Evidence map›Paper›PMID 26848771›Full record

ArticleOncotarget2016

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

Chi-Kang Lin, Meng-Yi Bai, Teh-Min Hu, Yu-Chi Wang, Tai-Kuang Chao, Shao-Ju Weng, Rui-Lan Huang, Po-Hsuan Su, Hung-Cheng Lai

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
8.4field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 88 citations in OpenAlex.

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  7. Navigating the Molecular Signaling: Deciphering Cancer Stem Cell Self-Renewal Pathways.International journal of molecular and cellular medicine · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Chi-Kang LinGraduate Institute of Medical Sciences, National Defense Medical Center, Taipei, Taiwan.
Meng-Yi BaiGraduate Institute of Biomedical Engineering, National Taiwan University of Science and Technology, Taipei, Taiwan.
Teh-Min HuSchool of Pharmacy, National Defense Medical Center, Taipei, Taiwan.
Yu-Chi WangGraduate Institute of Medical Sciences, National Defense Medical Center, Taipei, Taiwan.
Tai-Kuang ChaoDepartment of Pathology, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
Shao-Ju WengGraduate Institute of Medical Sciences, National Defense Medical Center, Taipei, Taiwan.
Rui-Lan HuangDepartment of Obstetrics and Gynecology, Shuang-Ho Hospital, Taipei Medical University, New Taipei City, Taiwan.
Po-Hsuan SuDepartment of Obstetrics and Gynecology, Shuang-Ho Hospital, Taipei Medical University, New Taipei City, Taiwan.
Hung-Cheng LaiGraduate Institute of Medical Sciences, National Defense Medical Center, Taipei, Taiwan.
National Defense Medical Center · TWTaipei Medical University · TWNational Taiwan University of Science and Technology · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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 μM 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.

Indexed as

AnimalsAntineoplastic AgentsBiological AvailabilityCell Line, TumorCell ProliferationDrug Evaluation, PreclinicalEnergy MetabolismFemaleGlycolysisHumansMiceMice, Inbred NODMice, SCIDNiclosamideOvarian NeoplasmsOxygen ConsumptionAntineoplastic AgentsNiclosamideSuspensionscancer metabolismnanoformulationnanomedicineniclosamideovarian cancer

Identifiers

PMID26848771
PMCPMC4891020
OpenAlexW2286764804

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.