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Research Article
Open Access

A Novel Anionic-phosphate-platinum Complex Effectively Targets a Cisplatinum-resistant Osteosarcoma in a Patient-derived Orthotopic Xenograft Mouse Model

KENTARO IGARASHI, KEI KAWAGUCHI, NORIO YAMAMOTO, KATSUHIRO HAYASHI, HIROAKI KIMURA, SHINJI MIWA, TAKASHI HIGUCHI, YUTA TANIGUCHI, HIROTAKA YONEZAWA, YOSHIHIRO ARAKI, SEI MORINAGA, SWETA MISRA, SCOTT D. NELSON, SARAH M. DRY, YUNFENG LI, AKIRA ODANI, SHREE RAM SINGH, HIROYUKI TSUCHIYA and ROBERT M. HOFFMAN
Cancer Genomics & Proteomics May 2020, 17 (3) 217-223; DOI: https://doi.org/10.21873/cgp.20182
KENTARO IGARASHI
1AntiCancer, Inc., San Diego, CA, U.S.A.
2Department of Surgery, University of California, San Diego, CA, U.S.A.
3Department of Orthopaedic Surgery, Kanazawa University, Kanazawa, Japan
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KEI KAWAGUCHI
1AntiCancer, Inc., San Diego, CA, U.S.A.
2Department of Surgery, University of California, San Diego, CA, U.S.A.
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NORIO YAMAMOTO
3Department of Orthopaedic Surgery, Kanazawa University, Kanazawa, Japan
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KATSUHIRO HAYASHI
3Department of Orthopaedic Surgery, Kanazawa University, Kanazawa, Japan
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HIROAKI KIMURA
3Department of Orthopaedic Surgery, Kanazawa University, Kanazawa, Japan
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SHINJI MIWA
3Department of Orthopaedic Surgery, Kanazawa University, Kanazawa, Japan
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TAKASHI HIGUCHI
3Department of Orthopaedic Surgery, Kanazawa University, Kanazawa, Japan
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YUTA TANIGUCHI
3Department of Orthopaedic Surgery, Kanazawa University, Kanazawa, Japan
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HIROTAKA YONEZAWA
3Department of Orthopaedic Surgery, Kanazawa University, Kanazawa, Japan
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YOSHIHIRO ARAKI
3Department of Orthopaedic Surgery, Kanazawa University, Kanazawa, Japan
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SEI MORINAGA
3Department of Orthopaedic Surgery, Kanazawa University, Kanazawa, Japan
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SWETA MISRA
4Mouse Cancer Genetics Program, National Cancer Institute, Frederick, MD, U.S.A.
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SCOTT D. NELSON
5Department of Pathology, University of California, Los Angeles, CA, U.S.A.
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SARAH M. DRY
5Department of Pathology, University of California, Los Angeles, CA, U.S.A.
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YUNFENG LI
5Department of Pathology, University of California, Los Angeles, CA, U.S.A.
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AKIRA ODANI
6Division of Pharmaceutical Sciences, Kanazawa University, Kanazawa, Japan
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SHREE RAM SINGH
7Basic Research Laboratory, National Cancer Institute, Frederick, MD, U.S.A.
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  • For correspondence: all@anticancer.com singhshr@mail.nih.gov tsuchi@med.kanazawa-u.ac.jp
HIROYUKI TSUCHIYA
3Department of Orthopaedic Surgery, Kanazawa University, Kanazawa, Japan
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  • For correspondence: all@anticancer.com singhshr@mail.nih.gov tsuchi@med.kanazawa-u.ac.jp
ROBERT M. HOFFMAN
1AntiCancer, Inc., San Diego, CA, U.S.A.
2Department of Surgery, University of California, San Diego, CA, U.S.A.
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  • For correspondence: all@anticancer.com singhshr@mail.nih.gov tsuchi@med.kanazawa-u.ac.jp
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Abstract

Background/Aim: We have previously developed a novel bone-targeting platinum compound, 3Pt, and showed that it has strong inhibitory activity against osteosarcoma cells and orthotopic cell-line xenograft mouse models. In the present report, we compared the efficacy of 3Pt to cisplatinum (CDDP) in a CDDP-resistant relapsed osteosarcoma patient-derived orthotopic xenograft (PDOX) mouse model. Patients and Methods: The tumor of a patient with osteosarcoma of the distal femur was treated with CDDP-based chemotherapy followed by surgery. The surgical specimen was used to establish a PDOX model. An osteosarcoma cell line was also established from the original patient tumor. Osteosarcoma cell viability was assessed with the WST-8 assay and the IC50 values were calculated. The PDOX models were randomized into three groups: untreated control, CDDP-treated group, and 3Pt-treated group. Tumor size and body weight were measured twice a week. Results: 3Pt had a strong concentration-dependent cytocidal effect in vitro. The IC50 value of 3Pt was significantly lower than that of CDDP. On day 14 of the treatment, 3Pt caused a significantly greater tumor growth inhibition compared to the untreated control and CDDP-treated mice. Conclusion: 3Pt is a promising clinical candidate for the treatment of recalcitrant osteosarcoma.

  • Osteosarcoma
  • cisplatinum-resistant
  • platinum complex
  • efficacy
  • 3Pt
  • PDOX
  • Received December 27, 2019.
  • Revision received February 19, 2020.
  • Accepted February 20, 2020.
  • Copyright© 2020, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved

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Cancer Genomics - Proteomics: 17 (3)
Cancer Genomics & Proteomics
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May-June 2020
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A Novel Anionic-phosphate-platinum Complex Effectively Targets a Cisplatinum-resistant Osteosarcoma in a Patient-derived Orthotopic Xenograft Mouse Model
KENTARO IGARASHI, KEI KAWAGUCHI, NORIO YAMAMOTO, KATSUHIRO HAYASHI, HIROAKI KIMURA, SHINJI MIWA, TAKASHI HIGUCHI, YUTA TANIGUCHI, HIROTAKA YONEZAWA, YOSHIHIRO ARAKI, SEI MORINAGA, SWETA MISRA, SCOTT D. NELSON, SARAH M. DRY, YUNFENG LI, AKIRA ODANI, SHREE RAM SINGH, HIROYUKI TSUCHIYA, ROBERT M. HOFFMAN
Cancer Genomics & Proteomics May 2020, 17 (3) 217-223; DOI: 10.21873/cgp.20182

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A Novel Anionic-phosphate-platinum Complex Effectively Targets a Cisplatinum-resistant Osteosarcoma in a Patient-derived Orthotopic Xenograft Mouse Model
KENTARO IGARASHI, KEI KAWAGUCHI, NORIO YAMAMOTO, KATSUHIRO HAYASHI, HIROAKI KIMURA, SHINJI MIWA, TAKASHI HIGUCHI, YUTA TANIGUCHI, HIROTAKA YONEZAWA, YOSHIHIRO ARAKI, SEI MORINAGA, SWETA MISRA, SCOTT D. NELSON, SARAH M. DRY, YUNFENG LI, AKIRA ODANI, SHREE RAM SINGH, HIROYUKI TSUCHIYA, ROBERT M. HOFFMAN
Cancer Genomics & Proteomics May 2020, 17 (3) 217-223; DOI: 10.21873/cgp.20182
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Keywords

  • Osteosarcoma
  • cisplatinum-resistant
  • platinum complex
  • efficacy
  • 3Pt
  • PDOX
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