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Endometrial Cancer Patient-Derived Xenograft Models: A Systematic Review
Background: Because patient-derived xenograft (PDX) models resemble the original tumors, they can be used as platforms to find target agents for precision medicine and to study characteristics of tumor biology such as clonal evolution and microenvironment interactions. The aim of this review was to...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9100787/ https://www.ncbi.nlm.nih.gov/pubmed/35566732 http://dx.doi.org/10.3390/jcm11092606 |
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author | Tanaka, Tomohito Nishie, Ruri Ueda, Shoko Miyamoto, Shunsuke Hashida, Sousuke Konishi, Hiromi Terada, Shinichi Kogata, Yuhei Sasaki, Hiroshi Tsunetoh, Satoshi Taniguchi, Kohei Komura, Kazumasa Ohmichi, Masahide |
author_facet | Tanaka, Tomohito Nishie, Ruri Ueda, Shoko Miyamoto, Shunsuke Hashida, Sousuke Konishi, Hiromi Terada, Shinichi Kogata, Yuhei Sasaki, Hiroshi Tsunetoh, Satoshi Taniguchi, Kohei Komura, Kazumasa Ohmichi, Masahide |
author_sort | Tanaka, Tomohito |
collection | PubMed |
description | Background: Because patient-derived xenograft (PDX) models resemble the original tumors, they can be used as platforms to find target agents for precision medicine and to study characteristics of tumor biology such as clonal evolution and microenvironment interactions. The aim of this review was to identify articles on endometrial cancer PDXs (EC-PDXs) and verify the methodology and outcomes. Methods: We used PubMed to research and identify articles on EC-PDX. The data were analyzed descriptively. Results: Post literature review, eight studies were selected for the systematic review. Eighty-five EC-PDXs were established from 173 patients with EC, with a total success rate of 49.1%. A 1–10 mm(3) fragment was usually implanted. Fresh-fragment implantation had higher success rates than using overnight-stored or frozen fragments. Primary tumors were successfully established with subcutaneous implantation, but metastasis rarely occurred; orthotopic implantation via minced tumor cell injection was better for metastatic models. The success rate did not correspond to immunodeficiency grades, and PDXs using nude mice reduced costs. The tumor growth period ranged from 2 weeks to 13 months. Similar characteristics were observed between primary tumors and PDXs, including pathological findings, gene mutations, and gene expression. Conclusion: EC-PDXs are promising tools for translational research because they closely resemble the features of tumors in patients and retain molecular and histological features of the disease. |
format | Online Article Text |
id | pubmed-9100787 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-91007872022-05-14 Endometrial Cancer Patient-Derived Xenograft Models: A Systematic Review Tanaka, Tomohito Nishie, Ruri Ueda, Shoko Miyamoto, Shunsuke Hashida, Sousuke Konishi, Hiromi Terada, Shinichi Kogata, Yuhei Sasaki, Hiroshi Tsunetoh, Satoshi Taniguchi, Kohei Komura, Kazumasa Ohmichi, Masahide J Clin Med Review Background: Because patient-derived xenograft (PDX) models resemble the original tumors, they can be used as platforms to find target agents for precision medicine and to study characteristics of tumor biology such as clonal evolution and microenvironment interactions. The aim of this review was to identify articles on endometrial cancer PDXs (EC-PDXs) and verify the methodology and outcomes. Methods: We used PubMed to research and identify articles on EC-PDX. The data were analyzed descriptively. Results: Post literature review, eight studies were selected for the systematic review. Eighty-five EC-PDXs were established from 173 patients with EC, with a total success rate of 49.1%. A 1–10 mm(3) fragment was usually implanted. Fresh-fragment implantation had higher success rates than using overnight-stored or frozen fragments. Primary tumors were successfully established with subcutaneous implantation, but metastasis rarely occurred; orthotopic implantation via minced tumor cell injection was better for metastatic models. The success rate did not correspond to immunodeficiency grades, and PDXs using nude mice reduced costs. The tumor growth period ranged from 2 weeks to 13 months. Similar characteristics were observed between primary tumors and PDXs, including pathological findings, gene mutations, and gene expression. Conclusion: EC-PDXs are promising tools for translational research because they closely resemble the features of tumors in patients and retain molecular and histological features of the disease. MDPI 2022-05-06 /pmc/articles/PMC9100787/ /pubmed/35566732 http://dx.doi.org/10.3390/jcm11092606 Text en © 2022 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 Tanaka, Tomohito Nishie, Ruri Ueda, Shoko Miyamoto, Shunsuke Hashida, Sousuke Konishi, Hiromi Terada, Shinichi Kogata, Yuhei Sasaki, Hiroshi Tsunetoh, Satoshi Taniguchi, Kohei Komura, Kazumasa Ohmichi, Masahide Endometrial Cancer Patient-Derived Xenograft Models: A Systematic Review |
title | Endometrial Cancer Patient-Derived Xenograft Models: A Systematic Review |
title_full | Endometrial Cancer Patient-Derived Xenograft Models: A Systematic Review |
title_fullStr | Endometrial Cancer Patient-Derived Xenograft Models: A Systematic Review |
title_full_unstemmed | Endometrial Cancer Patient-Derived Xenograft Models: A Systematic Review |
title_short | Endometrial Cancer Patient-Derived Xenograft Models: A Systematic Review |
title_sort | endometrial cancer patient-derived xenograft models: a systematic review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9100787/ https://www.ncbi.nlm.nih.gov/pubmed/35566732 http://dx.doi.org/10.3390/jcm11092606 |
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