Evidence map›Paper›PMID 35386230›Full record

ArticleDisease markers2022

The Higher Expression of CDCA2 Associated with Poor Prognosis in Glioma.

Xin Jin, Zhen-Qing Sun, Gui-Liang Zhou, Guo-Jun Li, Shi-Feng Deng

RetractedOpen access · hybridAbstract readRetracted Publication
In one paragraph

Article in Disease markers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 44% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Novel Functional Features of cGMP Substrate Proteins IRAG1 and IRAG2.International journal of molecular sciences · 2023
    Review
  2. Article
  3. Review
4 · The record

Corrections and comments

  • Retraction · 2023-07-19Concerns/Issues about Data · Concerns/Issues about Results and/or Conclusions · Concerns/Issues about Referencing/Attributions · Concerns/Issues about Peer Review · Investigation by Journal/Publisher · Investigation by Third Party · Paper Mill · Computer-Aided Content or Computer-Generated Content · Unreliable Results and/or Conclusions · · See also: https://pubpeer.com/publications/62CECC3FB5FAC919D177428469EF16
  • Retracted
5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Xin JinDepartment of Neurosurgery, Guangdong 999 Brain Hospital, Guangzhou, Guangdong, China.ORCID https://orcid.org/0000-0002-7967-3296
Zhen-Qing SunDepartment of Neurosurgery, Guangdong 999 Brain Hospital, Guangzhou, Guangdong, China.
Gui-Liang ZhouDepartment of Bioinformation, Guangdong South China New Drug Development Center, Guangzhou, Guangdong, China.
Guo-Jun LiDepartment of Neurosurgery, Guangdong 999 Brain Hospital, Guangzhou, Guangdong, China.
Shi-Feng DengDepartment of Neurosurgery, Guangdong 999 Brain Hospital, Guangzhou, Guangdong, China.
Guangdong 999 Brain Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioma is the most common primary intracranial tumor and is related to poor clinical outcomes. The developments of sensitive markers can be applied to reveal the mechanisms involved in the progression of glioma. This study examined CDCA2 expression in glioma samples and its significance in predicting glioma patient outcome. GEPIA and GEO datasets were used to explore the expression of CDCA2 in glioma. Kaplan-Meier and multivariate assays were applied to delve into the prognostic values of CDCA2 expression in glioma patients using CGGA datasets. Our group also determined the associations between CDCA2 and clinical characteristics. Coexpression analysis was performed. In this research, we observed that CDCA2 expression was distinctly upregulated in glioma specimens compared with nontumor specimens. The prognosis of glioma with high CDCA2 expression was distinctly worse compared with that of glioma with low CDCA2 expression. Additionally, multivariate Cox regression analysis revealed that high CDCA2 expression was an independent poor prognostic indicator for glioma patients. High expression of CDCA2 was positively associated with advanced clinical progression. Coexpression analysis revealed that CDCA2 could be positively related to ASPM, SKA1, DLGAP5, NCAPG, and CDCA8 and was negatively associated with ETNPPL, LDHD, MRVI1, CBX7, and CENPJ. Overall, our findings revealed that CDCA2 might serve as an independent prognosis indicator for glioma.

Indexed as

Brain NeoplasmsGliomaCarrier ProteinsCell Cycle ProteinsChromosomal Proteins, Non-HistoneHumansNuclear ProteinsPolycomb Repressive Complex 1PrognosisCarrier ProteinsCBX7 protein, humanCDCA2 protein, humanCell Cycle ProteinsChromosomal Proteins, Non-HistoneNuclear ProteinsPolycomb Repressive Complex 1SKA1 protein, human

Identifiers

PMID35386230
PMCPMC8977301
OpenAlexW4220833452

What OpenQuestion holds

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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.