Medical School of Chinese People's Liberation Army (PLA), Beijing, China.
Senior Department of Otolaryngology-Head & Neck Surgery, Chinese People's Liberation Army (PLA) General Hospital, National Clinical Research Center for Otolaryngologic Diseases, State Key Lab of Hearing Science, Beijing Key Lab of Hearing Impairment Prevention and Treatment, Ministry of Education, Beijing, China.
Front Immunol. 2022 Aug 26;13:975847. doi: 10.3389/fimmu.2022.975847. eCollection 2022.
Despite tremendous progress made in the diagnosis and managements, head and neck squamous cell carcinoma (HNSC) remains a global medical dilemma with dismal clinical prognosis and high mortality. Gene NT5E encodes the ecto-5'-nucleotidase (CD73), which facilitates the formation of immunosuppressive tumor microenvironment (TME) permissive for tumor progression in various malignancies. Nevertheless, the cell subsets NT5E expressed on and the potential function of NT5E in the TME of HNSC remain virgin lands in HNSC. In this study, we comprehensively performed integrated prognostic analysis and elucidated that NT5E was an independent prognostic indicator for HNSC, for which a high NT5E level predicted poor overall survival (OS), disease-specific survival (DSS) and progression-free interval (PFI) in HNSC patients (<0.05). Enrichment analyses revealed the close correlation between NT5E and ECM remodeling, and the latent function of NT5E may involve in epithelial-to-mesenchymal transition (EMT) and metastasis during HNSC progression. HNSC-related immune infiltration analysis and single-cell type analysis demonstrated that NT5E expression was significantly positively associated with cancer-associated fibroblasts (CAFs) in HNSC (<0.01). NT5E-related TME analysis revealed that NT5E-high group are characterized by low neoantigen loads (NAL, <0.001) and tumor mutation burden (TMB, <0.01), indicating high-NT5E-expression HNSC patients may be recalcitrant to immunotherapy. multicolor immunofluorescence staining was later conducted and the results further verified our findings. Taken together, NT5E could be a novel biomarker in HNSC. Predominantly expressed on CAFs, the upregulation of NT5E might predict an immunosuppressive TME for HNSC patients who may benefit little from immunotherapy. Targeting CAFs with high NT5E expression might be a novel therapeutic strategy for HNSC patients.
尽管在诊断和治疗方面取得了巨大进展,但头颈部鳞状细胞癌(HNSC)仍然是一个全球性的医学难题,临床预后不佳,死亡率高。基因 NT5E 编码外切 5'-核苷酸酶(CD73),它促进了免疫抑制性肿瘤微环境(TME)的形成,有利于各种恶性肿瘤的肿瘤进展。然而,NT5E 在 HNSC 的 TME 中表达的细胞亚群以及 NT5E 的潜在功能仍处于 HNSC 的处女地。在这项研究中,我们全面进行了综合预后分析,并阐明 NT5E 是 HNSC 的独立预后指标,高水平的 NT5E 预示着 HNSC 患者的总生存期(OS)、疾病特异性生存期(DSS)和无进展生存期(PFI)较差(<0.05)。富集分析显示 NT5E 与 ECM 重塑密切相关,NT5E 的潜在功能可能涉及 HNSC 进展过程中的上皮-间充质转化(EMT)和转移。HNSC 相关免疫浸润分析和单细胞类型分析表明,NT5E 表达与 HNSC 中的癌症相关成纤维细胞(CAFs)显著正相关(<0.01)。NT5E 相关的 TME 分析表明,NT5E-高表达组的新生抗原负荷(NAL,<0.001)和肿瘤突变负荷(TMB,<0.01)较低,这表明高-NT5E 表达的 HNSC 患者可能对免疫治疗有抗性。随后进行了多色免疫荧光染色,结果进一步验证了我们的发现。总之,NT5E 可以成为 HNSC 的一种新的生物标志物。主要表达在 CAFs 上,NT5E 的上调可能预示着 HNSC 患者的免疫抑制性 TME,他们可能从免疫治疗中获益有限。针对高 NT5E 表达的 CAFs 可能是 HNSC 患者的一种新的治疗策略。