Evidence map›Paper›PMID 38598342›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

Identification and removal of unexpected proliferative off-target cells emerging after iPSC-derived pancreatic islet cell implantation.

Hideyuki Hiyoshi, Kensuke Sakuma, Shinya Asano, Stephanie C Napier, Shuhei Konagaya, Taisuke Mochida, Hikaru Ueno, Takeshi Watanabe, Yoshiaki Kassai, Hirokazu Matsumoto and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

7 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
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  6. Direct in vivo reprogramming to relieve tissue ischemia via induced vasculogenesis.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  7. 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

12 authors at 2 institutions in 1 country.

Hideyuki HiyoshiTakeda-CiRA Discovery and Innovation, Takeda Pharmaceutical Company Limited, Fujisawa, Kanagawa 251-8555, Japan.ORCID 0000-0002-9416-0894
Kensuke SakumaTakeda-CiRA Discovery and Innovation, Takeda Pharmaceutical Company Limited, Fujisawa, Kanagawa 251-8555, Japan.
Shinya AsanoAxcelead Drug Discovery Partners, Inc., Fujisawa, Kanagawa 251-8555, Japan.
Stephanie C NapierTakeda-CiRA Discovery and Innovation, Takeda Pharmaceutical Company Limited, Fujisawa, Kanagawa 251-8555, Japan.
Shuhei KonagayaTakeda-CiRA Joint Program for iPS Cell Applications, Fujisawa, Kanagawa 251-8555, Japan.
Taisuke MochidaTakeda-CiRA Discovery and Innovation, Takeda Pharmaceutical Company Limited, Fujisawa, Kanagawa 251-8555, Japan.
Hikaru UenoTakeda-CiRA Discovery and Innovation, Takeda Pharmaceutical Company Limited, Fujisawa, Kanagawa 251-8555, Japan.
Takeshi WatanabeDrug Safety Research and Evaluation, Takeda Pharmaceutical Company Limited, Fujisawa, Kanagawa 251-8555, Japan.
Yoshiaki KassaiTakeda-CiRA Discovery and Innovation, Takeda Pharmaceutical Company Limited, Fujisawa, Kanagawa 251-8555, Japan.
Hirokazu MatsumotoTakeda-CiRA Discovery and Innovation, Takeda Pharmaceutical Company Limited, Fujisawa, Kanagawa 251-8555, Japan.
Ryo ItoTakeda-CiRA Discovery and Innovation, Takeda Pharmaceutical Company Limited, Fujisawa, Kanagawa 251-8555, Japan.
Taro ToyodaTakeda-CiRA Joint Program for iPS Cell Applications, Fujisawa, Kanagawa 251-8555, Japan.ORCID 0000-0002-2948-0525
Takeda (Japan) · JPKyoto University · JP

Funding

T-CiRA budget from Takeda Pharmaceutical Company Limited
6 · The paper itself

Abstract

Differentiation of pancreatic endocrine cells from human pluripotent stem cells (PSCs) has been thoroughly investigated for application in cell therapy against diabetes. In the context of induced pancreatic endocrine cell implantation, previous studies have reported graft enlargement resulting from off-target pancreatic lineage cells. However, there is currently no documented evidence of proliferative off-target cells beyond the pancreatic lineage in existing studies. Here, we show that the implantation of seven-stage induced PSC-derived pancreatic islet cells (s7-iPICs) leads to the emergence of unexpected off-target cells with proliferative capacity via in vivo maturation. These cells display characteristics of both mesenchymal stem cells (MSCs) and smooth muscle cells (SMCs), termed proliferative MSC- and SMC-like cells (PMSCs). The frequency of PMSC emergence was found to be high when 10

Indexed as

Induced Pluripotent Stem CellsIslets of LangerhansCell DifferentiationDocetaxelEmbryo ImplantationHumansDocetaxelcell-based therapyinduced pluripotent stem cell–derived pancreatic islet cellslong-term safetytype 1 diabetes mellitus

Identifiers

PMID38598342
PMCPMC11032438
OpenAlexW4394681117

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.