Evidence map›Paper›PMID 29452418›Full record

ArticleJournal of molecular cell biology2018

PHF20 collaborates with PARP1 to promote stemness and aggressiveness of neuroblastoma cells through activation of SOX2 and OCT4.

Wenyong Long, Wei Zhao, Bo Ning, Jing Huang, Junjun Chu, Linfeng Li, Qianquan Ma, Changsheng Xing, Helen Y Wang, Qing Liu and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of molecular cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

24 citing papers in PubMed, 31 citations in OpenAlex.

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  17. JMJD3: a critical epigenetic regulator in stem cell fate.Cell communication and signaling : CCS · 2021
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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

11 authors at 5 institutions in 2 countries.

Wenyong LongDepartment of Neurosurgery in Xiangya Hospital, Central South University, Changsha 410008, China.
Wei ZhaoCenter for Inflammation and Epigenetics, Houston Methodist Research Institute, Houston, TX 77030, USA.
Bo NingCenter for Inflammation and Epigenetics, Houston Methodist Research Institute, Houston, TX 77030, USA.
Jing HuangCenter for Inflammation and Epigenetics, Houston Methodist Research Institute, Houston, TX 77030, USA.
Junjun ChuKey Laboratory of Stem Cells and Tissue Engineering, Ministry of Education, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.
Linfeng LiCenter for Inflammation and Epigenetics, Houston Methodist Research Institute, Houston, TX 77030, USA.
Qianquan MaDepartment of Neurosurgery in Xiangya Hospital, Central South University, Changsha 410008, China.
Changsheng XingCenter for Inflammation and Epigenetics, Houston Methodist Research Institute, Houston, TX 77030, USA.
Helen Y WangCenter for Inflammation and Epigenetics, Houston Methodist Research Institute, Houston, TX 77030, USA.
Qing LiuDepartment of Neurosurgery in Xiangya Hospital, Central South University, Changsha 410008, China.
Rong-Fu WangCenter for Inflammation and Epigenetics, Houston Methodist Research Institute, Houston, TX 77030, USA.
Houston Methodist · USCentral South University · CNSun Yat-sen University · CNTexas A&M University · USXiangya Hospital Central South University · CN

Funding

Transport Oncophysics CoreU54CA210181 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI CHANG, JENNY C-N · 2016 to 2020
$9.3M
NCI NIH HHS U54 CA210181
6 · The paper itself

Abstract

The differentiation status of neuroblastoma (NB) strongly correlates with its clinical outcomes; however, the molecular mechanisms driving maintenance of stemness and differentiation remain poorly understood. Here, we show that plant homeodomain finger-containing protein 20 (PHF20) functions as a critical epigenetic regulator in sustaining stem cell-like phenotype of NB by using CRISPR/Cas9-based targeted knockout (KO) for high-throughput screening of gene function in NB cell differentiation. The expression of PHF20 in NB was significantly associated with high aggressiveness of the tumor and poor outcomes for NB patients. Deletion of PHF20 inhibited NB cell proliferation, invasive migration, and stem cell-like traits. Mechanistically, PHF20 interacts with poly(ADP-ribose) polymerase 1 (PARP1) and directly binds to promoter regions of octamer-binding transcription factor 4 (OCT4) and sex determining region Y-box 2 (SOX2) to modulate a histone mark associated with active transcription, trimethylation of lysine 4 on histone H3 protein subunit (H3K4me3). Overexpression of OCT4 and SOX2 restored growth and progression of PHF20 KO tumor cells. Consistently, OCT4 and SOX2 protein levels in clinical NB specimens were positively correlated with PHF20 expression. Our results establish PHF20 as a key driver of NB stem cell-like properties and aggressive behaviors, with implications for prognosis and therapy.

Indexed as

Protein Interaction MapsAnimalsAntigens, NeoplasmBiomarkers, TumorDNA-Binding ProteinsFemaleGene Expression Regulation, NeoplasticHumansMaleMiceNeoplasm InvasivenessNeoplastic Stem CellsNeuroblastomaOctamer Transcription Factor-3Poly (ADP-Ribose) Polymerase-1SOXB1 Transcription FactorsAntigens, NeoplasmBiomarkers, TumorDNA-Binding ProteinsOctamer Transcription Factor-3PARP1 protein, humanPHF20 protein, humanPoly (ADP-Ribose) Polymerase-1POU5F1 protein, humanSOX2 protein, humanSOXB1 Transcription FactorsTranscription Factors

Identifiers

PMID29452418
PMCPMC5951121
OpenAlexW2791224813

What OpenQuestion holds

Textmetadata
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.