Research Papers:

Protease nexin 1 induces apoptosis of prostate tumor cells through inhibition of X-chromosome-linked inhibitor of apoptosis protein

Chad M. McKee _, Yunchuan Ding, Jianfeng Zhou, Chunrui Li, Liang Huang, Xiangke Xin, Jing He, Joshua E. Allen, Wafik S. El-Deiry, Yunhong Cao, Ruth J. Muschel and Danmei Xu

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Oncotarget. 2015; 6:3784-3796. https://doi.org/10.18632/oncotarget.2921

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Chad M. McKee2,*, Yunchuan Ding1,*, Jianfeng Zhou1, Chunrui Li1, Liang Huang1, Xiangke Xin1, Jing He1, Joshua E. Allen3, Wafik S. El-Deiry3, Yunhong Cao2, Ruth J. Muschel2, Danmei Xu1

1Department of Internal Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Hubei, China

2Gray Institute of Radiation Oncology and Biology, Medical Science Division, University of Oxford, Oxford, United Kingdom

3Penn State Hershey Cancer Institute, Penn State University, Hershey, PA, USA

*These authors have contributed equally to this work

Correspondence to:

Ruth J. Muschel, e-mail: [email protected]

Danmei Xu, e-mail: [email protected]

Keywords: PN1, XIAP, prostate cancer, NF-κB, AKT

Received: November 18, 2014     Accepted: December 11, 2014     Published: February 17, 2015


Protease nexin 1 (PN1) is an endogenous serine protease inhibitor (SERPIN), expressed at high levels in the prostate, and capable of inhibiting the proliferation of prostate cancer cells. We previously showed that PN1-uPA complexes inhibited Sonic Hedgehog (SHH) signalling through engagement of the LRP receptor. Here, we describe an alternative anti-proliferative mechanism through which PN1 expression leads to apoptosis. In prostate cancer cells, increased expression of PN1 led to substantial reduction of XIAP levels and apoptosis mediated through the uPAR, but not the LRP receptor. The alterations in XIAP were effected in two ways 1) via alteration in the NF-κB pathway, a pathway known to signal XIAP transcription and 2) by promoting XIAP instability. The AKT pathway is known to phosphorylate XIAP at serine 87 leading to protein stability and PN1 expression is shown to interfere with this process. As a result of both mechanisms, programmed cell death is substantially increased. Consistent with these observations, reduced PN1 protein correlated with elevated p65/XIAP expression and with higher Gleason scores in human prostate tissue arrays. Thus, PN1 expression appears to differentially down-regulate distinct oncogenic pathways depending upon the cell surface receptor engaged by its complexes and demonstrates a novel molecular mechanism by which the protein can promote tumor cell apoptosis.

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