Evidence map›Paper›PMID 35365622›Full record

ArticleCell death & disease2022

CDC42EP3 promotes glioma progression via regulation of CCND1.

Zhigang Yang, Tao Xu, Tao Xie, Liangliang Yang, Guiping Wang, Yang Gao, Gangming Xi, Xiaobiao Zhang

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. The Role of the PAX Genes in Renal Cell Carcinoma.International journal of molecular sciences · 2024
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. 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

8 authors at 3 institutions in 1 country.

Zhigang Yang *Department of Neurosurgery, Zhongshan Hospital, Fudan University, Shanghai, China.ORCID 0000-0002-6278-3130
Tao Xu *Department of Neurosurgery, Changzheng Hospital, Naval Medical University, Shanghai, China.ORCID 0000-0003-1984-1689
Tao XieDepartment of Neurosurgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Liangliang YangDepartment of Neurosurgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Guiping WangDepartment of Neurology, Shanghai Xuhui Central Hospital, Shanghai, China.
Yang GaoDepartment of Neurosurgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Gangming XiDepartment of Neurology, Shanghai Xuhui Central Hospital, Shanghai, China. xgmsys@163.com.ORCID 0000-0001-7397-0292
Xiaobiao ZhangDepartment of Neurosurgery, Zhongshan Hospital, Fudan University, Shanghai, China. xiaobiao_zhang@163.com.ORCID 0000-0003-3970-1106
Sun Yat-sen University · CNShanghai Xuhui Central Hospital · CNSecond Military Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gliomas are the most common brain malignancies characterized by high degree of aggressiveness and high mortality. However, the underlying mechanism of glioma progression remains unclear. Here, we probed the role of CDC42EP3 (CDC42 effector protein 3) played in glioma development and its potential downstream mechanism. The expression of CDC42EP3 in tumor and normal brain tissues were examined through immunohistochemistry and we found the likelihood of CDC42EP3 overexpression was positively correlated with pathological grading. Patients with higher expression of CDC42EP3 were more likely to suffer from recurrence as well. Through constructing CDC42EP3-knockdown cell models, we discovered that silencing CDC42EP3 significantly restricted cell proliferation and migration but facilitated cell apoptosis in vitro. Inhibition on tumor growth mediated by CDC42EP3 depletion was further verified in vivo. Regarding downstream target of CDC42EP3, we found that it may positively regulate the expression of CCND1 through c-Myc-mediated transcription. Furthermore, our findings affirmed that effects of CDC42EP3 overexpression on cell proliferation, migration and apoptosis could be confined by depleting CCND1. In a word, this study reported the tumor-promoting role of CDC42EP3 in glioma progression which probably functioned through targeting CCND1.

Indexed as

Brain NeoplasmsGliomaApoptosisCell Line, TumorCell ProliferationCyclin D1Gene Expression Regulation, NeoplasticGTP-Binding Protein RegulatorsHumansCCND1 protein, humanCDC42EP3 protein, humanCyclin D1GTP-Binding Protein Regulators

Identifiers

PMID35365622
PMCPMC8975815
OpenAlexW4220715547

What OpenQuestion 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 OpenQuestion graph.