The expression and prognostic significance of platelet-derived growth factor receptor alpha in mature T- and natural killer-cell lymphomas

被引:12
作者
Chen, Ya-Ping [1 ]
Chang, Kung-Chao [2 ]
Su, Wu-Chou [1 ]
Chen, Tsai-Yun [1 ]
机构
[1] Natl Cheng Kung Univ Hosp, Div Hematol Oncol, Dept Internal Med, Tainan 704, Taiwan
[2] Natl Cheng Kung Univ Hosp, Dept Pathol, Tainan 704, Taiwan
关键词
Mature T- and NK-cell lymphoma; Platelet-derived growth factor receptor alpha; PDGFRA;
D O I
10.1007/s00277-008-0539-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Platelet-derived growth factor receptor alpha (PDGFRA) is important in numerous malignancies and can serve as a target for therapeutic strategy. We aimed to assess the role of PDGFRA expression in mature T- and natural killer (NK)-cell lymphomas. We used immunohistochemistry to analyze PDGFRA expression in mature T- and NK-cell lymphomas in tissue samples from 50 patients. In positive samples, we then did a mutational analysis of the PDGFRA gene on exons 10, 12, 14, and 18. The relationship between PDGFRA expression and overall survival in mature T- and NK-cell lymphomas was statistically analyzed in the study. We analyzed PDGFRA expression in four subtypes: angioimmunoblastic T-cell lymphoma (3/8, 37.5%); anaplastic large cell lymphoma (5/7, 71.4%); NK/T-cell lymphoma, nasal type (9/12, 75%); and peripheral T-cell lymphoma, unspecified (PTCLu; 7/23, 30.4%). It was lower in PTCLu than in other subtypes (30.4% vs. 63%, p=0.022). PDGFRA expression was not related to PDGFRA gene mutation. Overall survival in mature T- and NK-cell lymphomas correlated significantly with disease subtypes and an international prognostic index but not PDGFRA expression. Our study showed that PDGFRA expression was different in mature T- and NK-cell lymphomas. PDGFRA expression in PTCLu was lower in the present study than in previous reports done in Western countries. It suggests that this disease is biologically distinct in different races (30.4% vs. 91-100%).
引用
收藏
页码:985 / 990
页数:6
相关论文
共 30 条
[1]   Biology of platelet-derived growth factor and its involvement in disease [J].
Alvarez, Ricardo H. ;
Kantarjian, Hagop M. ;
Cortes, Jorge E. .
MAYO CLINIC PROCEEDINGS, 2006, 81 (09) :1241-1257
[2]   Regulation of PDGF and its receptors in fibrotic diseases [J].
Bonner, JC .
CYTOKINE & GROWTH FACTOR REVIEWS, 2004, 15 (04) :255-273
[3]  
Brown RE, 2002, ANN CLIN LAB SCI, V32, P339
[4]   Glivec (ST1571, Imatinib), a rationally developed, targeted anticancer drug [J].
Capdeville, R ;
Buchdunger, E ;
Zimmermann, J ;
Matter, A .
NATURE REVIEWS DRUG DISCOVERY, 2002, 1 (07) :493-502
[5]   DIRECT COMPARISONS OF PERIPHERAL T-CELL LYMPHOMA WITH DIFFUSE B-CELL LYMPHOMA OF COMPARABLE HISTOLOGICAL GRADES - SHOULD PERIPHERAL T-CELL LYMPHOMA BE CONSIDERED SEPARATELY [J].
CHENG, AL ;
CHEN, YC ;
WANG, CH ;
SU, IJ ;
HSIEH, HC ;
CHANG, JY ;
HWANG, WS ;
SU, WC ;
LIU, TW ;
TIEN, HF ;
TSAI, W ;
SHEN, MC ;
LIU, CH .
JOURNAL OF CLINICAL ONCOLOGY, 1989, 7 (06) :725-731
[6]   PDGFRA mutations in gastrointestinal stromal tumors: Frequency, spectrum and in vitro sensitivity to imatinib [J].
Corless, CL ;
Schroeder, A ;
Griffith, D ;
Town, A ;
McGreevey, L ;
Harrell, P ;
Shiraga, S ;
Bainbridge, T ;
Morich, J ;
Heinrich, MC .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (23) :5357-5364
[7]  
Dagher R, 2002, CLIN CANCER RES, V8, P3034
[8]   The World Health Organization classification of malignant lymphomas in Japan: Incidence of recently recognized entities [J].
Fujita, M ;
Yamashiro, K ;
Ichinohasama, R ;
Nakamura, N ;
Abe, M ;
Wakasa, H ;
Kojima, M ;
Motoori, T ;
Izumo, T ;
Tamaru, J ;
Mikata, A ;
Takeuchi, K ;
Kakiuchi, C ;
Mori, S ;
Matsuno, Y ;
Nakamura, S ;
Yatabe, Y ;
Ichimura, K ;
Suchi, T ;
Tajima, K ;
Mori, N ;
Takasaki, K ;
Tsurumi, K ;
Takami, T ;
Haga, H ;
Sakurai, T ;
Yamabe, H ;
Kobashi, Y ;
Ohsawa, M ;
Kanno, H ;
Aozasa, K ;
Nakamine, H ;
Yoshino, T ;
Akagi, T ;
Sasaki, N ;
Namba, K ;
Agatsuma, Y ;
Iwata, K ;
Suzumiya, J ;
Ohshima, K ;
Kikuchi, M ;
Takeshita, M ;
Hasui, K ;
Sato, E ;
Sueyoshi, K ;
Tokunaga, M .
PATHOLOGY INTERNATIONAL, 2000, 50 (09) :696-702
[9]  
Gisselbrecht C, 1998, BLOOD, V92, P76
[10]  
GRONWALD RGK, 1990, HUM GENET, V85, P383