Evidence map›Paper›PMID 38973154›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

EGR3 Inhibits Tumor Progression by Inducing Schwann Cell-Like Differentiation.

Cai-Hong Chen, Yang Chen, Yi-Nan Li, Heng Zhang, Xiu Huang, Ying-Ying Li, Zhi-Yang Li, Jing-Xia Han, Xin-Ying Wu, Hui-Juan Liu and 1 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. EGR3 Inhibits Tumor Progression by Inducing Schwann Cell-Like Differentiation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    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

11 authors.

Cai-Hong ChenTianjin Nankai University State Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Tianjin, 300350, China.
Yang ChenTianjin Nankai University State Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Tianjin, 300350, China.
Yi-Nan LiTianjin Nankai University State Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Tianjin, 300350, China.
Heng ZhangTianjin Nankai University State Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Tianjin, 300350, China.
Xiu HuangTianjin Nankai University State Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Tianjin, 300350, China.
Ying-Ying LiTianjin Nankai University State Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Tianjin, 300350, China.
Zhi-Yang LiTianjin Nankai University State Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Tianjin, 300350, China.
Jing-Xia HanTianjin Nankai University State Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Tianjin, 300350, China.
Xin-Ying WuTianjin Nankai University State Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Tianjin, 300350, China.
Hui-Juan LiuTianjin Nankai University State Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Tianjin, 300350, China.
Tao SunTianjin Nankai University State Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Tianjin, 300350, China.ORCID 0000-0002-8962-2193

Funding

Fundamental Research Funds for the Central UniversitiesNankai University 63241645National Natural Science Foundation of China 82272934
6 · The paper itself

Abstract

The mechanism and function of the expression of Schwann characteristics by nevus cells in the mature zone of the dermis are unknown. Early growth response 3 (EGR3) induces Schwann cell-like differentiation of melanoma cells by simulating the process of nevus maturation, which leads to a strong phenotypic transformation of the cells, including the formation of long protrusions and a decrease in cell motility, proliferation, and melanin production. Meanwhile, EGR3 regulates the levels of myelin protein zero (MPZ) and collagen type I alpha 1 chain (COL1A1) through SRY-box transcription factor 10 (SOX10)-dependent and independent mechanisms, by binding to non-strictly conserved motifs, respectively. Schwann cell-like differentiation demonstrates significant benefits in both in vivo and clinical studies. Finally, a CD86-P2A-EGR3 recombinant mRNA vaccine is developed which leads to tumor control through forced cell differentiation and enhanced immune infiltration. Together, these data support further development of the recombinant mRNA as a treatment for cancer.

Indexed as

Cell DifferentiationEarly Growth Response Protein 3MelanomaSchwann CellsAnimalsCell Line, TumorCell ProliferationDisease Models, AnimalDisease ProgressionHumansMiceEarly Growth Response Protein 3EGR3 protein, humanEGR3melanomamRNA vaccineschwann cell‐like differentiation

Identifiers

PMID38973154
PMCPMC11425834

What Socratic 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 Socratic graph.