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Genes, chromosomes & cancer v.56 no.4, 2017년, pp.303 - 313   SCI SCIE SCOPUS
본 등재정보는 저널의 등재정보를 참고하여 보여주는 베타서비스로 정확한 논문의 등재여부는 등재기관에 확인하시기 바랍니다.

Genomic and transcriptomic analysis of imatinib resistance in gastrointestinal stromal tumors

Takahashi, Tsuyoshi (Department of Gastroenterological Surgery, Osaka University Graduate School of Medicine, 2‐2 E2, Yamadaoka, Suita City, Osaka, 565‐0871, Japan ) ; Elzawahry, Asmaa (Department of Bioinformatics, National Cancer Center Research Institute, 5‐1‐1 Tsukiji, Chuo‐ku, Tokyo, 104‐0045, Japan ) ; Mimaki, Sachiyo (Division of Translational Research, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center, 6‐5‐1 Kashiwanoha, Kashiwa, Chiba, 277‐8577, Japan ) ; Furukawa, Eisaku (Department of Bioinformatics, National Cancer Center Research Institute, 5‐1‐1 Tsukiji, Chuo‐ku, Tokyo, 104‐0045, Japan ) ; Nakatsuka, Rie (Department of Gastroenterological Surgery, Osaka University Graduate School of Medicine, 2‐2 E2, Yamadaoka, Suita City, Osaka, 565‐0871, Japan ) ; Nakamura, Hiromi (D ) ; Nishigaki, Takahiko ; Serada, Satoshi ; Naka, Tetsuji ; Hirota, Seiichi ; Shibata, Tatsuhiro ; Tsuchihara, Katsuya ; Nishida, Toshirou ; Kato, Mamoru ;
  • 초록  

    Gastrointestinal stromal tumors represent the most common mesenchymal tumor of the digestive tract, driven by gain‐of‐function mutations in KIT . Despite its proven benefits, half of the patients treated with imatinib show disease progression within 2 years due to secondary resistance mutations in KIT . It remains unclear how the genomic and transcriptomic features change during the acquisition of imatinib resistance. Here, we performed exome sequencing and microarray transcription analysis for four imatinib‐resistant cell lines and one cell line briefly exposed to imatinib. We also performed exome sequencing of clinical tumor samples. The cell line briefly exposed to imatinib exhibited few single‐nucleotide variants and copy‐number alterations, but showed marked upregulation of genes related to detoxification and downregulation of genes involved in cell cycle progression. Meanwhile, resistant cell lines harbored numerous genomic changes: amplified genes related to detoxification and deleted genes with cyclin‐dependent kinase activity. Some variants in the resistant samples were traced back to the drug‐sensitive samples, indicating the presence of ancestral subpopulations. The subpopulations carried variants associated with cell death. Pre‐existing cancer cells with genetic alterations promoting apoptosis resistance may serve as a basis whereby cancer cells with critical mutations, such as secondary KIT mutations, can establish full imatinib resistance. ⓒ 2017 The Authors Genes, Chromosomes and Cancer Published by Wiley Periodicals, Inc.


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