Expression of MET in alveolar soft part sarcoma

被引:22
作者
Jun, Hyun Jung [1 ]
Lee, Jeeyun [1 ]
Lim, Do Hyoung [1 ]
Park, Joon Oh [1 ]
Ahn, Geunghwan [2 ]
Seo, Sung Wook [3 ]
Sung, Ki-Sun [3 ]
Lim, Do Hoon [4 ]
Yoo, Keon Hee [5 ]
Choi, Yoon-La [2 ]
机构
[1] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Med,Div Hematol Oncol, Seoul 135710, South Korea
[2] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pathol, Seoul 135710, South Korea
[3] Sungkyunkwan Univ, Sch Med, Dept Orthoped Surg, Seoul 135710, South Korea
[4] Sungkyunkwan Univ, Sch Med, Dept Radiat Oncol, Seoul 135710, South Korea
[5] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pediat, Seoul 135710, South Korea
关键词
Alveolar soft part sarcoma; MET; TFE3; Immunohistochemistry; Therapeutic target; FUSION; GENE;
D O I
10.1007/s12032-009-9234-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Alveolar soft part sarcoma (ASPS) is a rare soft tissue sarcoma which is characterized by the presence of a specific chromosomal translocation encoding the chimeric transcription factor (ASPL-TFE3) that activates expression of MET. We reviewed the clinical features and treatment outcome of 12 ASPS patients. The presence of ASPL-TFE3 fusion transcripts was assessed by reverse transcriptase polymerase chain reaction. In addition, we performed immunohistochemical studies for MET, TFE3, Ki-67, and EGFR expression. Lower extremity was the most commonly affected primary site (2 thigh, 3 lower leg, and 1 foot). Of four patients who received primary cytotoxic chemotherapy, no patient demonstrated treatment response. With follow-up duration of 94.4 months, median overall survival was 53.2 (95% C.I. 40.9-65.5) months. The immunohistochemical staining demonstrated 100% TFE3 positivity (8 of 8), 75% MET positivity (6 of 8) with a strong association between TFE3 expression and MET positivity with correlation coefficient of 0.808 (P = 0.02). The high expression of MET in ASPL-TFE3 (+) ASPS may further support the potential role of targeted agents against MET in this rare, chemoresistant tumor.
引用
收藏
页码:459 / 465
页数:7
相关论文
共 23 条
[1]  
AUERBACH HE, 1987, CANCER-AM CANCER SOC, V60, P66, DOI 10.1002/1097-0142(19870701)60:1<66::AID-CNCR2820600112>3.0.CO
[2]  
2-9
[3]   Functional cloning of TUG as a regulator of GLUT4 glucose transporter trafficking [J].
Bogan, JS ;
Hendon, N ;
McKee, AE ;
Tsao, TS ;
Lodish, HF .
NATURE, 2003, 425 (6959) :727-733
[4]   Alveolar soft part sarcoma in children and adolescents: A report from the Soft-Tissue Sarcoma Italian Cooperative Group [J].
Casanova, M ;
Ferrari, A ;
Bisogno, G ;
Cecchetto, G ;
Basso, E ;
De Bernardi, B ;
Indolfi, P ;
Bellani, FF ;
Carli, M .
ANNALS OF ONCOLOGY, 2000, 11 (11) :1445-1449
[5]   MET amplification leads to gefitinib resistance in lung cancer by activating ERBB3 signaling [J].
Engelman, Jeffrey A. ;
Zejnullahu, Kreshnik ;
Mitsudomi, Tetsuya ;
Song, Youngchul ;
Hyland, Courtney ;
Park, Joon Oh ;
Lindeman, Neal ;
Gale, Christopher-Michael ;
Zhao, Xiaojun ;
Christensen, James ;
Kosaka, Takayuki ;
Holmes, Alison J. ;
Rogers, Andrew M. ;
Cappuzzo, Federico ;
Mok, Tony ;
Lee, Charles ;
Johnson, Bruce E. ;
Cantley, Lewis C. ;
Janne, Pasi A. .
SCIENCE, 2007, 316 (5827) :1039-1043
[6]  
EVANS HL, 1985, CANCER-AM CANCER SOC, V55, P912, DOI 10.1002/1097-0142(19850215)55:4<912::AID-CNCR2820550434>3.0.CO
[7]  
2-G
[8]   HGF/SF-Met signaling in tumor progression [J].
Gao, CF ;
Vande Woude, GF .
CELL RESEARCH, 2005, 15 (01) :49-51
[9]  
GREENE FL, 2002, AJCC CANC STAGING MA, P193
[10]  
Hashimoto H, 1995, Curr Top Pathol, V89, P1