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PPM1D is a prognostic marker and therapeutic target in colorectal cancer
Author(s) -
Tianshu Peng,
Yongheng He,
Tian Nie,
XIANG-DANG HU,
HAI-YAN LU,
Jian Yi,
YUN-FEI SHUAI,
Min Luo
Publication year - 2014
Publication title -
experimental and therapeutic medicine
Language(s) - English
Resource type - Journals
eISSN - 1792-1015
pISSN - 1792-0981
DOI - 10.3892/etm.2014.1762
Subject(s) - oncogene , colorectal cancer , hazard ratio , molecular medicine , gene silencing , survival analysis , immunohistochemistry , oncology , carcinogenesis , cancer , biology , medicine , predictive marker , cancer research , cell cycle , confidence interval , gene , genetics
Protein phosphatase, Mg 2+ /Mn 2+ dependent, 1D (PPM1D) has been associated with carcinogenesis. The present study investigated PPM1D expression as a potential biomarker in colorectal cancer (CRC). PPM1D expression was assessed using immunohistochemistry in 368 patients with CRC. The correlation between PPM1D expression, clinicopathological features and prognosis was analyzed. PPM1D small interfering (si)RNA-induced PPM1D silencing was performed in CRC cell lines to assess the effect of PPM1D on tumor cell proliferation and invasion in vitro . A total of 68.48% (252/368) of the CRC samples displayed high PPM1D expression. By contrast, only 9.24% (34/368) of the matched non-cancerous tissue samples exhibited high PPM1D expression. High PPM1D expression was correlated with node metastasis (P=0.0024), distant metastasis (P<0.001) and TNM stage (P=0.0016). Kaplan-Meier survival analysis revealed that patients with low PPM1D expression had significantly longer survival than those with high PPM1D expression (P=0.012). Moreover, multivariate analyses demonstrated that high PPM1D expression was an independent prognostic factor for overall survival (hazard ratio = 0.24; 95% confidence interval, 0.13-0.86; P=0.004). Furthermore, PPM1D gene silencing was found to significantly reduce the proliferation and invasion of CRC cells in vitro . These findings suggest a role for PPM1D as a prognostic marker and potential therapeutic target in CRC.

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