IndraLab

Statements


USP7 activates MDM4. 7 / 8
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"However, the ability of USP7 to prevent proteasomal degradation of HdmX (as well as Hdm2) was abolished following DNA damage."

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"Specifically, HAUSP inhibition drives the proteolysis of both negative regulators of p53, Mdm2 and Mdmx, which subsequently decreases the ubiquitinated-p53forms leading to a total increase in p53 protein levels."

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"Because HAUSP rescues Hdm2-mediated degradation of Hdmx, we wondered whether an increase in HAUSP expression would also prevent the degradation of Hdmx after DNA damage."

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"In cases where p53 is of the wild type (Wt-p53) in tumors, inhibiting USP7 promotes the degradation of MDM2/MDMX, leading to the activation of p53 signaling."

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"It could be hypothesized that not the decrease in HAUSP activity triggers the degradation of Hdmx but rather an increase in Hdm2 activity."

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"USP7 inhibition promotes the degradation of MDM2 and MDMX, activates the p53 signaling, and causes cell cycle arrest and apoptosis, making USP7 a potential target for cancer therapy."

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"These results indicate that HAUSP rescues Hdmx from degradation by Hdm2 and that HAUSP increases the endogenous protein levels of Hdmx.To investigate a putative function for endogenous HAUSP in the re[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"