GDF15 promotes corneal neovascularization and RB cell progression via AKT/ERK signal pathway

In this study, we aim to explore the involvement of growth differentiation factor 15 (GDF15) in both corneal neovascularization (CNV) and retinoblastoma (RB) progression. Cell migration and proliferation were assessed through Scratch assays and CCK-8 assays. Apoptosis was quantified using flow cytometry. In vitro angiogenesis was evaluated through a tube formation assay. RT-PCR and western blot analyses were employed to assess the angiogenesis-related factors. Results demonstrated that RhGDF15 has a promotional effect on the migration of RB cells. Conversely, si-GDF15 demonstrated an opposite effect. RhGDF15 exhibited an enhancement the tube formation, the levels of HIF-1α and SDF, as well as cell migration. Conversely, si-GDF15 demonstrated an opposite effect. The levels of factors were elevated by rhGDF15 in both HREC and RB cell lines. In conclusion, the downregulation of GDF15 has the potential to inhibit corneal angiogenesis and impede the migration of RB cells. These effects may be dependent on the AKT/ERK pathway.

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Publication Details

Journal
Growth Factors
Published
2024-10-01
DOI
https://doi.org/10.1080/08977194.2024.2432948
Primary Topic
Connective Tissue Growth Factor Research
Type
article
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article

GDF15 promotes corneal neovascularization and RB cell progression via AKT/ERK signal pathway

Haijian Zheng, Shiliang Cheng, Meng Li, Yanluan Wan et al.
Growth Factors
Connective Tissue Growth Factor Research
article

GDF15 promotes corneal neovascularization and RB cell progression via AKT/ERK signal pathway

Haijian Zheng, Shiliang Cheng, Meng Li, Yanluan Wan, Ling Wang, Guanglan Liu, Chun Guang Li, Fangfang Li, Miao Yu, Wen Zheng, Xinfeng Liu
article en

Abstract

In this study, we aim to explore the involvement of growth differentiation factor 15 (GDF15) in both corneal neovascularization (CNV) and retinoblastoma (RB) progression. Cell migration and proliferation were assessed through Scratch assays and CCK-8 assays. Apoptosis was quantified using flow cytometry. In vitro angiogenesis was evaluated through a tube formation assay. RT-PCR and western blot analyses were employed to assess the angiogenesis-related factors. Results demonstrated that RhGDF15 has a promotional effect on the migration of RB cells. Conversely, si-GDF15 demonstrated an opposite effect. RhGDF15 exhibited an enhancement the tube formation, the levels of HIF-1α and SDF, as well as cell migration. Conversely, si-GDF15 demonstrated an opposite effect. The levels of factors were elevated by rhGDF15 in both HREC and RB cell lines. In conclusion, the downregulation of GDF15 has the potential to inhibit corneal angiogenesis and impede the migration of RB cells. These effects may be dependent on the AKT/ERK pathway.

Growth FactorsVol. 42(4)
Soochow University (CN), Shandong Provincial Hospital (CN), The First People’s Hospital of Lianyungang (CN), First Affiliated Hospital of Soochow University (CN), Qilu Hospital of Shandong University (CN)
Zero hunger
Openalex Percentile: Top 78%
Connective Tissue Growth Factor Research
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