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

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 inv...

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Detalles Bibliográficos
Autores principales: Noh, Byeong-Joo, Choi, Gun Moo, Jang, Hyuk Jai, Ma, Chung Hyeun, Oh, Ho-Suk, Kim, Moonho, Eom, Dae-Woon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9494626/
https://www.ncbi.nlm.nih.gov/pubmed/36238847
http://dx.doi.org/10.3892/ol.2022.13493
Descripción
Sumario: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.