Evidence map›Paper›PMID 26024952›Full record

ArticleHearing research2015

Variation analysis of transcriptome changes reveals cochlear genes and their associated functions in cochlear susceptibility to acoustic overstimulation.

Shuzhi Yang, Qunfeng Cai, Jonathan Bard, Jennifer Jamison, Jianmin Wang, Weiping Yang, Bo Hua Hu

Abstract read
In one paragraph

Article in Hearing research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Clinical and Genome-wide Analysis of Cisplatin-induced Tinnitus Implicates Novel Ototoxic Mechanisms.Clinical cancer research : an official journal of the American Association for Cancer Research · 2019
    Article
  9. The protective effect of metformin against the noise-induced hearing loss.European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2018
    Article
  10. Article
  11. 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

7 authors.

Shuzhi YangCenter for Hearing and Deafness, University at Buffalo, NY, 14214, USA. Electronic address: qits-002@163.com.
Qunfeng CaiCenter for Hearing and Deafness, University at Buffalo, NY, 14214, USA. Electronic address: qunfengcai@gmail.com.
Jonathan BardNext-Generation Sequencing and Expression Analysis Core, New York State Center of Excellence in Bioinformatics and Life Sciences, University at Buffalo, Buffalo, NY, 14263, USA. Electronic address: jbard@buffalo.edu.
Jennifer JamisonNext-Generation Sequencing and Expression Analysis Core, New York State Center of Excellence in Bioinformatics and Life Sciences, University at Buffalo, Buffalo, NY, 14263, USA. Electronic address: jjamison@buffalo.edu.
Jianmin WangDepartment of Biostatistics and Bioinformatics, Roswell Park Cancer Institute, Elm & Carlton Streets, Buffalo, NY, 14263, USA. Electronic address: Jianmin.Wang@RoswellPark.org.
Weiping YangCenter for Hearing and Deafness, University at Buffalo, NY, 14214, USA. Electronic address: yangwp301@126.com.
Bo Hua HuCenter for Hearing and Deafness, University at Buffalo, NY, 14214, USA. Electronic address: bhu@buffalo.edu.

Funding

Noise-induced acute hair cell DeathR01DC010154 · NIDCD · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI HU, BO HUA · 2010 to 2014
$2.0M
NIDCD NIH HHS 1R01DC010154NIDCD NIH HHS R01 DC010154
6 · The paper itself

Abstract

Individual variation in the susceptibility of the auditory system to acoustic overstimulation has been well-documented at both the functional and structural levels. However, the molecular mechanism responsible for this variation is unclear. The current investigation was designed to examine the variation patterns of cochlear gene expression using RNA-seq data and to identify the genes with expression variation that increased following acoustic trauma. This study revealed that the constitutive expressions of cochlear genes displayed diverse levels of gene-specific variation. These variation patterns were altered by acoustic trauma; approximately one-third of the examined genes displayed marked increases in their expression variation. Bioinformatics analyses revealed that the genes that exhibited increased variation were functionally related to cell death, biomolecule metabolism, and membrane function. In contrast, the stable genes were primarily related to basic cellular processes, including protein and macromolecular syntheses and transport. There was no functional overlap between the stable and variable genes. Importantly, we demonstrated that glutamate metabolism is related to the variation in the functional response of the cochlea to acoustic overstimulation. Taken together, the results indicate that our analyses of the individual variations in transcriptome changes of cochlear genes provide important information for the identification of genes that potentially contribute to the generation of individual variation in cochlear responses to acoustic overstimulation.

Indexed as

Acoustic StimulationGene Expression ProfilingTranscriptomeAnimalsCochleaComputational BiologyEarEvoked Potentials, Auditory, Brain StemFemaleGenetic VariationGlutamic AcidHair Cells, AuditoryHearing Loss, Noise-InducedMacromolecular SubstancesMaleMiceGlutamic AcidMacromolecular SubstancesRNACochleaGeneGlutamateNoiseRNA-sequenceSusceptibility

Identifiers

PMID26024952
PMCPMC4662632

What OpenQuestion holds

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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.