Indoleamine 2,3-dioxygenase is a novel prognostic indicator for endometrial cancer

被引:221
作者
Ino, K.
Yoshida, N.
Kajiyama, H.
Shibata, K.
Yamamoto, E.
Kidokoro, K.
Takahashi, N.
Terauchi, M.
Nawa, A.
Nomura, S.
Nagasaka, T.
Takikawa, O.
Kikkawa, F.
机构
[1] Nagoya Univ, Grad Sch Med, Dept Obstet & Gynecol, Nagoya, Aichi 4668550, Japan
[2] Nagoya Univ, Grad Sch Med, Div Pathol, Clin Lab, Nagoya, Aichi, Japan
[3] Natl Inst Longev Sci, Natl Ctr Geriatr & Gerontol, Obu, Japan
关键词
indoleamine 2,3-dioxygenase (IDO); endometrial cancer; prognostic factor; progression-free survival (PFS);
D O I
10.1038/sj.bjc.6603477
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Indoleamine 2,3-dioxygenase (IDO) is a tryptophan-catabolising enzyme inducing immune tolerance. The present study aimed to investigate IDO expression and its prognostic significance in endometrial cancer. Indoleamine 2,3-dioxygenase expression in endometrial cancer tissues (n = 80) was immunohistochemically scored as four groups (IDO-, 1+ , 2+ , and 3+). The high IDO expression (IDO2 + or 3 +) in tumour cells was found in 37 (46.3%) of the 80 cases, and was positively correlated with surgical stage, myometrial invasion, lymph-vascular space involvement, and lymph node metastasis, but not with the histological grade. Patients with high IDO expression had significantly impaired overall survival and progression-free survival (PFS) (P = 0.002 and P = 0.001, respectively) compared to patients with no or weak expression of IDO (IDO- or 1 +). The 5-year PFS for IDO-/1 +, 2 +, and 3 + were 97.7, 72.9, and 36.4%, respectively. Even in patients with early-stage disease (International Federation of Gynecology and Obstetrics I/II, n = 64), the PFS for IDO2 +/3 + was significantly poor (P = 0.001) compared to that for IDO-/1 +. On multivariate analysis, IDO expression was an independent prognostic factor for PFS (P = 0.020). These results indicated that the high IDO expression was involved in the progression of endometrial cancer and correlated with the impaired clinical outcome, suggesting that IDO is a novel and reliable prognostic indicator for endometrial cancer.
引用
收藏
页码:1555 / 1561
页数:7
相关论文
共 28 条
[1]   Eosinophil granulocytes account for indoleamine 2,3-dioxygenase-mediated immune escape in human non-small cell lung cancer [J].
Astigiano, S ;
Morandi, B ;
Costa, R ;
Mastracci, L ;
D'Agostino, A ;
Ratto, GB ;
Melioli, G ;
Frumento, G .
NEOPLASIA, 2005, 7 (04) :390-396
[2]   Prognostic value of indoleamine 2,3-dioxygenase expression in colorectal cancer:: Effect on tumor-infiltrating T cells [J].
Brandacher, G ;
Perathoner, A ;
Ladurner, R ;
Schneeberger, S ;
Obrist, P ;
Winkler, C ;
Werner, ER ;
Werner-Felmayer, G ;
Weiss, HG ;
Göbel, G ;
Margreiter, R ;
Königsrainer, A ;
Fuchs, D ;
Amberger, A .
CLINICAL CANCER RESEARCH, 2006, 12 (04) :1144-1151
[3]   Is observation and salvage (when necessary) an appropriate approach to intermediate risk endometrial cancer? [J].
Cardenes, H ;
Randall, ME .
GYNECOLOGIC ONCOLOGY, 2003, 89 (02) :199-200
[4]   Surgery and postoperative radiotherapy versus surgery alone for patients with stage-1 endometrial carcinoma:: multicentre randomised trial [J].
Creutzberg, CL ;
van Putten, WLJ ;
Koper, PCM ;
Lybeert, MLM ;
Jobsen, JJ ;
Wárlám-Rodenhuis, CC ;
De Winter, KAJ ;
Lutgens, LCHW ;
van den Bergh, ACM ;
van de Steen-Banasik, E ;
Beerman, H ;
van Lent, M .
LANCET, 2000, 355 (9213) :1404-1411
[5]   Stratification of intermediate-risk endometrial cancer patients into groups at high risk or low risk for recurrence based on tumor gene expression profiles [J].
Ferguson, SE ;
Olshen, AB ;
Viale, A ;
Barakat, RR ;
Boyd, J .
CLINICAL CANCER RESEARCH, 2005, 11 (06) :2252-2257
[6]   Indoleamine 2,3-dioxygenase contributes to tumor cell evasion of T cell-mediated rejection [J].
Friberg, M ;
Jennings, R ;
Alsarraj, M ;
Dessureault, S ;
Cantor, A ;
Extermann, M ;
Mellor, AL ;
Munn, DH ;
Antonia, SJ .
INTERNATIONAL JOURNAL OF CANCER, 2002, 101 (02) :151-155
[7]   CLINICAL STAGE-I ENDOMETRIAL CANCER - PROGNOSTIC FACTORS FOR LOCAL-CONTROL AND DISTANT METASTASIS AND IMPLICATIONS OF THE NEW FIGO SURGICAL STAGING SYSTEM [J].
GRIGSBY, PW ;
PEREZ, CA ;
KUTEN, A ;
SIMPSON, JR ;
GARCIA, DM ;
CAMEL, HM ;
KAO, MS ;
GALAKATOS, AE .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1992, 22 (05) :905-911
[8]   Cancer statistics, 2004 [J].
Jemal, A ;
Tiwari, RC ;
Murray, T ;
Ghafoor, A ;
Samuels, A ;
Ward, E ;
Feuer, EJ ;
Thun, MJ .
CA-A CANCER JOURNAL FOR CLINICIANS, 2004, 54 (01) :8-29
[9]   A phase III trial of surgery with or without adjunctive external pelvic radiation therapy in intermediate risk endometrial adenocarcinoma: a Gynecologic Oncology Group study [J].
Keys, HM ;
Roberts, JA ;
Brunetto, VL ;
Zaino, RJ ;
Spirtos, NM ;
Bloss, JD ;
Pearlman, A ;
Maiman, MA ;
Bell, JG .
GYNECOLOGIC ONCOLOGY, 2004, 92 (03) :744-751
[10]   Human placental indoleamine 2,3-dioxygenase: cellular localization and characterization of an enzyme preventing fetal rejection [J].
Kudo, Y ;
Boyd, CAR .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2000, 1500 (01) :119-124