Evidence map›Paper›PMID 37012138›Full record

ReviewSeminars in perinatology2023

Unlocking the potential of induced pluripotent stem cells for neonatal disease modeling and drug development.

Ziyi Liu, Bonny Lami, Laertis Ikonomou, Mingxia Gu

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in perinatology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 43% of its field
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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Review
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

4 authors at 3 institutions in 1 country.

Ziyi LiuPerinatal Institute, Division of Pulmonary Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States; Center for Stem Cell and Organoid Medicine, CuSTOM, Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States; Department of Pediatrics, University of Cincinnati School of Medicine, Cincinnati, OH, United States.
Bonny LamiPerinatal Institute, Division of Pulmonary Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States; Center for Stem Cell and Organoid Medicine, CuSTOM, Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States; Department of Pediatrics, University of Cincinnati School of Medicine, Cincinnati, OH, United States.
Laertis IkonomouDepartment of Oral Biology, University at Buffalo, The State University of New York, Buffalo, NY, United States; Division of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine, University at Buffalo, The State University of New York, Buffalo, NY, United States; Cell, Gene and Tissue Engineering Center, University at Buffalo, The State University of New York, Buffalo, NY, United States. Electronic address: laertisi@buffalo.edu.
Mingxia GuPerinatal Institute, Division of Pulmonary Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States; Center for Stem Cell and Organoid Medicine, CuSTOM, Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States; Department of Pediatrics, University of Cincinnati School of Medicine, Cincinnati, OH, United States. Electronic address: mingxia.gu@cchmc.org.
Cincinnati Children's Hospital Medical Center · USUniversity at Buffalo, State University of New York · USUniversity of Cincinnati · US

Funding

Gene regulatory networks in early lung epithelial cell fate decisionsR01HL158965 · NHLBI · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI Laertis Ikonomou · 2023 to 2026
$2.5M
Elucidating the FOXF1 gene regulatory network in human alveologenesisR01HL166283 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Mingxia Gu · 2023 to 2026
$1.9M
Uncovering compensatory mechanisms in family members with disease causing mutations of pulmonary hypertensionR00HL135258 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI GU, MINGXIA · 2020 to 2022
$747k
Mechanisms of Cell Death and Inflammation in Chemotherapy-Induced Oral MucositisR56DE028545 · NIDCR · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI DIAZ, PATRICIA · 2020 to 2020
$657k
NHLBI NIH HHS R00 HL135258NHLBI NIH HHS R01 HL158965NHLBI NIH HHS R01 HL166283NIDCR NIH HHS R56 DE028545
6 · The paper itself

Abstract

Neonatal lung and heart diseases, albeit rare, can result in poor quality of life, often require long-term management and/or organ transplantation. For example, Congenital Heart Disease (CHD) is one of the most common type of congenital disabilities, affecting nearly 1% of the newborns, and has complex and multifactorial causes, including genetic predisposition and environmental influences. To develop new strategies for heart and lung regeneration in CHD and neonatal lung disease, human induced pluripotent stem cells (hiPSCs) provide a unique and personalized platform for future cell replacement therapy and high-throughput drug screening. Additionally, given the differentiation potential of iPSCs, cardiac cell types such as cardiomyocytes, endothelial cells, and fibroblasts and lung cell types such Type II alveolar epithelial cells can be derived in a dish to study the fundamental pathology during disease progression. In this review, we discuss the applications of hiPSCs in understanding the molecular mechanisms and cellular phenotypes of CHD (e.g., structural heart defect, congenital valve disease, and congenital channelopathies) and congenital lung diseases, such as surfactant deficiencies and Brain-Lung-Thyroid syndrome. We also provide future directions for generating mature cell types from iPSCs, and more complex hiPSC-based systems using three-dimensional (3D) organoids and tissue-engineering. With these potential advancements, the promise that hiPSCs will deliver new CHD and neonatal lung disease treatments may soon be fulfilled.

Indexed as

Heart Defects, CongenitalInduced Pluripotent Stem CellsInfant, Newborn, DiseasesLung DiseasesDrug DevelopmentEndothelial CellsHumansInfant, NewbornQuality of LifeCongenital heart diseaseCongenital lung disorderDisease modelingDrug developmentHuman induced pluripotent stem cells

Identifiers

PMID37012138
PMCPMC10133195
OpenAlexW4323926481

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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 Socratic graph.