Evidence map›Paper›PMID 35173547›Full record

ArticleInternational journal of biological sciences2022

HJURP Promotes Malignant Progression and Mediates Sensitivity to Cisplatin and WEE1-inhibitor in Serous Ovarian Cancer.

Zhiyuan Dou, Chunping Qiu, Xun Zhang, Shu Yao, Chen Zhao, Zixiang Wang, Ran Chu, Jingying Chen, Zhongshao Chen, Rongrong Li and 5 more

Open access · goldAbstract read
In one paragraph

Article in International journal of biological sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

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  16. Cancer genomics & proteomics
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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

15 authors at 1 institution in 1 country.

Zhiyuan DouDepartment of Obstetrics and Gynecology, Qilu Hospital of Shandong University, Jinan, P.R. China.
Chunping QiuDepartment of Obstetrics and Gynecology, Qilu Hospital of Shandong University, Jinan, P.R. China.
Xun ZhangDepartment of Obstetrics and Gynecology, Qilu Hospital of Shandong University, Jinan, P.R. China.
Shu YaoDepartment of Obstetrics and Gynecology, Qilu Hospital of Shandong University, Jinan, P.R. China.
Chen ZhaoDepartment of Obstetrics and Gynecology, Qilu Hospital of Shandong University, Jinan, P.R. China.
Zixiang WangDepartment of Obstetrics and Gynecology, Qilu Hospital of Shandong University, Jinan, P.R. China.
Ran ChuDepartment of Obstetrics and Gynecology, Qilu Hospital of Shandong University, Jinan, P.R. China.
Jingying ChenDepartment of Obstetrics and Gynecology, Qilu Hospital of Shandong University, Jinan, P.R. China.
Zhongshao ChenDepartment of Obstetrics and Gynecology, Qilu Hospital of Shandong University, Jinan, P.R. China.
Rongrong LiDepartment of Obstetrics and Gynecology, Qilu Hospital of Shandong University, Jinan, P.R. China.
Kun WangDepartment of Obstetrics and Gynecology, Qilu Hospital of Shandong University, Jinan, P.R. China.
Penglin LiuDepartment of Obstetrics and Gynecology, Qilu Hospital of Shandong University, Jinan, P.R. China.
Chang LiuDepartment of Obstetrics and Gynecology, Qilu Hospital of Shandong University, Jinan, P.R. China.
Kun SongDepartment of Obstetrics and Gynecology, Qilu Hospital of Shandong University, Jinan, P.R. China.
Beihua KongDepartment of Obstetrics and Gynecology, Qilu Hospital of Shandong University, Jinan, P.R. China.
Qilu Hospital of Shandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ovarian cancer is the most lethal gynecological malignancy. Recurrence and chemoresistance are tough challenges leading to poor prognosis. HJURP is a molecular chaperone of CENP-A, which is associated with aggressive progression in multiple tumors. However, the function of HJURP in ovarian cancer has not been elucidated. In our study, we found HJURP was over-expressed in ovarian cancer and high expression of HJURP was correlated to unfavorable prognosis. HJURP knockdown could inhibit proliferation, metastasis and induce G0/G1 stagnation of ovarian cancer cells. Besides, next-generation sequencing (NGS) unveiled that WEE1 was down-regulated by silencing HJURP. Further mechanistic research revealed that HJURP regulated WEE1 through MYC, and luciferase assay indicated that MYC was a transcription factor of WEE1. Additionally, we investigated that silencing HJURP increased sensitivity of ovarian cancer cells to cisplatin via MYC/WEE1 axis, and HJURP participated in DNA repair of cisplatin-induced damage. More interestingly, silencing HJURP could enhance sensitivity of ovarian cancer cells to AZD1775 and improve the synergistic effect of cisplatin plus AZD1775 combined therapy. Collectively, our data displays that HJURP promotes tumor progression and chemoresistance of ovarian cancer, and HJURP has potential to be a novel therapeutic target in the combined treatment with cisplatin and AZD1775 in ovarian cancer.

Indexed as

Cystadenocarcinoma, SerousOvarian NeoplasmsCell Cycle ProteinsCell Line, TumorCisplatinFemaleHumansProtein-Tyrosine KinasesCell Cycle ProteinsCisplatinProtein-Tyrosine KinasesWEE1 protein, humanAZD1775chemoresistanceDNA damage repairHJURPWEE1

Identifiers

PMID35173547
PMCPMC8771849
OpenAlexW4206318356

What OpenQuestion holds

Textmetadata
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.