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Physiomimetic Models of Adenomyosis

Authors :
Clara Ives
Linda G. Griffith
Alexander Thomas Brown
Juan S. Gnecco
Lauren M. Baugh
M. Loring
Ellen L. Kan
Source :
Thieme Medical Publishers, Seminars in Reproductive Medicine
Publication Year :
2020
Publisher :
Georg Thieme Verlag KG, 2020.

Abstract

© 2020 by Thieme Medical Publishers, Inc., 333 Seventh Avenue, New York, NY 10001, USA. 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.

Details

ISSN :
15264564 and 15268004
Volume :
38
Database :
OpenAIRE
Journal :
Seminars in Reproductive Medicine
Accession number :
edsair.doi.dedup.....bde4900b8ed3d89ad033b64f52489f1a
Full Text :
https://doi.org/10.1055/s-0040-1719084