Evidence map›Paper›PMID 41859310›Full record

ArticleInternational journal of general medicine2026

The Association of EGFL7 Polymorphism and Expression with Cervical Cancer Susceptibility and Pathogenesis.

Weipeng Liu, Zhixin Niu, Zhiling Yan, Lei Shi, Shao Zhang, Chao Hong, Shuying Dai, Li Shi, Yufeng Yao

Abstract read
In one paragraph

Article in International journal of general medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Weipeng Liu *Institute of Medical Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Kunming, People's Republic of China.ORCID 0009-0006-4194-6291
Zhixin Niu *Institute of Medical Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Kunming, People's Republic of China.
Zhiling YanDepartment of Gynaecologic Oncology, No.3 Affiliated Hospital of Kunming Medical University, Kunming, People's Republic of China.
Lei ShiInstitute of Medical Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Kunming, People's Republic of China.
Shao ZhangDepartment of Gynaecologic Oncology, No.3 Affiliated Hospital of Kunming Medical University, Kunming, People's Republic of China.
Chao HongInstitute of Medical Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Kunming, People's Republic of China.
Shuying DaiDepartment of Pathogen Biology and Immunology Faculty of Basic Medical Science, Kunming Medical University, Kunming, People's Republic of China.
Li ShiInstitute of Medical Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Kunming, People's Republic of China.
Yufeng YaoInstitute of Medical Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Kunming, People's Republic of China.ORCID 0000-0003-4508-1409

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Previous studies have highlighted diverse roles for EGFL7 in various cancers, but its specific function in cervical cancer remains unclear. This study aimed to elucidate the role of EGFL7 in cervical cancer susceptibility and pathogenesis. Methods: We genotyped three EGFL7 SNPs in 694 healthy controls, 408 cervical intraepithelial neoplasia (CIN) patients, and 934 cervical cancer (CC) patients using TaqMan probe-based real-time PCR. EGFL7 expression was measured in tumor tissues and cell lines via qRT-PCR. RNA sequencing was used to explore the biological functions of EGFL7 in cervical cancer. Results: The G allele frequency of rs9411260 was significantly elevated in both the cervical cancer (CC) (P = 0.006) and cervical intraepithelial neoplasia (CIN) (P = 0.016) groups compared to the control group. EGFL7 mRNA expression was markedly downregulated in cervical cancer tissues and HeLa/C33A cells compared to normal tissues and ECT1/E6E7 cells. Furthermore, modulation of EGFL7 expression was found to alter pathways associated with cell adhesion, migration, and ECM-receptor interaction. Conclusion: EGFL7 polymorphisms and expression are associated with cervical cancer susceptibility. Dysregulated EGFL7 appears to contribute to cervical cancer progression by affecting cell adhesion and migration, offering new insights into its pathogenesis and potential therapeutic targets.

Indexed as

cell adhesioncervical cancerEGFL7migrationSNPs

Identifiers

PMID41859310
PMCPMC12998470

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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.