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Indoleamine 2,3-Dioxygenase 2 Immunohistochemical Expression in Resected Human Non-small Cell Lung Cancer: A Potential New Prognostic Tool

机译:indolemine 2,3-二恶英酶2在切除的人非小细胞肺癌中免疫组织化学表达:潜在的新预后工具

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摘要

Indoleamine 2,3-dioxygenase 2 (IDO2) is an analog of the tryptophan degrading and immunomodulating enzyme indoleamine 2,3-dioxygenase 1 (IDO1). Although the role of IDO1 is largely understood, the function of IDO2 is not yet well-elucidated. IDO2 overexpression was documented in some human tumors, but the linkage between IDO2 expression and cancer progression is still unclear, in particular in non-small cell lung cancer (NSCLC). Immunohistochemical expression and cellular localization of IDO2 was evaluated on 191 formalin-fixed and paraffin-embedded resected NSCLC. Correlations between IDO2 expression, clinical-pathological data, tumor-infiltrating lymphocytes (TILs), immunosuppressive tumor molecules (IDO1 and programmed cell death ligand-1 – PD-L1 –) and patients' prognosis were evaluated. IDO2 high expression is strictly related to high PD-L1 level among squamous cell carcinomas group (p = 0.012), to either intratumoral or mixed localization of TILs (p < 0.001) and to adenocarcinoma histotype (p < 0.001). Furthermore, a significant correlation between IDO2 high expression and poor non-small cell lung cancer prognosis was detected (p = 0.011). The current study reaches interesting knowledge about IDO2 in non-small cell lung cancer. The close relationship between IDO2 expression, PD-L1 increased levels, TILs localization and NSCLC poor prognosis, assumed IDO2 as a potential prognostic biomarker to be exploited for optimizing innovative combined therapies with immune checkpoint inhibitors.
机译:吲哚胺2,3-二氧合酶2(IDO2)是色氨酸降解和免疫调节酶Indoleamine 2,3-二氧合酶1(IDO1)的类似物。虽然IDO1的作用在很大程度上被理解,但IDO2的功能尚未得到良好。在一些人肿瘤中记录了IDO2过表达,但IDO2表达和癌症进展之间的连锁仍然不清楚,特别是在非小细胞肺癌(NSCLC)中。 IDO2的免疫组织化学表达和细胞定位在191型福尔马林固定和石蜡嵌入切除的NMSCLC中评价。评估了IDO2表达,临床病理数据,肿瘤浸润性淋巴细胞(TILS),免疫抑制肿瘤分子(IDO1和编程细胞死亡配体-1 - PD-1 - PD-1 - PD-L1 - )和患者预后之间的相关性。 IDO2高表达与鳞状细胞癌组(P = 0.012)中的高PD-L1水平严格相关,直到腹部或混合定位(P <0.001)和腺癌组合型(P <0.001)。此外,检测到IDO2高表达和非小细胞肺癌预后差的显着相关性(P = 0.011)。目前的研究达到了关于非小细胞肺癌IDO2的有趣知识。 IDO2表达,PD-L1增加的水平,直到定位和NSCLC预后的密切关系假设IDO2作为潜在的预后生物标志物,用于利用免疫检查点抑制剂优化创新组合疗法。

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