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The EML4‐ALK fusion gene is involved in various histologic types of lung cancers from nonsmokers with wild‐type EGFR and KRAS
Open accessAbstract
BACKGROUND: The echinoderm microtubule‐associated protein‐like 4‐anaplastic lymphoma kinase ( EML4‐ALK ) fusion gene resulting from the chromosome inversion inv(2)(p21;p23) recently was identified in nonsmall cell lung cancer (NSCLC). The authors of this study investigated the frequency, genetic and clinicopathologic profiles of EML4‐ALK in Chinese patients with NSCLC. METHODS: EML4‐ALK was investigated in 266 resected primary NSCLC, including adenocarcinomas (AD), lymphoepithelioma‐like carcinomas, squamous cell carcinomas, mucoepidermoid carcinomas, and adenosquamous carcinomas, by reverse transcriptase‐polymerase chain reaction and was verified by sequencing. EML4‐ALK protein expression was studied by immunohistochemistry. RESULTS: Thirteen tumors (4.9%) had EML4‐ALK comprising 4 fusion transcript variants with fusion of the variable segments from 5′ EML4 to 3′ ALK and with preservation of the ALK kinase domain. The most common variant consisted of 8 tumors with variant 3 that involved EML4 exon 6. The others included 2 tumors with variant 1 (exon 13), 2 tumors with variant 2 (exon 20), and 1 tumor with the novel variant 5 (exon 18). There were 11 ADs and 2 unusual carcinomas with mixed squamous and glandular components. Immunohistochemistry demonstrated diffuse ALK fusion proteins in the tumor cell cytoplasm. EML4‐ALK was associated with nonsmokers ( P = .009). Tumors with the fusion gene had the wild‐type epidermal growth factor receptor ( EGFR ) ( P = .001) and v‐Ki‐ ras 2/Kirsten rat sarcoma viral oncogene homolog ( KRAS ) genes. Patients who had EML4‐ALK ‐positive AD had a younger median age ( P = .018) compared with patients who did not have the fusion gene. CONCLUSIONS: The EML4‐ALK fusion gene was present in various histologic types of NSCLC. It occurred in mutual exclusion to EGFR and KRAS mutations and was associated with nonsmokers. The authors concluded that EML4‐ALK may be useful for predicting the potential response to ALK inhibitors as a therapeutic option for patients with lung cancer. Cancer 2009. © 2009 American Cancer Society.
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Identification of the transforming EML4–ALK fusion gene in non-small-cell lung cancer
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Recurrent Fusion of TMPRSS2 and ETS Transcription Factor Genes in Prostate Cancer
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Global Survey of Phosphotyrosine Signaling Identifies Oncogenic Kinases in Lung Cancer
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The impact of translocations and gene fusions on cancer causation
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EML4-ALK Fusion Gene and Efficacy of an ALK Kinase Inhibitor in Lung Cancer
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TPM3-ALK and TPM4-ALK Oncogenes in Inflammatory Myofibroblastic Tumors
Lawrence, B., Perez-Atayde, A., Hibbard, M. K., Rubin, B. P., Dal Cin, P., Pinkus, J. L., Pinkus, G. S., Xiao, S., Yi, E. S., Fletcher, C. D. M., et al. (2000) · The American Journal of Pathology · doi:10.1016/s0002-9440(10)64550-6 · Cited by 714
EML4-ALK Fusion Is Linked to Histological Characteristics in a Subset of Lung Cancers
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Identification of Novel Isoforms of the EML4-ALK Transforming Gene in Non–Small Cell Lung Cancer
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Crizotinib versus Chemotherapy in Advanced ALK -Positive Lung Cancer
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Shaw, A. T., Kim, D.-W., Mehra, R., Tan, D. S. W., Felip, E., Chow, L. Q. M., Camidge, D. R., Vansteenkiste, J., Sharma, S., De Pas, T., et al. (2014) · New England Journal of Medicine · doi:10.1056/nejmoa1311107 · Cited by 1,495
Mechanisms of Acquired Crizotinib Resistance in ALK-Rearranged Lung Cancers
Katayama, R., Shaw, A. T., Khan, T. M., Mino-Kenudson, M., Solomon, B. J., Halmos, B., Jessop, N. A., Wain, J. C., Yeo, A. T., Benes, C., et al. (2012) · Science Translational Medicine · doi:10.1126/scitranslmed.3003316 · Cited by 1,309
Lung cancer: Biology and treatment options
Lemjabbar-Alaoui, H., Hassan, O. U., Yang, Y.-W., & Buchanan, P. (2015) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2015.08.002 · Cited by 1,014
Metadata
- Authors
- Wong, D. W., Leung, E. L., So, K. K., Tam, I. Y., Sihoe, A. D., Cheng, L., Ho, K., Au, J. S., Chung, L., Pik Wong, M., & University of Hong Kong Lung Cancer Study Group
- Venue
- Cancer
- Publisher
- Wiley
- Published
- 2009-04-06
- Volume
- 115
- Issue
- 8
- Pages
- 1723-1733
- ISSN
- 0008-543X (ISSN-L)
- 1097-0142
- OpenAlex
- W2031494655
- Cited by
- 719
- References
- 23
- FWCI
- 50.31
- Type
- journal article
- Language
- en
- Open access
- bronze
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- Wong, D. W., Leung, E. L., So, K. K., Tam, I. Y., Sihoe, A. D., Cheng, L., Ho, K., Au, J. S., Chung, L., Pik Wong, M., & University of Hong Kong Lung Cancer Study Group. (2009). The EML4‐ALK fusion gene is involved in various histologic types of lung cancers from nonsmokers with wild‐type EGFR and KRAS. Cancer. https://doi.org/10.1002/cncr.24181
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