Evidence map›Paper›PMID 35848906›Full record

ArticleCancer science2022

N4BP3 promotes angiogenesis in hepatocellular carcinoma by binding with KAT2B.

Hexu Han, Wei Zhu, Ting Lin, Cuixia Liu, Hengyong Zhai

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

15 citing papers in PubMed, 20 citations in OpenAlex.

  1. Fine-tuning neuron number:bioRxiv : the preprint server for biology · 2026
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  3. SLA2 is Associated With Immune evasion and Exhaustion of CD8Journal of cellular and molecular medicine · 2026
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  4. Review
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  10. NSUN5 Facilitates Hepatocellular Carcinoma Progression by Increasing SMAD3 Expression.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. 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

5 authors at 3 institutions in 1 country.

Hexu HanDepartment of Gastroenterology, Taizhou People's Hospital, Taizhou, China.ORCID https://orcid.org/0000-0002-5812-0123
Wei ZhuDepartment of Pathology, Xishan People's Hospital of Wuxi City, Wuxi, China.
Ting LinDepartment of Basic Medicine, Jiangsu College of Nursing, Huai'an, China.
Cuixia LiuDepartment of Gastroenterology, Taizhou People's Hospital, Taizhou, China.
Hengyong ZhaiDepartment of Gastroenterology, Taizhou People's Hospital, Taizhou, China.ORCID https://orcid.org/0000-0002-6882-9785
Nantong University · CNJiangsu Vocational College of Medicine · CNWuxi People's Hospital · CN

Funding

Taizhou People's Hospital QDJJ202106
6 · The paper itself

Abstract

Although angiogenesis is a critical event in hepatocellular carcinoma (HCC), and this process provides the tumor with sufficient oxygen and nutrients, the precise molecular mechanism by which it occurs is not fully understood. NEDD4 binding protein 3 (N4BP3) was identified in this study as a novel pro-angiogenic factor in HCC cell lines and tissues. We discovered that N4BP3 was significantly expressed in HCC and that its level of expression was positively correlated with the density of tumor microvessels in HCC tissues. Cell biology experiments have shown that N4BP3 knockdown in HCC cells significantly inhibits the formation of complete tubular structures by HUVECs in vitro and HCC angiogenesis in vivo. In HCC cells, overexpression of N4BP3 has the opposite effects. Further cell and molecular biology experiments have revealed that N4BP3 interacts with KAT2B (lysine acetyltransferase 2B), increasing signal transducer and activator of transcription 3 (STAT3) expression by regulating the distribution of acetyl-histone H3 (Lys27) (H3K27ac) in its promoter region. This, in addition, regulates the activity of the STAT3 signaling pathway, which promotes the proliferation of microvessels in HCC and accelerates the malignant process of the tumor. In vivo experiments in nude mice have confirmed our findings, and also suggested that N4BP3 could be a potential target for the treatment of HCC in combination with sorafenib.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsLysine AcetyltransferasesAngiogenesis Inducing AgentsAnimalsCell Line, TumorCell ProliferationHistonesHumansMiceMice, NudeNeovascularization, PathologicOxygenSorafenibSTAT3 Transcription FactorAngiogenesis Inducing AgentsHistonesLysine AcetyltransferasesOxygenSorafenibSTAT3 Transcription Factorangiogenesishepatocellular carcinomametastasisN4BP3STAT3

Identifiers

PMID35848906
PMCPMC9530875
OpenAlexW4285800551

What OpenQuestion holds

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LicenceCC BY-NC
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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.