Identification of the transforming EML4-ALK fusion gene in non-small-cell lung cancer

被引:4229
作者
Soda, Manabu
Choi, Young Lim
Enomoto, Munehiro
Takada, Shuji
Yamashita, Yoshihiro
Ishikawa, Shunpei
Fujiwara, Shin-ichiro
Watanabe, Hideki
Kurashina, Kentaro
Hatanaka, Hisashi
Bando, Masashi
Ohno, Shoji
Ishikawa, Yuichi
Aburatani, Hiroyuki
Niki, Toshiro
Sohara, Yasunori
Sugiyama, Yukihiko
Mano, Hiroyuki [1 ]
机构
[1] Jichi Med Univ, Div Funct Genom, Tochigi 3290498, Japan
[2] Jichi Med Univ, Div Pulm Med, Tochigi 3290498, Japan
[3] Jichi Med Univ, Dept Pathol, Tochigi 3290498, Japan
[4] Jichi Med Univ, Div Gen Thorac Surg, Tochigi 3290498, Japan
[5] Univ Tokyo, Adv Sci & Technol Res Ctr, Tokyo 1538904, Japan
[6] Japanese Fdn Canc Res, Inst Canc, Tokyo 1358550, Japan
[7] Japan Sci & Technol Agcy, CREST, Saitama 3320012, Japan
关键词
D O I
10.1038/nature05945
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Improvement in the clinical outcome of lung cancer is likely to be achieved by identification of the molecular events that underlie its pathogenesis. Here we show that a small inversion within chromosome 2p results in the formation of a fusion gene comprising portions of the echinoderm microtubule-associated protein-like 4 (EML4) gene and the anaplastic lymphoma kinase (ALK) gene in non-small-cell lung cancer (NSCLC) cells. Mouse 3T3 fibroblasts forced to express this human fusion tyrosine kinase generated transformed foci in culture and subcutaneous tumours in nude mice. The EML4-ALK fusion transcript was detected in 6.7% (5 out of 75) of NSCLC patients examined; these individuals were distinct from those harbouring mutations in the epidermal growth factor receptor gene. Our data demonstrate that a subset of NSCLC patients may express a transforming fusion kinase that is a promising candidate for a therapeutic target as well as for a diagnostic molecular marker in NSCLC.
引用
收藏
页码:561 / U3
页数:7
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