4.3 Article

Preclinical evaluation of a nanoformulated antihelminthic, niclosamide, in ovarian cancer

Journal

ONCOTARGET
Volume 7, Issue 8, Pages 8993-9006

Publisher

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.7113

Keywords

nanoformulation; nanomedicine; niclosamide; ovarian cancer; cancer metabolism

Funding

  1. National Health Research Institution of Taiwan
  2. National Science Council of Taiwan
  3. Taipei Medical University
  4. Tri-Service General Hospital
  5. Tri-Service General Hospital-National Taiwan University of Science and Technology Joint Research Program [TSGH-NTUST-104-04]
  6. [NHRI-EX104-10406BI]
  7. [TMU-NDMC-104-05]
  8. [104TMU-SHH-07]
  9. [TMUTOP103005-1]
  10. [TMU103-AE1-B06 TSGH-C104-006-006-008-S01,-S02,-S03]
  11. [TSGH-C104-012]
  12. [NSC 102-2314-B-016-043 (NLAC102)]

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Ovarian cancer treatment remains a challenge and targeting cancer stem cells presents a promising strategy. Niclosamide is an old antihelminthic drug that uncouples mitochondria of intestinal parasites. Although recent studies demonstrated that niclosamide could be a potential anticancer agent, its poor water solubility needs to be overcome before further preclinical and clinical investigations can be conducted. Therefore, we evaluated a novel nanosuspension of niclosamide (nano-NI) for its effect against ovarian cancer. Nano-NI effectively inhibited the growth of ovarian cancer cells in which it induced a metabolic shift to glycolysis at a concentration of less than 3 mu M in vitro and suppressed tumor growth without obvious toxicity at an oral dose of 100 mg/kg in vivo. In a pharmacokinetic study after oral administration, nano-NI showed rapid absorption (reaching the maximum plasma concentration within 5 min) and improved the bioavailability (the estimated bioavailability for oral nano-NI was 25%). In conclusion, nano-NI has the potential to be a new treatment modality for ovarian cancer and, therefore, further clinical trials are warranted.

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