Evidence map›Paper›PMID 36853485›Full record

ArticleEsophagus : official journal of the Japan Esophageal Society2023

Comprehensive analysis of CDK5 as a novel biomarker for progression in esophageal cancer.

Rui Ling, Yucheng Sheng, Yuwen Hu, Deqian Wang, Yuepeng Zhou, Yang Shu

Open access · hybridAbstract read
PubMed Publisher
In one paragraph

Article in Esophagus : official journal of the Japan Esophageal Society, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 31% 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

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 2 citations in OpenAlex.

  1. Pooled it
  2. 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 at 1 institution in 1 country.

Rui Ling *Department of Central Laboratory, Affiliated Hospital of Jiangsu University, 438 Jiefang Road, Zhenjiang, 212001, China.
Yucheng Sheng *Department of Central Laboratory, Affiliated Hospital of Jiangsu University, 438 Jiefang Road, Zhenjiang, 212001, China.
Yuwen Hu *Department of Central Laboratory, Affiliated Hospital of Jiangsu University, 438 Jiefang Road, Zhenjiang, 212001, China.
Deqian WangDepartment of Central Laboratory, Affiliated Hospital of Jiangsu University, 438 Jiefang Road, Zhenjiang, 212001, China.
Yuepeng ZhouDepartment of Central Laboratory, Affiliated Hospital of Jiangsu University, 438 Jiefang Road, Zhenjiang, 212001, China. yuepeng_zhou@ujs.edu.cn.
Yang ShuDepartment of Central Laboratory, Affiliated Hospital of Jiangsu University, 438 Jiefang Road, Zhenjiang, 212001, China. ushyang@ujs.edu.cn.ORCID 0000-0002-7816-0763
Jiangsu University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCyclin-dependent kinase 5 (CDK5) is a member of the cyclin-dependent kinase family, and unlike the rest of the members of the family, its kinase activity is independent of cyclins. Accumulating evidence has shown that CDK5 plays a significant role in the progress of tumorigenesis except in nervous system. In particular, the expression of CDK5 and its function in esophageal cancer (ESCA) remain unknown.

methodsWith TCGA and GEO databases, CDK5 was analyzed with the expression, predicted value, clinical relationship, functional enrichment, immune cell infiltration and immune molecules in ESCA. In addition, we explored the CDK5 expression with local datasets and the influence of CDK5 on proliferation, migration and invasion behaviors of the esophageal squamous cell carcinoma (ESCC) cells in vitro and in vivo experiments.

resultsCDK5 expression was upregulated in ESCA, and this regulation has been verified in cell lines of ESCC. Further analysis has found that the expression of CDK5 was correlated with race, weight, BMI, histological type and tumor central location in ESCA. KEGG analysis revealed that CDK5 was involved in the progress of cancers, innate immune system and PI3K-Akt signaling pathway. CDK5 was closely related to immune cells and immune molecules in ESCA. Functional experiments confirmed CDK5 was an oncogene in ESCC by in vivo and in vitro models.

conclusionsThis study shows that CDK5 is a risk factor to promote tumor progression, and Roscovitine could be one of the effective tools in the therapy of ESCA.

Indexed as

Esophageal NeoplasmsEsophageal Squamous Cell CarcinomaBiomarkersCyclin-Dependent Kinase 5HumansPhosphatidylinositol 3-KinasesBiomarkersCyclin-Dependent Kinase 5Phosphatidylinositol 3-KinasesCyclin-dependent kinase 5Esophageal cancerInvasionMigrationProliferation

Identifiers

PMID36853485
OpenAlexW4322616696

What OpenQuestion 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 OpenQuestion graph.