1. Academic Validation
  2. Identification of the transforming EML4-ALK fusion gene in non-small-cell lung cancer

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

  • Nature. 2007 Aug 2;448(7153):561-6. doi: 10.1038/nature05945.
Manabu Soda 1 Young Lim Choi Munehiro Enomoto Shuji Takada Yoshihiro Yamashita Shunpei Ishikawa Shin-ichiro Fujiwara Hideki Watanabe Kentaro Kurashina Hisashi Hatanaka Masashi Bando Shoji Ohno Yuichi Ishikawa Hiroyuki Aburatani Toshiro Niki Yasunori Sohara Yukihiko Sugiyama Hiroyuki Mano
Affiliations

Affiliation

  • 1 Division of Functional Genomics, Jichi Medical University, Tochigi 329-0498, Japan.
Abstract

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.

Figures