Evidence map›Paper›PMID 29660270›Full record

ArticleACS chemical neuroscience2018

Protective Effect of a Mitochondria-Targeted Peptide against the Development of Chemotherapy-Induced Peripheral Neuropathy in Mice.

Satoshi Toyama, Naohito Shimoyama, Hazel H Szeto, Peter W Schiller, Megumi Shimoyama

Abstract read
In one paragraph

Article in ACS chemical neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
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  6. Targeting the organelle for radiosensitization in cancer radiotherapy.Asian journal of pharmaceutical sciences · 2024
    Review
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  18. Mitochondria-Targeted Antioxidants: A Step towards Disease Treatment.Oxidative medicine and cellular longevity · 2020
    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

5 authors at 4 institutions in 3 countries.

Satoshi ToyamaDepartment of Neuroscience , Jikei University School of Medicine , 3-25-8 Nishi-Shimbashi, Minato-Ku , Tokyo 105-8471 , Japan.
Naohito ShimoyamaDepartment of Palliative Medicine , Jikei University Hospital , 3-19-18 Nishi-Shimbashi, Minato-Ku , Tokyo 105-8471 , Japan.
Hazel H SzetoBurke Medical Research Institute , 785 Mamaroneck Avenue , White Plains , New York 10605 , United States.
Peter W SchillerLaboratory of Chemical Biology and Peptide Research , Montreal Clinical Research Institute , 110 Pine Avenue West , Montreal , Quebec , Canada H2W 1R7.
Megumi ShimoyamaDepartment of Palliative Medicine , Jikei University Hospital , 3-19-18 Nishi-Shimbashi, Minato-Ku , Tokyo 105-8471 , Japan.ORCID 0000-0003-3511-4721
The Jikei University Hospital · JPBurke Medical Research Institute · USJikei University School of Medicine · JPMontreal Clinical Research Institute · CA

Funding

DEVELOPMENT OF RECEPTOR-SPECIFIC OPIOID PEPTIDE ANALOGSR01DA004443 · NIDA · CLINICAL RESEARCH INSTITUTE OF MONTREAL · PI SCHILLER, PETER W · 1987 to 2016
$2.0M
DEVELOPMENT OF RECEPTOR SPECIFIC OPIOID PEPTIDE ANALOGSR37DA004443 · NIDA · CLINICAL RESEARCH INSTITUTE OF MONTREAL · PI SCHILLER, PETER W · 1997 to 2003
$621k
Canadian Institutes of Health Research MOP-89716NIDA NIH HHS R01 DA004443NIDA NIH HHS R37 DA004443
6 · The paper itself

Abstract

Several chemotherapeutic agents used for cancer treatment induce dose-limiting peripheral neuropathy that compromises patients' quality of life and limits cancer treatment. Recently, mitochondrial dysfunction has been shown to be involved in the mechanism of chemotherapy-induced peripheral neuropathy. SS-20 is a mitochondria-targeted peptide that promotes mitochondrial respiration and restores mitochondrial bioenergetics. In the present study, we examined the protective effect of SS-20 against the development of chemotherapy-induced peripheral neuropathy utilizing a murine model of peripheral neuropathy induced by oxaliplatin, a first-line chemotherapy agent for colon cancer. Weekly administrations of oxaliplatin induced peripheral neuropathy as demonstrated by the development of neuropathic pain and loss of intraepidermal nerve fibers in the hind paw. Continuous administration of SS-20 protected against the development of oxaliplatin-induced neuropathic pain and mitigated the loss of intraepidermal nerve fibers to normal levels. Our findings suggest that SS-20 may be a drug candidate for the prevention of chemotherapy-induced peripheral neuropathy.

Indexed as

AnimalsAntineoplastic AgentsDisease Models, AnimalHyperalgesiaMaleMice, Inbred BALB CMitochondriaMolecular StructureNeuralgiaOligopeptidesOxaliplatinPeripheral NervesPeripheral Nervous System DiseasesProtective AgentsAntineoplastic AgentsOligopeptidesOxaliplatinphenylalanyl-arginyl-phenylalanyllysinamideProtective Agentschemotherapychemotherapy-induced peripheral neuropathymitochondrianeuropathic painOxaliplatinpain

Identifiers

PMID29660270
PMCPMC6051920
OpenAlexW2801860620

What OpenQuestion holds

Textmetadata
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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.