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Current status and future outlook for patient‐derived cancer models from a rare cancer research perspective
Rare cancers are a group of approximately 200 malignancies with extremely low incidences and with a wide variety of genotypes and phenotypes. Collectively, they are more common than any single malignancy. However, given the small numbers of individuals diagnosed with rare cancers, it is difficult to...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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John Wiley and Sons Inc.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7935796/ https://www.ncbi.nlm.nih.gov/pubmed/32986888 http://dx.doi.org/10.1111/cas.14669 |
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author | Kondo, Tadashi |
author_facet | Kondo, Tadashi |
author_sort | Kondo, Tadashi |
collection | PubMed |
description | Rare cancers are a group of approximately 200 malignancies with extremely low incidences and with a wide variety of genotypes and phenotypes. Collectively, they are more common than any single malignancy. However, given the small numbers of individuals diagnosed with rare cancers, it is difficult to design clinical trials with sufficient patient numbers. Therefore, few effective anticancer drugs have been developed, and evidence‐based medicine is not always feasible for rare cancers. Consequently, their clinical outcomes are generally poorer. Cancer research requires adequate models that faithfully recapitulate molecular features and reproduce treatment responses of the original tumors. Such models allow us to focus on more efficacious drugs in the clinical studies. For rare cancers, patient‐derived cancer models are particularly important because the enrollment of sufficient patients is rarely attainable within a reasonable period of time. However, extremely few models are available for rare cancers. For example, cell lines and xenografts are available for only a limited number of histological subtypes of sarcomas; therefore, most sarcoma research is performed without such models, and a lack of adequate cancer models causes a lag in therapeutic development. The establishment of novel rare cancer models will dramatically facilitate rare cancer research and treatment development in the near future. This review focuses on the status of patient‐derived rare cancer models and discusses their pivotal problems and possibilities, using sarcomas as a representative rare cancer type. Multi‐institutional collaboration will help address the scarcity of patient‐derived rare cancer models. |
format | Online Article Text |
id | pubmed-7935796 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79357962021-03-15 Current status and future outlook for patient‐derived cancer models from a rare cancer research perspective Kondo, Tadashi Cancer Sci Review Articles Rare cancers are a group of approximately 200 malignancies with extremely low incidences and with a wide variety of genotypes and phenotypes. Collectively, they are more common than any single malignancy. However, given the small numbers of individuals diagnosed with rare cancers, it is difficult to design clinical trials with sufficient patient numbers. Therefore, few effective anticancer drugs have been developed, and evidence‐based medicine is not always feasible for rare cancers. Consequently, their clinical outcomes are generally poorer. Cancer research requires adequate models that faithfully recapitulate molecular features and reproduce treatment responses of the original tumors. Such models allow us to focus on more efficacious drugs in the clinical studies. For rare cancers, patient‐derived cancer models are particularly important because the enrollment of sufficient patients is rarely attainable within a reasonable period of time. However, extremely few models are available for rare cancers. For example, cell lines and xenografts are available for only a limited number of histological subtypes of sarcomas; therefore, most sarcoma research is performed without such models, and a lack of adequate cancer models causes a lag in therapeutic development. The establishment of novel rare cancer models will dramatically facilitate rare cancer research and treatment development in the near future. This review focuses on the status of patient‐derived rare cancer models and discusses their pivotal problems and possibilities, using sarcomas as a representative rare cancer type. Multi‐institutional collaboration will help address the scarcity of patient‐derived rare cancer models. John Wiley and Sons Inc. 2021-02-06 2021-03 /pmc/articles/PMC7935796/ /pubmed/32986888 http://dx.doi.org/10.1111/cas.14669 Text en © 2020 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Review Articles Kondo, Tadashi Current status and future outlook for patient‐derived cancer models from a rare cancer research perspective |
title | Current status and future outlook for patient‐derived cancer models from a rare cancer research perspective |
title_full | Current status and future outlook for patient‐derived cancer models from a rare cancer research perspective |
title_fullStr | Current status and future outlook for patient‐derived cancer models from a rare cancer research perspective |
title_full_unstemmed | Current status and future outlook for patient‐derived cancer models from a rare cancer research perspective |
title_short | Current status and future outlook for patient‐derived cancer models from a rare cancer research perspective |
title_sort | current status and future outlook for patient‐derived cancer models from a rare cancer research perspective |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7935796/ https://www.ncbi.nlm.nih.gov/pubmed/32986888 http://dx.doi.org/10.1111/cas.14669 |
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