Prognostic role of indoleamine 2,3-dioxygenase in endometrial carcinoma

被引:38
|
作者
de Jong, Renske A. [1 ]
Kema, Ido P. [2 ]
Boerma, Annemarie [1 ]
Boezen, H. Marike [3 ]
van der Want, Johannes J. L. [4 ]
Gooden, Marloes J. M. [1 ]
Hollema, Harry [5 ]
Nijman, Hans W. [1 ]
机构
[1] Univ Groningen, Dept Gynecol Oncol, Univ Med Ctr Groningen, NL-9700 RB Groningen, Netherlands
[2] Univ Groningen, Dept Lab Med, Univ Med Ctr Groningen, NL-9700 RB Groningen, Netherlands
[3] Univ Groningen, Dept Epidemiol, Univ Med Ctr Groningen, NL-9700 RB Groningen, Netherlands
[4] Univ Groningen, Univ Med Ctr Groningen, Dept Cell Biol Mol Imaging & Electron Microscopy, NL-9713 AV Groningen, Netherlands
[5] Univ Groningen, Dept Pathol, Univ Med Ctr Groningen, NL-9700 RB Groningen, Netherlands
关键词
Endometrial carcinoma; Indoleamine 2,3-dioxygenase; T-lymphocytes; Prognosis; T-CELL PROLIFERATION; DENDRITIC CELLS; TRYPTOPHAN CATABOLISM; EXPRESSION; CANCER; INHIBITION; SURVIVAL; KYNURENINE;
D O I
10.1016/j.ygyno.2012.05.034
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective. Indoleamine-2,3-dioxygenase (IDO) suppresses the function of T-lymphocytes and is an important immune escape mechanism for cancer. Therefore, it is to be expected that IDO influences prognosis of cancer patients. This study aimed to investigate the prognostic role of IDO expression in a large cohort of endometrial carcinoma (EC) patients. Methods. A tissue microarray containing primary EC tissue of 355 patients treated in a single institution was used to evaluate IDO expression. Expression of IDO was associated with clinicopathological characteristics, survival and previously determined numbers of CD8(+) and Foxp3(+) T-lymphocytes. Results. IDOhigh expression was associated with lower numbers of intratumoral CD8(+) T-lymphocytes (p = 0.031). Next to well-known prognostic parameters, IDOhigh expression was independently associated with poor disease specific survival in the general cohort of EC patients (HR 2.62, 95% C.I. 1.48-4.66, p = 0.001) and among patients with early stage EC (HR 3.06, 95% C.I. 1.10-8.54, p = 0.032). Conclusion. Our results show that IDO expression is associated with poor survival. This provides evidence that further research into the use of IDO blocking agents in cancer treatment is valid where it might be a promising new therapeutic strategy. (c) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:474 / 480
页数:7
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