Microarray and bioinformatic analysis of conventional ameloblastoma: an observational analysis

被引:2
作者
Fernando Jacinto-Aleman, Luis [1 ]
Portilla-Robertson, Javier [1 ]
Rosa Leyva-Huerta, Elba [1 ]
Orlando Ramirez-Jarquin, Josue [2 ]
German Villanueva-Sanchez, Francisco [3 ]
机构
[1] Univ Nacl Autonoma Mexico, Fac Odontol, Div Estudios Posgrad & Invest, Dept Patol & Med Bucal, Ciudad De Mexico 04510, Mexico
[2] Univ Nacl Autonoma Mexico, Div Neurociencias, Inst Fisiol Celular, Ciudad De Mexico, Mexico
[3] Univ Nacl Autonoma Mexico, Escuela Nacl Estudios Super, Guanajuato, Mexico
关键词
Ameloblastoma; Computational Biology; Platelet-derived growth factor Alpha; IL2RA protein; human; GROWTH-FACTOR; EXPRESSION;
D O I
10.1590/1678-7757-2022-0308
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Ameloblastoma is a highly aggressive odontogenic tumor, and its pathogenesis is associated with many participating genes. Objective: We aimed to identify and validate new critical genes of conventional ameloblastoma using microarray and bioinformatics analysis. Methodology: Gene expression microarray and bioinformatic analysis were performed using CHIP H10KA and DAVID software for enrichment. Protein-protein interactions (PPI) were visualized using STRING-Cytoscape with MCODE plugin, followed by Kaplan-Meier and GEPIA analyses that were used for the candidate's postulation. RT-qPCR and IHC assays were performed to validate the bioinformatic approach. Results: 376 upregulated genes were identified. PPI analysis revealed 14 genes that were validated by Kaplan-Meier and GEPIA resulting in PDGFA and IL2RA as candidate genes. The RT-qPCR analysis confirmed their intense expression. Immunohistochemistry analysis showed that PDGFA expression is parenchyma located. Conclusion: With bioinformatics methods, we can identify upregulated genes in conventional ameloblastoma, and with RT-qPCR and immunoexpression analysis validate that PDGFA could be a more specific and localized therapeutic target.
引用
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页数:11
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