Evidence map›Paper›PMID 36862329›Full record

ArticleStem cell reviews and reports2023

TPX2 Amplification-Driven Aberrant Mitosis in Culture Adapted Human Embryonic Stem Cells with gain of 20q11.21.

Ho-Chang Jeong, Young-Hyun Go, Joong-Gon Shin, Yun-Jeong Kim, Min-Guk Cho, Dasom Gwon, Hyun Sub Cheong, Haeseung Lee, Jae-Ho Lee, Chang-Young Jang and 2 more

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In one paragraph

Article in Stem cell reviews and reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

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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

12 authors at 6 institutions in 1 country.

Ho-Chang Jeong *Department of Life Science, Sogang University, Seoul, 04107, Republic of Korea.
Young-Hyun Go *Research Institute of Pharmaceutical Science, Seoul National University, Seoul, 08826, Republic of Korea.
Joong-Gon ShinResearch Institute for Basic Science, Sogang University, 35 Baekbum ro, Mapo-gu, Seoul, 04107, South Korea.
Yun-Jeong KimCollege of Pharmacy, Seoul National University, 1 Gwanak-ro Gwanak-gu, Seoul, 08826, South Korea.
Min-Guk ChoDepartment of Biochemistry and Molecular Biology, Ajou University School of Medicine, Suwon, 16499, Republic of Korea.
Dasom GwonDrug Information Research Institute, College of Pharmacy, Sookmyung Women's University, Seoul, 04310, Republic of Korea.
Hyun Sub CheongDepartment of Genetic Epidemiology, SNP Genetics, Inc., Seoul, 04107, Republic of Korea.
Haeseung LeeCollege of Pharmacy, Pusan Nati, onal University, Pusan, Korea.
Jae-Ho LeeDepartment of Biochemistry and Molecular Biology, Ajou University School of Medicine, Suwon, 16499, Republic of Korea.
Chang-Young JangDrug Information Research Institute, College of Pharmacy, Sookmyung Women's University, Seoul, 04310, Republic of Korea.
Hyoung Doo ShinResearch Institute for Basic Science, Sogang University, 35 Baekbum ro, Mapo-gu, Seoul, 04107, South Korea. hdshin@sogang.ac.kr.
Hyuk-Jin ChaCollege of Pharmacy, Seoul National University, 1 Gwanak-ro Gwanak-gu, Seoul, 08826, South Korea. hjcha93@snu.ac.kr.ORCID 0000-0001-9277-2662
Seoul National University · KRSogang University · KRAjou University · KRSookmyung Women's University · KRPusan National University · KRSNP Genetics (South Korea) · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDespite highly effective machinery for the maintenance of genome integrity in human embryonic stem cells (hESCs), the frequency of genetic aberrations during in-vitro culture has been a serious issue for future clinical applications.

methodBy passaging hESCs over a broad range of timepoints (up to 6 years), the isogenic hESC lines with different passage numbers with distinct cellular characteristics, were established.

resultWe found that mitotic aberrations, such as the delay of mitosis, multipolar centrosomes, and chromosome mis-segregation, were increased in parallel with polyploidy compared to early-passaged hESCs (EP-hESCs) with normal copy number. Through high-resolution genome-wide approaches and transcriptome analysis, we found that culture adapted-hESCs with a minimal amplicon in chromosome 20q11.21 highly expressed TPX2, a key protein for governing spindle assembly and cancer malignancy. Consistent with these findings, the inducible expression of TPX2 in EP-hESCs reproduced aberrant mitotic events, such as the delay of mitotic progression, spindle stabilization, misaligned chromosomes, and polyploidy.

conclusionThese studies suggest that the increased transcription of TPX2 in culture adapted hESCs could contribute to an increase in aberrant mitosis due to altered spindle dynamics.

Indexed as

Human Embryonic Stem CellsCell CycleCell Cycle ProteinsHumansMicrotubule-Associated ProteinsMitosisPolyploidyCell Cycle ProteinsMicrotubule-Associated ProteinsTPX2 protein, human20q11.21 ampliconChromosome instabilityCulture adaptationEmbryonic stem cellsTPX2

Identifiers

PMID36862329
OpenAlexW4322758758

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Registered trials

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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.