| Literature DB >> 19176394 |
Seung-Woo Hong1, Chang-Jae Kim, Won-Sang Park, Jae-Sik Shin, Soon-Duck Lee, Seong-Gyu Ko, Sam-Il Jung, In-Chul Park, Sung-Kwan An, Won-Keun Lee, Wang-Jae Lee, Dong-Hoon Jin, Myeong-Sok Lee.
Abstract
The p34(SEI-1) protein exerts oncogenic effects via regulation of the cell cycle, which occurs through a direct interaction with cyclin-dependent kinase 4. Such regulation can increase the survival of various types of tumor cells. Here, we show that the antiapoptotic function of p34(SEI-1) increases tumor cell survival by protecting the X-linked inhibitor of apoptosis protein (XIAP) from degradation. Our findings show that p34(SEI-1) inhibits apoptosis. This antiapoptotic effect was eliminated by the suppression of p34(SEI-1) expression. We also determined that direct binding of p34(SEI-1) to the BIR2 domain prevents ubiquitination of XIAP. Interestingly, p34(SEI-1) expression is absent or weak in normal tissues but is strongly expressed in tissues obtained from patients with breast cancer. Furthermore, the expression levels of p34(SEI-1) and XIAP seem to be coordinated in human breast cancer cell lines and tumor tissues. Thus, our findings reveal that p34(SEI-1) uses a novel apoptosis-inhibiting mechanism to stabilize XIAP.Entities:
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Year: 2009 PMID: 19176394 DOI: 10.1158/0008-5472.CAN-08-1189
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701