1. Academic Validation
  2. 2-Hydroxypropyl-β-Cyclodextrin Acts as a Novel Anticancer Agent

2-Hydroxypropyl-β-Cyclodextrin Acts as a Novel Anticancer Agent

  • PLoS One. 2015 Nov 4;10(11):e0141946. doi: 10.1371/journal.pone.0141946.
Masako Yokoo 1 Yasushi Kubota 1 2 Keiichi Motoyama 3 Taishi Higashi 3 Masatoshi Taniyoshi 3 Hiroko Tokumaru 3 Rena Nishiyama 3 Yoko Tabe 4 Sakiko Mochinaga 5 Akemi Sato 1 Naoko Sueoka-Aragane 1 Eisaburo Sueoka 2 6 Hidetoshi Arima 3 7 Tetsumi Irie 3 7 Shinya Kimura 1
Affiliations

Affiliations

  • 1 Division of Hematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan.
  • 2 Department of Transfusion Medicine, Saga University Hospital, Saga, Japan.
  • 3 Graduate School of Pharmaceutical Sciences, Kumamoto University, Kumamoto, Japan.
  • 4 Department of Clinical Laboratory Medicine, Juntendo University School of Medicine, Tokyo, Japan.
  • 5 Department of Pharmacy, Saga University Hospital, Saga, Japan.
  • 6 Department of Clinical Laboratory Medicine, Faculty of Medicine, Saga University, Saga, Japan.
  • 7 Program for Leading Graduate Schools "HIGO (Health life science: Interdisciplinary and Global Oriented) Program", Kumamoto University, Kumamoto, Japan.
Abstract

2-Hydroxypropyl-β-cyclodextrin (HP-β-CyD) is a cyclic oligosaccharide that is widely used as an enabling excipient in pharmaceutical formulations, but also as a Cholesterol modifier. HP-β-CyD has recently been approved for the treatment of Niemann-Pick Type C disease, a lysosomal lipid storage disorder, and is used in clinical practice. Since Cholesterol accumulation and/or dysregulated Cholesterol metabolism has been described in various malignancies, including leukemia, we hypothesized that HP-β-CyD itself might have Anticancer effects. This study provides evidence that HP-β-CyD inhibits leukemic cell proliferation at physiologically available doses. First, we identified the potency of HP-β-CyD in vitro against various leukemic cell lines derived from acute myeloid leukemia (AML), acute lymphoblastic leukemia and chronic myeloid leukemia (CML). HP-β-CyD treatment reduced intracellular Cholesterol resulting in significant leukemic cell growth inhibition through G2/M cell-cycle arrest and Apoptosis. Intraperitoneal injection of HP-β-CyD significantly improved survival in leukemia mouse models. Importantly, HP-β-CyD also showed Anticancer effects against CML cells expressing a T315I Bcr-Abl mutation (that confers resistance to most ABL tyrosine kinase inhibitors), and hypoxia-adapted CML cells that have characteristics of leukemic stem cells. In addition, colony forming ability of human primary AML and CML cells was inhibited by HP-β-CyD. Systemic administration of HP-β-CyD to mice had no significant adverse effects. These data suggest that HP-β-CyD is a promising Anticancer agent regardless of disease or cellular characteristics.

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