Evidence map›Paper›PMID 42862339›Full record

ArticleActa diabetologica2026

Clinical significance and biological role of circFNDC3B in diabetic retinopathy.

Fang Liu, Dongxu Guan, Zhiyu Yang, Dan Zou

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Article in Acta diabetologica, 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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5 · Who and what money

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4 authors.

Fang LiuDepartment of Eye Disease Center, Affiliated HongQi Hospital of Mudanjiang Medical University, Mudanjiang, 157011, China.
Dongxu GuanDepartment of Eye Disease Center, Affiliated HongQi Hospital of Mudanjiang Medical University, Mudanjiang, 157011, China.
Zhiyu YangDepartment of Gastroenterology, Mudanjiang First People's Hospital, Mudanjiang, 157011, China.
Dan ZouNursing Department, Affiliated HongQi Hospital of Mudanjiang Medical University, No. 5, Tongxiang Road, Aimin District, Mudanjiang, 157011, Heilongjiang, China. zoudandr@163.com.ORCID http://orcid.org/0009-0009-4785-914X

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6 · The paper itself

Abstract

objectiveThis paper investigates the clinical significance and role of circFNDC3B in diabetic retinopathy (DR).

methodsExpression levels of circFNDC3B, miR-578, and PIK3CA were detected in serum from DR patients and in HRMECs under high glucose (HG) conditions via qRT-PCR. Diagnostic value of circFNDC3B were assessed using ROC curves and logistic regression analysis. Cell proliferation, migration, and invasion capabilities of HRMECs were assessed using CCK-8 assays and Transwell experiments. Cellular inflammation was measured via ELISA. The interrelationship among circFNDC3B, miR-578, and PIK3CA was validated through dual-luciferase reporter and RNA immunoprecipitation experiments.

resultsIn the serum of patients with DR, circFNDC3B was markedly upregulated, and it has potential as a diagnostic biomarker for DR. miR-578 was identified as a direct target miRNA of circFNDC3B, showing downregulated expression in both DR patient serum and HG-induced HRMECs. Inhibition of miR-578 partially reversed the suppression of circFNDC3B downregulation on proliferation, migration, invasion, and inflammatory responses in HG-induced HRMECs circFNDC3B regulated PIK3CA expression by sponging miR-578.

conclusioncircFNDC3B may serve as a potential biomarker for DR diagnosis and treatment. Its involvement in HG-induced HRMEC injury, through interacting with miR-578, provides new insights into the pathogenesis of DR.

Indexed as

circFNDC3BDiabetic retinopathymiR-578PIK3CA

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