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dc.contributor.authorGnecco, Juan S
dc.contributor.authorBrown, Alex T
dc.contributor.authorKan, Ellen L
dc.contributor.authorBaugh, Lauren
dc.contributor.authorIves, Clara
dc.contributor.authorLoring, Megan
dc.contributor.authorGriffith, Linda G
dc.date.accessioned2022-01-26T15:37:18Z
dc.date.available2021-10-27T19:53:20Z
dc.date.available2022-01-26T15:37:18Z
dc.date.issued2020-11
dc.identifier.issn1526-8004
dc.identifier.urihttps://hdl.handle.net/1721.1/133525.2
dc.description.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.en_US
dc.language.isoen
dc.publisherGeorg Thieme Verlag KGen_US
dc.relation.isversionofhttp://dx.doi.org/10.1055/S-0040-1719084en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourceThieme Medical Publishersen_US
dc.titlePhysiomimetic Models of Adenomyosisen_US
dc.typeArticleen_US
dc.contributor.departmentMassachusetts Institute of Technology. Center for Gynepathology Research
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineering
dc.relation.journalSeminars in Reproductive Medicineen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2021-09-03T12:14:58Z
dspace.orderedauthorsGnecco, JS; Brown, AT; Kan, EL; Baugh, L; Ives, C; Loring, M; Griffith, LGen_US
dspace.date.submission2021-09-03T12:14:59Z
mit.journal.volume38en_US
mit.journal.issue02/03en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work Neededen_US


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