Oncogenic mutations of ALK kinase in neuroblastoma (original) (raw)
- Letter
- Published: 16 October 2008
- Junko Takita1,2,3 na1,
- Young Lim Choi4 na1,
- Motohiro Kato1,3,
- Miki Ohira5,
- Masashi Sanada2,3,6,
- Lili Wang2,3,6,
- Manabu Soda4,
- Akira Kikuchi7,
- Takashi Igarashi1,
- Akira Nakagawara5,
- Yasuhide Hayashi8,
- Hiroyuki Mano4,6 &
- …
- Seishi Ogawa2,3,6
Nature volume 455, pages 971–974 (2008)Cite this article
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Abstract
Neuroblastoma in advanced stages is one of the most intractable paediatric cancers, even with recent therapeutic advances1. Neuroblastoma harbours a variety of genetic changes, including a high frequency of MYCN amplification, loss of heterozygosity at 1p36 and 11q, and gain of genetic material from 17q, all of which have been implicated in the pathogenesis of neuroblastoma2,3,4,5. However, the scarcity of reliable molecular targets has hampered the development of effective therapeutic agents targeting neuroblastoma. Here we show that the anaplastic lymphoma kinase (ALK), originally identified as a fusion kinase in a subtype of non-Hodgkin’s lymphoma (NPM–ALK)6,7,8 and more recently in adenocarcinoma of lung (EML4–ALK)9,10, is also a frequent target of genetic alteration in advanced neuroblastoma. According to our genome-wide scans of genetic lesions in 215 primary neuroblastoma samples using high-density single-nucleotide polymorphism genotyping microarrays11,12,13,14, the ALK locus, centromeric to the MYCN locus, was identified as a recurrent target of copy number gain and gene amplification. Furthermore, DNA sequencing of ALK revealed eight novel missense mutations in 13 out of 215 (6.1%) fresh tumours and 8 out of 24 (33%) neuroblastoma-derived cell lines. All but one mutation in the primary samples (12 out of 13) were found in stages 3–4 of the disease and were harboured in the kinase domain. The mutated kinases were autophosphorylated and displayed increased kinase activity compared with the wild-type kinase. They were able to transform NIH3T3 fibroblasts as shown by their colony formation ability in soft agar and their capacity to form tumours in nude mice. Furthermore, we demonstrate that downregulation of ALK through RNA interference suppresses proliferation of neuroblastoma cells harbouring mutated ALK. We anticipate that our findings will provide new insights into the pathogenesis of advanced neuroblastoma and that _ALK_-specific kinase inhibitors might improve its clinical outcome.
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Data deposits
The nucleotide sequences of ALK mutations detected in this study have been deposited in GenBank under the accession numbers EU788003 (K1062M), EU788004 (T1087I), EU788005 (F1174L; TTC/TTA), EU788006 (F1174L; TTC/TTG), EU788007 (F1174C), EU788008 (F1174V), EU788009 (F1245L) and EU788010 (R1275Q). The copy number data as well as the raw microarray data will be accessible from http://www.ncbi.nlm.nih.gov/geo/ with the accession number GSE12494.
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Acknowledgements
We thank H. P. Koeffler for critically reading and editing the manuscript. We also thank M. Matsumura, Y. Ogino, S. Ichimura, S. Sohma, E. Matsui, Y. Yin, N. Hoshino and Y. Nakamura for their technical assistance. This work was supported by the Core Research for Evolutional Science and Technology, Japan Science and Technology Agency and by a Grant-in-Aid from the Ministry of Health, Labor and Welfare of Japan for the third-term Comprehensive 10-year Strategy for Cancer Control.
Author Contributions Y.C., Y.L.C. and J.T. contributed equally to this work. M.K. and M.Sa. performed microarray experiments and subsequent data analyses. Y.C. and J.T. performed mutation analysis of ALK. Y.C., Y.L.C., J.T., M.So., L.W. and H.M. conducted functional assays of mutant ALK. A.N., M.O., T.I., A.K. and Y.H. prepared tumour specimens and were involved in statistical analysis. A.N., Y.H., H.M., J.T. and S.O. designed the overall study, and S.O. and J.T. wrote the manuscript. All authors discussed the results and commented on the manuscript.
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- Yuyan Chen, Junko Takita and Young Lim Choi: These authors contributed equally to this work.
Authors and Affiliations
- Department of Pediatrics,,
Yuyan Chen, Junko Takita, Motohiro Kato & Takashi Igarashi - Cell Therapy and Transplantation Medicine,,
Yuyan Chen, Junko Takita, Masashi Sanada, Lili Wang & Seishi Ogawa - Cancer Genomics Project, Graduate School of Medicine, The University of Tokyo, Tokyo 113-8655, Japan ,
Yuyan Chen, Junko Takita, Motohiro Kato, Masashi Sanada, Lili Wang & Seishi Ogawa - Division of Functional Genomics, Jichi Medical University, Toguchi 329-0498, Japan
Young Lim Choi, Manabu Soda & Hiroyuki Mano - Division of Biochemistry, Chiba Cancer Center Research Institute, Chiba 260-8717, Japan
Miki Ohira & Akira Nakagawara - Core Research for Evolutional Science and Technology, Japan Science and Technology Agency, Saitama, 332-0012, Japan
Masashi Sanada, Lili Wang, Hiroyuki Mano & Seishi Ogawa - Division of Hematology/Oncology, Saitama Children’s Medical Center, Saitama 339-8551, Japan
Akira Kikuchi - Gunma Children’s Medical Center, Shibukawa 377-8577, Japan
Yasuhide Hayashi
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Chen, Y., Takita, J., Choi, Y. et al. Oncogenic mutations of ALK kinase in neuroblastoma.Nature 455, 971–974 (2008). https://doi.org/10.1038/nature07399
- Received: 03 June 2008
- Accepted: 28 August 2008
- Issue Date: 16 October 2008
- DOI: https://doi.org/10.1038/nature07399
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Editorial Summary
Neuroblastoma: a genetic link to ALK
Neuroblastoma is the most common childhood cancer. There is a strong familial association and it was predicted over 30 years ago that there was a genetic element to the disease. Four groups now report the identification of mutations in the tyrosine kinase receptor ALK (anaplastic lymphoma kinase) in neuroblastoma patients. ALK acts as a neuroblastoma predisposition gene, and somatic point mutations occur in sporadic neuroblastoma cases. These mutations promote ALK's kinase activity and can transform cells and display tumorigenic activity in vivo. ALK inhibitors decrease neuroblastoma cell proliferation, so have potential as anticancer drugs.