DUSP1 and cancer: Similarly, ERK activation by (E)-2-benzylidene-3-(cyclohexylamino)-2,3-dihydro-1H-inden-1-one (BCI), a dual MKP1/6 phosphatase inhibitor that targets exclusively ERK1/2 [20,21], also induced concentration-dependent toxicity in different cancer cell lines including MDA-MB-231 (Figure 7E).