang, X. (2020) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2020.12.002 · Cited by 40
Semiconducting polymer nanoparticles for photothermal ablation of colorectal cancer organoids
McCarthy, B., Cudykier, A., Singh, R. N., Levi‐Polyachenko, N. H., & Söker, S. (2021) · Scientific Reports · doi:10.1038/s41598-021-81122-w · Cited by 39
Patient-derived Tumour Organoids: A Bridge between Cancer Biology and Personalised Therapy
Wu, W., Li, X., & Yu, S. (2022) · Acta Biomaterialia · doi:10.1016/j.actbio.2022.04.050 · Cited by 40
The Efficacy of Using Patient-Derived Organoids to Predict Treatment Response in Colorectal Cancer
Su, C., Olsen, K. A., Bond, C., & Whitehall, V. (2023) · Cancers · doi:10.3390/cancers15030805 · Cited by 37
Systematic review: predictive value of organoids in colorectal cancer
Sakshaug, B. C., Folkesson, E., Haukaas, T. H., Visnes, T., & Flobak, Å. (2023) · Scientific Reports · doi:10.1038/s41598-023-45297-8 · Cited by 40
Drug persistence – From antibiotics to cancer therapies
Kochanowski, K., Morinishi, L. S., Altschuler, S. J., & Wu, L. F. (2018) · Current Opinion in Systems Biology · doi:10.1016/j.coisb.2018.03.003 · Cited by 39
IPO11 mediates βcatenin nuclear import in a subset of colorectal cancers
Mis, M., O’Brien, S., Steinhart, Z., Lin, S., Hart, T., Moffat, J., & Angers, S. (2019) · The Journal of Cell Biology · doi:10.1083/jcb.201903017 · Cited by 37
Joshi, R. S., de Moura, M. C., Piñeyro, D., Álvarez‐Errico, D., Arribas, C., & Esteller, M. (2020) · Epigenetics · doi:10.1080/15592294.2020.1762398 · Cited by 39
Hou, Y., Ai, X., Zhao, L., Gao, Z., Wang, Y., Lu, Y., Tu, P., & Jiang, Y. (2020) · Lab on a Chip · doi:10.1039/d0lc00288g · Cited by 38
Lee, T. W., Lai, A., Harms, J. K., Singleton, D. C., Dickson, B. D., Macann, A., Hay, M. P., & Jamieson, S. M. F. (2020) · Cancers · doi:10.3390/cancers12123743 · Cited by 38
Patient-Derived Organoid Models of Human Neuroendocrine Carcinoma
Dijkstra, K. K., van den Berg, J. G., Weeber, F., van de Haar, J., Velds, A., Kaing, S., Peters, D. D. G. C., Eskens, F. A. L. M., de Groot, D. J., Tesselaar, M. E. T., et al. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.627819 · Cited by 42
Hong, H. K., Yun, N. H., Jeong, Y., Park, J., Doh, J., Lee, W. Y., & Cho, Y. B. (2021) · Cancer Medicine · doi:10.1002/cam4.4114 · Cited by 37
In vitro assays for investigating the FLASH effect
Adrian, G., Ruan, J.-L., Paillas, S., Cooper, C. R., & Petersson, K. (2022) · Expert Reviews in Molecular Medicine · doi:10.1017/erm.2022.5 · Cited by 38
Stem cells: the new “model organism”
Drubin, D. G., & Hyman, A. A. (2017) · Molecular Biology of the Cell · doi:10.1091/mbc.e17-03-0183 · Cited by 34
A protracted war against cancer drug resistance
Tian, Y., Wang, X., Wu, C., Qiao, J., Jin, H. D., & Li, H. (2024) · Cancer Cell International · doi:10.1186/s12935-024-03510-2 · Cited by 39
Kabiljo, J., Theophil, A., Homola, J., Renner, A. F., Stürzenbecher, N., Ammon, D., Zirnbauer, R., Stang, S., Tran, L., Laengle, J., et al. (2024) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2024-009494 · Cited by 38
Organoids as a Model for Colorectal Cancer
Young, M. A., & Reed, K. R. (2016) · Current Colorectal Cancer Reports · doi:10.1007/s11888-016-0335-4 · Cited by 40
Generation of an equine biobank to be used for Functional Annotation of Animal Genomes project
Burns, E., Bordbari, M. H., Mienaltowski, M. J., Affolter, V. K., Barro, M. V., Gianino, F., Gianino, G., Giulotto, E., Kalbfleisch, T., Katzman, S. A., et al. (2018) · Animal Genetics · doi:10.1111/age.12717 · Cited by 36
2D- and 3D-Based Intestinal Stem Cell Cultures for Personalized Medicine
Liu, Y., & Chen, Y.-G. (2018) · Cells · doi:10.3390/cells7120225 · Cited by 37
Propagation of human prostate tissue from induced pluripotent stem cells
Hepburn, A. C., Curry, E. L., Moad, M., Steele, R. E., Franco, O. E., Wilson, L., Singh, P., Buskin, A., Crawford, S. E., Gaughan, L., et al. (2020) · Stem Cells Translational Medicine · doi:10.1002/sctm.19-0286 · Cited by 36
Boos, S. L., Loevenich, L. P., Vosberg, S., Engleitner, T., Öllinger, R., Kumbrink, J., Rokavec, M., Michl, M., Greif, P. A., Jung, A., et al. (2021) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2021.10.008 · Cited by 39
Targeting cancer drug resistance utilizing organoid technology
Chai, C., Ji, P., Xu, H., Tang, H., Wang, Z., Zhang, H., & Zhou, W. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.114098 · Cited by 35
Decoding the basis of histological variation in human cancer
Fujii, M., Sekine, S., & Sato, T. (2023) · Nature reviews. Cancer · doi:10.1038/s41568-023-00648-5 · Cited by 35
Organoid‐Guided Precision Medicine: From Bench to Bedside
Tao, B., Li, X., Hao, M., Tian, T., Li, Y., Li, X., Yang, C., Li, Q., Feng, Q., Zhou, H., et al. (2025) · MedComm · doi:10.1002/mco2.70195 · Cited by 38
Libouban, M. A. A., de Roos, J. A. D. M., Uitdehaag, J. C. M., Willemsen‐Seegers, N., Mainardi, S., Dylus, J., de Man, J., Tops, B. B. J., Meijerink, J. P. P., Štorchová, Z., et al. (2017) · Oncotarget · doi:10.18632/oncotarget.16213 · Cited by 36
Organoids Provide an Important Window on Inflammation in Cancer
Baker, K. (2018) · Cancers · doi:10.3390/cancers10050151 · Cited by 37
More than fishing for a cure: The promises and pitfalls of high throughput cancer cell line screens
Ling, A. L., Gruener, R. F., Fessler, J. L., & Huang, R. S. (2018) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2018.06.014 · Cited by 35
Linxweiler, J., Hammer, M., Muhs, S., Kohn, M., Pryalukhin, A. E., Veith, C., Bohle, R. M., Stöckle, M., Junker, K., & Saar, M. (2018) · Journal of Cancer Research and Clinical Oncology · doi:10.1007/s00432-018-2803-5 · Cited by 36
Dzobo, K., Rowe, A., Senthebane, D. A., AlMazyadi, M., Patten, V. A., & Parker, M. I. (2018) · OMICS A Journal of Integrative Biology · doi:10.1089/omi.2018.0172 · Cited by 37
Organoids: Past Learning and Future Directions
O’Connell, L., & Winter, D. C. (2019) · Stem Cells and Development · doi:10.1089/scd.2019.0227 · Cited by 39
Comprehensive Analysis of MEN1 Mutations and Their Role in Cancer
Nelakurti, D. D., Pappula, A. L., Rajasekaran, S., Miles, W. O., & Petreaca, R. C. (2020) · Cancers · doi:10.3390/cancers12092616 · Cited by 35
Cho, E. J., Kim, M., Jo, D., Kim, J., Oh, J., Chung, H. C., Lee, S.-H., Kim, D., Chun, S., Kim, J., et al. (2021) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-021-02034-1 · Cited by 36
Organ-Chip Models: Opportunities for Precision Medicine in Pancreatic Cancer
Haque, M. R., Rempert, T. H., Al-Hilal, T. A., Wang, C., Bhushan, A., & Bishehsari, F. (2021) · Cancers · doi:10.3390/cancers13174487 · Cited by 39
Decellularized normal and cancer tissues as tools for cancer research
Gentilin, E., D’Angelo, E., Agostini, M., & Astolfi, L. (2021) · Cancer Gene Therapy · doi:10.1038/s41417-021-00398-2 · Cited by 37
CFTR and Gastrointestinal Cancers: An Update
Bhattacharya, R., Blankenheim, Z., Scott, P. M., & Cormier, R. T. (2022) · Journal of Personalized Medicine · doi:10.3390/jpm12060868 · Cited by 38
Patient-derived cancer models: Valuable platforms for anticancer drug testing
Genta, S., Coburn, B. A., Cescon, D. W., & Spreafico, A. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.976065 · Cited by 39
Three‐dimensional pancreas organogenesis models
Grapin‐Botton, A. (2016) · Diabetes Obesity and Metabolism · doi:10.1111/dom.12720 · Cited by 41
Individualized medicine using intestinal responses to CFTR potentiators and correctors
Beekman, J. M. (2016) · Pediatric Pulmonology · doi:10.1002/ppul.23553 · Cited by 36
Chen, K.-Y., Srinivasan, T., Lin, C., Tung, K.-L., Gao, Z., Hsu, D. S., Lipkin, S. M., & Shen, X. (2018) · 2018 40th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/embc.2018.8512784 · Cited by 35
Tao, M., & Wu, X. (2021) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-021-02139-7 · Cited by 35
Flanagan, D. J., Woodcock, S. A., Phillips, C., Eagle, C., & Sansom, O. J. (2022) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2022.108179 · Cited by 36
Patient-derived organoids for therapy personalization in inflammatory bowel diseases
Lucafò, M., Muzzo, A., Marcuzzi, M., Giorio, L., Decorti, G., & Stocco, G. (2022) · World Journal of Gastroenterology · doi:10.3748/wjg.v28.i24.2636 · Cited by 38
Progress and promise of alternative animal and non-animal methods in biomedical research
Freires, I. A., Colón, D. F., Soares, L. F. F., Costa, I. S., de Araújo, L. P., Breseghello, I., Abdalla, H. B., Lazarini, J. G., Rosalen, P. L., Pigossi, S. C., et al. (2023) · Archives of Toxicology · doi:10.1007/s00204-023-03532-1 · Cited by 36
Patient-Derived Organoids Predict Treatment Response in Metastatic Colorectal Cancer
Smabers, L. P., Wensink, G. E., Verissimo, C. S., Doorn, M., Yang, T., Voskuilen, T., Huismans, M. A., Iersel, L. V., Cirkel, G. A., Gootjes, E. C., et al. (2025) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-25-1564 · Cited by 41
Self-citationA Biosensor for the Mitotic Kinase MPS1 Reveals Spatiotemporal Activity Dynamics and Regulation
Kuijt, T. E. F., Lambers, M. L. A., Weterings, S. D. C., Ponsioen, B., Bolhaqueiro, A. C. F., Staijen, D. H. M., & Kops, G. J. P. L. (2020) · Current Biology · doi:10.1016/j.cub.2020.07.062 · Cited by 31
Patient-derived tumour models for personalized therapeutics in urological cancers
van de Merbel, A. F., van der Horst, G., & van der Pluijm, G. (2020) · Nature Reviews Urology · doi:10.1038/s41585-020-00389-2 · Cited by 35
Pituitary Remodeling Throughout Life: Are Resident Stem Cells Involved?
Laporte, E., Vennekens, A., & Vankelecom, H. E. J. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.604519 · Cited by 41
Dorrigiv, D., Simeone, K., Communal, L., Kendall‐Dupont, J., St‐Georges‐Robillard, A., Péant, B., Carmona, E., Mes‐Masson, A., & Gervais, T. (2021) · Cancers · doi:10.3390/cancers13164208 · Cited by 40
Regenerative Engineering: Current Applications and Future Perspectives
Goldenberg, D., McLaughlin, C., Koduru, S. V., & Ravnic, D. J. (2021) · Frontiers in Surgery · doi:10.3389/fsurg.2021.731031 · Cited by 37
Verteporfin inhibits gastric cancer cell growth by suppressing adhesion molecule FAT1
Kang, M.-H., Jeong, G. S., Smoot, D. T., Ashktorab, H., Hwang, C. M., Kim, B. S., Kim, H. S., & Park, Y. (2017) · Oncotarget · doi:10.18632/oncotarget.21946 · Cited by 35
MLH1 Deficiency Induces Cetuximab Resistance in Colon Cancer via Her‐2/PI3K/AKT Signaling
Han, Y., Peng, Y., Fu, Y., Cai, C., Guo, C., Liu, S., Li, Y., Chen, Y., Shen, E., Long, K., et al. (2020) · Advanced Science · doi:10.1002/advs.202000112 · Cited by 34
Xu, N.-Y., Li, J., Wang, M., Chen, X., Tang, R., & Liu, X. (2024) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.3c17863 · Cited by 37
Gut microbial-derived N-acetylmuramic acid alleviates colorectal cancer via the AKT1 pathway
Hu, M., Xu, Y., Wang, Y., Huang, Z., Wang, L., Zeng, F., Qiu, B., Liu, Z., Yuan, P., yu, W., et al. (2025) · Gut · doi:10.1136/gutjnl-2024-332891 · Cited by 34
Tashiro, T., Okuyama, H., Endo, H., Kawada, K., Ashida, Y., Ohue, M., Sakai, Y., & Inoue, M. (2017) · PLoS ONE · doi:10.1371/journal.pone.0174151 · Cited by 31
Human-cell-derived organoids as a new ex vivo model for drug assays in oncology
Mebarki, M., Griscelli, A. B., & Bonhomme‐Faivre, L. (2018) · Drug Discovery Today · doi:10.1016/j.drudis.2018.02.003 · Cited by 34
Moorefield, E., Blue, R. E., Quinney, N. L., Gentzsch, M., & Ding, S. (2018) · BMC Cell Biology · doi:10.1186/s12860-018-0165-0 · Cited by 34
Linden, C. V., & Corbet, C. (2019) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2019.05.016 · Cited by 34
Targeting Protein Synthesis in Colorectal Cancer
Schmidt, S., Denk, S., & Wiegering, A. (2020) · Cancers · doi:10.3390/cancers12051298 · Cited by 36
Kast, F., Klein, C., Umaña, P., Gros, A., & Gasser, S. (2021) · OncoImmunology · doi:10.1080/2162402x.2020.1869389 · Cited by 34
Zhao, Y., Zhang, B., Ma, Y., Zhao, F., Chen, J., Wang, B., Jin, H., Zhou, F., Guan, J., Zhao, Q., et al. (2022) · Advanced Science · doi:10.1002/advs.202201539 · Cited by 34
Patient-derived organoid analysis of drug resistance in precision medicine: is there a value?
Abugomaa, A., & Elbadawy, M. (2020) · Expert Review of Precision Medicine and Drug Development · doi:10.1080/23808993.2020.1715794 · Cited by 35
Wensink, G. E., Bond, M. J. G., Küçükköse, E., May, A. M., Vink, G. R., Koopman, M., Kranenburg, O., & Roodhart, J. M. L. (2021) · Cancer Treatment Reviews · doi:10.1016/j.ctrv.2021.102174 · Cited by 35
Brain Organoids: A Game-Changer for Drug Testing
Giorgi, C., Lombardozzi, G., Ammannito, F., Scenna, M. S., Maceroni, E., Quintiliani, M., d’Angelo, M., Cimini, A., & Castelli, V. (2024) · Pharmaceutics · doi:10.3390/pharmaceutics16040443 · Cited by 34
Interferon-responsive intestinal BEST4/CA7+ cells are targets of bacterial diarrheal toxins
Wang, D., Spoelstra, W. K., Lin, L., Akkerman, N., Krueger, D., Dayton, T. L., van Zon, J. S., Tans, S. J., van Es, J. H., & Clevers, H. C. (2025) · Cell stem cell · doi:10.1016/j.stem.2025.02.003 · Cited by 35
Self-citationAn emerging role for cytopathology in precision oncology
Pauli, C., Puca, L., Mosquera, J. M., Robinson, B. D., Beltran, H., Rubin, M. A., & Rao, R. A. (2015) · Cancer Cytopathology · doi:10.1002/cncy.21647 · Cited by 33
Rodenhizer, D., Dean, T., Xu, B., Cojocari, D., & McGuigan, A. P. (2018) · Nature Protocols · doi:10.1038/s41596-018-0022-9 · Cited by 35
Organoids for Advanced Therapeutics and Disease Models
Kim, S., Cho, A., Min, S., Kim, S., & Cho, S. (2018) · Advanced Therapeutics · doi:10.1002/adtp.201800087 · Cited by 33
Baker, L. A., Tiriac, H., & Tuveson, D. A. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-8879-2_9 · Cited by 34
Parker, R. N., Cairns, D. M., Wu, W. A., Jordan, K. E., Guo, C., Huang, W., Martín‐Moldes, Z., & Kaplan, D. L. (2020) · Advanced Healthcare Materials · doi:10.1002/adhm.202000266 · Cited by 33
Three-Dimensional Culture Systems in Gastric Cancer Research
Alzeeb, G., Metges, J., Corcos, L., & Jossic-Corcos, C. L. (2020) · Cancers · doi:10.3390/cancers12102800 · Cited by 38
Curvello, R., & Garnier, G. (2020) · Biomacromolecules · doi:10.1021/acs.biomac.0c01510 · Cited by 35
Recent developments in cancer research: Expectations for a new remedy
Ando, K., Hu, Q., Kasagi, Y., Oki, E., & Mori, M. (2021) · Annals of Gastroenterological Surgery · doi:10.1002/ags3.12440 · Cited by 33
Rao, S., Hossain, T., & Mahmoudi, T. (2021) · Cancer Letters · doi:10.1016/j.canlet.2021.02.024 · Cited by 34
Organoids of the Female Reproductive Tract: Innovative Tools to Study Desired to Unwelcome Processes
Heremans, R., Jan, Ž., Timmerman, D., & Vankelecom, H. E. J. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.661472 · Cited by 36
Emerging liver organoid platforms and technologies
Lam, D. T. U. H., Dan, Y. Y., Chan, Y.-S., & Ng, H. (2021) · Cell Regeneration · doi:10.1186/s13619-021-00089-1 · Cited by 36
Personalized Immunotherapy in Colorectal Cancers: Where Do We Stand?
Hu, L., Lan, H., Huang, D., Li, X., & Jin, K. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.769305 · Cited by 34
Geevimaan, K., Guo, J.-Y., Shen, C., Jiang, J., Fann, C. S. J., Hwang, M., Shui, J., Lin, H.-T., Wang, M.-J. S., Shih, H.-C., et al. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.883437 · Cited by 34
The Roles of Secreted Wnt Ligands in Cancer
Werner, J., Boonekamp, K. E., Zhan, T., & Boutros, M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24065349 · Cited by 37
Lorenzi, F., Babaei‐Jadidi, R., Sheard, J., Spencer‐Dene, B., & Nateri, A. S. (2016) · Molecular Therapy — Methods & Clinical Development · doi:10.1038/mtm.2016.24 · Cited by 32
Utilizing gastric cancer organoids to assess tumor biology and personalize medicine
Lin, M., Gao, M., Cavnar, M. J., & Kim, J. (2019) · World Journal of Gastrointestinal Oncology · doi:10.4251/wjgo.v11.i7.509 · Cited by 33
Mapping oncogenic protein interactions for precision medicine
Tabar, M. S., Francis, H., Yeo, D., Bailey, C. G., & Rasko, J. E. J. (2022) · International Journal of Cancer · doi:10.1002/ijc.33954 · Cited by 30
Zhu, C., Teng, L., Lai, Y., Yao, X., Fang, Y., Wang, Z., Lin, S., Zhang, H., Li, Q., Li, Y., et al. (2024) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-024-05215-1 · Cited by 32
Mizutani, T., Boretto, M., Lim, S., Drost, J., González, D. M., Oka, R., Geurts, M. H., Begthel, H., Korving, J., van Es, J. H., et al. (2024) · Nature Cancer · doi:10.1038/s43018-024-00841-x · Cited by 37
Self-citationReimagining human-centric drug development with new approach methodologies
Wu, X., Wu, M. A., Zou, J., Kleinstreuer, N., & Wu, J. C. (2026) · Science · doi:10.1126/science.aeb0045 · Cited by 37
The third dimension: new developments in cell culture models for colorectal research
Pereira, J., Awatade, N. T., Loureiro, C. A., Matos, P., Amaral, M. D., & Jordan, P. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2258-2 · Cited by 32
Tumor Organoids Fill the Niche
Shroyer, N. F. (2016) · Cell stem cell · doi:10.1016/j.stem.2016.05.020 · Cited by 32
A precision approach to tumour treatment
Dienstmann, R., & Tabernero, J. M. (2017) · Nature · doi:10.1038/nature23101 · Cited by 32
Roelofs, C., Hollande, F., Redvers, R. P., Anderson, R. L., & Mérino, D. (2019) · Biochemical Society Transactions · doi:10.1042/bst20180375 · Cited by 32
Design Approaches for Generating Organ Constructs
Xia, Y. F., & Belmonte, J. C. I. (2019) · Cell stem cell · doi:10.1016/j.stem.2019.05.016 · Cited by 32
BTK inhibitors synergise with 5‐FU to treat drug‐resistant TP53‐null colon cancers
Lavitrano, M., Ianzano, L., Bonomo, S., Cialdella, A., Cerrito, M. G., Pisano, F., Missaglia, C., Giovannoni, R., Romano, G., McLean, C. M., et al. (2019) · The Journal of Pathology · doi:10.1002/path.5347 · Cited by 32
The Interleukin 22 Pathway Interacts with Mutant KRAS to Promote Poor Prognosis in Colon Cancer
McCuaig, S., Barras, D., Mann, E. H., Friedrich, M., Bullers, S. J., Janney, A., Garner, L. C., Domingo, E., Koelzer, V. H., Delorenzi, M., et al. (2020) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-19-1086 · Cited by 34
A fully defined 3D matrix for ex vivo expansion of human colonic organoids from biopsy tissue
Bergenheim, F. H., Fregni, G., Buchanan, C. F., Riis, L. B., Heulot, M., Touati, J., Seidelin, J. B., Rizzi, S. C., & Nielsen, O. H. (2020) · Biomaterials · doi:10.1016/j.biomaterials.2020.120248 · Cited by 33
Electromembrane Extraction and Mass Spectrometry for Liver Organoid Drug Metabolism Studies
Skottvoll, F. S., Hansen, F. A., Harrison, S. P., Boger, I. C. S., Mrsa, A., Restan, M. S., Stein, M., Lundanes, E., Pedersen‐Bjergaard, S., Aizenshtadt, A., et al. (2021) · Analytical Chemistry · doi:10.1021/acs.analchem.0c05082 · Cited by 33
Pham, N., Radulovich, N., Ibrahimov, E., Martins-Filho, S. N., Li, Q., Pintilie, M., Weiss, J., Raghavan, V., Cabanero, M., Denroche, R. E., et al. (2021) · Scientific Reports · doi:10.1038/s41598-021-90049-1 · Cited by 33
Use of preclinical models for malignant pleural mesothelioma
Shamseddin, M., Obacz, J., Garnett, M. J., Rintoul, R. C., Francies, H. E., & Marciniak, S. J. (2021) · Thorax · doi:10.1136/thoraxjnl-2020-216602 · Cited by 30
Self-citationOrganoids, Where We Stand and Where We Go
Kaluthantrige Don, F., & Huch, M. (2021) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2021.03.001 · Cited by 32
Intestinal multicellular organoids to study colorectal cancer
Idris, M., Alves, M. M., Hofstra, R. M. W., Mahé, M. M., & Melotte, V. (2021) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2021.188586 · Cited by 33
Metadata
- Authors
- 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., McLaren-Douglas, A., Blokker, J., Jaksani, S., Bartfeld, S., Volckman, R., van Sluis, P., Li, V. S. W., Seepo, S., Sekhar Pedamallu, C., Cibulskis, K., Carter, S. L., McKenna, A., Lawrence, M. S., Lichtenstein, L., Stewart, C., Koster, J., Versteeg, R., van Oudenaarden, A., Saez-Rodriguez, J., Vries, R. G. J., Getz, G., Wessels, L., Stratton, M. R., McDermott, U., Meyerson, M., Garnett, M. J., & Clevers, H.
- Affiliations
- Wellcome Sanger Institute (GB)
- Broad Institute (US)
- The Netherlands Cancer Institute (NL)
- European Bioinformatics Institute (GB)
- Diakonessenhuis hospital (NL)
- Royal Netherlands Academy of Arts and Sciences (NL)
- National Institute for Medical Research (GB)
- Amsterdam UMC Location University of Amsterdam (NL)
- Corresponding author
- Garnett, Mathew J.
- Clevers, Hans
- ORCID
- Francis, Joshua M.
- Iorio, Francesco
- Pronk, Apollo
- Taylor-Weiner, Amaro
- Kester, Lennart
- Bartfeld, Sina
- Li, Vivian S.W.
- Cibulskis, Kristian
- Carter, Scott L.
- McKenna, Aaron
- Lawrence, Michael S.
- Stewart, Chip
- Versteeg, Rogier
- Vries, Robert G.J.
- Getz, Gad
- Wessels, Lodewyk
- Stratton, Michael R.
- McDermott, Ultan
- Meyerson, Matthew
- Garnett, Mathew J.
- Clevers, Hans
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2015-05
- Volume
- 161
- Issue
- 4
- Pages
- 933-945
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC6428276
- OpenAlex
- W1741548448
- Cited by
- 2,408
- References
- 64
- Citations by year
- 2026: 196 · 2025: 233 · 2024: 232 · 2023: 220 · 2022: 267 · 2021: 343 · 2020: 260 · 2019: 181 · 2018: 173 · 2017: 154 · 2016: 108 · 2015: 39
- FWCI
- 69.01
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- KNAW research portal (Royal Academy of Art and Sciences (KNAW)) (publishedVersion, other-oa)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion, other-oa)
- Utrecht University Repository (Utrecht University) (submittedVersion, other-oa)
- Figshare (submittedVersion, cc-by)
- RWTH Publications (RWTH Aachen) (submittedVersion)
- Pure Amsterdam UMC (submittedVersion)
- Utrecht University Repository (Utrecht University) (submittedVersion)
- Funders
- Francis Crick Institute (10105)
- Topics
- Health Sciences › Medicine › Oncology › Cancer Cells and Metastasis
- Health Sciences › Medicine › Oncology › Colorectal Cancer Treatments and Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Wnt/β-catenin signaling in development and cancer
- Keywords
- colorectal cancer, tumor organoids, organoid biobank, Lgr5+ stem cells, R-spondin, Wnt signaling, porcupine inhibitor, RNF43 mutation, APC mutation, drug screening, personalized treatment, molecular subtypes, gene expression profiling
- MeSH terms
- DNA-Binding Proteins, Drug Screening Assays, Antitumor, Humans, Organ Culture Techniques, Organoids, Colorectal Neoplasms, Oncogene Proteins, Biological Specimen Banks, Ubiquitin-Protein Ligases, Precision Medicine
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