Evidence map›Paper›PMID 19245717›Full record

ArticleMolecular pain2009

Mice with cisplatin and oxaliplatin-induced painful neuropathy develop distinct early responses to thermal stimuli.

Lauren E Ta, Philip A Low, Anthony J Windebank

Open access · goldAbstract read
In one paragraph

Article in Molecular pain, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 88 papers.

0numbers the graph read from it
0cells of the map it votes in
88citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

88 citing papers in PubMed, 144 citations in OpenAlex.

  1. Clinical Course of Oxaliplatin-Induced Neuropathy: Results From the Randomized Phase III Trial N08CB (Alliance).Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2015
    Trial
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  7. Animal models of cisplatin-induced neuropathic pain.Animal models and experimental medicine · 2025
    Review
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  14. Research progress of ginger in the treatment of gastrointestinal tumors.World journal of gastrointestinal oncology · 2023
    Review
  15. Does statin suppress oxaliplatin-induced peripheral neuropathy in patients with colorectal cancer? A single-center observational study.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2023
    Observational
  16. Article
  17. Kinin BPharmaceutics · 2023
    Article
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28 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

Lauren E TaProgram in Molecular Neuroscience, Mayo Graduate School and Cellular Neurobiology Laboratory, Department of Neurology, Mayo Clinic, College of Medicine, Rochester, MN 55905, USA. ta.lauren@mayo.edu
Philip A Low
Anthony J Windebank
Mayo Clinic · US

Funding

MECHANISMS OF NEURONAL DEATH AND NEUROPROTECTIONR01NS040471 · NINDS · MAYO CLINIC ROCHESTER · PI WINDEBANK, ANTHONY JOHN · 2000 to 2010
$2.5M
Endoplasmic Reticulum Calcium Pools in Neuropathic PainK08DE014571 · NIDCR · MAYO CLINIC ROCHESTER · PI TA, LAUREN E · 2003 to 2007
$594k
NIDCR NIH HHS K08 DE014571NIDCR NIH HHS K08 DE14571-05NINDS NIH HHS R01 NS040471NINDS NIH HHS R01 NS 40471-04
6 · The paper itself

Abstract

backgroundCisplatin has been in use for 40 years for treatment of germ line and other forms of cancer. Oxaliplatin is approved for treatment of metastatic colorectal cancer. Thirty to forty percent of cancer patients receiving these agents develop pain and sensory loss. Oxaliplatin induces distinctive cold-associated dysesthesias in up to 80% of patients.

resultsWe have established mouse models of cisplatin and oxaliplatin-induced neuropathy using doses similar to those used in patients. Adult male C57BL6J mice were treated with daily intraperitoneal injection for 5 days, followed by 5 days of rest, for two cycles. Total cumulative doses of 23 mg/kg cisplatin and 30 mg/kg oxaliplatin were used. Behavioral evaluations included cold plate, von Frey, radiant heat, tail immersion, grip strength and exploratory behavior at baseline and at weekly intervals for 8 weeks. Following two treatment cycles, mice in the cisplatin and oxaliplatin treatment groups demonstrated significant mechanical allodynia compared to control mice. In addition, the cisplatin group exhibited significant thermal hyperalgesia in hind paws and tail, and the oxaliplatin group developed significant cold hyperalgesia in hind paws.

conclusionWe have therefore established a model of platinum drug-induced painful peripheral neuropathy that reflects the differences in early thermal pain responses that are observed in patients treated with either cisplatin or oxaliplatin. This model should be useful in studying the molecular basis for these different pain responses and in designing protective therapeutic strategies.

Indexed as

AnimalsCisplatinDisease Models, AnimalDrug Therapy, CombinationHot TemperatureHyperalgesiaMaleMiceMice, Inbred C57BLOrganoplatinum CompoundsOxaliplatinPeripheral Nervous System DiseasesCisplatinOrganoplatinum CompoundsOxaliplatin

Identifiers

PMID19245717
PMCPMC2655284
OpenAlexW2096610541

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.