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Physiomimetic Models of Adenomyosis
Adenomyosis remains an enigmatic disease in the clinical and research communities. The high prevalence, diversity of morphological and symptomatic presentations, array of potential etiological explanations, and variable response to existing interventions suggest that different subgroups of patients...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Thieme Medical Publishers, Inc.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803459/ https://www.ncbi.nlm.nih.gov/pubmed/33176387 http://dx.doi.org/10.1055/s-0040-1719084 |
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author | Gnecco, Juan S. Brown, Alex T. Kan, Ellen L. Baugh, Lauren Ives, Clara Loring, Megan Griffith, Linda G. |
author_facet | Gnecco, Juan S. Brown, Alex T. Kan, Ellen L. Baugh, Lauren Ives, Clara Loring, Megan Griffith, Linda G. |
author_sort | Gnecco, Juan S. |
collection | PubMed |
description | Adenomyosis remains an enigmatic disease in the clinical and research communities. The high prevalence, diversity of morphological and symptomatic presentations, array of potential etiological explanations, and variable response to existing interventions suggest that different subgroups of patients with distinguishable mechanistic drivers of disease may exist. These factors, combined with the weak links to genetic predisposition, make the entire spectrum of the human condition challenging to model in animals. Here, after an overview of current approaches, a vision for applying physiomimetic modeling to adenomyosis is presented. Physiomimetics combines a system's biology analysis of patient populations to generate hypotheses about mechanistic bases for stratification with in vitro patient avatars to test these hypotheses. A substantial foundation for three-dimensional (3D) tissue engineering of adenomyosis lesions exists in several disparate areas: epithelial organoid technology; synthetic biomaterials matrices for epithelial–stromal coculture; smooth muscle 3D tissue engineering; and microvascular tissue engineering. These approaches can potentially be combined with microfluidic platform technologies to model the lesion microenvironment and can potentially be coupled to other microorgan systems to examine systemic effects. In vitro patient-derived models are constructed to answer specific questions leading to target identification and validation in a manner that informs preclinical research and ultimately clinical trial design. |
format | Online Article Text |
id | pubmed-7803459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Thieme Medical Publishers, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78034592021-01-14 Physiomimetic Models of Adenomyosis Gnecco, Juan S. Brown, Alex T. Kan, Ellen L. Baugh, Lauren Ives, Clara Loring, Megan Griffith, Linda G. Semin Reprod Med Adenomyosis remains an enigmatic disease in the clinical and research communities. The high prevalence, diversity of morphological and symptomatic presentations, array of potential etiological explanations, and variable response to existing interventions suggest that different subgroups of patients with distinguishable mechanistic drivers of disease may exist. These factors, combined with the weak links to genetic predisposition, make the entire spectrum of the human condition challenging to model in animals. Here, after an overview of current approaches, a vision for applying physiomimetic modeling to adenomyosis is presented. Physiomimetics combines a system's biology analysis of patient populations to generate hypotheses about mechanistic bases for stratification with in vitro patient avatars to test these hypotheses. A substantial foundation for three-dimensional (3D) tissue engineering of adenomyosis lesions exists in several disparate areas: epithelial organoid technology; synthetic biomaterials matrices for epithelial–stromal coculture; smooth muscle 3D tissue engineering; and microvascular tissue engineering. These approaches can potentially be combined with microfluidic platform technologies to model the lesion microenvironment and can potentially be coupled to other microorgan systems to examine systemic effects. In vitro patient-derived models are constructed to answer specific questions leading to target identification and validation in a manner that informs preclinical research and ultimately clinical trial design. Thieme Medical Publishers, Inc. 2020-05 2020-11-09 /pmc/articles/PMC7803459/ /pubmed/33176387 http://dx.doi.org/10.1055/s-0040-1719084 Text en The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. ( https://creativecommons.org/licenses/by-nc-nd/4.0/ ) https://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License, which permits unrestricted reproduction and distribution, for non-commercial purposes only; and use and reproduction, but not distribution, of adapted material for non-commercial purposes only, provided the original work is properly cited. |
spellingShingle | Gnecco, Juan S. Brown, Alex T. Kan, Ellen L. Baugh, Lauren Ives, Clara Loring, Megan Griffith, Linda G. Physiomimetic Models of Adenomyosis |
title | Physiomimetic Models of Adenomyosis |
title_full | Physiomimetic Models of Adenomyosis |
title_fullStr | Physiomimetic Models of Adenomyosis |
title_full_unstemmed | Physiomimetic Models of Adenomyosis |
title_short | Physiomimetic Models of Adenomyosis |
title_sort | physiomimetic models of adenomyosis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803459/ https://www.ncbi.nlm.nih.gov/pubmed/33176387 http://dx.doi.org/10.1055/s-0040-1719084 |
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