Evidence map›Paper›PMID 29125463›Full record

ArticleeLife2017

Pharmacological augmentation of nicotinamide phosphoribosyltransferase (NAMPT) protects against paclitaxel-induced peripheral neuropathy.

Peter M LoCoco, April L Risinger, Hudson R Smith, Teresa S Chavera, Kelly A Berg, William P Clarke

Open access · goldAbstract read
In one paragraph

Article in eLife, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 11% 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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 52 citations in OpenAlex.

  1. Pooled it
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  17. Application of P7C3 Compounds to Investigating and Treating Acute and Chronic Traumatic Brain Injury.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2023
    Review
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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

6 authors at 1 institution in 1 country.

Peter M LoCocoDepartment of Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, United States.ORCID http://orcid.org/0000-0002-5678-791X
April L RisingerDepartment of Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, United States.ORCID http://orcid.org/0000-0002-4363-3268
Hudson R SmithDepartment of Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, United States.
Teresa S ChaveraDepartment of Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, United States.
Kelly A BergDepartment of Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, United States.
William P ClarkeDepartment of Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, United States.ORCID https://orcid.org/0000-0002-8861-8256
Harvard University · US

Funding

TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Robin Jean Leach · 1991 to 2026
$59.1M
Institutional Research Training GrantT32DE014318 · NIDCR · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Kenneth M Hargreaves · 2002 to 2026
$12.1M
Institute for Integration of Medicine & Science: A Partnership to Improve HealthUL1TR000149 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CLARK, ROBERT A · 2012 to 2013
$6.8M
NCATS NIH HHS UL1 TR000149NCI NIH HHS P30 CA054174NIDCR NIH HHS T32 DE014318
6 · The paper itself

Abstract

Chemotherapy-induced peripheral neuropathy (CIPN) arises from collateral damage to peripheral afferent sensory neurons by anticancer pharmacotherapy, leading to debilitating neuropathic pain. No effective treatment for CIPN exists, short of dose-reduction which worsens cancer prognosis. Here, we report that stimulation of nicotinamide phosphoribosyltransferase (NAMPT) produced robust neuroprotection in an aggressive CIPN model utilizing the frontline anticancer drug, paclitaxel (PTX). Daily treatment of rats with the first-in-class NAMPT stimulator, P7C3-A20, prevented behavioral and histologic indicators of peripheral neuropathy, stimulated tissue NAD recovery, improved general health, and abolished attrition produced by a near maximum-tolerated dose of PTX. Inhibition of NAMPT blocked P7C3-A20-mediated neuroprotection, whereas supplementation with the NAMPT substrate, nicotinamide, potentiated a subthreshold dose of P7C3-A20 to full efficacy. Importantly, P7C3-A20 blocked PTX-induced allodynia in tumored mice without reducing antitumoral efficacy. These findings identify enhancement of NAMPT activity as a promising new therapeutic strategy to protect against anticancer drug-induced peripheral neurotoxicity.

Indexed as

AnimalsAntineoplastic Agents, PhytogenicBehavior, AnimalCarbazolesDisease Models, AnimalEnzyme ActivatorsHistocytochemistryNeuroprotective AgentsNicotinamide PhosphoribosyltransferasePaclitaxelPeripheral Nervous System DiseasesRatsTreatment OutcomeAntineoplastic Agents, PhytogenicCarbazolesEnzyme ActivatorsNeuroprotective AgentsNicotinamide PhosphoribosyltransferaseP7C3 compoundPaclitaxelcancer biologychemotherapymouseNADNAMPTneuropathyneuroprotectionneuroscienceneurotoxicitypainrat

Identifiers

PMID29125463
PMCPMC5701795
OpenAlexW2767477183

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.