KIAA1199 Correlates With Tumor Microenvironment and Immune Infiltration in Lung Adenocarcinoma as a Potential Prognostic Biomarker.

Pathology oncology research : POR Pub Date : 2022-11-07 eCollection Date: 2022-01-01 DOI:10.3389/pore.2022.1610754
Xiaoju Shen, Xiaocheng Mo, Weidan Tan, Xiaoxiang Mo, Li Li, Fei Yu, Jingchuan He, Zhihua Deng, Shangping Xing, Zhiquan Chen, Jie Yang
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引用次数: 2

Abstract

Background: KIAA1199 has been considered a key regulator of carcinogenesis. However, the relationship between KIAA1199 and immune infiltrates, as well as its prognostic value in lung adenocarcinoma (LUAD) remains unclear. Methods: The expression of KIAA1199 and its influence on tumor prognosis were analyzed using a series of databases, comprising TIMER, GEPIA, UALCAN, LCE, Prognoscan and Kaplan-Meier Plotter. Further, immunohistochemistry (IHC), western blot (WB) and receiver operating characteristic (ROC) curve analyses were performed to verify our findings. The cBioPortal was used to investigate the genomic alterations of KIAA1199. Prediction of candidate microRNA (miRNAs) and transcription factor (TF) targeting KIAA1199, as well as GO and KEGG analyses, were performed based on LinkedOmics. TIMER and TISIDB databases were used to explore the relationship between KIAA1199 and tumor immune infiltration. Results: High expression of KIAA1199 was identified in LUAD and Lung squamous cell carcinoma (LUSC) patients. High expression of KIAA1199 indicated a worse prognosis in LUAD patients. The results of IHC and WB analyses showed that the expression level of KIAA1199 in tumor tissues was higher than that in adjacent tissues. GO and KEGG analyses indicated KIAA1199 was mainly involved in extracellular matrix (ECM)-receptor interaction and extracellular matrix structure constituent. KIAA1199 was positively correlated with infiltrating levels of CD4+ T cells, macrophages, neutrophil cells, dendritic cells, and showed positive relationship with immune marker subsets expression of a variety of immunosuppressive cells. Conclusion: High expression of KIAA1199 predicts a poor prognosis of LUAD patients. KIAA1199 might exert its carcinogenic role in the tumor microenvironment via participating in the extracellular matrix formation and regulating the infiltration of immune cells in LUAD. The results indicate that KIAA1199 might be a novel biomarker for evaluating prognosis and immune cell infiltration in LUAD.

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KIAA1199与肺腺癌肿瘤微环境和免疫浸润相关,作为潜在的预后生物标志物
背景:KIAA1199被认为是致癌的关键调节因子。然而,KIAA1199与免疫浸润的关系及其在肺腺癌(LUAD)中的预后价值尚不清楚。方法:采用TIMER、GEPIA、UALCAN、LCE、Prognoscan、Kaplan-Meier Plotter等数据库分析KIAA1199的表达及其对肿瘤预后的影响。此外,免疫组织化学(IHC)、免疫印迹(WB)和受试者工作特征(ROC)曲线分析验证了我们的发现。利用基因门户研究KIAA1199的基因组变化。基于LinkedOmics进行候选microRNA (mirna)和靶向KIAA1199的转录因子(TF)预测,以及GO和KEGG分析。利用TIMER和TISIDB数据库探讨KIAA1199与肿瘤免疫浸润的关系。结果:KIAA1199在LUAD和Lung squamous cell carcinoma (LUSC)患者中高表达。KIAA1199的高表达表明LUAD患者预后较差。IHC和WB分析结果显示,KIAA1199在肿瘤组织中的表达水平高于邻近组织。GO和KEGG分析表明KIAA1199主要参与细胞外基质(ECM)-受体相互作用和细胞外基质结构组成。KIAA1199与CD4+ T细胞、巨噬细胞、中性粒细胞、树突状细胞的浸润水平呈正相关,与多种免疫抑制细胞的免疫标记亚群表达呈正相关。结论:KIAA1199高表达预示LUAD患者预后不良。KIAA1199可能通过参与LUAD细胞外基质的形成和调节免疫细胞的浸润,在肿瘤微环境中发挥致癌作用。结果提示KIAA1199可能是评估LUAD预后和免疫细胞浸润的一种新的生物标志物。
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