XMU-MP-1 induces growth arrest in a model human mini-organ and antagonises cell cycle-dependent paclitaxel cytotoxicity

Cell Division

Ellen Mitchell¹  Talveen S. Purba¹  Charlotte E. L. Mellor¹ 

[1] Centre for Dermatology Research, University of Manchester & NIHR Biomedical Research Centre, Manchester, M13 9PT, UK;

关键词: XMU-MP-1;    Hippo;    YAP1;    Cell cycle;    Proliferation;    Hair follicle;    MST1/2;    Aurora B;    Chemotherapy;    Alopecia;   

DOI  :  10.1186/s13008-020-00067-0

来源: Springer

【 摘 要 】

BackgroundXMU-MP-1 is an inhibitor of the Hippo pathway kinases MST1/2 and has been shown to promote the downstream activation of the pro-proliferative, pro-regenerative and anti-apoptotic transcriptional regulator YAP1. We tested whether XMU-MP-1 can activate YAP1 in a model human mini-organ, namely the hair follicle, to determine whether it can be pharmacologically exploited to promote regeneration in the hair follicle as a novel strategy to treat pathological hair loss disorders.ResultsXMU-MP-1 treatment inhibited MOB1 phosphorylation but did not increase active YAP1 in the hair follicle. Rather than promote proliferation, XMU-MP-1 serendipitously decreased the number of Ki-67+, EdU+ and phospho histone H3+ hair matrix keratinocytes and antagonised the cytotoxic effects of paclitaxel.ConclusionsXMU-MP-1 perturbs epithelial cell cycle progression in a model human mini-organ. This may arise as an off-target effect, especially when XMU-MP-1 has been described to strongly inhibit 21 additional kinases beyond MST1/2. Therefore, whilst these effects may be dependent on tissue context, researchers should exercise caution when interpreting the effects of XMU-MP-1, especially in tissues with actively proliferating cell populations.

【 授权许可】

CC BY