2014
DOI: 10.1016/j.bbagen.2014.02.006
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Curcusone D, a novel ubiquitin–proteasome pathway inhibitor via ROS-induced DUB inhibition, is synergistic with bortezomib against multiple myeloma cell growth

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Cited by 24 publications
(12 citation statements)
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References 46 publications
(62 reference statements)
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“…Our data also suggest that EAAT3 may regulate the extinction of morphine-induced CPP. This finding is in agreement with our previous results that EAAT3 may regulate learning and memory (Lee et al, 2012; Cao et al, 2014; Wang et al, 2014) and add additional evidence for its role in learning and memory. In addition, our results suggest that EAAT3 can be a target for developing interventions to speed up the recovery from morphine addiction.…”
Section: Discussionsupporting
confidence: 93%
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“…Our data also suggest that EAAT3 may regulate the extinction of morphine-induced CPP. This finding is in agreement with our previous results that EAAT3 may regulate learning and memory (Lee et al, 2012; Cao et al, 2014; Wang et al, 2014) and add additional evidence for its role in learning and memory. In addition, our results suggest that EAAT3 can be a target for developing interventions to speed up the recovery from morphine addiction.…”
Section: Discussionsupporting
confidence: 93%
“…Although EAATs that can regulate glutamatergic neurotransmission have been shown to participate in the development of addiction to drugs, such as cocaine (Fujio et al, 2005, Fischer et al, 2013), it is not clear whether EAATs play a role in morphine addiction. Our recent studies have shown that EAAT3, the major neuronal EAAT, may be an important component in the biochemical processes for learning and memory (Lee et al, 2012, Cao et al, 2014, Wang et al, 2014). Thus, EAAT3 may regulate morphine addiction.…”
Section: Discussionmentioning
confidence: 99%
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“…6.30) [100]. It was suggested that curcusone D (54) induces reactive oxygen species (ROS), which may correlate with its inhibition of DUBs and the UPS to induce cellular growth inhibition and apoptosis [100]. Investigation of the mechanism of UPS inhibition revealed that curcusone D (54) did not inhibit the proteasome's chymotrypsin-like, trypsin-like, or caspaselike activities, but it reduced the activity of cellular DUBs.…”
Section: Deubiquitinase Inhibitorsmentioning
confidence: 99%
“…However, if this clearance event is disrupted, immature immunoglobulin would promptly accumulate, which causes cell death eventually [3]. There are two intracellular mechanisms to degrade such harmful proteins after their ubiquitination, namely, ubiquitin-proteasome system (UPS) and autophagy-lysosome system [4][5][6].…”
Section: Introductionmentioning
confidence: 99%