Evidence map›Paper›PMID 30805989›Full record

ArticleStem cells (Dayton, Ohio)2019

Somatic MIWI2 Hinders Direct Lineage Reprogramming From Fibroblast to Hepatocyte.

Xiaojie Shi, Zipei Xiao, Francesco Zonta, Wei Wang, Yue Wan, Yu Li, Nan Wang, Yuanyuan Kuang, Mingjuan Du, Jian Dong and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2019. 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
0.2field-weighted citation impact, top 49% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. PiRNA-63049 inhibits bone formation through Wnt/β-catenin signaling pathway.International journal of biological sciences · 2021
    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 3 institutions in 1 country.

Xiaojie ShiShanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, People's Republic of China.ORCID 0000-0002-9760-7989
Zipei XiaoShanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, People's Republic of China.
Francesco ZontaShanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, People's Republic of China.
Wei WangShanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, People's Republic of China.
Yue WanShanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, People's Republic of China.
Yu LiShanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, People's Republic of China.
Nan WangShanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, People's Republic of China.
Yuanyuan KuangShanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, People's Republic of China.
Mingjuan DuShanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, People's Republic of China.
Jian DongDepartment of Medical Oncology, Kunming Cancer Hospital, Kunming Medical University, Kunming, People's Republic of China.
Ju WangShanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, People's Republic of China.
Guang YangShanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, People's Republic of China.
ShanghaiTech University · CNChinese Academy of Sciences · CNKunming Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Remodeling of the gene regulatory network in cells is believed to be a prerequisite for their lineage reprogramming. However, its key regulatory factors are not yet elucidated. In this article, we investigate the role of PIWI proteins and provide evidence that one of them, MIWI2, is elicited during transdifferentiation of fibroblasts into hepatocyte-like cells. In coincidence with the peak expression of MIWI2, we identified the appearance of a unique intermediate epigenetic state characterized by a specific Piwi-interacting RNA (piRNA) profile consisting of 219 novel sequences. Knockout of MIWI2 greatly improved the formation of the induced hepatocytes, whereas overexpression of exogenous MIWI2 completely abolished the stimulated effect. A bioinformatics analysis of piRNA interaction network, followed by experimental validation, revealed the Notch signaling pathway as one of the immediate effectors of MIWI2. Altogether, our results show for the first time that temporal expression of MIWI2 contributes negatively to cell plasticity not only in germline, but also in developed cells, such as mouse fibroblasts. Stem Cells 2019;37:803-812.

Indexed as

Epigenesis, GeneticAlbuminsAnimalsArgonaute ProteinsCell LineageCell TransdifferentiationCellular ReprogrammingCRISPR-Cas SystemsFibroblastsGene Regulatory NetworksGenetic VectorsHepatocyte Nuclear Factor 1-alphaHepatocyte Nuclear Factor 3-gammaHepatocytesLentivirusMiceAlbuminsArgonaute ProteinsFoxa3 protein, mouseHepatocyte Nuclear Factor 1-alphaHepatocyte Nuclear Factor 3-gammaHnf1a protein, mousePIWIL4 protein, mouseReceptors, NotchRNA, Small InterferingCell fate conversioniHepLineage reprogrammingMIWI2piRNAPIWITransdifferentiation

Identifiers

PMID30805989
PMCPMC6850183
OpenAlexW2917713686

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.