Title : Ubiquitin proteasomal pathway mediated degradation of p53 in melanoma.

Pub. Date : 2011 Apr 15

PMID : 21167122






4 Functional Relationships(s)
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1 Treatment of 8B20 cells with the UPP inhibitors, MG132 and clasto-lactacystin-beta-lactone, led to an increase in levels of p53 while treatment with non-proteasomal inhibitors did not alter p53 levels. benzyloxycarbonylleucyl-leucyl-leucine aldehyde tumor protein p53 Homo sapiens
2 Treatment of 8B20 cells with MG132 led to an increase in the half-life of p53. benzyloxycarbonylleucyl-leucyl-leucine aldehyde tumor protein p53 Homo sapiens
3 In vivo studies showed that MG132 induced p53 overexpression and reduced tumor growth, suggesting an important role of p53 stabilization in controlling melanoma. benzyloxycarbonylleucyl-leucyl-leucine aldehyde tumor protein p53 Homo sapiens
4 In vivo studies showed that MG132 induced p53 overexpression and reduced tumor growth, suggesting an important role of p53 stabilization in controlling melanoma. benzyloxycarbonylleucyl-leucyl-leucine aldehyde tumor protein p53 Homo sapiens