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Potential mechanisms underlying the promoting effects of 3D collagen scaffold culture on stemness and drug resistance of glioma cells

胶质瘤 生物 癌症研究 抗药性 基因 遗传学
作者
Wei Jia,Hecheng Zhu,Ming Zhao,Quanwei Zhou,Wen Yin,Weidong Liu,Lei Wang,Zhifeng Xiao,Xingjun Jiang,Jianwu Dai,Chao Ren
出处
期刊:Biochimica Et Biophysica Acta: Molecular Basis Of Disease [Elsevier BV]
卷期号:1868 (11): 166522-166522 被引量:5
标识
DOI:10.1016/j.bbadis.2022.166522
摘要

3D collagen scaffold culture is a good tool to study glioma metastasis and recurrence in vitro.The effect of 3D collagen culture on the colony formation, the sphere formation, and drug sensitivity of glioma cells was observed by soft-agar colony formation assays, sphere formation assays, and CCK-8 assays, respectively. 3D-glioma-drug genes were identified by previous results and online databases. Gene enrichment and PPI analyses were performed by R software and Metacsape. Hub 3D-glioma-drug genes were screened by STRING and Cytoscape. TCGA and CGGA databases and R software were used to analyze the distribution of hub genes in glioma and their effects on the prognosis. Western Blot was used to verify the effect of 3D collagen culture on the expression of hub genes. miRNAs targeting hub genes were predicted by ENCORI.3D collagen scaffold culture promoted colony formation, sphere formation, and drug resistance of glioma cells. There were 77 3D-glioma-drug genes screened, and the pathways enriched in the protein interaction network mainly included responses to stressors, DNA damage and repair, and drug metabolism. Hub 3D-glioma-drug genes were AKT1, ATM, CASP3, CCND1, EGFR, PARP1, and TP53. These genes and predicted miRNAs were expressed differentially in glioma samples and partially affected the prognosis of patients with glioma. These findings suggested these hub genes and miRNAs may play a key role in the effects generated by the 3D culture model and become new markers for glioma diagnosis and treatment.

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