Evidence map›Paper›PMID 34187415›Full record

ArticleBMC cancer2021

CypB promotes cell proliferation and metastasis in endometrial carcinoma.

Jing Liu, Ying Zuo, Gui-Mei Qu, Xiao Song, Zhong-Hui Liu, Ting-Guo Zhang, Zhu-Hua Zheng, Hong-Kun Wang

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 42% 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

6 citing papers in PubMed, 6 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 6 institutions in 1 country.

Jing Liu *Department of Pathology, Affiliated Yantai Yuhuangding Hospital, Medical College of Qingdao University, Yantai, China.
Ying Zuo *Department of Gynecology, Affiliated Yantai Yuhuangding Hospital, Medical College of Qingdao University, Yantai, China.
Gui-Mei QuDepartment of Pathology, Affiliated Yantai Yuhuangding Hospital, Medical College of Qingdao University, Yantai, China.
Xiao SongDepartment of Pathology, People's Hospital of Rong cheng, Weihai, China.
Zhong-Hui LiuDepartment of Pathology, Yantai Muping District Traditional Chinese Medicine Hospital, Yantai, China.
Ting-Guo ZhangDepartment of Pathology, School of Medicine, Shandong University, Jinan, Shandong, China.
Zhu-Hua ZhengDepartment of Pediatrics, Traditional Chinese Medicine Hospital of Rushan, Weihai, China.
Hong-Kun WangDepartment of Gynaecology and Obstetrics, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China. annie_coco@163.com.
Qingdao University · CNShandong University · CNShanghai Jiao Tong University · CNWeifang Chinese Medicine Hospital · CNYantaishan Hospital · CNYuhuangding Hospital · CN

Funding

Natural Science Foundation of Shandong Province (CN) ZR2016HL39
6 · The paper itself

Abstract

backgroundThe molecular pathogenesis of endometrial cancer is not completely understood. CypB upregulated in many cancers, however, its role in endometrial carcinoma has not been studied. Here, we determine the effect of CypB on the growth of endometrial cancer.

methodsIn this study, we examined the expression of CypB in endometrial cancer tissues using immunohistochemistry. CypB silenced in HEC-1-B cell line by shRNA. CCK-8, colony formation assays, wound healing assays, and transwell analysis were performed to assess its effect on tumor cell proliferation and metastasis. Furthermore, microarray analysis was carried out to compare the global mRNA expression profile between the HEC-1-B and CypB-silenced HEC-1-B cells. Gene ontology and KEGG pathway enrichment analysis were performed to determine the potential function of differentially expressed genes related to CypB.

resultsWe found that CypB was upregulated in endometrial cancer, inhibit CypB expression could significantly suppress cell proliferation, metastasis, and migration. We identified 1536 differentially expressed genes related to CypB (onefold change, p < 0.05), among which 652 genes were upregulated and 884 genes were downregulated. The genes with significant difference in top were mainly enriched in the cell cycle, glycosphingolipid biosynthesis, adherens junctions, and metabolism pathways.

conclusionThe results of our study suggest that CypB may serve as a novel regulator of endometrial cell proliferation and metastasis, thus representing a novel target for gene-targeted endometrial therapy.

trial registrationYLYLLS [2018] 008. Registered 27 November 2017.

Indexed as

Cell ProliferationCyclophilinsEndometrial NeoplasmsFemaleHumansNeoplasm Metastasiscyclophilin BCyclophilinsCyclophilin BEndometrial cancerMicroarrayProliferation

Identifiers

PMID34187415
PMCPMC8240271
OpenAlexW3134253434

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.