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pmid:37354488
An integrated bioinformatic investigation of focal adhesion-related genes in glioma followed by preliminary validation of COL1A2 in tumorigenesis.
Guojun Yao · Ling Deng · Xinquan Long · Yufan Zhou · Xiang Zhou
Aging · 2023 doi:10.18632/aging.204834
Paper
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Experiment
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Data
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Analysis
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Execution
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Complete file
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In addition, FAs are associated with changes in the tumor microenvironment (TME) that lead to malignant progression and drug resistance in tumors. However, there are still few studies on the comprehensive analysis of focal adhesion-related genes (FARGs) in glioma. Expression data and clinical information of glioma samples were downloaded from public databases. Two distinct molecular subtypes were identified based on FARGs using an unsupervised consensus clustering algorithm. A scoring system consisting of nine FARGs was constructed using integrated LASSO regression and multivariate Cox regression. It not only has outstanding prognostic value but also can guide immunotherapy of glioma patients, which was verified in TCGA, CGGA, GSE16011, and IMvigor210 cohorts. The results of bioinformatics analysis, immunohistochemistry staining, and western blotting all revealed that the expression of COL1A2 was up-regulated in glioblastoma and related to poor prognosis outcomes in patients from public datasets. COL1A2 promotes the proliferation, migration, and invasion of glioblastoma cells. A positive correlation between COL1A2 and CD8 was determined in GBM specimens from eight patients. Moreover, the results of cell co-cultured assay showed that COL1A2 participated in the killing of GBM cells by Jurkat cells. Our study indicates that the FARGs have prominent application value in the identification of molecular subtypes and prediction of survival outcomes in glioma patients. 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Cell culture, transfection, and activation Normal human astrocytes (NHA", "were added to the culture medium. The COL1A2 knockdown and overexpression plasmids were constructed"], "order_basis": "paper_text_order:5837", "id": "assay:4"}, {"role": "data_generation", "definition_id": "cell_culture", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.99, "evidence": ["ed with RPMI-1640 medium (Gibco, USA), other cell lines were cultured with MEM (Gibco, USA) or DMEM (Gibco, USA).", "source Center. Except that Jurkat cells were cultured with RPMI-1640 medium (Gibco, USA), other cell li", "0 medium (Gibco, USA), other cell lines were cultured with MEM (Gibco, USA) or DMEM (Gibco, USA). 50 IU", "s proliferated. 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