Laboratory of Molecular Immuno-Oncology, Faculty of Medicine of Monastir, University of Monastir, Monastir, Tunisia.
Higher Institute of Biotechnology of Monastir, University of Monastir, Monastir, Tunisia.
Immun Inflamm Dis. 2022 Sep;10(9):e690. doi: 10.1002/iid3.690.
Indoleamine 2,3-dioxygenase (IDO) is an immunosuppressive tryptophan-depleting enzyme expressed in nasopharyngeal carcinoma (NPC) tissue. However, IDO has not been reported in the peripheral blood of NPC patients. The aim of this study was to analyze, IDO1 and IDO2 messenger RNA (mRNA) expression, the kynurenine (Kyn) and tryptophan (Trp) plasma levels, their clinical values and their relationship with cytokine levels in NPC.
We evaluated IDO1 and IDO2 mRNA expression in peripheral blood mononuclear cells (PBMC) by quantitative real-time PCR, plasma Trp and Kyn levels by HPLC, and cytokine levels by ELISA in 75 NPC patients and 51 healthy controls.
Compared to controls, IDO1 mRNA expression was significantly upregulated and IDO2 mRNA expression was significantly downregulated in PBMC of patients. Also compared to controls, plasma Kyn levels and Kyn/Trp ratio were significantly higher in patients. At the time of diagnosis, the plasma Kyn/Trp ratio was associated with advanced cancer status and was an independent prognostic factor for worse disease-specific survival. According to cancer stages, IDO1 mRNA expression was positively correlated with plasma Kyn/Trp ratio in patients with earlier stages (I-II-III) but negatively correlated in patients with the late-stage cancer (IV). Tumor necrosis factor-α, interleukin (IL)-6 and IL-10 levels were significantly higher in patients compared to controls. Moreover, and despite treatment, patients simultaneously carrying high plasma Kyn/Trp ratio and high plasma IL-6 and IL-10 levels at diagnosis died approximately 1 year after first diagnosis.
Measuring blood IDO mRNA expression and Kyn/Trp ratio at diagnosis could be a potential marker to evaluate NPC progression and predict survival outcome.
色氨酸 2,3-双加氧酶(IDO)是一种免疫抑制性色氨酸耗竭酶,在鼻咽癌(NPC)组织中表达。然而,IDO 尚未在 NPC 患者的外周血中报道。本研究旨在分析 IDO1 和 IDO2 信使 RNA(mRNA)表达、犬尿氨酸(Kyn)和色氨酸(Trp)血浆水平、它们的临床价值及其与 NPC 中细胞因子水平的关系。
我们通过定量实时 PCR 评估了 75 名 NPC 患者和 51 名健康对照者外周血单个核细胞(PBMC)中的 IDO1 和 IDO2 mRNA 表达、HPLC 检测血浆 Trp 和 Kyn 水平、ELISA 检测细胞因子水平。
与对照组相比,患者 PBMC 中的 IDO1 mRNA 表达显著上调,IDO2 mRNA 表达显著下调。与对照组相比,患者的血浆 Kyn 水平和 Kyn/Trp 比值也明显升高。在诊断时,血浆 Kyn/Trp 比值与晚期癌症状态相关,是疾病特异性生存的独立预后因素。根据癌症分期,IDO1 mRNA 表达与早期(I-II-III 期)患者的血浆 Kyn/Trp 比值呈正相关,与晚期癌症(IV 期)患者的血浆 Kyn/Trp 比值呈负相关。与对照组相比,患者的肿瘤坏死因子-α、白细胞介素(IL)-6 和 IL-10 水平明显升高。此外,尽管进行了治疗,但同时在诊断时具有高血浆 Kyn/Trp 比值和高血浆 IL-6 和 IL-10 水平的患者在首次诊断后约 1 年内死亡。
在诊断时测量血液 IDO mRNA 表达和 Kyn/Trp 比值可能是评估 NPC 进展和预测生存结果的潜在标志物。