Evidence map›Paper›PMID 41631213›Full record

ReviewBiochemistry and biophysics reports2026

TDP-43 in neurodegeneration and cancer: Decoding the mechanism of mRNA localization and translation.

Panjiao Pang, Mingyang Yu, Huixin Ma, Longkai Wei, Jiali Huang, Lingxin Zhao, Ying-Hua Zhang

Abstract readReview
In one paragraph

Review in Biochemistry and biophysics reports, 2026. 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

7 authors.

Panjiao PangXinxiang Key Laboratory of Molecular Neurology, School of Basic Medical Sciences, Henan Medical University, Xinxiang, 453003, People's Republic of China.
Mingyang YuXinxiang Key Laboratory of Molecular Neurology, School of Basic Medical Sciences, Henan Medical University, Xinxiang, 453003, People's Republic of China.
Huixin MaXinxiang Key Laboratory of Molecular Neurology, School of Basic Medical Sciences, Henan Medical University, Xinxiang, 453003, People's Republic of China.
Longkai WeiXinxiang Key Laboratory of Molecular Neurology, School of Basic Medical Sciences, Henan Medical University, Xinxiang, 453003, People's Republic of China.
Jiali HuangXinxiang Key Laboratory of Molecular Neurology, School of Basic Medical Sciences, Henan Medical University, Xinxiang, 453003, People's Republic of China.
Lingxin ZhaoXinxiang Key Laboratory of Molecular Neurology, School of Basic Medical Sciences, Henan Medical University, Xinxiang, 453003, People's Republic of China.
Ying-Hua ZhangXinxiang Key Laboratory of Molecular Neurology, School of Basic Medical Sciences, Henan Medical University, Xinxiang, 453003, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The localization and translation of mRNAs play crucial roles in maintaining cellular phenotype and function, with RNA-binding protein (RBP) contributing significantly to these processes. TAR DNA-binding protein of 43 kDa (TDP-43) is an RNA/DNA-binding protein that is primarily localized in the nucleus, where it performs essential functions in pre-mRNA splicing, mRNA transport, and the stabilization and localized translation of mRNA. Its mis-localization from the cytoplasm, as well as mutations, protein misfolding, and posttranslational modifications, is closely linked to a reduction in its RNA-binding ability. This functional impairment is implicated in the initiation and progression of neurodegenerative diseases and cancer. In this review, we begin with a retrospective analysis of the molecular mechanism by which distinct domains of TDP-43 contribute to the initiation and progression of disease, particularly because its overexpression in tumors significantly influences disease progression. We subsequently elucidate the classical mechanisms of mRNA localization and translation, while clarifying the role of TDP-43 in these processes. Finally, we summarize the mechanisms by which TDP-43 facilitates the formation of ribonucleoprotein particles and this protein's involvement in mRNA localization and translation, as well as its associated molecular pathways. In conclusion, this review highlights the critical roles of TDP-43 and subsequent therapeutic strategies for treatment of neurodegenerative diseases and tumors.

Indexed as

Liquid-liquid phase separationLocal translationMolecular mechanismmRNA localizationProtein aggregationTDP-43

Identifiers

PMID41631213
PMCPMC12860977

What Socratic 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 Socratic graph.