Evidence map›Paper›PMID 34413913›Full record

ArticleDisease markers2021

Cysteine-Rich Intestinal Protein 1 Served as an Epithelial Ovarian Cancer Marker via Promoting Wnt/

Yujuan Liu, Wenyu Li, Ji Luo, Yiguo Wu, Yuanyuan Xu, Tingtao Chen, Wei Zhang, Fen Fu

Open access · hybridAbstract read
In one paragraph

Article in Disease markers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

14 citing papers in PubMed, 18 citations in OpenAlex.

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  6. Wnt/β-catenin-driven EMT regulation in human cancers.Cellular and molecular life sciences : CMLS · 2024
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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.

Yujuan LiuDepartment of Gynaecology and Obstetrics, The Second Affiliated Hospital of Nanchang University, No. 1 Mingde Road, Nanchang 330006, China.ORCID https://orcid.org/0000-0002-4597-7240
Wenyu LiQueen Mary School, Nanchang University, No. 999 Xuefu Avenue, Nanchang 330031, China.ORCID https://orcid.org/0000-0001-5914-703X
Ji LuoDepartment of Gynaecology and Obstetrics, The Second Affiliated Hospital of Nanchang University, No. 1 Mingde Road, Nanchang 330006, China.ORCID https://orcid.org/0000-0001-7425-9929
Yiguo WuDepartment of Gynaecology and Obstetrics, The Second Affiliated Hospital of Nanchang University, No. 1 Mingde Road, Nanchang 330006, China.ORCID https://orcid.org/0000-0001-7523-3042
Yuanyuan XuDepartment of Gynaecology and Obstetrics, The Second Affiliated Hospital of Nanchang University, No. 1 Mingde Road, Nanchang 330006, China.ORCID https://orcid.org/0000-0001-5011-4389
Tingtao ChenInstitute of Translational Medicine, Nanchang University, No. 999 Xuefu Avenue, Nanchang 330031, China.ORCID https://orcid.org/0000-0002-0506-8536
Wei ZhangDepartment of Gynaecology and Obstetrics, The Second Affiliated Hospital of Nanchang University, No. 1 Mingde Road, Nanchang 330006, China.ORCID https://orcid.org/0000-0002-1606-7774
Fen FuDepartment of Gynaecology and Obstetrics, The Second Affiliated Hospital of Nanchang University, No. 1 Mingde Road, Nanchang 330006, China.ORCID https://orcid.org/0000-0002-7823-1816
Nanchang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo explore the expression, functions, and the possible mechanisms of cysteine-rich intestinal protein 1 (CRIP1) in epithelial ovarian cancer.

methodsUsing open microarray datasets from The Cancer Genome Atlas (TCGA), we identified the tumorigenic genes in ovarian cancer. Then, we detected CRIP1 expression in 26 pairs of epithelial ovarian cancer tissue samples by immunohistochemistry (IHC) and performed a correlation analysis between CRIP1 and the clinicopathological features. In addition, epithelial ovarian cancer cell lines A2780 and OVCAR3 were used to examine CRIP1 expression by western blot and qRT-PCR. Various cell function experiments related to tumorigenesis were performed including the CCK8 assay, EdU, Annexin V-FITC/PI apoptosis assay, wound healing, and Transwell assay. In addition, the expression of epithelial-mesenchymal transition (EMT) markers was detected by western blot to illustrate the relationship between CRIP1 and EMT. Furthermore, KEGG pathway enrichment analysis and western blot were conducted to reveal the signaling pathways in which CRIP1 is involved in ovarian cancer pathogenesis.

resultsCRIP1 was identified as an oncogene from the TCGA database. The IHC score demonstrated that the CRIP1 protein was expressed at a higher level in tumours than in tumour-adjacent tissues and was associated with a higher pathological stage, grade, and positive lymphatic metastasis. In cell models, CRIP1 was overexpressed in serous epithelial ovarian cancer. Cell function experiments showed that the knockdown of CRIP1 did not significantly affect cell proliferation or apoptosis but could exert an inhibitory effect on cell migration and invasion, and also induce changes in EMT markers. Furthermore, KEGG pathway enrichment analysis and western blot showed that CRIP1 could induce ovarian cancer cell metastasis through activation of the Wnt/

conclusionThis study is the first to demonstrate that CRIP1 acts as an oncogene and may promote tumour metastasis by regulating the EMT-related Wnt/

Indexed as

Biomarkers, TumorCarcinoma, Ovarian EpithelialCarrier ProteinsCell Line, TumorCell MovementCell ProliferationDisease ProgressionEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticHumansLIM Domain ProteinsNeoplasm GradingNeoplasm MetastasisOvarian NeoplasmsUp-RegulationBiomarkers, TumorCarrier ProteinsCRIP1 protein, humanLIM Domain Proteins

Identifiers

PMID34413913
PMCPMC8369172
OpenAlexW3187943506

What OpenQuestion holds

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LicenceCC BY
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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.