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Novel gene fusions in human oropharyngeal carcinoma.
Masago, Katsuhiro; Kuroda, Hiroaki; Sasaki, Eiichi; Fujita, Yasuko; Fujita, Shiro; Horio, Yoshitsugu; Endo, Motoyoshi; Ishihara, Hiromasa; Hanai, Nobuhiro; Matsushita, Hirokazu.
Affiliation
  • Masago K; Department of Pathology and Molecular Diagnostics, Aichi Cancer Center, Nagoya, Japan; Division of Translational Oncoimmunology, Aichi Cancer Research Institute, Nagoya, Japan. Electronic address: masago@aichi-cc.jp.
  • Kuroda H; Department of Respiratory Surgery, Aichi Cancer Center Hospital, Nagoya, Japan; Division of Translational Oncoimmunology, Aichi Cancer Research Institute, Nagoya, Japan; Department of Thoracic Surgery, Teikyo University Mizonokuchi Hospital, Kawasaki, Japan.
  • Sasaki E; Department of Pathology and Molecular Diagnostics, Aichi Cancer Center, Nagoya, Japan.
  • Fujita Y; Department of Pathology and Molecular Diagnostics, Aichi Cancer Center, Nagoya, Japan.
  • Fujita S; Department of Respiratory Medicine, Kobe Central Hospital, Kobe, Japan.
  • Horio Y; Department of Respiratory Medicine, Aichi Cancer Center Hospital, Nagoya, Japan; Division of Translational Oncoimmunology, Aichi Cancer Research Institute, Nagoya, Japan.
  • Endo M; Department of Molecular Biology, University of Occupational and Environmental Health, Kitakyushu, Japan.
  • Ishihara H; Division of Translational Oncoimmunology, Aichi Cancer Research Institute, Nagoya, Japan.
  • Hanai N; Department of Head and Neck Surgery, Aichi Cancer Center Hospital, Nagoya, Japan.
  • Matsushita H; Division of Translational Oncoimmunology, Aichi Cancer Research Institute, Nagoya, Japan.
Cancer Genet ; 286-287: 29-34, 2024 Jul 01.
Article in En | MEDLINE | ID: mdl-38971117
ABSTRACT
Few reports have analyzed the fusion genes involved in carcinogenesis in the oropharynx, where the incidence of human papillomavirus-associated tumors is relatively low. The aim of this study was to identify novel driver fusion genes in patients with oropharyngeal cancer. The study enrolled fifty-seven patients who were diagnosed with oropharyngeal carcinoma. RNA sequencing data from fresh-frozen specimens were used to identify candidate fusion genes via the JAFFA, arriba, and STAR-Fusion pipelines. Candidate fusion genes were confirmed by direct sequencing. The expression level of a candidate fusion gene was compared to that of tumors without fusion genes. Finally, filtering was performed for driver genes using the annoFuse pipeline. In addition, the VIRTUS pipeline was used to analyze the presence of human papillomavirus in the tumors. We identified 5 (8.8 %) novel potential driver in-frame fusion genes, MKNK2MOB3A, ICMTRPS6KA3, ATP1B3GRK7, CSNK2A1KIF16B, and FGFR3MAEA, and 1 (1.8 %) known in-frame fusion gene, FGFR3TACC3, in 57 patients with pharyngeal carcinoma. Our results suggest that sporadic fusion genes may contribute to tumorigenesis in oropharyngeal carcinomas.
Key words

Full text: 1 Database: MEDLINE Language: En Journal: Cancer Genet Year: 2024 Type: Article

Full text: 1 Database: MEDLINE Language: En Journal: Cancer Genet Year: 2024 Type: Article