Pinin facilitated proliferation and metastasis of colorectal cancer through activating EGFR/ERK signaling pathway
PDF | HTML | Supplementary Files | How to cite
Metrics: PDF 1603 views | HTML 1961 views | ?
Zhigang Wei1,*, Wenhui Ma1,*, Xiaolong Qi1,*, Xianjun Zhu1, Yutian Wang2, Zhuoluo Xu1, Jun Luo1, Da Wang1, Weihong Guo1, Xiaomei Li2, Sainan Xin2, Jiang Yu1,2, Guoxin Li1
1Department of General Surgery, Nanfang Hospital, Southern Medical University, Guangzhou, China
2Department of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, China
*These authors have contributed equally to this work
Guoxin Li, email: [email protected]
Jiang Yu, email: [email protected]
Keywords: colorectal cancer, PNN, EGFR/ERK, metastasis
Received: January 16, 2016 Accepted: March 28, 2016 Published: April 15, 2016
Increasing emphasis has been put on the influence of desmosome related proteins on progress of colorectal cancer (CRC). Pinin (PNN) is a desmosome-associated molecule that has been reported its overexpression could increase desmoglein 2 (DSG2) and E-cadherin (E-ca) levels. However, it was documented that DSG2 and E-ca had opposite functions in CRC. Thus, we attempted to elucidate function and mechanism of PNN in CRC. Herein, we revealed that overexpression of PNN was significantly correlated with the aggressive characteristics and indicated poor overall survival of CRC patients. In addition, the proliferation, invasion in vitro, and tumorigenic growth, metastasis in vivo were also promoted by the up-regulation of PNN. It was also verified that up-regulation of PNN increased the expression of DSG2 and activated the EGFR/ERK signaling pathway. Our findings suggested that PNN, as a valuable marker of prognosis, has important influence on the progression of CRC.
All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 3.0 License.