Evidence map›Paper›PMID 34099634›Full record

ArticleCell death & disease2021

HJURP promotes proliferation in prostate cancer cells through increasing CDKN1A degradation via the GSK3β/JNK signaling pathway.

Wenjie Lai, Weian Zhu, Chutian Xiao, Xiaojuan Li, Yu Wang, Yuefu Han, Jiayu Zheng, Yingqiu Li, Mingqiang Li, Xingqiao Wen

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.9field-weighted citation impact, top 7% 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

25 citing papers in PubMed, 42 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

10 authors at 3 institutions in 1 country.

Wenjie LaiDepartment of Urology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Weian ZhuDepartment of Urology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Chutian XiaoDepartment of Urology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Xiaojuan LiDepartment of Health Care, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Yu WangDepartment of Urology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Yuefu HanDepartment of Urology, Yue Bei People's Hospital, Shaoguan, China.
Jiayu ZhengDepartment of Urology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Yingqiu LiState Key Laboratory of Biocontrol, Key Laboratory of Gene Engineering of the Ministry of Education, School of Life Sciences, Sun Yat-sen University, Guangzhou, China.
Mingqiang LiLaboratory of Biomaterials and Translational Medicine, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China. limq567@mail.sysu.edu.cn.ORCID 0000-0002-5178-4138
Xingqiao WenDepartment of Urology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China. wenxq@mail.sysu.edu.cn.ORCID 0000-0003-1809-9208
Sun Yat-sen University · CNShantou University · CNSouthern Medical University Shenzhen Hospital · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82072820
6 · The paper itself

Abstract

Genes with cross-cancer aberrations are most likely to be functional genes or potential therapeutic targets. Here, we found a total of 137 genes were ectopically expressed in eight cancer types, of which Holliday junction recognition protein (HJURP) was significantly upregulated in prostate cancer (PCa). Moreover, patients with higher HJURP mRNA and protein levels had poorer outcomes, and the protein levels served as an independent prognosis factor for the overall survival of PCa patients. Functionally, ectopic HJURP expression promoted PCa cells proliferation in vitro and in vivo. Mechanistically, HJURP increased the ubiquitination of cyclin-dependent kinase inhibitor 1 (CDKN1A) via the GSK3β/JNK signaling pathway and decreased its stability. This study investigated the role of HJURP in PCa proliferation and may provide a novel prognostic and therapeutic target for PCa.

Indexed as

MAP Kinase Signaling SystemAgedBiomarkers, TumorCell ProliferationCyclin-Dependent Kinase Inhibitor p21DNA-Binding ProteinsGlycogen Synthase Kinase 3 betaHumansMalePrognosisProstatic NeoplasmsBiomarkers, TumorCDKN1A protein, humanCyclin-Dependent Kinase Inhibitor p21DNA-Binding ProteinsGlycogen Synthase Kinase 3 betaHJURP protein, human

Identifiers

PMID34099634
PMCPMC8184824
OpenAlexW3171725454

What OpenQuestion holds

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LicenceCC BY
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.