Evidence map›Paper›PMID 36918705›Full record

ReviewMolecular psychiatry2023

Friend or foe: role of pathological tau in neuronal death.

Moxin Wu, Zhiying Chen, Min Jiang, Bing Bao, Dongling Li, Xiaoping Yin, Xueren Wang, Dan Liu, Ling-Qiang Zhu

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular psychiatry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

18 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Kinetic modeling ofEJNMMI research · 2025
    Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. 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 at 3 institutions in 1 country.

Moxin Wu *Department of Medical Laboratory, Affiliated Hospital of Jiujiang University, Jiujiang, 332000, China.
Zhiying Chen *Jiujiang Clinical Precision Medicine Research Center, Jiujiang, 332000, China.
Min Jiang *Jiujiang Clinical Precision Medicine Research Center, Jiujiang, 332000, China.
Bing BaoJiujiang Clinical Precision Medicine Research Center, Jiujiang, 332000, China.
Dongling LiJiujiang Clinical Precision Medicine Research Center, Jiujiang, 332000, China.
Xiaoping YinJiujiang Clinical Precision Medicine Research Center, Jiujiang, 332000, China. xiaopingbuxiao@126.com.
Xueren WangDepartment of Anesthesiology, Shanxi Bethune Hospital, Taiyuan, 030032, China. xrwang@hust.edu.cn.
Dan LiuDepartment of Medical Genetics, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China. liudan_echo@mail.hust.edu.cn.
Ling-Qiang ZhuDepartment of Pathophysiology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China. zhulq@mail.hust.edu.cn.ORCID 0000-0001-9964-9229
Jiujiang University · CNHuazhong University of Science and Technology · CNShanxi Academy of Medical Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuronal death is one of the most common pathological hallmarks of diverse neurological diseases, which manifest varying degrees of cognitive or motor dysfunction. Neuronal death can be classified into multiple forms with complicated and unique regulatory signaling pathways. Tau is a key microtubule-associated protein that is predominantly expressed in neurons to stabilize microtubules under physiological conditions. In contrast, pathological tau always detaches from microtubules and is implicated in a series of neurological disorders that are characterized by irreversible neuronal death, such as necrosis, apoptosis, necroptosis, pyroptosis, ferroptosis, autophagy-dependent neuronal death and phagocytosis by microglia. However, recent studies have also revealed that pathological tau can facilitate neuron escape from acute apoptosis, delay necroptosis through its action on granulovacuolar degeneration bodies (GVBs), and facilitate iron export from neurons to block ferroptosis. In this review, we briefly describe the current understanding of how pathological tau exerts dual effects on neuronal death by acting as a double-edged sword in different neurological diseases. We propose that elucidating the mechanism by which pathological tau affects neuronal death is critical for exploring novel and precise therapeutic strategies for neurological disorders.

Indexed as

ApoptosisNervous System DiseasesHumansMicrotubulesNerve DegenerationNeuronstau Proteinstau Proteins

Identifiers

PMID36918705
OpenAlexW4324144260

What Socratic holds

Textmetadata
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.