Synergistic effect of plasma-activated medium and novel indirubin derivatives on human skin cancer cells by activation of the AhR pathway (vol 12, 2528, 2022)

被引:1
|
作者
Rebl, Henrike
Sawade, Marie
Hein, Martin
Bergemann, Claudia
Wende, Manuela
Lalk, Michael
Langer, Peter
Emmert, Steffen
Nebe, Barbara
机构
[1] Department of Cell Biology, Rostock University Medical Center, Rostock
[2] Institute for Chemistry, University of Rostock, Rostock
[3] Institute for Biochemistry, University of Greifswald, Greifswald
[4] Clinic and Polyclinic for Dermatology and Venerology, Rostock University Medical Center, Rostock
关键词
D O I
10.1038/s41598-022-08218-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Due to the increasing number of human skin cancers and the limited effectiveness of therapies, research into innovative therapeutic approaches is of enormous clinical interest. In recent years, the use of cold atmospheric pressure plasma has become increasingly important as anti-cancer therapy. The combination of plasma with small molecules offers the potential of an effective, tumour-specific, targeted therapy. The synthesised glycosylated and non glycosylated thia-analogous indirubin derivatives KD87 and KD88, respectively, were first to be investigated for their pharmaceutical efficacy in comparison with Indirubin-3'-monoxime (I3M) on human melanoma (A375) and squamous cell carcinoma (A431) cells. In combinatorial studies with plasma-activated medium (PAM) and KD87 we determined significantly decreased cell viability and cell adhesion. Cell cycle analyses revealed a marked G2/M arrest by PAM and a clear apoptotic effect by the glycosylated indirubin derivative KD87 in both cell lines and thus a synergistic anti-cancer effect. I3M had a pro-apoptotic effect only in A431 cells, so we hypothesize a different mode of action of the indirubin derivatives in the two skin cancer cells, possibly due to a different level of the aryl hydrocarbon receptor and an activation of this pathway by nuclear translocation of this receptor and subsequent activation of gene expression. © 2022, The Author(s).
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    Henrike Rebl
    Marie Sawade
    Martin Hein
    Claudia Bergemann
    Manuela Wende
    Michael Lalk
    Peter Langer
    Steffen Emmert
    Barbara Nebe
    Scientific Reports, 12
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