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Role of Prognostic Marker PRR11 in Immune Infiltration for Facilitating Lung Adenocarcinoma Progression / 生物医学与环境科学(英文)
Artigo em Inglês | WPRIM (Pacífico Ocidental) | ID: wpr-1007859
Biblioteca responsável: WPRO
ABSTRACT
The PRR11 gene (Proline Rich 11) has been implicated in lung cancer; however, relationship between PRR11 and immune infiltration is not clearly understood. In this study, we used The Cancer Genome Atlas (TCGA) data to analyze the lung adenocarcinoma patients; PRR11 gene expression, clinicopathological findings, enrichment, and immune infiltration were also studied. PRR11 immune response expression assays in lung adenocarcinoma (LUAD) were performed using TIMER, and statistical analysis and visualization were conducted using R software. All data were verified using Gene Expression Profiling Interactive Analysis (GEPIA), and the Human Protein Atlas (HPA). We found that PRR11 was an important prognostic factor in patients with LUAD. PRR11 expression was correlated with tumor stage and progression. Gene Set Enrichment Analysis (GSEA) showed that PRR11 was enriched in the cell cycle regulatory pathways. Immune infiltration analysis revealed that the number of T helper 2 (Th2) cells increased when PRR11 was overexpressed. These results confirm the role of PRR11 as a prognostic marker of lung adenocarcinoma by controlling the cell cycle and influencing the immune system to facilitate lung cancer progression.
Assuntos

Texto completo: Disponível Base de dados: WPRIM (Pacífico Ocidental) Assunto principal: Prognóstico / Bioensaio / Ciclo Celular / Adenocarcinoma de Pulmão / Neoplasias Pulmonares Limite: Humanos Idioma: Inglês Revista: Biomedical and Environmental Sciences Ano de publicação: 2023 Tipo de documento: Artigo
Texto completo: Disponível Base de dados: WPRIM (Pacífico Ocidental) Assunto principal: Prognóstico / Bioensaio / Ciclo Celular / Adenocarcinoma de Pulmão / Neoplasias Pulmonares Limite: Humanos Idioma: Inglês Revista: Biomedical and Environmental Sciences Ano de publicação: 2023 Tipo de documento: Artigo
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