Evidence map›Paper›PMID 34944048›Full record

ReviewCells2021

Clever Experimental Designs: Shortcuts for Better iPSC Differentiation.

Ryota Yasui, Keisuke Sekine, Hideki Taniguchi

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
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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

3 authors at 3 institutions in 1 country.

Ryota YasuiDepartment of Regenerative Medicine, Yokohama City University Graduate School of Medicine, Yokohama 236-0004, Japan.
Keisuke SekineDepartment of Regenerative Medicine, Yokohama City University Graduate School of Medicine, Yokohama 236-0004, Japan.ORCID 0000-0001-5133-0876
Hideki TaniguchiDepartment of Regenerative Medicine, Yokohama City University Graduate School of Medicine, Yokohama 236-0004, Japan.
National Cancer Centre Japan · JPThe University of Tokyo · JPYokohama City University · JP

Funding

Japan Agency for Medical Research and Development NoneMinistry of Education, Culture, Sports, Science and Technology of Japan 18K19589
6 · The paper itself

Abstract

For practical use of pluripotent stem cells (PSCs) for disease modelling, drug screening, and regenerative medicine, the cell differentiation process needs to be properly refined to generate end products with consistent and high quality. To construct and optimize a robust cell-induction process, a myriad of cell culture conditions should be considered. In contrast to inefficient brute-force screening, statistical design of experiments (DOE) approaches, such as factorial design, orthogonal array design, response surface methodology (RSM), definitive screening design (DSD), and mixture design, enable efficient and strategic screening of conditions in smaller experimental runs through multifactorial screening and/or quantitative modeling. Although DOE has become routinely utilized in the bioengineering and pharmaceutical fields, the imminent need of more detailed cell-lineage specification, complex organoid construction, and a stable supply of qualified cell-derived material requires expedition of DOE utilization in stem cell bioprocessing. This review summarizes DOE-based cell culture optimizations of PSCs, mesenchymal stem cells (MSCs), hematopoietic stem cells (HSCs), and Chinese hamster ovary (CHO) cells, which guide effective research and development of PSC-derived materials for academic and industrial applications.

Indexed as

Cell DifferentiationAnimalsCell ProliferationDecision TreesHumansInduced Pluripotent Stem CellsResearch Designcell differentiationChinese hamster ovary (CHO) celldesign of experiments (DOE)embryonic stem cell (ESC)hematopoietic stem cell (HSC)induced pluripotent stem cell (iPSC)mesenchymal stem cell (MSC)

Identifiers

PMID34944048
PMCPMC8700474
OpenAlexW4200223777

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.