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pmid:39090419

LINC01370 suppresses hepatocellular carcinoma proliferation and metastasis by regulating the PI3K/AKT pathway.

Fei Xiao · Zhuoyun Zhang · Luqian Li · Xiaojie He · Yufeng Chen

Discover oncology · 2024 doi:10.1007/s12672-024-01193-9

Paper

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LINC01370 suppresses hepatocellular carcinoma proliferation and metastasis by regulating the PI3K/AKT pathway.
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10.1007/s12672-024-01193-9
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Fei Xiao
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Zhuoyun Zhang
[2]
Luqian Li
[3]
Xiaojie He
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Yufeng Chen
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Discover oncology
year
2024
abstract
BACKGROUND: Hepatocellular carcinoma (HCC) poses a serious threat to human health worldwide. lncRNA dysregulation is frequently observed in various cancers, including HCC. However, the function of LINC01370 in HCC progression and its underlying mechanisms remain unclear. METHODS: LINC01370 expression in HCC tissues with cells was analyzed by applying the GEO and GEPIA databases and qRT-PCR. CCK-8 and Transwell assays were used to assess HCC cell proliferation, migration, and invasion. The PI3K, AKT, with p-AKT protein expression were analyzed by western blotting. RESULTS: Gene Expression Omnibus (GEO) and Gene Expression Profiling Interactive Analysis (GEPIA) showed that LINC01370 expression was significantly lower in HCC tissues than in normal tissues. LINC01370 overexpression markedly repressed HepG2 SMMC-7721 cells proliferation, migration, and invasion. To understand the downstream mechanism of LINC01370 regulation, we further analyzed the genes co-expressed with LINC01370 in GSE136247 and GSE132037 and then performed KEGG analysis. The PA pathway was found to be a downstream pathway regulated by LINC01370 in GSE136247 and GSE132037 via gene co-expression and KEGG analysis. Furthermore, PI3K and p-AKT protein levels decreased after LINC01370 overexpression. Importantly, rescue experiments showed that activation of the PI3K/AKT pathway disrupted the repressive effect of LINC01370 overexpression on the proliferation, migration, and invasion of HepG2 of SMMC-7721 cells. CONCLUSIONS: This study verified that LINC01370 suppresses HCC proliferation with metastasis by regulating the PI3K/AKT pathway.
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However, the function of LINC01370 in HCC progression and its underlying mechanisms remain unclear.\nMETHODS: LINC01370 expression in HCC tissues with cells was analyzed by applying the GEO and GEPIA databases and qRT-PCR. CCK-8 and Transwell assays were used to assess HCC cell proliferation, migration, and invasion. The PI3K, AKT, with p-AKT protein expression were analyzed by western blotting.\nRESULTS: Gene Expression Omnibus (GEO) and Gene Expression Profiling Interactive Analysis (GEPIA) showed that LINC01370 expression was significantly lower in HCC tissues than in normal tissues. LINC01370 overexpression markedly repressed HepG2 SMMC-7721 cells proliferation, migration, and invasion. To understand the downstream mechanism of LINC01370 regulation, we further analyzed the genes co-expressed with LINC01370 in GSE136247 and GSE132037 and then performed KEGG analysis. 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Importantly, rescue experiments showed that activation of the PI3K/AKT pathway disrupted the repressive effect of LINC01370 overexpression on the proliferation, migration, and invasion of HepG2 of SMMC-7721 cells.\nCONCLUSIONS: This study verified that LINC01370 suppresses HCC proliferation with metastasis by regulating the PI3K/AKT pathway.", "claims": [{"id": "claim-method", "statement": "Divergence was assessed using a t-test with a one-way ANOVA.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:39090419", "locator": "sections[9] \"Statistical analysis\" paragraph 2", "quote": "Divergence was assessed using a t-test with a one-way ANOVA."}], "state": "complete"}, {"id": "claim-data-access", "statement": "All data generated or analysed during this study are included in this published article [and its supplementary information files].", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:39090419", "locator": "sections[23] \"notes\" paragraph 1", "quote": "All data generated or analysed during this study are included in this published article [and its supplementary information files]."}], "state": "complete"}, {"id": "claim-target-result", "statement": "LINC01370 suppresses HCC proliferation and metastasis by regulating the PI3K/AKT pathway.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:39090419", "locator": "sections[0] \"Abstract\" paragraph 4", "quote": "This study verified that LINC01370 suppresses HCC proliferation with metastasis by regulating the PI3K/AKT pathway."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "partial", "objective": "LINC01370 suppresses HCC proliferation and metastasis by regulating the PI3K/AKT pathway.", "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:39090419"], "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": "blocked", "blocked_on": "data:accession_absent", "description": "The GEO series accession resolves and its sample accessions are listed. 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CONCLUSIONS: This study", "fe Science (Shanghai, China). The cells were cultured in DMEM (Gibco, Gaithersburg, MD, USA) suppleme", "cubation for 5 h, the transdected-cells were cultured in complete culture medium for further study. 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