Oncotarget

Research Papers:

PRSS3 is a prognostic marker in invasive ductal carcinoma of the breast

Li Qian, Xiangxiang Gao, Hua Huang, Shumin Lu, Yin Cai, Yu Hua, Yifei Liu and Jianguo Zhang _

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Oncotarget. 2017; 8:21444-21453. https://doi.org/10.18632/oncotarget.15590

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Abstract

Li Qian1,*, Xiangxiang Gao2,*, Hua Huang1, Shumin Lu3, Yin Cai3, Yu Hua3, Yifei Liu1, Jianguo Zhang1

1Department of Clinical Pathology, Affiliated Hospital of Nantong University, Nantong, Jiangsu, China

2Department of Oncology, Affiliated Tumor Hospital of Nantong University, Nantong Tumor Hospital, Nantong, Jiangsu, China

3Research Center of Clinical Medicine, Affiliated Hospital of Nantong University, Nantong, Jiangsu, China

*These authors contributed equally to this work

Correspondence to:

Jianguo Zhang, email: [email protected]

Yifei Liu, email: [email protected]

Keywords: invasive ductal carcinoma, immunohistochemistry, PRSS3, prognosis

Received: November 08, 2016     Accepted: January 27, 2017     Published: February 21, 2017

ABSTRACT

Objective: Serine protease 3 (PRSS3) is an isoform of trypsinogen, and plays an important role in the development of many malignancies. The objective of this study was to determine PRSS3 mRNA and protein expression levels in invasive ductal carcinoma of the breast and normal surrounding tissue samples.

Results: Both PRSS3 mRNA and protein levels were significantly higher in invasive ductal carcinoma of the breast tissues than in normal or benign tissues (all P < 0.05). High PRSS3 protein levels were associated with patients’ age, histological grade, Her-2 expression level, ki-67 expression, and the 5.0-year survival rate. These high protein levels are independent prognostic markers in invasive ductal carcinoma of the breast.

Materials and Methods: We used real-time quantitative polymerase chain reactions (N = 40) and tissue microarray immunohistochemistry analysis (N = 286) to determine PRSS3 mRNA and protein expression, respectively. PRSS3 protein levels in invasive ductal carcinoma of the breast tissues were correlated with the clinical characteristics of patients with invasive ductal carcinoma of the breast and their 5.0-year survival rate.

Conclusions: PRSS3 acts as an oncogene in invasive ductal carcinoma of the breast development and progression. This finding implies that detection of PRSS3 expression can be a useful prognosis marker and the targeting of PRSS3 can potentially represent a new strategy for invasive ductal carcinoma of the breast treatment.


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