Evidence map›Paper›PMID 38025687›Full record

ArticlePeerJ2023

Metabolomic analyses uncover an inhibitory effect of niclosamide on mitochondrial membrane potential in cholangiocarcinoma cells.

Thanaporn Kulthawatsiri, Yingpinyapat Kittirat, Jutarop Phetcharaburanin, Jittima Tomacha, Bundit Promraksa, Arporn Wangwiwatsin, Poramate Klanrit, Attapol Titapun, Watcharin Loilome, Nisana Namwat

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

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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

10 authors at 2 institutions in 1 country.

Thanaporn KulthawatsiriCholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Khon Kaen, Thailand.
Yingpinyapat KittiratCholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Khon Kaen, Thailand.
Jutarop PhetcharaburaninCholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Khon Kaen, Thailand.
Jittima TomachaCholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Khon Kaen, Thailand.
Bundit PromraksaDepartment of Medical Sciences/Regional Medical Sciences Center 2, Ministry of Public Health, Phitsanulok, Phitsanulok, Thailand.
Arporn WangwiwatsinCholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Khon Kaen, Thailand.ORCID 0000-0003-4536-4492
Poramate KlanritCholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Khon Kaen, Thailand.
Attapol TitapunCholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Khon Kaen, Thailand.
Watcharin LoilomeCholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Khon Kaen, Thailand.
Nisana NamwatCholangiocarcinoma Research Institute, Khon Kaen University, Khon Kaen, Khon Kaen, Thailand.ORCID 0000-0002-6743-5047
Khon Kaen University · THMinistry of Public Health · TH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Niclosamide is an oral anthelminthic drug that has been used for treating tapeworm infections. Its mechanism involves the disturbance of mitochondrial membrane potential that in turn inhibits oxidative phosphorylation leading to ATP depletion. To date, niclosamide has been validated as the potent anti-cancer agent against several cancers. However, the molecular mechanisms underlying the effects of niclosamide on the liver fluke Materials and Methods: The inhibitory effect of niclosamide on CCA cells was determined using SRB assay. A mitochondrial membrane potential using tetramethylrhodamine, ethyl ester-mitochondrial membrane potential (TMRE-MMP) assay was conducted. Liquid chromatography-mass spectrometry-based metabolomics was employed to investigate the global metabolic changes upon niclosamide treatment. ATP levels were measured using CellTiter-Glo Results: Niclosamide strongly inhibited CCA cell growth and reduced the MMP of CCA cells. An orthogonal partial-least square regression analysis revealed that the effects of niclosamide on suppressing cell viability and MMP of CCA cells were significantly associated with an increase in niacinamide, a precursor in NAD synthesis that may disrupt the electron transport system leading to suppression of NAD Conclusion: Our findings unravel the mode of action of niclosamide in the energy depletion that could potentially serve as the promising therapeutic strategy for CCA treatment.

Indexed as

Bile Duct NeoplasmsCholangiocarcinomaOpisthorchiasisAdenosine TriphosphateAnimalsBile Ducts, IntrahepaticMembrane Potential, MitochondrialNADNiclosamideAdenosine TriphosphateNADNiclosamideCholangiocarcinomaLC-MSMetabolomicsNiclosamide

Identifiers

PMID38025687
PMCPMC10676079
OpenAlexW4388906734

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.