Evidence map›Paper›PMID 34080290›Full record

ArticleJournal of cellular and molecular medicine2021

Identification and assessment of PLK1/2/3/4 in lung adenocarcinoma and lung squamous cell carcinoma: Evidence from methylation profile.

Sisi Deng, Xiaoli Lu, Zhi Zhang, Rui Meng, Mi Li, Shilin Xia

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

13 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Article
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  4. Immune Escape-Related Gene NXT1 as a Potential Prognostic and Therapeutic Target in Hepatocellular Carcinoma.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2025
    Article
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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 3 institutions in 2 countries.

Sisi DengCancer Center, Tongji Medical College, Union Hospital, Huazhong University of Science and Technology, Wuhan, China.
Xiaoli LuCancer Center, Tongji Medical College, Union Hospital, Huazhong University of Science and Technology, Wuhan, China.
Zhi ZhangCancer Center, Tongji Medical College, Union Hospital, Huazhong University of Science and Technology, Wuhan, China.
Rui MengCancer Center, Tongji Medical College, Union Hospital, Huazhong University of Science and Technology, Wuhan, China.
Mi LiDepartment of Orthopedics, Tongji Medical College, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China.ORCID 0000-0003-0952-230X
Shilin XiaClinical Laboratory of Integrative Medicine, The First Affiliated Hospital of Dalian Medical University, Dalian, China.
Union Hospital · CNDalian Medical University · CNTongji Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer is a very aggressive cancer characterized with molecular heterogeneities in different subtypes, including lung adenocarcinoma and lung squamous cell carcinoma. However, few related molecular signatures have been established for the treatment of lung cancer subtypes. Polo-like kinase (PLK) family is a crucial regulator during cell division. Aberrant genetic and epigenetic alteration of PLK members plays a controversial role among different cancers. In this study, we performed an analysis of transcriptional and protein expression to identify overexpressed PLK1/4 and under-expressed PLK2/3 in lung cancer subtypes. We then analysed biological function of PLKs and related genes. Besides, we estimated a correlation of PLKs with patient's genders and TP53 mutation in lung cancer. Higher PLK1/4 expression was significantly associated with male patient and TP53 mutant status, separately. Moreover, we carried out a methylation profile analysis including methylation level, DNA methyltransferases correlation and survival analysis of global methylation. Global methylation survival analysis showed that prognostic value of PLK1/2/4 methylation remained the same significant trend between two lung cancer subtypes, whereas prognostic value of PLK3 methylation lacked consistency. Taken together, these results provided instructive insights into a comprehensive evaluation for advanced therapeutic strategy based on epigenetic evidences.

Indexed as

Adenocarcinoma of LungCarcinoma, Non-Small-Cell LungCell Cycle ProteinsDisease-Free SurvivalDNA MethylationFemaleGene Expression Regulation, NeoplasticHumansMalePolo-Like Kinase 1Polo-like KinasesPrognosisProtein Serine-Threonine KinasesProto-Oncogene ProteinsTumor Suppressor Protein p53Tumor Suppressor ProteinsCell Cycle ProteinsPLK2 protein, humanPLK3 protein, humanPLK4 protein, humanPolo-Like Kinase 1Polo-like KinasesProtein Serine-Threonine KinasesProto-Oncogene ProteinsTP53 protein, humanTumor Suppressor Protein p53Tumor Suppressor Proteinslung adenocarcinomalung squamous cell carcinomamethylationPLK1/2/3/4

Identifiers

PMID34080290
PMCPMC8278123
OpenAlexW3165613780

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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.