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John L. Darling

Researcher at University of Wolverhampton

Publications -  48
Citations -  1834

John L. Darling is an academic researcher from University of Wolverhampton. The author has contributed to research in topics: Cancer & Cell culture. The author has an hindex of 21, co-authored 46 publications receiving 1598 citations. Previous affiliations of John L. Darling include University of London & University College London.

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Disulfiram modulated ROS-MAPK and NFκB pathways and targeted breast cancer cells with cancer stem cell-like properties.

TL;DR: Disulfiram/copper inhibited BCSCs and enhanced cytotoxicity of PAC in BC cell lines and may be caused by simultaneous induction of ROS and inhibition of NFκB.
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Cytotoxic effect of disulfiram/copper on human glioblastoma cell lines and ALDH-positive cancer-stem-like cells.

TL;DR: The findings indicate that the cytotoxicity of DS/Cu and the enhancing effect ofDS/Cu on the cytOToxicity of dFdC in GBM stem-like cells may be caused by induction of ROS and inhibition of both ALDH and the NFkB pathway.
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Disulfiram targets cancer stem-like cells and reverses resistance and cross-resistance in acquired paclitaxel-resistant triple-negative breast cancer cells

TL;DR: Disulfiram abolished CSC characters and completely reversed PAC and CDDP resistance in MDA-MB-231PAC10 cells, suggesting cancer stem cells may be responsible for acquired pan-chemoresistance.
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Disulfiram/copper complex inhibiting NFκB activity and potentiating cytotoxic effect of gemcitabine on colon and breast cancer cell lines

TL;DR: The data from this study indicated that DS may be used in clinic to improve the therapeutic effect of dFdC in breast and colon cancer patients.
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Liposome encapsulated Disulfiram inhibits NFκB pathway and targets breast cancer stem cells in vitro and in vivo.

TL;DR: A liposome-encapsulated DS (Lipo-DS) was developed and its anticancer effect and mechanisms in vitro and in vivo showed very strong anticancer efficacy and no significant in vivo nonspecific toxicity was observed.