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Identification of prophylactic drugs for oxaliplatin-induced peripheral neuropathy using big data.
Zamami, Yoshito; Niimura, Takahiro; Kawashiri, Takehiro; Goda, Mitsuhiro; Naito, Yutaro; Fukushima, Keijo; Ushio, Soichiro; Aizawa, Fuka; Hamano, Hirofumi; Okada, Naoto; Yagi, Kenta; Miyata, Koji; Takechi, Kenshi; Chuma, Masayuki; Koyama, Toshihiro; Kobayashi, Daisuke; Shimazoe, Takao; Fujino, Hiromichi; Izawa-Ishizawa, Yuki; Ishizawa, Keisuke.
Afiliación
  • Zamami Y; Department of Clinical Pharmacy, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama, Japan; Department of Pharmacy, Okayama University Hospital, Okayama, Japan.
  • Niimura T; Department of Pharmacy, Tokushima University Hospital, Tokushima, Japan.
  • Kawashiri T; Department of Clinical Pharmacy and Pharmaceutical Care, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.
  • Goda M; Department of Clinical Pharmacology and Therapeutics, Tokushima University Graduate School of Biomedical Sciences, Tokushima, Japan.
  • Naito Y; Department of Clinical Pharmacology and Therapeutics, Tokushima University Graduate School of Biomedical Sciences, Tokushima, Japan.
  • Fukushima K; Department of Pharmacology for Life Sciences, Tokushima University Graduate School of Biomedical Sciences, Tokushima, Japan.
  • Ushio S; Department of Pharmacy, Okayama University Hospital, Okayama, Japan.
  • Aizawa F; Department of Pharmacy, Tokushima University Hospital, Tokushima, Japan.
  • Hamano H; Clinical Research Center for Developmental Therapeutics, Tokushima University Hospital, Tokushima, Japan.
  • Okada N; Department of Pharmacy, Tokushima University Hospital, Tokushima, Japan.
  • Yagi K; Clinical Research Center for Developmental Therapeutics, Tokushima University Hospital, Tokushima, Japan.
  • Miyata K; Department of Clinical Pharmacology and Therapeutics, Tokushima University Graduate School of Biomedical Sciences, Tokushima, Japan.
  • Takechi K; Department of Drug Information Analysis, College of Pharmaceutical Sciences, Matsuyama University, Matsuyama, Japan.
  • Chuma M; Department of Hospital Pharmacy and Pharmacology, Asahikawa Medical University, Asahikawa, Japan.
  • Koyama T; Department of Pharmaceutical Biomedicine, Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University, Okayama, Japan.
  • Kobayashi D; Department of Clinical Pharmacy and Pharmaceutical Care, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.
  • Shimazoe T; Department of Clinical Pharmacy and Pharmaceutical Care, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.
  • Fujino H; Department of Pharmacology for Life Sciences, Tokushima University Graduate School of Biomedical Sciences, Tokushima, Japan.
  • Izawa-Ishizawa Y; Department of Pharmacology, University of Tokushima Graduate School of Biomedical Sciences, Tokushima, Japan.
  • Ishizawa K; Department of Pharmacy, Tokushima University Hospital, Tokushima, Japan; Department of Clinical Pharmacology and Therapeutics, Tokushima University Graduate School of Biomedical Sciences, Tokushima, Japan. Electronic address: ishizawa@tokushima-u.ac.jp.
Biomed Pharmacother ; 148: 112744, 2022 Apr.
Article en En | MEDLINE | ID: mdl-35240525
ABSTRACT

BACKGROUND:

Drug repositioning is a cost-effective method to identify novel disease indications for approved drugs; it requires a shorter developmental period than conventional drug discovery methods. We aimed to identify prophylactic drugs for oxaliplatin-induced peripheral neuropathy by drug repositioning using data from large-scale medical information and life science information databases.

METHODS:

Herein, we analyzed the reported data between 2007 and 2017 retrieved from the FDA's database of spontaneous adverse event reports (FAERS) and the LINCS database provided by the National Institute of Health. The efficacy of the drug candidates for oxaliplatin-induced peripheral neuropathy obtained from the database analysis was examined using a rat model of peripheral neuropathy. Additionally, we compared the incidence of peripheral neuropathy in patients who received oxaliplatin at the Tokushima University Hospital, Japan. The effects of statins on the animal model were examined in six-week-old male Sprague-Dawley rats and seven or eight-week-old male BALB/C mice. Retrospective medical chart review included clinical data from Tokushima University Hospital from April 2009 to March 2018.

RESULTS:

Simvastatin, indicated for dyslipidemia, significantly reduced the severity of peripheral neuropathy and oxaliplatin-induced hyperalgesia. In the nerve tissue of model rats, the mRNA expression of Gstm1 increased with statin administration. A retrospective medical chart review using clinical data revealed that the incidence of peripheral neuropathy decreased with statin use. CONCLUSION AND RELEVANCE Thus, drug repositioning using data from large-scale basic and clinical databases enables the discovery of new indications for approved drugs with a high probability of success.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedades del Sistema Nervioso Periférico / Reposicionamiento de Medicamentos / Profilaxis Pre-Exposición / Oxaliplatino Tipo de estudio: Diagnostic_studies / Observational_studies / Risk_factors_studies Límite: Animals / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Biomed Pharmacother Año: 2022 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedades del Sistema Nervioso Periférico / Reposicionamiento de Medicamentos / Profilaxis Pre-Exposición / Oxaliplatino Tipo de estudio: Diagnostic_studies / Observational_studies / Risk_factors_studies Límite: Animals / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Biomed Pharmacother Año: 2022 Tipo del documento: Article País de afiliación: Japón