Evidence map›Paper›PMID 42090086›Full record

ArticleDiscover oncology2026

Exosomal circVANGL1 promotes cisplatin resistance in osteosarcoma cells by regulating the miR-145-5p/E2F3 axis.

Fan Mo, Hao Wang, Qi Xie, Dahong Huang, Yuan Yang

Abstract read
In one paragraph

Article in Discover oncology, 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
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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Fan Mo *Department of Orthopedics, Guangxi Medical University Kaiyuan Langdong Hospital, Langdong, Nanning, 530028, Guangxi, China.
Hao Wang *Department of Orthopedics and Traumatology, Jieyang City Chinese Medicine Hospital, Jieyang, 522000, Guangdong, China.
Qi XieDepartment of Orthopedics, Guangxi Medical University Kaiyuan Langdong Hospital, Langdong, Nanning, 530028, Guangxi, China.
Dahong HuangDepartment of Orthopedics, Guangxi Medical University Kaiyuan Langdong Hospital, Langdong, Nanning, 530028, Guangxi, China.
Yuan YangDepartment of Orthopedics, Guangxi Medical University Kaiyuan Langdong Hospital, Langdong, Nanning, 530028, Guangxi, China. yangyuannn@yeah.net.

Funding

Self-funded scientific research project of Guangxi Health Commission Z-A20221074
6 · The paper itself

Abstract

BACKGROUND AND

objectivesOsteosarcoma (OS) is a malignant bone tumor originating directly from bone tissue, predominantly affecting adolescents. Cisplatin (DDP)-based chemotherapy is commonly used in the treatment of OS, but the emergence of DDP resistance poses a significant challenge to effective management. The study aimed to investigate the role of circRNA VANGL1 (circVANGL1) in mediating DDP resistance in OS in vitro. MATERIALS AND

methodsThe OS cell lines U2OS and MG-63 were used, and DDP-resistant cell models (U2OS-DR and MG-63-DR) were established. Transfection with circVANGL1 siRNA was performed to silence circVANGL1 expression, and its impact on cell proliferation, apoptosis, DDP resistance, and miR-145-5p level was studied. Fluorescence in situ hybridization was employed to localize circVANGL1. TargetScan prediction was utilized to identify the interaction between circVANGL1 and miR-145-5p. Co-transfection experiments of si-circVANGL1 with anti-miR-145-5p or E2F3 overexpression vector (E2F3-oe) were conducted to assess their effects on DDP-resistant cells.

resultsCompared to the parental cells, the expression of circVANGL1 was increased by approximately 2.2-fold and 2.5-fold in U2OS-DR and MG-63-DR cells, respectively (P < 0.01). Transfection with si-circVANGL1 effectively suppressed cell proliferation and DDP resistance while promoting apoptosis in DDP-resistant cells. circVANGL1 is transferred via exosomes and primarily localized in the cytoplasm of U2OS and MG-63 cells. TargetScan prediction indicated a target relationship between circVANGL1 and miR-145-5p. Co-transfection of si-circVANGL1 with anti-miR-145-5p or E2F3-oe counteracted the changes in proliferation and apoptosis observed with si-circVANGL1 transfection alone in DDP-resistant cells.

conclusionIn vitro findings preliminarily suggest that exosomal circVANGL1 may promote DDP resistance in OS cells by regulating the miR-145-5p/E2F3 axis.

Indexed as

circRNAcircVANGL1CisplatinDrug resistanceE2F3miR-145-5pOsteosarcoma

Identifiers

PMID42090086
PMCPMC13315029

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