Reduced expression of uroplakin 1A is associated with the poor prognosis of gastric adenocarcinoma patients

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Abstract

Background: The aim of this study was to investigate the expression and prognostic significance of Uroplakin1A (UPK1A) in gastric adenocarcinoma patients. Functional studies were also analyzed in vitro. Methodology/Principal Findings: Real-time quantitative PCR (RT-qPCR), western blotting, and immunohistochemical (IHC) staining methods were used to analyze the expression of UPK1A in primary gastric adenocarcinoma tissue samples. Compared with matched adjacent non-tumor, the expression of UPK1A in fresh surgical specimens was reduced, which was confirmed by RT-qPCR (P<0.01) and western blotting analysis (P<0.01). The paraffin specimens from a consecutive series of 445 gastric adenocarcinoma patients who underwent surgery between 2003 and 2006 were analyzed by IHC staining. The relationship between UPK1A expression, clinicopathological factors, and survival were evaluated. IHC staining analysis revealed that the reduced expression of UPK1A was observed in 224 cases (50.3%). Additionally, the correlation analysis of clinicopathological factors demonstrated that reduced expression of UPK1A was significantly associated with histological grade (P = 0.022), node metastasis (P<0.001) and tumor node metastasis (TNM) stage (P = 0.008) (7th edition of the International Union Against Cancer (UICC)). Furthermore, Kaplan-Meier survival analysis revealed that the reduced expression of UPK1A was significantly associated with poor prognosis (P = 0.043). Cox hazards model analysis indicated that UPK1A expression was an independent risk factor at the 0.1 level (P = 0.094). The function of UPK1A in cell cycle, migration, and invasion was investigated by overexpressing UPK1A in the MKN45 gastric cancer cell line. The elevated expression of UPK1A cells induced G1 phase arrest and significantly inhibited migration and invasion. Conclusions/Significance: The reduced expression of UPK1A might play a role in the progression of gastric cancer. Thus, UPK1A could be a potential favorable biomarker associated with gastric cancer prognosis. © 2014 Zheng et al.

Figures

  • Figure 1. Decreased UPK1A mRNA expression in gastric cancer tumor tissues was detected by RT-qPCR (n = 51, p,0.01, gastric cancer tumor compared with adjacent non-tumor tissue, Wilcoxon matched-pairs signed-rank test). The small box inside the outside box represents the mean. doi:10.1371/journal.pone.0093073.g001
  • Figure 2. Decreased expression of UPK1A protein in GC tumor tissues was detected by western blotting (n = 29, p,0.01, gastric cancer tumor compared with tissue, Wilcoxon matched-pairs signed-rank test). (A) Expression of UPK1A protein in gastric tumor and adjacent non-tumor tissues. (B) The relative expression of UPK1A in comparison with the expression level of normal paracancerous tissues. (N, normal paracancerous tissues; T, tumor). doi:10.1371/journal.pone.0093073.g002
  • Figure 3. The in situ expression of UPK1A protein in gastric cancer specimens was assessed by immunohistochemistry. (A) and (E), Immuno-staining of a GC tumor and the adjacent non-tumorous area. (B) and (F), Strong UPK1A staining was observed in well-differentiated GC. (C) and (G), Weak UPK1A staining in moderately differentiated gastric cancer. (D) and (H), Negative UPK1A staining in poorly differentiated GC. (A–D with 2006magnification; E–H with 4006magnification). doi:10.1371/journal.pone.0093073.g003
  • Table 1. The Expression of UPK1A and the Clinicopathologic Characteristics of Patients with Gastric Cancer.
  • Figure 4. Kaplan-Meier survival analysis of gastric cancer patients (n = 445). The survival rate of patients in the UPK1A-high group was higher than that of the patients in the UPK1A-low group (log-rank test, P = 0.043). doi:10.1371/journal.pone.0093073.g004
  • Table 2. Univariate and multivariate analyses of overall survival in 445 cases of gastric cancer patients.
  • Figure 5. In the wound healing assay, representative images were photographed 0, 24, 48 and 72 hours after scratching. The result demonstrated that the high expression of UPK1A inhibited the cell motility. doi:10.1371/journal.pone.0093073.g005
  • Figure 6. Matrigel invasion assays of vector-MNK45 and UPK1A-overexpressed MNK45 cells. The invading cells were fixed and stained with crystal violet (magnification, 2006) on the left. The right images present the quantification of 10 randomly selected fields. The results represent the mean 6 SD of three independent experiments. *, P,0.05. doi:10.1371/journal.pone.0093073.g006

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Zheng, Y., Wang, D. D., Wang, W., Pan, K., Huang, C. Y., Li, Y. F., … Zhou, Z. W. (2014). Reduced expression of uroplakin 1A is associated with the poor prognosis of gastric adenocarcinoma patients. PLoS ONE, 9(4). https://doi.org/10.1371/journal.pone.0093073

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