Evidence map›Paper›PMID 40823305›Full record

ReviewFrontiers in neurology2025

Eukaryotic initiation factors: central factor associating mRNA translational plasticity during neuropathic pain progression.

Xinshuo Li, Haibo Zhan, Xindan Zhang, Jiayi Li, Xiangrui Li, Xihua Lu, Changhong Miao, Chunli Zhou, Zhen Zhang

Abstract readReview
In one paragraph

Review in Frontiers in neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

9 authors.

Xinshuo Li *Department of Anesthesiology, The Affiliated Cancer Hospital of Zhengzhou University & Henan Cancer Hospital, Zhengzhou, Henan, China.
Haibo Zhan *Department of Anesthesiology, Huadu District People's Hospital of Guangzhou, Huadu Institute of Medical Sciences, Guangzhou, Guangdong, China.
Xindan Zhang *The 1st Clinical Department, China Medical University, Shenyang, Liaoning, China.
Jiayi LiDepartment of Anesthesiology, The Affiliated Cancer Hospital of Zhengzhou University & Henan Cancer Hospital, Zhengzhou, Henan, China.
Xiangrui LiDepartment of Anesthesiology, The Affiliated Cancer Hospital of Zhengzhou University & Henan Cancer Hospital, Zhengzhou, Henan, China.
Xihua LuDepartment of Anesthesiology, The Affiliated Cancer Hospital of Zhengzhou University & Henan Cancer Hospital, Zhengzhou, Henan, China.
Changhong MiaoDepartment of Anesthesia and Perioperative Medicine, Zhongshan Hospital, Fudan University, Shanghai, China.
Chunli ZhouDepartment of Anesthesiology, Xiangyang Central Hospital, Affiliated Hospital of Hubei University of Arts and Science, Xiangyang, Hubei, China.
Zhen ZhangDepartment of Anesthesiology, The Affiliated Cancer Hospital of Zhengzhou University & Henan Cancer Hospital, Zhengzhou, Henan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuropathic pain causes plasticity in the nervous system, which is often associated with altered protein synthesis. Proteins are the key executors of cellular functions, and their alteration is closely related to the occurrence of neuropathic pain. Protein synthesis is a finely regulated process involving the interaction of multiple biomolecules. Among them, the eukaryotic translation initiation factors (eIFs) are a group of key regulatory proteins that control the initiation phase of protein translation and thus influence the rate and type of protein synthesis. Recent studies have shown that the eIFs are involved in the regulation of neuropathic pain regulating translation through phosphorylation and affecting the transmission and processing of neuropathic pain signals. Among them, eIF4E and eIF2α, as core initiation factors, changes in their expression and activity are closely associated with various neuropathic pain. This review aims to summarize the evidence for the involvement of the eIFs, especially eIF4E and eIF2α, in pain-associated mRNA translational plasticity, and to propose relevant therapeutic approaches. We hope that this review will provide important ideas for future research on the mechanisms of neuropathic pain and new targets for the treatment of neuropathic pain.

Indexed as

eIF2αeIF4EeIF4Gneuropathic painplasticitytranslation

Identifiers

PMID40823305
PMCPMC12351134

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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.