RT Journal Article SR Electronic T1 Identification of Novel Isoforms of the EML4-ALK Transforming Gene in Non–Small Cell Lung Cancer JF Cancer Research JO Cancer Res FD American Association for Cancer Research SP 4971 OP 4976 DO 10.1158/0008-5472.CAN-07-6158 VO 68 IS 13 A1 Choi, Young Lim A1 Takeuchi, Kengo A1 Soda, Manabu A1 Inamura, Kentaro A1 Togashi, Yuki A1 Hatano, Satoko A1 Enomoto, Munehiro A1 Hamada, Toru A1 Haruta, Hidenori A1 Watanabe, Hideki A1 Kurashina, Kentaro A1 Hatanaka, Hisashi A1 Ueno, Toshihide A1 Takada, Shuji A1 Yamashita, Yoshihiro A1 Sugiyama, Yukihiko A1 Ishikawa, Yuichi A1 Mano, Hiroyuki YR 2008 UL http://cancerres.aacrjournals.org/content/68/13/4971.abstract AB The genome of a subset of non–small-cell lung cancers (NSCLC) harbors a small inversion within chromosome 2 that gives rise to a transforming fusion gene, EML4-ALK, which encodes an activated protein tyrosine kinase. Although breakpoints within EML4 have been identified in introns 13 and 20, giving rise to variants 1 and 2, respectively, of EML4-ALK, it has remained unclear whether other isoforms of the fusion gene are present in NSCLC cells. We have now screened NSCLC specimens for other in-frame fusion cDNAs that contain both EML4 and ALK sequences. Two slightly different fusion cDNAs in which exon 6 of EML4 was joined to exon 20 of ALK were each identified in two individuals of the cohort. Whereas one cDNA contained only exons 1 to 6 of EML4 (variant 3a), the other also contained an additional 33-bp sequence derived from intron 6 of EML4 (variant 3b). The protein encoded by the latter cDNA thus contained an insertion of 11 amino acids between the EML4 and ALK sequences of that encoded by the former. Both variants 3a and 3b of EML4-ALK exhibited marked transforming activity in vitro as well as oncogenic activity in vivo. A lung cancer cell line expressing endogenous variant 3 of EML4-ALK underwent cell death on exposure to a specific inhibitor of ALK catalytic activity. These data increase the frequency of EML4-ALK–positive NSCLC tumors and bolster the clinical relevance of this oncogenic kinase. [Cancer Res 2008;68(13):4971–6] ©2008 American Association for Cancer Research.