Evidence map›Paper›PMID 42694293›Full record

ReviewBiomaterials research2026

Female Reproductive Tract Modeling through Advanced 3D Biomimetic Platforms.

Chaeyoun Lee, Yoonseo Choi, Hyejin Lee, Seunghee Kim, Jeong Su Park, Young Min Shin, Dae Hyeok Yang, Gun-Jae Jeong, Dong Nyoung Heo, Jeong-Kee Yoon and 6 more

Abstract readReview
In one paragraph

Review in Biomaterials research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Chaeyoun LeeDepartment of Biological Sciences, Sookmyung Women's University, Seoul 04312, Republic of Korea.
Yoonseo ChoiDepartment of Biological Sciences, Sookmyung Women's University, Seoul 04312, Republic of Korea.
Hyejin LeeDepartment of Biological Sciences, Sookmyung Women's University, Seoul 04312, Republic of Korea.
Seunghee KimDepartment of Biological Sciences, Sookmyung Women's University, Seoul 04312, Republic of Korea.ORCID https://orcid.org/0009-0004-4148-247X
Jeong Su ParkPLCOskin Co. Ltd., Seoul 03721, Republic of Korea.
Young Min ShinDepartment of Biological Sciences, Sookmyung Women's University, Seoul 04312, Republic of Korea.
Dae Hyeok YangDepartment of Biologics and Engineering, The Catholic University of Korea, Bucheon-si 14662, Gyeonggi-do, Republic of Korea.
Gun-Jae JeongSchool of Nanomedical Engineering, Korea National University of Transportation, Chungju 27469, Republic of Korea.
Dong Nyoung HeoDepartment of Dental Materials, School of Dentistry, Kyung Hee University, Seoul 02447, Republic of Korea.ORCID https://orcid.org/0000-0002-7717-7184
Jeong-Kee YoonDepartment of Systems Biotechnology, Chung-Ang University, Anseong-Si, Gyeonggi-Do 17546, Republic of Korea.
Junhyeong YimDepartment of Biological Sciences, Sookmyung Women's University, Seoul 04312, Republic of Korea.
Jongmin KimDepartment of Biological Sciences, Sookmyung Women's University, Seoul 04312, Republic of Korea.
Yonghwan KimDepartment of Biological Sciences, Sookmyung Women's University, Seoul 04312, Republic of Korea.
Kyung Hyun YooDepartment of Biological Sciences, Sookmyung Women's University, Seoul 04312, Republic of Korea.
Jung Bok LeeDepartment of Biological Sciences, Sookmyung Women's University, Seoul 04312, Republic of Korea.
Byung-Chul LeeDepartment of Biological Sciences, Sookmyung Women's University, Seoul 04312, Republic of Korea.ORCID https://orcid.org/0000-0003-0358-6855

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The female reproductive tract (FRT) is an intricate and highly regulated network comprising the ovaries, fallopian tubes, uterus, cervix, and placenta, which work in concert to govern complex reproductive functions. Dysfunction within any of these organs can lead to serious pathological conditions, including infertility, pregnancy complications, and gynecological cancers. Although conventional 2-dimensional (2D) cultures and animal models have provided foundational insights, they are limited in their ability to recapitulate human-specific 3D tissue architecture and dynamic biochemical microenvironments. To address these limitations, organoid and organ-on-a-chip (OoC) technologies have emerged as a powerful 3D biomimetic platform. Organoids preserve epithelial identity, cellular heterogeneity, and patient-specific phenotypes, whereas OoC systems incorporate microfluidic flow, mechanical stimulation, and multicompartmental interfaces to model organ-level physiology. This review provides an organ-specific overview of recent advances in organoid and OoC systems across the FRT, discusses their advantages and current limitations relative to traditional models, and highlights their potential to transform reproductive biology research, disease modeling, and translational applications.

Identifiers

PMID42694293
PMCPMC13538936

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.