Evidence map›Paper›PMID 32565963›Full record

ArticleOncology letters2020

Claudin 10 acts as a novel biomarker for the prognosis of patients with ovarian cancer.

Zhongjun Li, Wenting Xuan, Lishan Huang, Niankun Chen, Zhiyong Hou, Biyan Lu, Chuangyu Wen, Suran Huang

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.0field-weighted citation impact, top 28% 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

15 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
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  6. Claudin-10 is a new candidate prognostic marker in metastatic high-grade serous carcinoma.Virchows Archiv : an international journal of pathology · 2023
    Article
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  15. circKMT2D contributes to HExperimental and therapeutic medicine · 2020
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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 1 institution in 1 country.

Zhongjun LiDepartment of Obstetrics and Gynecology, Dongguan Affiliated Hospital, Southern Medical University, Dongguan, Guangdong 523059, P.R. China.
Wenting XuanDepartment of Obstetrics and Gynecology, Dongguan Affiliated Hospital, Southern Medical University, Dongguan, Guangdong 523059, P.R. China.
Lishan HuangDepartment of Obstetrics and Gynecology, Dongguan Affiliated Hospital, Southern Medical University, Dongguan, Guangdong 523059, P.R. China.
Niankun ChenDepartment of Obstetrics and Gynecology, Dongguan Affiliated Hospital, Southern Medical University, Dongguan, Guangdong 523059, P.R. China.
Zhiyong HouDepartment of Obstetrics and Gynecology, Dongguan Affiliated Hospital, Southern Medical University, Dongguan, Guangdong 523059, P.R. China.
Biyan LuDepartment of Basic Medical Sciences, Dongguan Polytechnic, Dongguan, Guangdong 523808, P.R. China.
Chuangyu WenDepartment of Obstetrics and Gynecology, Dongguan Affiliated Hospital, Southern Medical University, Dongguan, Guangdong 523059, P.R. China.
Suran HuangDepartment of Obstetrics and Gynecology, Dongguan Affiliated Hospital, Southern Medical University, Dongguan, Guangdong 523059, P.R. China.
Southern Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ovarian cancer (OC) is one of the most fatal gynecological malignancies in the world and confers a poor 5-year survival rate. The present study was designed to discover novel prognostic markers for patients with OC in order to estimate disease metastasis or recurrence. Based on the large cohorts of transcriptome data from multicenter sources, a comprehensive analysis was performed to explore potential prognostic markers. A total of 269 differentially expressed genes were identified, of which 32 were upregulated and 237 downregulated in OC tissues compared with the corresponding expression in normal tissues. Kaplan-Meier analysis, log-rank test and nomogram analysis were employed to demonstrate that low expression levels of claudin 10 (CLDN10) were associated with a less favorable disease prognosis. The most promising prognostic marker for OC was subsequently selected. Additionally, the prognostic nomogram was constructed in order to assess the 5-year survival rate using CLDN10 expression as a prognostic marker for OC. Furthermore, gene set enrichment analysis and analysis of the tumor-associated competing endogenous RNA network were performed to elucidate the potential biological processes associated with CLDN10 expression. The current results indicated that CLDN10 may influence OC progression via transforming growth factor-β (TGF-β)- or WNT/β-catenin-induced epithelial-to-mesenchymal transition (EMT). The associations among CLDN10, microRNA-486-5p, TGF-β, WNT/β-catenin and EMT should be further investigated in future studies.

Indexed as

claudin 10competing endogenous RNAovarian cancerprognosissignaling pathways

Identifiers

PMID32565963
PMCPMC7285858
OpenAlexW3017931821

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.