Evidence map›Paper›PMID 22562580›Full record

ReviewCellular and molecular life sciences : CMLS2012

siRNA-mediated knock-down of NOX3: therapy for hearing loss?

Leonard P Rybak, Debashree Mukherjea, Sarvesh Jajoo, Tejbeer Kaur, Vickram Ramkumar

Abstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.5field-weighted citation impact, top 23% 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

23 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. NADPH Oxidase 3: Beyond the Inner Ear.Antioxidants (Basel, Switzerland) · 2024
    Review
  9. Review
  10. Article
  11. Review
  12. NOX Inhibitors: From Bench to Naxibs to Bedside.Handbook of experimental pharmacology · 2021
    Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Adenosine A1 Receptor Protects Against Cisplatin Ototoxicity by Suppressing the NOX3/STAT1 Inflammatory Pathway in the Cochlea.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    Article
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 1 institution in 1 country.

Leonard P RybakDepartment of Surgery, Division of Otolaryngology, Southern Illinois University, School of Medicine, Springfield, IL 62794-9649, USA. lrybak@sumed.edu
Debashree Mukherjea
Sarvesh Jajoo
Tejbeer Kaur
Vickram Ramkumar
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
Targeting Inflammation for the Amelioration of Cisplatin-Hearing LossR15DC011412 · NIDCD · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI RAMKUMAR, VICKRAM · 2011 to 2011
$437k
Novel Approaches for Prevention and Treatment of Noise Induced Hearing lossR03DC011621 · NIDCD · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI MUKHERJEA, DEBASHREE · 2012 to 2014
$429k
Amelioration of cisplatin ototoxicity by transplatinF32DC009950 · NIDCD · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI MUKHERJEA, DEBASHREE · 2009 to 2010
$113k
NIDCD NIH HHS F32 DC 009950NIDCD NIH HHS F32 DC009950NIDCD NIH HHS R01 DC002396NIDCD NIH HHS R01-DC02396NIDCD NIH HHS R03 DC011621NIDCD NIH HHS R15 DC011412
6 · The paper itself

Abstract

Cisplatin is a widely used chemotherapeutic agent that causes significant hearing loss. Previous studies have shown that cisplatin exposure is associated with increase in reactive oxygen species (ROS) in the cochlea. The inner ear expresses a unique isoform of NADPH oxidase, NOX3. This enzyme may be the primary source of ROS generation in the cochlea. The knockdown of NOX3 by pretreatment with siRNA prevented cisplatin ototoxicity, as demonstrated by preservation of hearing thresholds and inner ear sensory cells. Trans-tympanic NOX3 siRNA reduced the expression of NOX3 and biomarkers of cochlear damage, including transient receptor vanilloid 1 (TRPV1) channel and kidney injury molecule-1 (KIM-1) in cochlear tissues. In addition, siRNA against NOX3 reduced apoptosis as demonstrated by TUNEL staining, and prevented the increased expression of Bax and abrogated the decrease in Bcl2 expression following cisplatin administration. Trans-tympanic administration of siRNA directed against NOX3 may provide a useful method of attenuating cisplatin ototoxicity. In this paper, we review recent publications dealing with the role of NOX3 in ototoxicity and the effects of siRNA against cisplatin-induced hearing loss.

Indexed as

CisplatinEar, InnerHearing LossHumansMembrane ProteinsNADPH OxidasesParaquatRNA InterferenceRNA, Small InterferingCisplatinMembrane ProteinsNADPH OxidasesNox3 protein, humanParaquatRNA, Small Interfering

Identifiers

PMID22562580
PMCPMC5441545
OpenAlexW1998209096

What OpenQuestion holds

Textmetadata
LicenceTDM
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.