Evidence map›Paper›PMID 38795132›Full record

ArticleCellular and molecular life sciences : CMLS2024

NEK2 promotes the development of ovarian endometriosis and impairs decidualization by phosphorylating FOXO1.

Mengxue Wang, Fangyuan Sun, Shucai Zhang, Xiaohui Zhang, Yujun Sun, Ting Yu, Yuanyuan Li, Aifang Jiang, Pengyun Qiao, Chune Ren and 1 more

Abstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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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

11 authors.

Mengxue Wang *Department of Reproductive Medicine, Affiliated Hospital of Shandong Second Medical University, Weifang, Shandong Province, P.R. China.
Fangyuan Sun *Department of Reproductive Medicine, Affiliated Hospital of Shandong Second Medical University, Weifang, Shandong Province, P.R. China.
Shucai Zhang *Emergency Department, Affiliated Hospital of Shandong Second Medical University, Weifang, Shandong Province, P.R. China.
Xiaohui Zhang *Department of Obstetrics and Gynecology, Zhucheng People's Hospital, Shandong Second Medical University, Weifang, Shandong Province, P.R. China.
Yujun SunDepartment of Reproductive Medicine, Affiliated Hospital of Shandong Second Medical University, Weifang, Shandong Province, P.R. China.
Ting YuDepartment of Reproductive Medicine, Affiliated Hospital of Shandong Second Medical University, Weifang, Shandong Province, P.R. China.
Yuanyuan LiDepartment of Reproductive Medicine, Affiliated Hospital of Shandong Second Medical University, Weifang, Shandong Province, P.R. China.
Aifang JiangDepartment of Reproductive Medicine, Affiliated Hospital of Shandong Second Medical University, Weifang, Shandong Province, P.R. China.
Pengyun QiaoDepartment of Reproductive Medicine, Affiliated Hospital of Shandong Second Medical University, Weifang, Shandong Province, P.R. China.
Chune RenDepartment of Reproductive Medicine, Affiliated Hospital of Shandong Second Medical University, Weifang, Shandong Province, P.R. China. wyfybaby@126.com.
Tingting YangDepartment of Reproductive Medicine, Affiliated Hospital of Shandong Second Medical University, Weifang, Shandong Province, P.R. China. y402115432@163.com.ORCID http://orcid.org/0000-0001-9927-3057

Funding

Clinical Research Center of Affiliated Hospital of Weifang Medical University 2021wyfylcyj01National Natural Science Foundation of China 81602301National Natural Science Foundation of China 81972489Natural Science Foundation of Shandong Province ZR2021MH235Shandong province college science and technology plan project J17KA254
6 · The paper itself

Abstract

Ovarian endometriosis is a common gynecological disease, and one of its most significant symptoms is infertility. In patients with endometriosis, defects in endometrial decidualization lead to impaired endometrial receptivity and embryo implantation, thus affecting early pregnancy and women's desire to have children. However, the mechanisms underlying the development of endometriosis and its associated defective decidualization are unclear. We find that NEK2 expression is increased in the ectopic and eutopic endometrium of patients with endometriosis. Meanwhile, NEK2 interacts with FOXO1 and phosphorylates FOXO1 at Ser184, inhibiting the stability of the FOXO1 protein. Importantly, NEK2-mediated phosphorylation of FOXO1 at Ser184 promotes cell proliferation, migration, invasion and impairs decidualization. Furthermore, INH1, an inhibitor of NEK2, inhibits the growth of ectopic lesions in mouse models of endometriosis and promotes endometrial decidualization in mouse models of artificially induced decidualization. Taken together, these findings indicate that NEK2 regulates the development of endometriosis and associated disorders of decidualization through the phosphorylation of FOXO1, providing a new therapeutic target for its treatment.

Indexed as

Cell ProliferationEndometriosisEndometriumForkhead Box Protein O1NIMA-Related KinasesAdultAnimalsCell MovementDeciduaDisease Models, AnimalFemaleHumansMicePhosphorylationForkhead Box Protein O1FOXO1 protein, humanNEK2 protein, humanNIMA-Related KinasesDecidualizationEndometriosisFOXO1NEK2

Identifiers

PMID38795132
PMCPMC11127904

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Registered trials

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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.