Evidence map›Paper›PMID 31492983›Full record

ReviewJournal of cancer research and clinical oncology2019

PLK4: a promising target for cancer therapy.

Yi Zhao, Xin Wang

Abstract readReview
In one paragraph

Review in Journal of cancer research and clinical oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
–field-weighted citation impact
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

39 citing papers in PubMed.

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  8. Role of PLK4 inhibition in cancer therapy.Cancer metastasis reviews · 2025
    Review
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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

2 authors.

Yi ZhaoDepartment of Hematology, Shandong Provincial Hospital Affiliated to Shandong University, No. 324, Jingwu Road, Jinan, 250021, Shandong, People's Republic of China.
Xin WangDepartment of Hematology, Shandong Provincial Hospital Affiliated to Shandong University, No. 324, Jingwu Road, Jinan, 250021, Shandong, People's Republic of China. xinw@sdu.edu.cn.ORCID http://orcid.org/0000-0001-5457-5799

Funding

Doctoral Foundation of Shandong Province (CN) 2017GSF18189Key Research and Development Program of Shandong Province 2018CXGC1213National Natural Science Foundation of China 81270598National Natural Science Foundation of China 81473486National Natural Science Foundation of China 81770210
6 · The paper itself

Abstract

purposePolo-like kinase 4 (PLK4) is a serine/threonine protein kinase that regulates centriole duplication. PLK4 deregulation causes centrosome number abnormalities, mitotic defects, chromosomal instability and, consequently, tumorigenesis. Therefore, PLK4 has emerged as a therapeutic target for the treatment of multiple cancers. In this review, we summarize the critical role of centrosome amplification and PLK4 in cancer. We also highlight recent advances in the development of PLK4 inhibitors and discuss potential combination therapies for cancer.

methodsThe relevant literature from PubMed is reviewed in this article. The ClinicalTrials.gov database was searched for clinical trials related to the specific topic.

resultsPLK4 is aberrantly expressed in multiple cancers and has prognostic value. Targeting PLK4 with inhibitors suppresses tumor growth in vitro and in vivo.

conclusionsPLK4 plays an important role in centrosome amplification and tumor progression. PLK4 inhibitors used alone or in combination with other drugs have shown significant anticancer efficacy, suggesting a potential therapeutic strategy for cancer. The results of relevant clinical trials await evaluation.

Indexed as

Biomarkers, TumorAnimalsAntineoplastic AgentsCell Transformation, NeoplasticCentrosomeGene Expression Regulation, NeoplasticHumansMolecular Targeted TherapyNeoplasm MetastasisNeoplasmsOrgan SpecificityProtein Kinase InhibitorsProtein Serine-Threonine KinasesStructure-Activity RelationshipTumor Suppressor Protein p53Antineoplastic AgentsBiomarkers, TumorPLK4 protein, humanProtein Kinase InhibitorsProtein Serine-Threonine KinasesTumor Suppressor Protein p53CancerCentrosomesCFI-400945PLK4PLK4 inhibitor

Identifiers

PMID31492983
PMCPMC11810395

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.