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Low temperature upregulating HSP70 expression to mitigate the paclitaxel-induced damages in NHEK cell

Scalp cooling is the most approved treatment for preventing chemotherapy-induced alopecia (CIA). However, the protective mechanism of scalp cooling has rarely been reported. The goal of the present study was to study the relationship between paclitaxel concentration and temperature and the inhibitor...

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Autores principales: Chen, Liang, Xu, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9854382/
https://www.ncbi.nlm.nih.gov/pubmed/36684674
http://dx.doi.org/10.7717/peerj.14630
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author Chen, Liang
Xu, Yi
author_facet Chen, Liang
Xu, Yi
author_sort Chen, Liang
collection PubMed
description Scalp cooling is the most approved treatment for preventing chemotherapy-induced alopecia (CIA). However, the protective mechanism of scalp cooling has rarely been reported. The goal of the present study was to study the relationship between paclitaxel concentration and temperature and the inhibitory effect of low temperature on paclitaxel-induced alopecia. The results showed that the dose of paclitaxel should not exceed 60–70 mg/mL during scalp cooling treatment, and the optimal cooling temperature under different paclitaxel concentrations was determined. Normal human epidermal keratinocytes (NHEK) cells were analyzed by global transcriptome analysis, functional annotation and pathway analysis of differentially expressed genes (DEGs) and ELISA kit to analyze the mechanism of low temperature therapy. The expression of HSPA8, HSPA1A and HSPA1B, which belongs to HSP70, was up-regulated by low temperature. These genes are important target genes of low temperature treatment, which were confirmed by ELISA. The up-regulation of PLK2 and the down-regulation of TXNIP expression are the upstream of mitochondrial dysfunction and ROS, inhibiting the accumulation of ROS and up-regulating the mitochondrial membrane potential. Our research partially elucidates the therapeutic mechanism of scalp cooling, which provides a new idea on the drug research and development in CIA.
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spelling pubmed-98543822023-01-21 Low temperature upregulating HSP70 expression to mitigate the paclitaxel-induced damages in NHEK cell Chen, Liang Xu, Yi PeerJ Biochemistry Scalp cooling is the most approved treatment for preventing chemotherapy-induced alopecia (CIA). However, the protective mechanism of scalp cooling has rarely been reported. The goal of the present study was to study the relationship between paclitaxel concentration and temperature and the inhibitory effect of low temperature on paclitaxel-induced alopecia. The results showed that the dose of paclitaxel should not exceed 60–70 mg/mL during scalp cooling treatment, and the optimal cooling temperature under different paclitaxel concentrations was determined. Normal human epidermal keratinocytes (NHEK) cells were analyzed by global transcriptome analysis, functional annotation and pathway analysis of differentially expressed genes (DEGs) and ELISA kit to analyze the mechanism of low temperature therapy. The expression of HSPA8, HSPA1A and HSPA1B, which belongs to HSP70, was up-regulated by low temperature. These genes are important target genes of low temperature treatment, which were confirmed by ELISA. The up-regulation of PLK2 and the down-regulation of TXNIP expression are the upstream of mitochondrial dysfunction and ROS, inhibiting the accumulation of ROS and up-regulating the mitochondrial membrane potential. Our research partially elucidates the therapeutic mechanism of scalp cooling, which provides a new idea on the drug research and development in CIA. PeerJ Inc. 2023-01-17 /pmc/articles/PMC9854382/ /pubmed/36684674 http://dx.doi.org/10.7717/peerj.14630 Text en ©2023 Chen and Xu https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Biochemistry
Chen, Liang
Xu, Yi
Low temperature upregulating HSP70 expression to mitigate the paclitaxel-induced damages in NHEK cell
title Low temperature upregulating HSP70 expression to mitigate the paclitaxel-induced damages in NHEK cell
title_full Low temperature upregulating HSP70 expression to mitigate the paclitaxel-induced damages in NHEK cell
title_fullStr Low temperature upregulating HSP70 expression to mitigate the paclitaxel-induced damages in NHEK cell
title_full_unstemmed Low temperature upregulating HSP70 expression to mitigate the paclitaxel-induced damages in NHEK cell
title_short Low temperature upregulating HSP70 expression to mitigate the paclitaxel-induced damages in NHEK cell
title_sort low temperature upregulating hsp70 expression to mitigate the paclitaxel-induced damages in nhek cell
topic Biochemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9854382/
https://www.ncbi.nlm.nih.gov/pubmed/36684674
http://dx.doi.org/10.7717/peerj.14630
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