Evidence map›Paper›PMID 25809464›Full record

ArticleGene therapy2015

Cochlear protection against cisplatin by viral transfection of X-linked inhibitor of apoptosis protein across round window membrane.

H Jie, S Tao, L Liu, L Xia, A Charko, Z Yu, M Bance, S Yin, G S Robertson, J Wang

Abstract read
PubMed Publisher
In one paragraph

Article in Gene therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 40% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Advancing precision ear medicine: leveraging animal models for disease insights and therapeutic innovations.Mammalian genome : official journal of the International Mammalian Genome Society · 2025
    Review
  5. Review
  6. Review
  7. Current Advances in Adeno-Associated Virus-Mediated Gene Therapy to Prevent Acquired Hearing Loss.Journal of the Association for Research in Otolaryngology : JARO · 2022
    Review
  8. Article
  9. Article
  10. Advances in Inner Ear Therapeutics for Hearing Loss in Children.Current otorhinolaryngology reports · 2020
    Article
  11. Review
  12. Review
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

10 authors at 3 institutions in 2 countries.

H JieDepartment of Otolaryngology, Affiliated Sixth People's Hospital of Shanghai Jiao Tong University, Shanghai, China.
S TaoDepartment of Physiology, Medical College, Southeast University, Nanjing, China.
L LiuDepartment of Physiology, Medical College, Southeast University, Nanjing, China.
L XiaDepartment of Otolaryngology, Affiliated Sixth People's Hospital of Shanghai Jiao Tong University, Shanghai, China.
A CharkoSchool of Human Communication Disorder, Dalhousie University, Halifax, Nova Scotia, Canada.
Z YuSchool of Human Communication Disorder, Dalhousie University, Halifax, Nova Scotia, Canada.
M BanceDepartment of Surgery, Division of Otolaryngology, Dalhousie University, Halifax, Nova Scotia, Canada.
S YinDepartment of Otolaryngology, Affiliated Sixth People's Hospital of Shanghai Jiao Tong University, Shanghai, China.
G S RobertsonDepartments of Psychiatry and Pharmacology, Dalhousie University, Halifax, Nova Scotia, Canada.
J Wang1] Department of Otolaryngology, Affiliated Sixth People's Hospital of Shanghai Jiao Tong University, Shanghai, China [2] School of Human Communication Disorder, Dalhousie University, Halifax, Nova Scotia, Canada.ORCID 0000000336336799
Dalhousie University · CAShanghai Jiao Tong University · CNSoutheast University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have previously demonstrated that both age-related and noise-induced hearing loss are reduced in transgenic mice that ubiquitously overexpress X-linked inhibitor of apoptosis protein (XIAP). In view of the therapeutic implications of these findings, we have developed a minimally invasive surgical method to deliver adenoid-associated virus (AAV) across the round window membrane (RWM) of the cochlea, enabling efficient gene transfer to hair cells and sensory neurons in this enclosed structure. This RWM approach was used in the present study to evaluate the effectiveness of AAV-mediated XIAP overexpression in protecting against cisplatin-induced ototoxicity. Two weeks following surgery, AAV-derived XIAP was detected in the majority of inner and outer hair cells, resulting in a threefold elevation of this antiapoptotic protein in the cochlea. The protection of AAV-mediated XIAP overexpression was evaluated in animals treated with cisplatin at a dose of 4 mg kg(-1) per day for 4-7 consecutive days. The XIAP overexpression was found to attenuate cisplatin-induced hearing loss by ~22 dB. This was accompanied by a reduction of the loss of vulnerable hair cells and sensory neurons in the cochlea by 13%.

Indexed as

AnimalsAntineoplastic AgentsCisplatinCochleaDependovirusGenetic TherapyGenetic VectorsGuinea PigsHair Cells, AuditoryHearing LossRound Window, EarSensory Receptor CellsTransfectionX-Linked Inhibitor of Apoptosis ProteinAntineoplastic AgentsCisplatinX-Linked Inhibitor of Apoptosis Protein

Identifiers

PMID25809464
OpenAlexW1994558354

What OpenQuestion holds

Textmetadata
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.