Abstract

Objective Since early diagnosis is very important for treating gastric cancer (GC), we aimed to detect serum small proline-rich protein2A (SPRR2A) to verify its diagnostic value for GC patients. Methods Serum samples were collected from 200 patients with GC, 100 patients with gastritis, 40 patients with rectal cancer (RC), 50 patients with colon cancer (CC), and 100 healthy controls. An enzyme-linked immunosorbent assay (ELISA) detection kit was applied to measure serum SPRR2A concentration. The correlations between serum SPRR2A and carcinoembryonic antigen (CEA), clinical pathological parameters of GC, and receiver operating characteristic (ROC) curve were also analyzed. Results The median serum SPRR2A concentration in GC patients was significantly higher than those in healthy controls and gastritis or colorectal cancer patients (P < 0.001). Serum SPRR2A concentration at a cut-off value of 80.7 pg/ml yielded an AUC of 0.851, with 75.7% sensitivity and 74.5% specificity for discriminating GC patients from healthy people. The AUC for the serum SPRR2A concentration combined with the CEA concentration was 0.876, with 79.7% sensitivity and 78.7% specificity. Similarly, serum SPRR2A discriminated GC patients from gastritis patients with an AUC of 0.820, with 90.5% sensitivity and 61.7% specificity. The AUC for the serum SPRR2A concentration combined with the CEA concentration was 0.848, with 87.8% sensitivity and 68.1% specificity. The serum SPRR2A levels in GC patients were associated with lymph node metastasis and the tumor-node-metastasis (TNM) stage (P < 0.05). There was an obvious difference in serum SPRR2A expression between GC patients before and after surgery (P < 0.0001). Conclusion These results suggest that serum SPRR2A can be used as an effective marker for GC.

Highlights

  • Gastric cancer (GC), an epithelial malignancy, is the third leading cause of cancer-related deaths globally, accounting for 7% of cancer cases and 9% of cancer-related deaths [1]

  • We found that the expression of small proline-rich protein2A (SPRR2A) was significantly increased in GC patients compared with healthy controls, while there was no significant difference between chronic gastritis and colorectal cancer patients and healthy

  • It is worth noting that our results showed that SPRR2A had low specificity between distinguishing gastritis and gastric cancer

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Summary

Introduction

Gastric cancer (GC), an epithelial malignancy, is the third leading cause of cancer-related deaths globally, accounting for 7% of cancer cases and 9% of cancer-related deaths [1]. It is important to identify oncogenes for the early diagnosis and treatment of cancer. Upper gastrointestinal endoscopy is a sensitive and specific diagnostic test for gastric cancer. Since peripheral blood can be noninvasively obtained and stored, detection of multiple serum biomarkers has become an alternative method for helping to make early diagnosis of GC. A common biomarker used for the diagnosis of GC is CEA. The sensitivity and specificity of CEA in GC detection are 30% and 70%, respectively. It cannot be used as a Disease Markers

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