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Tumor-targeting Salmonella typhimurium A1-R arrests a doxorubicin-resistant PDGFRA-amplified patient-derived orthotopic xenograft mouse model of pleomorphic liposarcoma

  • Tasuku Kiyuna
  • , Yasunori Tome
  • , Takashi Murakami
  • , Ming Zhao
  • , Kentaro Miyake
  • , Kentaro Igarashi
  • , Kei Kawaguchi
  • , Masuyo Miyake
  • , Hiromichi Oshiro
  • , Takashi Higuchi
  • , Yunfeng Li
  • , Sarah M. Dry
  • , Scott D. Nelson
  • , Tara A. Russell
  • , Mark A. Eckardt
  • , Arun S. Singh
  • , Fuminori Kanaya
  • , Fritz C. Eilber
  • , Robert M. Hoffman

研究成果: ジャーナルへの寄稿 › 学術論文 › 査読

抄録

Pleomorphic liposarcoma (PLPS) is a recalcitrant soft-tissue sarcoma (STS) subtype in need of transformative therapy. We have previously established a patient-derived orthotopic xenograft (PDOX) model, of PLPS with PDGFRA amplification, using surgical orthotopic implantation. In the current study, the PLPS PDOX model was randomized into 3 groups of 7 mice each: untreated control; doxorubicin (DOX)-treated; and treated with Salmonella typhimurium A1-R (S. typhimurium A1-R) expressing green fluorescent protein (GFP). Tumor volume and body weight were monitored during the treatment period. The PLPS PDOX was resistant to DOX. In contrast, the PLPS PDOX was highly sensitive to S. typhimurium A1-R. There was no significant body-weight loss among these 3 groups. Fluorescence imaging demonstrated that S. typhimurium A1-R-GFP was very effective to target the PLPS PDOX tumor. The current study demonstrates that a PLPS PDOX, resistant to first-line therapy DOX, was highly sensitive to tumor targeting S. typhimurium A1-R.

本文言語英語
ページ(範囲)7827-7833
ページ数7
ジャーナルJournal of Cellular Biochemistry
巻119
号9
DOI
出版ステータス出版済み - 09-2018
外部発表はい

All Science Journal Classification (ASJC) codes

  • 生化学
  • 分子生物学
  • 細胞生物学

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