Evidence map›Paper›PMID 40558550›Full record

ArticleCells2025

Transcriptomic Profiling of iPS Cell-Derived Hepatocyte-like Cells Reveals Their Close Similarity to Primary Liver Hepatocytes.

Saqlain Suleman, Sharmin Alhaque, Andrew Guo, Aaron Zhang, Serena Fawaz, Stefany Perera, Mohammad S Khalifa, Hassan Rashidi, David C Hay, Michael Themis

Abstract read
In one paragraph

Article in Cells, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

10 authors.

Saqlain SulemanSchool of Life Sciences, Faculty of Science and Engineering, Angila Ruskin University, Cambridge CB1 2PU, UK.ORCID 0000-0003-4610-9397
Sharmin AlhaqueDivision of Biosciences, Department of Life Sciences, College of Health, Medicine & Life Sciences, Brunel University of London, London UB8 3PH, UK.
Andrew GuoBiomavericks, 64 Nile Street, London N1 7SR, UK.
Aaron ZhangBiomavericks, 64 Nile Street, London N1 7SR, UK.
Serena FawazDivision of Biosciences, Department of Life Sciences, College of Health, Medicine & Life Sciences, Brunel University of London, London UB8 3PH, UK.
Stefany PereraDivision of Biosciences, Department of Life Sciences, College of Health, Medicine & Life Sciences, Brunel University of London, London UB8 3PH, UK.
Mohammad S KhalifaDivision of Biosciences, Department of Life Sciences, College of Health, Medicine & Life Sciences, Brunel University of London, London UB8 3PH, UK.
Hassan RashidiCentre for Regenerative Medicine, The University of Edinburgh, Edinburgh EH16 4UU, UK.ORCID 0000-0001-8078-6688
David C HayCentre for Regenerative Medicine, The University of Edinburgh, Edinburgh EH16 4UU, UK.ORCID 0000-0002-7593-5973
Michael ThemisDivision of Biosciences, Department of Life Sciences, College of Health, Medicine & Life Sciences, Brunel University of London, London UB8 3PH, UK.ORCID 0000-0002-6719-4271

Funding

National Centre for the Replacement Refinement and Reduction of Animals in Research SBRI CRACK-IT InMutaGene Challenge 21Testavec N/A
6 · The paper itself

Abstract

Human-induced pluripotent stem cell (iPSC)-derived hepatocyte-like cells (HLCs) have been shown to be useful for the development of cell-based regenerative strategies and for modelling drug discovery. However, stem cell-derived HLCs are not identical in nature to primary human hepatocytes (PHHs), which could affect the cell phenotype and, potentially, model reliability. Therefore, we employed the in-depth gene expression profiling of HLCs and other important and relevant cell types, which led to the identification of clear similarities and differences between them at the transcriptional level. Through gene set enrichment analysis, we identified that genes that are critical for immune signalling pathways become downregulated upon HLC differentiation. Our analysis also found that TAV.HLCs exhibit a mild gene signature characteristic of acute lymphoblastic leukaemia, but not other selected cancers. Importantly, HLCs present significant similarity to PHHs, making them genuinely valuable for modelling human liver biology in vitro and for the development of prototype cell-based therapies for pre-clinical testing.

Indexed as

Gene Expression ProfilingHepatocytesInduced Pluripotent Stem CellsLiverTranscriptomeCell DifferentiationCells, CulturedHumansdifferentiationliverstem cellstranscriptomic

Identifiers

PMID40558550
PMCPMC12190443

What OpenQuestion 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 OpenQuestion graph.