IDO1 与头颈部鳞状细胞癌的免疫状况相关:一项基于生物信息学分析的研究。

IF 3 Q1 DENTISTRY, ORAL SURGERY & MEDICINE Frontiers in oral health Pub Date : 2024-04-26 eCollection Date: 2024-01-01 DOI:10.3389/froh.2024.1335648
Georgia Vasiliki Gkountana, Lezhou Wang, Martina Giacomini, Aini Hyytiäinen, Krista Juurikka, Tuula Salo, Ahmed Al-Samadi
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引用次数: 0

摘要

背景:头颈部鳞状细胞癌(HNSCC)是一种死亡率高、预后差的常见癌症类型。最近的研究集中于免疫检查点在 HNSCC 进展中的作用,以及它们作为预后标志物和免疫治疗候选物的潜在用途。一些免疫检查点,如 PD-1 和 PD-L1,已在 HNSCC 中得到深入研究。而对其他分子,如吲哚胺 2,3-二氧化酶 1(IDO1)的研究则很少:方法:利用在线数据库(包括GEPIA、UALCAN、TIMER2.0、cBioPortal和LinkedOmics)探讨了IDO1的表达、预后潜力以及与HNSCC免疫特征的关联。为了进行验证,对 7 对原发性和转移性 HNSCC 进行了 IDO1 免疫染色:我们的分析表明,与健康对照组织相比,IDO1在HNSCC中的表达明显较高,尤其是在HPV+ SCC中。然而,IDO1的表达对HNSCC患者的总生存率和无病生存率的预后潜力很弱,甚至没有预后潜力。IDO1 在 HNSCC 中的表达与多种免疫相关分子呈正相关,包括大多数免疫检查点。此外,GO富集分析显示,在HNSCC中,一些免疫相关通路与IDO1的表达呈正相关,如对I型干扰素的反应和淋巴细胞介导的免疫通路。最后,IDO1的表达与HNSCC中大多数免疫细胞的浸润呈正相关,如CD4+ T细胞、CD8+ T细胞、M1和M2巨噬细胞、树突状细胞和B细胞:结论:IDO1的表达与HNSCC的免疫特征密切相关。结论:IDO1 的表达与 HNSCC 的免疫特征密切相关,应进一步探讨这一观察结果,以阐明靶向 IDO1 作为 HNSCC 新型免疫治疗方法的潜力。
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IDO1 correlates with the immune landscape of head and neck squamous cell carcinoma: a study based on bioinformatics analyses.

Background: Head and neck squamous cell carcinoma (HNSCCs) is a common cancer type with a high mortality rate and poor prognosis. Recent studies have focused on the role of immune checkpoints in HNSCC progression and in their potential use as prognostic markers and immunotherapeutic candidates. Some immune checkpoints, such as PD-1 and PD-L1, have been studied thoroughly in HNSCC. Other molecules, such as indoleamine 2,3-dioxygenase 1 (IDO1), have been investigated minimally.

Methods: IDO1 expression, prognostic potential, and association with the immune profile of HNSCC were explored using online databases, including GEPIA, UALCAN, TIMER2.0, cBioPortal, and LinkedOmics, which utilize TCGA datasets and are freely available for use. For validation purposes, seven pairs of primary and metastatic HNSCC were immunostained for IDO1.

Results: Our analysis revealed significantly higher expression of IDO1 in HNSCC, especially in HPV+ SCCs compared with healthy control tissue. However, IDO1 expression showed weak to no prognostic potential for overall and disease-free survival in HNSCC. IDO1 expression in HNSCC was positively correlated with several immune-related molecules, including most of the immune checkpoints. Additionally, GO enrichment analysis revealed that several immune-related pathways are positively correlated with IDO1 expression in HNSCC, such as response to type I interferon and lymphocyte-mediated immunity pathways. Finally, IDO1 expression positively correlated with infiltration of most of the immune cells in HNSCC, such as CD4+ T cells, CD8+ T cells, M1 and M2 macrophages, dendritic cells, and B cells.

Conclusion: IDO1 expression is closely correlated with the immune profile of the HNSCC. This observation should be explored further to elucidate the potential of targeting IDO1 as a novel immunotherapeutic approach for HNSCC.

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