Evidence map›Paper›PMID 39039334›Full record

ReviewDiscover oncology2024

Ataxin-2: a powerful RNA-binding protein.

Lulu Li, Meng Wang, Lai Huang, Xiaoli Zheng, Lina Wang, Hongming Miao

Abstract readReview
In one paragraph

Review in Discover oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. PolyQ-Expansion of Ataxin-2 Disrupts Microtubule Stability and Impairs Axon Outgrowth.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  6. Review
  7. Review
  8. Review
  9. 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

6 authors.

Lulu LiSchool of Basic Medical Science, Southwest Medical University, Luzhou, 646000, China.
Meng WangDepartment of Pathophysiology, College of High Altitude Military Medicine, Army Medical University, Chongqing, 400038, China.
Lai HuangDepartment of Clinical and Military Laboratory Medicine, College of Medical Laboratory Science, Army Medical University, Chongqing, 400038, China.
Xiaoli ZhengSchool of Basic Medical Science, Southwest Medical University, Luzhou, 646000, China. xlzheng1111@126.com.
Lina WangDepartment of Clinical and Military Laboratory Medicine, College of Medical Laboratory Science, Army Medical University, Chongqing, 400038, China. ninawongtmmu@163.com.
Hongming MiaoDepartment of Pathophysiology, College of High Altitude Military Medicine, Army Medical University, Chongqing, 400038, China. hongmingmiao@sina.com.

Funding

China National University Student Innovation & Entrepreneurship Development Program No. 202390035008Chongqing Fund for Outstanding Youth CSTB2022NSCQ-JQX0010 to H.M.Sichuan Science and Technology Program 2022YFS0622Special project of Scientific and Chongqing Postdoctoral Special Funding Project 2021XM1018Technological Innovation Capability Improvement of Army Military Medical University No. 2021XQN03the National Science Foundation of China No. 82003109The Science and Technology Strategic Cooperation Programs of Luzhou Municipal People's Government and Southwest Medical University 2019LZXNYDZ01
6 · The paper itself

Abstract

Ataxin-2 (ATXN2) was originally discovered in the context of spinocerebellar ataxia type 2 (SCA2), but it has become a key player in various neurodegenerative diseases. This review delves into the multifaceted roles of ATXN2 in human diseases, revealing its diverse molecular and cellular pathways. The impact of ATXN2 on diseases extends beyond functional outcomes; it mainly interacts with various RNA-binding proteins (RBPs) to regulate different stages of post-transcriptional gene expression in diseases. With the progress of research, ATXN2 has also been found to play an important role in the development of various cancers, including breast cancer, gastric cancer, pancreatic cancer, colon cancer, and esophageal cancer. This comprehensive exploration underscores the crucial role of ATXN2 in the pathogenesis of diseases and warrants further investigation by the scientific community. By reviewing the latest discoveries on the regulatory functions of ATXN2 in diseases, this article helps us understand the complex molecular mechanisms of a series of human diseases related to this intriguing protein.

Indexed as

ATXN2CancersMetabolism of RNANeurodegenerative diseasesRNA binding protein

Identifiers

PMID39039334
PMCPMC11263328

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.