Evidence map›Paper›PMID 29163050›Full record

ReviewFrontiers in cellular neuroscience2017

Mechanisms of Cisplatin-Induced Ototoxicity and Otoprotection.

Sandeep Sheth, Debashree Mukherjea, Leonard P Rybak, Vickram Ramkumar

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in cellular neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 191 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
191citing papers in PubMed, 4 pooled it
17.2field-weighted citation impact, top 1% 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

191 citing papers in PubMed, 4 syntheses or guidelines pooled it, 348 citations in OpenAlex.

  1. Pooled it
  2. N-acetylcysteine for the Prevention of Cisplatin-Induced Hearing Loss: A Systematic Review and Meta-analysis.Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery · 2025
    Pooled it
  3. Pooled it
  4. Pooled it
  5. [Efficacy of intratympanic infiltration of N-acetyl cysteine in cisplatin ototoxicity].Revista medica del Instituto Mexicano del Seguro Social · 2023
    Trial
  6. Trial
  7. Honokiol-mediated reversal of cisplatin-induced transcriptomic changes in outer hair cells.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2026
    Article
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  10. Article
  11. Review
  12. Article
  13. Review
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  18. Observational
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  20. Review

131 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

4 authors at 1 institution in 1 country.

Sandeep ShethDepartment of Pharmacology, Southern Illinois University School of Medicine, Springfield, IL, United States.
Debashree MukherjeaDepartment of Surgery (Otolaryngology), Southern Illinois University School of Medicine, Springfield, IL, United States.
Leonard P RybakDepartment of Pharmacology, Southern Illinois University School of Medicine, Springfield, IL, United States.
Vickram RamkumarDepartment of Pharmacology, Southern Illinois University School of Medicine, Springfield, IL, United States.
Southern Illinois University School of Medicine · US

Funding

ENDOGENOUS MODULATION OF OTOTOXICITY OF CISPLATINR01DC002396 · NIDCD · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI RYBAK, LEONARD P · 1994 to 2018
$4.7M
Oral Epigallocatechin Gallate (EGCG) for Treatment of Cisplatin OtotoxicityR01DC016835 · NIDCD · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI RYBAK, LEONARD P · 2018 to 2022
$2.2M
Transplatin: A Novel Agent to Mitigate Cisplatin ToxicityR01CA166907 · NCI · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI RAMKUMAR, VICKRAM · 2013 to 2017
$1.5M
NCI NIH HHS R01 CA166907NIDCD NIH HHS R01 DC002396NIDCD NIH HHS R01 DC016835
6 · The paper itself

Abstract

Evidence of significant hearing loss during the early days of use of cisplatin as a chemotherapeutic agent in cancer patients has stimulated research into the causes and treatment of this side effect. It has generally been accepted that hearing loss is produced by excessive generation of reactive oxygen species (ROS) in cell of the cochlea, which led to the development of various antioxidants as otoprotective agents. Later studies show that ROS could stimulate cochlear inflammation, suggesting the use of anti-inflammatory agents for treatment of hearing loss. In this respect, G-protein coupled receptors, such as adenosine A

Indexed as

anti-inflammatory agentsantioxidantsapoptosiscisplatinotoprotectionototoxicityoxidative stress

Identifiers

PMID29163050
PMCPMC5663723
OpenAlexW2765087544

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.