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Activation of the IRE1α-XBP1 branch of the unfolded protein response (UPR) has been implicated in multiple types of human cancers, including multiple myeloma (MM). Through an in silico drug discovery approach based on protein-compound virtual docking, we identified the anthracycline antibiotic doxorubicin as an in vitro and in vivo inhibitor of XBP1 activation, a previously unknown activity for this widely utilized cancer chemotherapeutic drug. Through a series of mechanistic and phenotypic studies, we showed that this novel activity of doxorubicin was not due to inhibition of topoisomerase II (Topo II). Consistent with its inhibitory activity on the IRE1α-XBP1 branch of the UPR, doxorubicin displayed more potent cytotoxicity against MM cell lines than other cancer cell lines that have lower basal IRE1α-XBP1 activity. In addition, doxorubicin significantly inhibited XBP1 activation in CD138(+) tumor cells isolated from MM patients. Our findings suggest that the UPR-modulating activity of doxorubicin may be utilized clinically to target IRE1α-XBP1-dependent tumors such as MM.

Original publication

DOI

10.1038/srep33353

Type

Journal article

Journal

Sci Rep

Publication Date

16/09/2016

Volume

6

Keywords

Cell Death, Cell Line, Tumor, Doxorubicin, Endoribonucleases, Etoposide, Humans, Protein-Serine-Threonine Kinases, RNA Splicing, Signal Transduction, Topoisomerase Inhibitors, Unfolded Protein Response, X-Box Binding Protein 1