Transcriptional landscape of TRPV1, TRPA1, TRPV4, and TRPM8 channels throughout human tissues.
Bioinformatics
Biomarkers
Dorsal root ganglia
Drug development
RNA-sequencing
TRP channels
Journal
Life sciences
ISSN: 1879-0631
Titre abrégé: Life Sci
Pays: Netherlands
ID NLM: 0375521
Informations de publication
Date de publication:
01 Nov 2022
01 Nov 2022
Historique:
received:
06
07
2022
revised:
02
09
2022
accepted:
14
09
2022
pubmed:
21
9
2022
medline:
7
10
2022
entrez:
20
9
2022
Statut:
ppublish
Résumé
This article aims to analyze the baseline distribution of TRPA1, TRPV1, TRPV4, and TRPM8 channels in human systems at the transcriptional level. Using the RNA-seq dataset from the National Center for Biotechnology Information (NCBI) gene database, we investigated and compared the transcriptional levels of TRPV1, TRPA1, TRPV4 and TRPM8 found in 95 human subjects representing 33 different tissues to determine the tissue specificity of all protein-coding genes. In this study, we observed higher transcriptional levels for TRPV1 (duodenum), TRPA1 (Urinary bladder), TRPV4 (Kidney) and TRPM8 (Prostate) compared to the other TRPs. These channels are involved in developing inflammatory and painful pathologies and seem to participate in cancer development. This information on transcriptional levels of TRPV1, TRPA1, TRPV4 and TRPM8 in human systems may provide essential suggestions for further studies on these proteins.
Identifiants
pubmed: 36126722
pii: S0024-3205(22)00677-4
doi: 10.1016/j.lfs.2022.120977
pii:
doi:
Substances chimiques
Membrane Proteins
0
TRPA1 Cation Channel
0
TRPA1 protein, human
0
TRPM Cation Channels
0
TRPM8 channel-associated factor 1 protein, human
0
TRPM8 protein, human
0
TRPV Cation Channels
0
TRPV1 protein, human
0
TRPV4 protein, human
0
Transient Receptor Potential Channels
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
120977Informations de copyright
Copyright © 2022 Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Conflicts of interest The authors declare no potential conflicts of interest.