Evidence map›Paper›PMID 40641603›Full record

ArticleFrontiers in cell and developmental biology2025

Comparative analysis of small molecule and growth factor-derived human induced pluripotent stem cell-derived hepatocyte-like cells.

Faizal Z Asumda, Shadia Alzoubi, Kiyasha Padarath, Kimya Jones, Ravindra Kolhe, Ashis Kumar Mondal, Ahmet Alptekin, Wenbo Zhi, Tae Jin Lee, Robert C Huebert and 3 more

Abstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2025. 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

13 authors.

Faizal Z Asumda *Medical College of Georgia-Augusta University Department of Pediatrics, Augusta, GA, United States.
Shadia AlzoubiMedical College of Georgia-Augusta University Department of Pediatrics, Augusta, GA, United States.
Kiyasha PadarathMedical College of Georgia-Augusta University Department of Pediatrics, Augusta, GA, United States.
Kimya JonesMedical College of Georgia-Augusta University Department of Pathology, Augusta, GA, United States.
Ravindra KolheMedical College of Georgia-Augusta University Department of Pathology, Augusta, GA, United States.
Ashis Kumar MondalMedical College of Georgia-Augusta University Department of Pathology, Augusta, GA, United States.
Ahmet AlptekinMedical College of Georgia-Augusta University Department of Pathology, Augusta, GA, United States.
Wenbo ZhiMedical College of Georgia-Augusta University Vascular Biology Center, Augusta, GA, United States.
Tae Jin LeeMedical College of Georgia-Augusta University Center for Biotechnology and Genomics, Augusta, GA, United States.
Robert C HuebertMayo Clinic Division of Gastroenterology and Hepatology, Rochester, MN, United States.
Nathan P StaffMayo Clinic Department of Neurology Rochester, Rochester, MN, United States.
Lewis R RobertsMayo Clinic Division of Gastroenterology and Hepatology, Rochester, MN, United States.
Lindsey A KirkebyMayo Clinic Center for Regenerative Biotherapeutics, Rochester, MN, United States.

Funding

Molecular Mechanisms of Cholestatic FibrogenesisR01DK117861 · NIDDK · MAYO CLINIC ROCHESTER · PI Robert Christian Huebert · 2019 to 2026
$2.8M
NIDDK NIH HHS R01 DK117861
6 · The paper itself

Abstract

The growth factor and small molecule protocol are the two primary approaches for generating human induced pluripotent stem cell-derived hepatocyte-like cells (iPSC-HLCs). We compared the efficacy of the growth factor and small molecule protocols across fifteen different human iPSC lines. Morphological assessment, relative quantification of gene expression, protein expression and proteomic studies were carried out. HLCs derived from the growth factor protocol displayed mature hepatocyte morphological features including a raised, polygonal shape with well-defined refractile borders, granular cytoplasm with lipid droplets and/or vacuoles with multiple spherical nuclei or a large centrally located nucleus; significantly elevated hepatocyte gene and protein expression including AFP, HNF4A, ALBUMIN, and proteomic and metabolic features that are more aligned with a mature phenotype. HLCs derived from the small molecule protocol showed a dedifferentiated, proliferative phenotype that is more akin to liver tumor-derived cell lines. These experimental results suggest that HLCs derived from growth factors are better suited for studies of metabolism, biotransformation, and viral infection.

Indexed as

growth factorshepatocyte-like cellshepatocytesinduced pluripotent stem cellssmall molecules

Identifiers

PMID40641603
PMCPMC12240953

What Socratic holds

Textmetadata
LicenceCC BY
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.