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Patient-derived rectal cancer organoids—applications in basic and translational cancer research
Colorectal cancer (CRC) is one of the most commonly diagnosed cancers and among the leading causes of death in both men and women. Rectal cancer (RC) is particularly challenging compared with colon cancer as the treatment after diagnosis of RC is more complex on account of its narrow anatomical loca...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9360321/ https://www.ncbi.nlm.nih.gov/pubmed/35957894 http://dx.doi.org/10.3389/fonc.2022.922430 |
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author | Yan, Yumeng Cheong, Io Hong Chen, Peizhan Li, Xiaoguang Wang, Xianli Wang, Hui |
author_facet | Yan, Yumeng Cheong, Io Hong Chen, Peizhan Li, Xiaoguang Wang, Xianli Wang, Hui |
author_sort | Yan, Yumeng |
collection | PubMed |
description | Colorectal cancer (CRC) is one of the most commonly diagnosed cancers and among the leading causes of death in both men and women. Rectal cancer (RC) is particularly challenging compared with colon cancer as the treatment after diagnosis of RC is more complex on account of its narrow anatomical location in the pelvis adjacent to the urogenital organs. More and more existing studies have begun to refine the research on RC and colon cancer separately. Early diagnosis and multiple treatment strategies optimize outcomes for individual patients. However, the need for more accurate and precise models to facilitate RC research is underscored due to the heterogeneity of clinical response and morbidity interrelated with radical surgery. Organoids generated from biopsies of patients have developed as powerful models to recapitulate many aspects of their primary tissue, consisting of 3-D self-organizing structures, which shed great light on the applications in both biomedical and clinical research. As the preclinical research models for RC are usually confused with colon cancer, research on patient-derived RC organoid models enable personalized analysis of cancer pathobiology, organizational function, and tumor initiation and progression. In this review, we discuss the various applications of patient-derived RC organoids over the past two years in basic cancer biology and clinical translation, including sequencing analysis, drug screening, precision therapy practice, tumor microenvironment studies, and genetic engineering opportunities. |
format | Online Article Text |
id | pubmed-9360321 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93603212022-08-10 Patient-derived rectal cancer organoids—applications in basic and translational cancer research Yan, Yumeng Cheong, Io Hong Chen, Peizhan Li, Xiaoguang Wang, Xianli Wang, Hui Front Oncol Oncology Colorectal cancer (CRC) is one of the most commonly diagnosed cancers and among the leading causes of death in both men and women. Rectal cancer (RC) is particularly challenging compared with colon cancer as the treatment after diagnosis of RC is more complex on account of its narrow anatomical location in the pelvis adjacent to the urogenital organs. More and more existing studies have begun to refine the research on RC and colon cancer separately. Early diagnosis and multiple treatment strategies optimize outcomes for individual patients. However, the need for more accurate and precise models to facilitate RC research is underscored due to the heterogeneity of clinical response and morbidity interrelated with radical surgery. Organoids generated from biopsies of patients have developed as powerful models to recapitulate many aspects of their primary tissue, consisting of 3-D self-organizing structures, which shed great light on the applications in both biomedical and clinical research. As the preclinical research models for RC are usually confused with colon cancer, research on patient-derived RC organoid models enable personalized analysis of cancer pathobiology, organizational function, and tumor initiation and progression. In this review, we discuss the various applications of patient-derived RC organoids over the past two years in basic cancer biology and clinical translation, including sequencing analysis, drug screening, precision therapy practice, tumor microenvironment studies, and genetic engineering opportunities. Frontiers Media S.A. 2022-07-26 /pmc/articles/PMC9360321/ /pubmed/35957894 http://dx.doi.org/10.3389/fonc.2022.922430 Text en Copyright © 2022 Yan, Cheong, Chen, Li, Wang and Wang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Yan, Yumeng Cheong, Io Hong Chen, Peizhan Li, Xiaoguang Wang, Xianli Wang, Hui Patient-derived rectal cancer organoids—applications in basic and translational cancer research |
title | Patient-derived rectal cancer organoids—applications in basic and translational cancer research |
title_full | Patient-derived rectal cancer organoids—applications in basic and translational cancer research |
title_fullStr | Patient-derived rectal cancer organoids—applications in basic and translational cancer research |
title_full_unstemmed | Patient-derived rectal cancer organoids—applications in basic and translational cancer research |
title_short | Patient-derived rectal cancer organoids—applications in basic and translational cancer research |
title_sort | patient-derived rectal cancer organoids—applications in basic and translational cancer research |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9360321/ https://www.ncbi.nlm.nih.gov/pubmed/35957894 http://dx.doi.org/10.3389/fonc.2022.922430 |
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