Abstract
Abstract
Background
Using human keratinocyte HaCaT cell line model, we screened for proteins that changed their content due to SDS exposure in non-toxic dose (25 μg/ml, as determined by the MTT assay and microscopic examination) during 48 h.
Methods
The altered level of proteins from HaCaT keratinocytes exposed to SDS was analyzed by LC-MS/MS approach and quantified using Progenesis LC software.
Results
The Pathview map of 131 upregulated proteins was built, and enhancement of glycolysis/gluconeogenesis was found.
Conclusions
The results of our study admit the possibility of promotion of the cutaneous neoplasia and/or the peculiarity of the response of immortalized keratinocytes to the SDS treatment and provide new insights into possible role of SDS as integrator of diverse signaling that influence cell fate decisions.
Publisher
Springer Science and Business Media LLC
Cited by
8 articles.
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