Evidence map›Paper›PMID 28501332›Full record

ArticleToxicology and applied pharmacology2017

Inhibition of nicotinamide phosphoribosyltransferase and depletion of nicotinamide adenine dinucleotide contribute to arsenic trioxide suppression of oral squamous cell carcinoma.

Xin Yue Wang, Jin Zhi Wang, Lu Gao, Fu Yin Zhang, Qi Wang, Ke Jian Liu, Bin Xiang

Open access · greenAbstract read
In one paragraph

Article in Toxicology and applied pharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

9 citing papers in PubMed, 16 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

7 authors at 3 institutions in 2 countries.

Xin Yue WangLaboratory of Oral and Maxillofacial Disease, Second Hospital of Dalian Medical University, Dalian, Liaoning 116023, PR China.
Jin Zhi WangDepartment of Oral and Maxillofacial Surgery, Second Hospital of Dalian Medical University, Dalian, Liaoning 116023, PR China.
Lu GaoDepartment of Oral Anatomy, School of Stomatology, Dalian Medical University, Dalian, Liaoning 116044, PR China.
Fu Yin ZhangDepartment of Oral and Maxillofacial Surgery, Second Hospital of Dalian Medical University, Dalian, Liaoning 116023, PR China.
Qi WangLaboratory of Oral and Maxillofacial Disease, Second Hospital of Dalian Medical University, Dalian, Liaoning 116023, PR China.
Ke Jian LiuDepartment of Pharmaceutical Sciences, College of Pharmacy, University of New Mexico Health Sciences Center, Albuquerque, NM 87131, USA. Electronic address: kliu@salud.unm.edu.
Bin XiangLaboratory of Oral and Maxillofacial Disease, Second Hospital of Dalian Medical University, Dalian, Liaoning 116023, PR China. Electronic address: xiangbin72@163.com.
Dalian Medical University · CNSecond Affiliated Hospital of Dalian Medical University · CNUniversity of New Mexico · US

Funding

Arsenic co-carcinogenesis with UVR: nitrosation and oxidation of target proteinsR01ES021100 · NIEHS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI HUDSON, LAURIE G, LIU, KE JIAN · 2012 to 2016
$2.4M
NIEHS NIH HHS R01 ES021100
6 · The paper itself

Abstract

Emerging evidence suggests that increased nicotinamide phosphoribosyltransferase (NAMPT) expression is associated with the development and prognosis of many cancers, but it remains unknown regarding its role in oral squamous cell carcinoma (OSCC). In the present study, the results from tissue microarray showed that NAMPT was overexpressed in OSCC patients and its expression level was directly correlated with differential grades of cancer. Interestingly, treatment of OSCC cells with chemotherapy agent arsenic trioxide (ATO) decreased the levels of NAMPT protein and increased cellular death in an ATO dose- and time-dependent manner. Most importantly, combination of low concentration ATO with FK866 (a NAMPT inhibitor) exerted enhanced inhibitive effect on NAMPT protein and mRNA expressions, leading to synergistic cytotoxicity on cancer cells through increasing cell apoptosis and depleting intracellular nicotinamide adenine dinucleotide levels. These findings demonstrate the crucial role of NAMPT in the prognosis of OSCC and reveal inhibition of NAMPT as a novel mechanism of ATO in suppressing cancer cell growth. Our results suggest that ATO can significantly enhance therapeutic efficacy of NAMPT inhibitor, and combined treatment may be a novel and effective therapeutic strategy for OSCC patients.

Indexed as

AdultArsenicalsArsenic TrioxideCarcinoma, Squamous CellCell Line, TumorCell SurvivalCytokinesDose-Response Relationship, DrugEnzyme InhibitorsFemaleHumansMaleMiddle AgedMouth NeoplasmsNADNicotinamide PhosphoribosyltransferaseArsenicalsArsenic TrioxideCytokinesEnzyme InhibitorsNADNicotinamide Phosphoribosyltransferasenicotinamide phosphoribosyltransferase, humanOxidesArsenic trioxideFK866Nicotinamide adenine dinucleotideNicotinamide phosphoribosyltransferaseSquamous cell carcinoma

Identifiers

PMID28501332
PMCPMC5568507
OpenAlexW2613495141

What OpenQuestion holds

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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.