作者: Rajash Pallai , Aishwarya Bhaskar , Natalie Barnett-Bernodat , Christina Gallo-Ebert , Michelle Pusey
DOI: 10.1007/S13277-015-3326-1
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摘要: Using yeast two-hybrid analysis, we identified several novel protein interactions for the oncoprotein Cancerous Inhibitor of PP2A (CIP2A) and confirmed a subset these in human cancer cell lines. Analysis interaction prostate carcinoma cells between CIP2A leucine-rich repeat-containing 59 (LRRC59) suggests that is translocated into nucleus at G2/M through its association with LRRC59. Recent work by others has demonstrated nuclear disrupts mitotic checkpoints, which promotes deregulation cycle increases cancerous phenotypes. Thus, provide therapeutic mechanism inhibiting function via targeting CIP2A-LRRC59 interaction.