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Organoid Models for Cancer Research—From Bed to Bench Side and Back
SIMPLE SUMMARY: Despite significant strides in multimodal therapy, cancers still rank within the first three causes of death especially in industrial nations. A lack of individualized approaches and accurate preclinical models are amongst the major barriers that limit the development of novel therap...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8507862/ https://www.ncbi.nlm.nih.gov/pubmed/34638297 http://dx.doi.org/10.3390/cancers13194812 |
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author | Kastner, Carolin Hendricks, Anne Deinlein, Hanna Hankir, Mohammed Germer, Christoph-Thomas Schmidt, Stefanie Wiegering, Armin |
author_facet | Kastner, Carolin Hendricks, Anne Deinlein, Hanna Hankir, Mohammed Germer, Christoph-Thomas Schmidt, Stefanie Wiegering, Armin |
author_sort | Kastner, Carolin |
collection | PubMed |
description | SIMPLE SUMMARY: Despite significant strides in multimodal therapy, cancers still rank within the first three causes of death especially in industrial nations. A lack of individualized approaches and accurate preclinical models are amongst the major barriers that limit the development of novel therapeutic options and drugs. Recently, the 3D culture system of organoids was developed which stably retains the genetic and phenotypic characteristics of the original tissue, healthy as well as diseased. In this review, we summarize current data and evidence on the relevance and reliability of such organoid culture systems in cancer research, focusing on their role in drug investigations (in a personalized manner). ABSTRACT: Organoids are a new 3D ex vivo culture system that have been applied in various fields of biomedical research. First isolated from the murine small intestine, they have since been established from a wide range of organs and tissues, both in healthy and diseased states. Organoids genetically, functionally and phenotypically retain the characteristics of their tissue of origin even after multiple passages, making them a valuable tool in studying various physiologic and pathophysiologic processes. The finding that organoids can also be established from tumor tissue or can be engineered to recapitulate tumor tissue has dramatically increased their use in cancer research. In this review, we discuss the potential of organoids to close the gap between preclinical in vitro and in vivo models as well as clinical trials in cancer research focusing on drug investigation and development. |
format | Online Article Text |
id | pubmed-8507862 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-85078622021-10-13 Organoid Models for Cancer Research—From Bed to Bench Side and Back Kastner, Carolin Hendricks, Anne Deinlein, Hanna Hankir, Mohammed Germer, Christoph-Thomas Schmidt, Stefanie Wiegering, Armin Cancers (Basel) Review SIMPLE SUMMARY: Despite significant strides in multimodal therapy, cancers still rank within the first three causes of death especially in industrial nations. A lack of individualized approaches and accurate preclinical models are amongst the major barriers that limit the development of novel therapeutic options and drugs. Recently, the 3D culture system of organoids was developed which stably retains the genetic and phenotypic characteristics of the original tissue, healthy as well as diseased. In this review, we summarize current data and evidence on the relevance and reliability of such organoid culture systems in cancer research, focusing on their role in drug investigations (in a personalized manner). ABSTRACT: Organoids are a new 3D ex vivo culture system that have been applied in various fields of biomedical research. First isolated from the murine small intestine, they have since been established from a wide range of organs and tissues, both in healthy and diseased states. Organoids genetically, functionally and phenotypically retain the characteristics of their tissue of origin even after multiple passages, making them a valuable tool in studying various physiologic and pathophysiologic processes. The finding that organoids can also be established from tumor tissue or can be engineered to recapitulate tumor tissue has dramatically increased their use in cancer research. In this review, we discuss the potential of organoids to close the gap between preclinical in vitro and in vivo models as well as clinical trials in cancer research focusing on drug investigation and development. MDPI 2021-09-26 /pmc/articles/PMC8507862/ /pubmed/34638297 http://dx.doi.org/10.3390/cancers13194812 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Kastner, Carolin Hendricks, Anne Deinlein, Hanna Hankir, Mohammed Germer, Christoph-Thomas Schmidt, Stefanie Wiegering, Armin Organoid Models for Cancer Research—From Bed to Bench Side and Back |
title | Organoid Models for Cancer Research—From Bed to Bench Side and Back |
title_full | Organoid Models for Cancer Research—From Bed to Bench Side and Back |
title_fullStr | Organoid Models for Cancer Research—From Bed to Bench Side and Back |
title_full_unstemmed | Organoid Models for Cancer Research—From Bed to Bench Side and Back |
title_short | Organoid Models for Cancer Research—From Bed to Bench Side and Back |
title_sort | organoid models for cancer research—from bed to bench side and back |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8507862/ https://www.ncbi.nlm.nih.gov/pubmed/34638297 http://dx.doi.org/10.3390/cancers13194812 |
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