Evidence map›Paper›PMID 31837068›Full record

ArticleCell proliferation2020

Systematic expression analysis of WEE family kinases reveals the importance of PKMYT1 in breast carcinogenesis.

Yu Liu, Jian Qi, Zhen Dou, Jiliang Hu, Li Lu, Haiming Dai, Hongzhi Wang, Wulin Yang

Open access · goldAbstract read
In one paragraph

Article in Cell proliferation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 6% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 69 citations in OpenAlex.

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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

8 authors at 4 institutions in 1 country.

Yu LiuAnhui Province Key Laboratory of Medical Physics and Technology, Center of Medical Physics and Technology, Hefei Institutes of Physical Science, Chinese Academy of Sciences, Hefei, China.
Jian QiAnhui Province Key Laboratory of Medical Physics and Technology, Center of Medical Physics and Technology, Hefei Institutes of Physical Science, Chinese Academy of Sciences, Hefei, China.
Zhen DouHefei National Science Center for Physical Sciences at the Microscale, University of Science and Technology of China, Hefei, China.
Jiliang HuDepartment of Neurosurgery, The Shenzhen People's Hospital (The Second Clinical Medical Collage of Jinan University), Shenzhen, China.
Li LuDepartment of Anatomy, Shanxi Medical University, Taiyuan, China.
Haiming DaiAnhui Province Key Laboratory of Medical Physics and Technology, Center of Medical Physics and Technology, Hefei Institutes of Physical Science, Chinese Academy of Sciences, Hefei, China.
Hongzhi WangAnhui Province Key Laboratory of Medical Physics and Technology, Center of Medical Physics and Technology, Hefei Institutes of Physical Science, Chinese Academy of Sciences, Hefei, China.
Wulin YangAnhui Province Key Laboratory of Medical Physics and Technology, Center of Medical Physics and Technology, Hefei Institutes of Physical Science, Chinese Academy of Sciences, Hefei, China.ORCID https://orcid.org/0000-0001-6520-7182
Chinese Academy of Sciences · CNUniversity of Science and Technology of China · CNJinan University · CNShanxi Medical University · CN

Funding

Anhui Province Key Laboratory of Medical Physics and Technology LMPT201702Innovative Program of Development Foundation of Hefei Center for Physical Science and Technology 2018CXFX006National Natural Science Foundation of China 81572948National Natural Science Foundation of China 81872276Natural Science Foundation of Anhui Province 1708085MH204Natural Science Foundation of Shanxi Province 2015011132Shanxi Scholarship Council of China 2014-033
6 · The paper itself

Abstract

objectivesMany cancer cells depend on G2 checkpoint mechanism regulated by WEE family kinases to maintain genomic integrity. The PKMYT1 gene, as a member of WEE family kinases, participates in G2 checkpoint surveillance and probably links with tumorigenesis, but its role in breast cancer remains largely unclear. MATERIALS AND

methodsIn this study, we used a set of bioinformatic tools to jointly analyse the expression of WEE family kinases and investigate the prognostic value of PKMYT1 in breast cancer.

resultsThe results indicated that PKMYT1 is the only frequently overexpressed member of WEE family kinases in breast cancer. KM plotter data suggests that abnormally high expression of PKMYT1 predicts poor prognosis, especially for some subtypes, such as luminal A/B and triple-negative (TNBC) types. Moreover, the up-regulation of PKMYT1 was associated with HER2-positive (HER2+), basal-like (Basal-like), TNBC statuses and increased classifications of Scarff, Bloom and Richardson (SBR). Co-expression analysis showed PKMYT1 has a strong positive correlation with Polo-like kinase 1 (PLK1), implying they may cooperate in regulating cancer cell proliferation by synchronizing rapid cell cycle with high quality of genome maintenance.

conclusionsCollectively, this study demonstrates that overexpression of PKMYT1 is always found in breast cancer and predicts unfavourable prognosis, implicating it as an appealing therapeutic target for breast carcinoma.

Indexed as

Breast NeoplasmsCarcinogenesisCell Line, TumorCell ProliferationFemaleHumansMembrane ProteinsPrognosisProtein Serine-Threonine KinasesProtein-Tyrosine KinasesUp-RegulationMembrane ProteinsPKMYT1 protein, humanProtein Serine-Threonine KinasesProtein-Tyrosine Kinasesbreast cancerG2M checkpointPKMYT1PLK1Prognostic biomarkerWEE family kinases

Identifiers

PMID31837068
PMCPMC7046476
OpenAlexW2995810260

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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.