Evidence map›Paper›PMID 40937143›Full record

ArticleDegenerative neurological and neuromuscular disease2025

TP73-AS1 Regulates MPP+-Induced Cell Inflammation and Apoptosis in SH-SY5Y Cells.

Xue Zhang, Li Xue, Haiyan Li, Xiaolong Yu, Kaixin Dou, Anmu Xie

Abstract read
In one paragraph

Article in Degenerative neurological and neuromuscular disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Xue ZhangDepartment of Neurology, Affiliated Hospital of Qingdao University, Qingdao, People's Republic of China.ORCID 0000-0002-5782-2174
Li XueDepartment of Internal Medicine, Affiliated Hospital of Qingdao University, Qingdao, People's Republic of China.
Haiyan LiDepartment of Neurology, Qingdao Central Hospital, University of Health and Rehabilitation Sciences, Qingdao, People's Republic of China.
Xiaolong YuDepartment of Neurology, Qingdao Central Hospital, University of Health and Rehabilitation Sciences, Qingdao, People's Republic of China.
Kaixin DouDepartment of Neurology, Affiliated Hospital of Qingdao University, Qingdao, People's Republic of China.
Anmu XieDepartment of Neurology, Affiliated Hospital of Qingdao University, Qingdao, People's Republic of China.ORCID 0000-0003-2591-467X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The aim was to investigate the potential role of TP73-AS1 in the pathogenesis of Parkinson's disease. Methods: Peripheral blood samples were obtained from three patients with early-onset Parkinson's disease (PD), three patients with late-onset PD, and three healthy controls for the extraction of total RNA. Genomic long non-coding RNA (lncRNA) expression levels were analyzed using the Illumina HiSeq2500 sequencing platform. Quantitative real-time polymerase chain reaction (qRT-PCR) was used to study the expression of TP73-AS1. Flow cytometry and Western blot analyses were conducted to assess the functional role of TP73-AS1 in SH-SY5Y cells in vitro. Moreover, the expression of inflammatory cytokines, such as IL-16, IL-6, and α-synuclein (SYN), was examined using cellular immunofluorescence techniques. Results: Among early-onset PD patients, 59 lncRNAs were significantly upregulated, and 57 lncRNAs were significantly downregulated compared to the control group. Similarly, late-onset PD patients showed 70 upregulated lncRNAs and 77 downregulated lncRNAs with statistical significance compared to the control group. In vitro studies indicated a significant increase in lncRNA TP73-AS1 expression in the MPP+-treated group in contrast with the control group (

Indexed as

apoptosishigh-throughput sequencinginflammationlong non-coding RNATP73-AS1

Identifiers

PMID40937143
PMCPMC12420920

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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.