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pmid:41092639

LAMC1 aggravates diabetic retinopathy through PI3K/AKT signaling-regulated epithelial-mesenchymal transition in retinal pigment epithelial cells.

Lei Liu · Yanlin Gao · Shiqi Yao

The journal of physiological sciences : JPS · 2025 doi:10.1016/j.jphyss.2025.100045

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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title
LAMC1 aggravates diabetic retinopathy through PI3K/AKT signaling-regulated epithelial-mesenchymal transition in retinal pigment epithelial cells.
doi
10.1016/j.jphyss.2025.100045
pmid
41092639
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[0]
Lei Liu
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Yanlin Gao
[2]
Shiqi Yao
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The journal of physiological sciences : JPS
year
2025
abstract
Diabetic retinopathy (DR), a leading cause of adult blindness, with LAMC1-mediated epithelial-mesenchymal transition (EMT) playing a key role. By analyzing DR-related microarray datasets (GSE60436/GSE102485) from GEO, we identified 685 differentially expressed genes (570 downregulated, 115 upregulated). Functional and WGCNA analyses linked these to PI3K/Akt signaling, revealing 11 diagnostic hub genes, including LAMC1. Western blot analysis confirmed that LAMC1 significantly upregulated in high glucose (HG)-treated ARPE-19 cells and diabetic mouse retinas. In vitro and in vivo experiments confirmed that LAMC1 promotes EMT in retinal pigment epithelial (RPE) cells via PI3K/Akt activation, enhancing migration and invasion. Conversely, LAMC1 knockdown alleviated retinal damage in diabetic mice. Our studies uncovered that LAMC1's role in DR progression through PI3K/Akt-driven EMT, suggesting its potential as a therapeutic target.
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LAMC1 promotes diabetic retinopathy through epithelial-mesenchymal transition regulated by PI3K/AKT signaling axis.
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Our studies uncovered that LAMC1’s role in DR progression through PI3K/Akt-driven EMT, suggesting its potential as a therapeutic target.
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LAMC1 promotes diabetic retinopathy through epithelial-mesenchymal transition regulated by PI3K/AKT signaling axis.
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LAMC1 promotes diabetic retinopathy through epithelial-mesenchymal transition regulated by PI3K/AKT signaling axis.
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Induced Expression of VEGFC, ANGPT, and EFNB2 and Their Receptors Characterizes Neovascularization in Proliferative Diabetic Retinopathy
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Gene Expression Profile of Fibrovascular Membrane Associated with Proliferative Diabetic Retinopathy
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playing a key role. By analyzing DR-related microarray datasets (GSE60436/GSE102485) from GEO, we i
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ng 11 diagnostic hub genes, including LAMC1. Western blot analysis confirmed that LAMC1 significantly
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ng migration and invasion. Conversely, LAMC1 knockdown alleviated retinal damage in diabetic mice.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:41092639", "kind": "science-record", "revision": 4, "content_hash": "sha256:2a27db5893efc43dd315f7f0ce07d1628136a55f60527c0aaf186821c3a04f08", "created_at": "2026-11-01T20:31:09Z", "updated_at": "2026-11-01T22:57:18Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "LAMC1 aggravates diabetic retinopathy through PI3K/AKT signaling-regulated epithelial-mesenchymal transition in retinal pigment epithelial cells.", "doi": "10.1016/j.jphyss.2025.100045", "pmid": "41092639", "authors": ["Lei Liu", "Yanlin Gao", "Shiqi Yao"], "journal": "The journal of physiological sciences : JPS", "year": 2025, "abstract": "Diabetic retinopathy (DR), a leading cause of adult blindness, with LAMC1-mediated epithelial-mesenchymal transition (EMT) playing a key role. By analyzing DR-related microarray datasets (GSE60436/GSE102485) from GEO, we identified 685 differentially expressed genes (570 downregulated, 115 upregulated). Functional and WGCNA analyses linked these to PI3K/Akt signaling, revealing 11 diagnostic hub genes, including LAMC1. Western blot analysis confirmed that LAMC1 significantly upregulated in high glucose (HG)-treated ARPE-19 cells and diabetic mouse retinas. In vitro and in vivo experiments confirmed that LAMC1 promotes EMT in retinal pigment epithelial (RPE) cells via PI3K/Akt activation, enhancing migration and invasion. Conversely, LAMC1 knockdown alleviated retinal damage in diabetic mice. Our studies uncovered that LAMC1's role in DR progression through PI3K/Akt-driven EMT, suggesting its potential as a therapeutic target.", "claims": [{"id": "claim-method", "statement": "The \"limma\" package was employed for this analysis, with the criteria of log2|(FC)|≥ 1 and an adjusted p-value less than 0.05.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:41092639", "locator": "sections[4] \"Data integration and differential expression analysis\" paragraph 2", "quote": "The \"limma\" package was employed for this analysis, with the criteria of log2|(FC)|≥ 1 and an adjusted p-value less than 0.05."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets used or analyzed during the current study are available from the corresponding author on reasonable request.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:41092639", "locator": "sections[41] \"Data availability\" paragraph 2", "quote": "The datasets used or analyzed during the current study are available from the corresponding author on reasonable request."}], "state": "complete"}, {"id": "claim-target-result", "statement": "LAMC1 promotes diabetic retinopathy through epithelial-mesenchymal transition regulated by PI3K/AKT signaling axis.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:41092639", "locator": "sections[0] \"Abstract\" paragraph 1", "quote": "Our studies uncovered that LAMC1’s role in DR progression through PI3K/Akt-driven EMT, suggesting its potential as a therapeutic target."}, {"asset": "source:pmid:41092639", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "LAMC1 promotes diabetic retinopathy through epithelial-mesenchymal transition regulated by PI3K/AKT signaling axis."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "LAMC1 promotes diabetic retinopathy through epithelial-mesenchymal transition regulated by PI3K/AKT signaling axis.", "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:41092639"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. 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By analyzing DR-related microarray datasets (GSE60436/GSE102485) from GEO, we i"], "order_basis": "paper_text_order:269", "id": "assay:1"}, {"role": "data_generation", "definition_id": "western_blot", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.99, "evidence": ["ng 11 diagnostic hub genes, including LAMC1. Western blot analysis confirmed that LAMC1 significantly", "apidly frozen at - 80°C and was reserved for Western blot analysis. Statistical analysis All statistic"], "order_basis": "paper_text_order:524", "id": "assay:2"}, {"role": "data_generation", "definition_id": "animal_model", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.99, "evidence": ["lls and diabetic mouse retinas. In vitro and in vivo experiments confirmed that LAMC1 promotes EM", "cose (HG)-treated ARPE-19 cells and diabetic mouse retinas. In vitro and in vivo experiments co", "wing a 7-day period of adaptive feeding, the mice were randomly allocated into 4 distinct groups, e", "ecutive days. In contrast, the Control group mice were injected with an equivalent volume of citrat"], "order_basis": "paper_text_order:649", "id": "assay:3"}, {"role": "data_generation", "definition_id": "transfection", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.85, "evidence": ["ng migration and invasion. 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