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Patient-Derived Bladder Cancer Organoid Models in Tumor Biology and Drug Testing : A Systematic Review

Medle, Benjamin LU ; Sjödahl, Gottfrid LU ; Eriksson, Pontus LU ; Liedberg, Fredrik LU ; Höglund, Mattias LU and Bernardo, Carina LU orcid (2022) In Cancers 14(9). p.1-19
Abstract

Bladder cancer is a common and highly heterogeneous malignancy with a relatively poor outcome. Patient-derived tumor organoid cultures have emerged as a preclinical model with improved biomimicity. However, the impact of the different methods being used in the composition and dynamics of the models remains unknown. This study aims to systematically review the literature regarding patient-derived organoid models for normal and cancer tissue of the bladder, and their current and potential future applications for tumor biology studies and drug testing. A PRISMA-compliant systematic review of the PubMED, Embase, Web of Sciences, and Scopus databases was performed. The results were analyzed based on the methodologies, comparison with primary... (More)

Bladder cancer is a common and highly heterogeneous malignancy with a relatively poor outcome. Patient-derived tumor organoid cultures have emerged as a preclinical model with improved biomimicity. However, the impact of the different methods being used in the composition and dynamics of the models remains unknown. This study aims to systematically review the literature regarding patient-derived organoid models for normal and cancer tissue of the bladder, and their current and potential future applications for tumor biology studies and drug testing. A PRISMA-compliant systematic review of the PubMED, Embase, Web of Sciences, and Scopus databases was performed. The results were analyzed based on the methodologies, comparison with primary tumors, functional analysis, and chemotherapy and immunotherapy testing. The literature search identified 536 articles, 24 of which met the inclusion criteria. Bladder cancer organoid models have been increasingly used for tumor biology studies and drug screening. Despite the heterogeneity between methods, organoids and primary tissues showed high genetic and phenotypic concordance. Organoid sensitivity to chemotherapy matched the response in patient-derived xenograft (PDX) models and predicted response based on clinical and mutation data. Advances in bioengineering technology, such as microfluidic devices, bioprinters, and imaging, are likely to further standardize and expand the use of organoids.

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author
; ; ; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
3D tumor models, bladder cancer, drug response, organoids, precision medicine, spheroids
in
Cancers
volume
14
issue
9
article number
2062
pages
1 - 19
publisher
MDPI AG
external identifiers
  • scopus:85128576993
  • pmid:35565191
ISSN
2072-6694
DOI
10.3390/cancers14092062
language
English
LU publication?
yes
additional info
Publisher Copyright: © 2022 by the authors. Licensee MDPI, Basel, Switzerland.
id
1b1ce426-0593-4acc-ad39-bde9a216b8bf
date added to LUP
2022-05-10 22:03:17
date last changed
2024-05-03 08:05:58
@article{1b1ce426-0593-4acc-ad39-bde9a216b8bf,
  abstract     = {{<p>Bladder cancer is a common and highly heterogeneous malignancy with a relatively poor outcome. Patient-derived tumor organoid cultures have emerged as a preclinical model with improved biomimicity. However, the impact of the different methods being used in the composition and dynamics of the models remains unknown. This study aims to systematically review the literature regarding patient-derived organoid models for normal and cancer tissue of the bladder, and their current and potential future applications for tumor biology studies and drug testing. A PRISMA-compliant systematic review of the PubMED, Embase, Web of Sciences, and Scopus databases was performed. The results were analyzed based on the methodologies, comparison with primary tumors, functional analysis, and chemotherapy and immunotherapy testing. The literature search identified 536 articles, 24 of which met the inclusion criteria. Bladder cancer organoid models have been increasingly used for tumor biology studies and drug screening. Despite the heterogeneity between methods, organoids and primary tissues showed high genetic and phenotypic concordance. Organoid sensitivity to chemotherapy matched the response in patient-derived xenograft (PDX) models and predicted response based on clinical and mutation data. Advances in bioengineering technology, such as microfluidic devices, bioprinters, and imaging, are likely to further standardize and expand the use of organoids.</p>}},
  author       = {{Medle, Benjamin and Sjödahl, Gottfrid and Eriksson, Pontus and Liedberg, Fredrik and Höglund, Mattias and Bernardo, Carina}},
  issn         = {{2072-6694}},
  keywords     = {{3D tumor models; bladder cancer; drug response; organoids; precision medicine; spheroids}},
  language     = {{eng}},
  number       = {{9}},
  pages        = {{1--19}},
  publisher    = {{MDPI AG}},
  series       = {{Cancers}},
  title        = {{Patient-Derived Bladder Cancer Organoid Models in Tumor Biology and Drug Testing : A Systematic Review}},
  url          = {{http://dx.doi.org/10.3390/cancers14092062}},
  doi          = {{10.3390/cancers14092062}},
  volume       = {{14}},
  year         = {{2022}},
}