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Article Open Access

Duplication of ALK F1245 missense mutation due to acquired uniparental disomy associated with aggressive progression in a patient with relapsed neuroblastoma

  • Authors:
    • Shunsuke Kimura
    • Daisuke Hasegawa
    • Yuri Yoshimoto
    • Masafumi Seki
    • Atsuro Daida
    • Masahiro Sekiguchi
    • Shinsuke Hirabayashi
    • Yosuke Hosoya
    • Masao Kobayashi
    • Satoru Miyano
    • Seishi Ogawa
    • Junko Takita
    • Atsushi Manabe
  • View Affiliations / Copyright

    Affiliations: Department of Pediatrics, St Luke's International Hospital, Tokyo 104‑8560, Japan, Department of Pediatrics, The University of Tokyo, Tokyo 113‑8654, Japan, Department of Pediatrics, Hiroshima University Graduate School of Biomedical Sciences, Minami, Hiroshima 734‑8553, Japan, Laboratory of DNA Information Analysis, Human Genome Center, Institute of Medical Science, The University of Tokyo, Tokyo 108‑8639, Japan, Department of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University, Sakyo, Kyoto 606‑8501, Japan
    Copyright: © Kimura et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 3323-3329
    |
    Published online on: January 29, 2019
       https://doi.org/10.3892/ol.2019.9985
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Abstract

Recent genome‑wide analysis of neuroblastoma (NBL) revealed amplification and heterozygous mutation of anaplastic lymphoma kinase (ALK) are responsible for oncogenicity, frequently observed during relapses. A 3‑year‑old girl with relapsed high‑risk NBL had a heterozygous ALK F1245L mutation at diagnosis, which became homozygous due to uniparental disomy (UPD) of the entire chromosome 2, confirmed by single nucleotide polymorphism array and variant allele frequency of this mutation. The ALK inhibitor, crizotinib, failed to control the tumor and the patient died of the disease. Further genomic analysis using targeted capture sequencing for 381 genes related to pediatric cancers identified more alterations acquired at relapse, such as TSC complex subunit 2 and protein tyrosine phosphatase receptor type D. In addition to these several acquired mutations, this extremely rare duplication of ALK mutation might explain the aggressive clinical course after relapse, because acquired UPD, resulting in the duplication of an oncogenic mutation, has been reported for various neoplasms. Although a clinical benefit of ALK inhibitors in patients with NBL has not been confirmed yet, a treatment based on the ALK mutation status will be promising in future using more potent next‑generation ALK inhibitors.
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Copy and paste a formatted citation
Spandidos Publications style
Kimura S, Hasegawa D, Yoshimoto Y, Seki M, Daida A, Sekiguchi M, Hirabayashi S, Hosoya Y, Kobayashi M, Miyano S, Miyano S, et al: Duplication of ALK F1245 missense mutation due to acquired uniparental disomy associated with aggressive progression in a patient with relapsed neuroblastoma. Oncol Lett 17: 3323-3329, 2019.
APA
Kimura, S., Hasegawa, D., Yoshimoto, Y., Seki, M., Daida, A., Sekiguchi, M. ... Manabe, A. (2019). Duplication of ALK F1245 missense mutation due to acquired uniparental disomy associated with aggressive progression in a patient with relapsed neuroblastoma. Oncology Letters, 17, 3323-3329. https://doi.org/10.3892/ol.2019.9985
MLA
Kimura, S., Hasegawa, D., Yoshimoto, Y., Seki, M., Daida, A., Sekiguchi, M., Hirabayashi, S., Hosoya, Y., Kobayashi, M., Miyano, S., Ogawa, S., Takita, J., Manabe, A."Duplication of ALK F1245 missense mutation due to acquired uniparental disomy associated with aggressive progression in a patient with relapsed neuroblastoma". Oncology Letters 17.3 (2019): 3323-3329.
Chicago
Kimura, S., Hasegawa, D., Yoshimoto, Y., Seki, M., Daida, A., Sekiguchi, M., Hirabayashi, S., Hosoya, Y., Kobayashi, M., Miyano, S., Ogawa, S., Takita, J., Manabe, A."Duplication of ALK F1245 missense mutation due to acquired uniparental disomy associated with aggressive progression in a patient with relapsed neuroblastoma". Oncology Letters 17, no. 3 (2019): 3323-3329. https://doi.org/10.3892/ol.2019.9985
Copy and paste a formatted citation
x
Spandidos Publications style
Kimura S, Hasegawa D, Yoshimoto Y, Seki M, Daida A, Sekiguchi M, Hirabayashi S, Hosoya Y, Kobayashi M, Miyano S, Miyano S, et al: Duplication of ALK F1245 missense mutation due to acquired uniparental disomy associated with aggressive progression in a patient with relapsed neuroblastoma. Oncol Lett 17: 3323-3329, 2019.
APA
Kimura, S., Hasegawa, D., Yoshimoto, Y., Seki, M., Daida, A., Sekiguchi, M. ... Manabe, A. (2019). Duplication of ALK F1245 missense mutation due to acquired uniparental disomy associated with aggressive progression in a patient with relapsed neuroblastoma. Oncology Letters, 17, 3323-3329. https://doi.org/10.3892/ol.2019.9985
MLA
Kimura, S., Hasegawa, D., Yoshimoto, Y., Seki, M., Daida, A., Sekiguchi, M., Hirabayashi, S., Hosoya, Y., Kobayashi, M., Miyano, S., Ogawa, S., Takita, J., Manabe, A."Duplication of ALK F1245 missense mutation due to acquired uniparental disomy associated with aggressive progression in a patient with relapsed neuroblastoma". Oncology Letters 17.3 (2019): 3323-3329.
Chicago
Kimura, S., Hasegawa, D., Yoshimoto, Y., Seki, M., Daida, A., Sekiguchi, M., Hirabayashi, S., Hosoya, Y., Kobayashi, M., Miyano, S., Ogawa, S., Takita, J., Manabe, A."Duplication of ALK F1245 missense mutation due to acquired uniparental disomy associated with aggressive progression in a patient with relapsed neuroblastoma". Oncology Letters 17, no. 3 (2019): 3323-3329. https://doi.org/10.3892/ol.2019.9985
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