Evidence map›Paper›PMID 30957190›Full record

ArticleMolecular medicine reports2019

Overexpression of CKS2 is associated with a poor prognosis and promotes cell proliferation and invasion in breast cancer.

Naiqi Huang, Zuli Wu, Hong Hong, Xiangming Wang, Fengqiang Yang, Hengguo Li

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.8field-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

18 citing papers in PubMed, 30 citations in OpenAlex.

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  13. OTUD6A Is an Aurora Kinase A-Specific Deubiquitinase.International journal of molecular sciences · 2021
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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 1 institution in 1 country.

Naiqi HuangDepartment of Pharmacy, Ninghai First Hospital, Ninghai, Zhejiang 315600, P.R. China.
Zuli WuDepartment of General Surgery, Ninghai First Hospital, Ninghai, Zhejiang 315600, P.R. China.
Hong HongDepartment of General Surgery, Ninghai First Hospital, Ninghai, Zhejiang 315600, P.R. China.
Xiangming WangDepartment of General Surgery, Ninghai First Hospital, Ninghai, Zhejiang 315600, P.R. China.
Fengqiang YangDepartment of Urology, Ninghai First Hospital, Ninghai, Zhejiang 315600, P.R. China.
Hengguo LiDepartment of Breast and Thyroid Surgery, Ninghai First Hospital, Ninghai, Zhejiang 315600, P.R. China.
Ninghai First Hospital Medicare and Health Group · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Growing evidence indicates that cyclin dependent kinases regulatory subunit 2 (CKS2) serves an essential role in the regulation of multiple cellular processes in diverse human cancer types. The present study investigated the contribution of CKS2 to breast cancer (BC) progression. In the present study, CKS2 expression in BC was detected using Oncomine and The Cancer Genome Atlas database. The association between expression levels and clinical features was explored using Kaplan‑Meier plotter and the Breast Cancer Gene‑Expression Miner Version 4.0 (bc‑GenExMiner) online database. In addition, the roles of CKS2 in BC progression were examined. It was identified that CKS2 expression was significantly increased in BC tissues at the mRNA and protein levels. Bc‑GenExMiner demonstrated that high CKS2 expression was associated with a positive estrogen receptor status, progesterone receptor status, nodal status and basal‑like status. High CKS2 expression was markedly associated with poor overall survival, relapse‑free survival, and distant metastasis‑free survival in patients with BC. Moreover, functional assays revealed that CKS2 inhibition suppressed cell proliferation and invasion ability in vitro and reduced tumor growth in vivo. Thus, the present findings suggested that CKS2 may act as a potential biomarker and therapeutic target for the treatment of BC.

Indexed as

AnimalsBiomarkers, TumorBreast NeoplasmsCarrier ProteinsCDC2-CDC28 KinasesCell Cycle ProteinsCell Line, TumorCell ProliferationFemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesHeterograftsHumansKaplan-Meier EstimateMice, Inbred BALB CPrognosisBiomarkers, TumorCarrier ProteinsCDC2-CDC28 KinasesCell Cycle ProteinsCKS2 protein, humanReceptors, EstrogenReceptors, ProgesteroneRNA, Messenger

Identifiers

PMID30957190
PMCPMC6522797
OpenAlexW2932253769

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.