Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2048496 | FEBS Letters | 2012 | 6 Pages |
Abstract
Hepatitis B X-interacting protein (HBXIP) is able to enhance migration of breast cancer cells. However, the role of HBXIP in regulation of complement-dependent cytotoxicity (CDC) in breast cancer is not understood. Here, we report that HBXIP contributes to protecting breast cancer cells from CDC by upregulating membrane-bound complement regulatory protein (mCRPs), including CD46, CD55 and CD59. We found that HBXIP upregulated mCRPs through activating p-ERK1/2/NF-κB. Interestingly, the knockdown of CD59 was able to block the HBXIP-enhanced breast tumor growth in animal. Thus, we conclude that HBXIP upregulates CD46, CD55 and CD59 through p-ERK1/2/NF-κB signaling to protect breast cancer from CDC.
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Authors
Wenjing Cui, Yu Zhao, Changliang Shan, Guangyao Kong, Nan Hu, Yiwen Zhang, Shuai Zhang, Weiying Zhang, Yingyi Zhang, Xiaodong Zhang, Lihong Ye,