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肝外胆管癌中基于 IDO1 表达的免疫分型的预后意义

英文原题:Prognostic implications of immune classification using IDO1 expression in extrahepatic bile duct carcinoma.

查看英文原题

Prognostic implications of immune classification using IDO1 expression in extrahepatic bile duct carcinoma.

PubMed 2022/09/05(内容时间) Oncol Lett Q3 · IF 2.1(JCR 2025)

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中文摘要

吲哚胺2,3-双加氧酶1(IDO1)是一种免疫调节酶,可催化色氨酸降解为犬尿氨酸,并诱导肿瘤细胞免疫耐受。IDO1在肝外胆管癌(EHBDC)中的作用尚未充分阐明。

因此,本研究旨在评估EHBDC中IDO1的表达及其预后意义。研究对76例手术切除的EHBDC样本进行IDO1免疫组化组织芯片分析,并结合CD8阳性TIL(肿瘤浸润淋巴细胞)状态进行评估。76例中有25例(32.9%)IDO1高表达。IDO1高表达与CD8阳性TIL数量减少(P=0.008)、较高pN分期(P=0.007)、较晚总体分期(P=0.001)及复发更常见(P=0.018)相关。

进一步按IDO1表达和CD8阳性TIL状态分层后,与IDO1高/CD8高、IDO1低/CD8高和IDO1低/CD8低亚组相比,IDO1高/CD8低亚组的总生存期(P=0.025)和无病生存期(P=0.015)均较短。IDO1高表达与CD8阳性TIL减少和不良预后相关。鉴于IDO1可能成为免疫治疗新靶点,IDO1/CD8阳性TIL分层可作为EHBDC患者有用的预后和预测工具。

展开英文摘要原文

Indoleamine 2, 3-dioxygenase 1 (IDO1) is an immunomodulatory enzyme that catalyzes the degradation of tryptophan to kynurenine and induces immune tolerance in tumor cells. The effects of IDO1 on extrahepatic bile duct carcinoma (EHBDC) are poorly understood.

Therefore, the present study aimed to investigate the expression and prognostic significance of IDO1 in EHBDC. An immunohistochemical microarray analysis of IDO1 expression was performed for 76 surgically resected cases of EHBDC. CD8 + tumor infiltrating lymphocytes (TILs) were also investigated through a combination analysis with IDO1 expression. IDO1 was highly expressed in 25 of 76 (32. 9%) cases. High expression of IDO1 was associated with decreased numbers of CD8 + TILs (P=0. 008), a higher pN category (P=0. 007), an advanced overall stage (P=0.

001) and frequent recurrence (P=0. 018). When IDO1 expression was further stratified with CD8 + TIL state, the IDO1 high /CD8 low subgroup was decreased in terms of overall survival (P=0. 025) and disease-free survival (P=0. 015) compared with IDO1 high /CD8 high , IDO1 low /CD8 high and IDO1 low /CD8 low subgroups.

High IDO1 expression was associated with a decreased number of CD8 + TILs and associated with a poor prognosis. As IDO1 may be a new target of immunotherapy applications, IDO1/CD8 + TIL subgrouping can be a useful prognostic and predictive tool in patients with EHBDC.

论文信息

作者
Noh BJ、Choi GM、Jang HJ、Ma CH、Oh HS、Kim M、Eom DW
单位
Department of Pathology, Gangneung Asan Hospital, University of Ulsan College of Medicine, Gangneung, Gangwon-do 25440, Republic of Korea.South Korea
期刊
Oncology letters2022 Oct
原文标识
PubMed 36238847 · DOI 10.3892/ol.2022.13493