Evidence map›Paper›PMID 41318742›Full record

ArticleCommunications biology2025

HuB serves as the central hub for connecting HuR-related mRNAs with translation machinery in inflammation.

Jing Zhang, Ximan Huang, Yunhan Tang, Xiyue Zhong, Jing Wang, Min Wei, Xiaoqing Han, Yueshuang Ke, Xueqing Ba

Abstract read
In one paragraph

Article in Communications biology, 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. 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

9 authors.

Jing ZhangKey Laboratory of Molecular Epigenetics of Ministry of Education (MOE), Northeast Normal University, Changchun, Jilin, China.
Ximan HuangKey Laboratory of Molecular Epigenetics of Ministry of Education (MOE), Northeast Normal University, Changchun, Jilin, China.
Yunhan TangKey Laboratory of Molecular Epigenetics of Ministry of Education (MOE), Northeast Normal University, Changchun, Jilin, China.
Xiyue ZhongKey Laboratory of Molecular Epigenetics of Ministry of Education (MOE), Northeast Normal University, Changchun, Jilin, China.
Jing WangDepartment of Respiratory Medicine, China-Japan Union Hospital of Jilin University, Changchun, Jilin, China.
Min WeiKey Laboratory of Molecular Epigenetics of Ministry of Education (MOE), Northeast Normal University, Changchun, Jilin, China.ORCID http://orcid.org/0000-0001-9945-6961
Xiaoqing HanKey Laboratory of Molecular Epigenetics of Ministry of Education (MOE), Northeast Normal University, Changchun, Jilin, China. hanxq115@nenu.edu.cn.ORCID http://orcid.org/0000-0003-4722-9083
Yueshuang KeKey Laboratory of Molecular Epigenetics of Ministry of Education (MOE), Northeast Normal University, Changchun, Jilin, China. keys585@nenu.edu.cn.ORCID http://orcid.org/0000-0003-1518-4271
Xueqing BaKey Laboratory of Molecular Epigenetics of Ministry of Education (MOE), Northeast Normal University, Changchun, Jilin, China. baxq755@nenu.edu.cn.ORCID http://orcid.org/0000-0002-1075-5496

Funding

National Natural Science Foundation of China (National Science Foundation of China) 32170591
6 · The paper itself

Abstract

The mRNAs of inflammatory factors often contain unstable AU-rich elements (AREs) within their 3' untranslated regions (3'UTRs), and HuR is a key ARE-binding protein to recognize such elements. However, the roles of other Hu family member (s) remain unclear. In this study, we show an inflammatory stimulation-induced short-form and cytoplasm-localized HuB (Hel-N2). In cytoplasm, HuB interacts with HuR as well as HuR-associated pro-inflammatory cytokine/chemokine mRNAs and facilitates the recruitment of these mRNAs into the translation machinery. Furthermore, HuB recruits RNA helicase DHX9 to unwind the secondary structures presented in the 5' untranslated regions (5'UTRs) of these mRNAs, thereby promoting their translation. The work has been carried out in human and mouse cell lines and female mice. Our finding not only broadens our understanding about how the Hu family members govern pro-inflammatory gene expression, but also suggests that targeting HuB is a viable strategy to treat inflammation-related diseases.

Indexed as

ELAV-Like Protein 1InflammationProtein BiosynthesisRNA, Messenger3' Untranslated Regions5' Untranslated RegionsAnimalsDEAD-box RNA HelicasesFemaleHumansMice3' Untranslated Regions5' Untranslated RegionsDEAD-box RNA HelicasesELAVL1 protein, humanELAV-Like Protein 1RNA, Messenger

Identifiers

PMID41318742
PMCPMC12764827

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Registered trials

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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.