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World J Surg Oncol. 2014 May 21;12:154. doi: 10.1186/1477-7819-12-154.

Expression of natriuretic peptide receptor-A in esophageal squamous cell carcinomas and the relationship with tumor invasion and migration.

Author information

1
Department of second Thoracic surgery, First Affiliated Hospital, Xi'an Jiaotong University, Yanta West Road no, 277, Xi'an, Shaanxi 710061, China. wangjsh@mail.xjtu.edu.cn.

Abstract

BACKGROUND:

The natriuretic peptide receptor-A (NPRA) has been investigated as a receptor of natriuretic peptides in the cardiovascular system. In this study, however, we analyze the expression status of NPRA and the relationship with tumor invasion in esophageal squamous cell carcinoma (ESCC) for the first time.

METHODS:

Western blots were used to examine the expression status of protein in human ESCC cell lines. Then, we used immunohistochemistry to detect the expression of NPRA in 45 ESCC specimens and 40 corresponding nontumor tissues. The clinical data were analyzed through statistical methods. Sh-RNA-NPRA was transfected into Eca109 cells to detect the relationship between NPRA and cell invasion through transwell assays.

RESULTS:

In esophageal squamous cells, the expression of NPRA was strongly detected in the cytoplasm, while undetectable or very weak in the nucleus. The positive rates of NPRA in cancer tissues are significantly higher than that in nontumor tissues (P<0.05). Clinicopathological analyses revealed that increased NPRA expression correlated with differentiation and TNM stage (P<0.05), while it showed no statistically significant association with age, gender, and lymph node metastasis. In analysis of prognosis, we found that highly.Transwell assays showed that NPRA promoted Eca109 cell migration and invasion in vitro and may be involved in MMP2 and MMP9 activation.

CONCLUSIONS:

NPRA protein is highly expressed in ESCC tissues and could promote Eca109 cell migration and invasion in vitro.

PMID:
24885858
PMCID:
PMC4038370
DOI:
10.1186/1477-7819-12-154
[Indexed for MEDLINE]
Free PMC Article

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