Abstract:Cytokeratin 18 (CK18) fragments are released into circulation during epithelial cell death. M30 (reflect caspase cleaved CK18 fragment) and M65 (reflect total CK18 fragment) enzyme-linked immunosorbent assay (ELISA) detects circulating CK18 fragments released during caspase-dependent or total cell death, respectively; thus, CK18 has the potential of being a biomarker for epithelial cancers. In the present study, we investigated the serum levels of M30 and M65 in patients with gastric cancer, determined correla… Show more
“…Even with surgical management, the prognosis of gastric cancer is still unsatisfactory, with an estimated 5-year survival rate of 20–25% in China (Hartgrink et al, 2009). Considerable efforts have been made to determine the risk factors for gastric cancer and to identify biomarkers in order to enhance screening and early detection and to better predict the clinical outcomes (Saragoni et al, 2013, Tiberio et al, 2015, Oyama et al, 2013, Hiraki et al, 2011, Lv et al, 2015). In addition to intensified screening for early detection, it is of timely and clinical importance to find novel approaches to improve the prognosis and prolong the survival of patients with gastric cancer.…”
Metabolic syndrome (MetS) has been shown to be associated with an increased risk of gastric cancer. However, the impact of MetS on gastric cancer mortality remains largely unknown. Here, we prospectively examined the prediction of preoperative MetS for gastric cancer mortality by analyzing a subset of data from the ongoing Fujian prospective investigation of cancer (FIESTA) study. This study was conducted among 3012 patients with gastric cancer who received radical gastrectomy between 2000 and 2010. The latest follow-up was completed in 2015. Blood/tissue specimens, demographic and clinicopathologic characteristics were collected at baseline. During 15-year follow-up, 1331 of 3012 patients died of gastric cancer. The median survival time (MST) of patients with MetS was 31.3 months, which was significantly shorter than that of MetS-free patients (157.1 months). The coexistence of MetS before surgery was associated with a 2.3-fold increased risk for gastric cancer mortality (P < 0.001). The multivariate-adjusted hazard ratios (HRs) were increased with invasion depth T1/T2 (HR = 2.78, P < 0.001), regional lymph node metastasis N0 (HR = 2.65, P < 0.001), positive distant metastasis (HR = 2.53, P < 0.001), TNM stage I/II (HR = 3.00, P < 0.001), intestinal type (HR = 2.96, P < 0.001), negative tumor embolus (HR = 2.34, P < 0.001), and tumor size ≤ 4.5 cm (HR = 2.49, P < 0.001). Further survival tree analysis confirmed the top splitting role of TNM stage, followed by MetS or hyperglycemia with remarkable discrimination ability. In this large cohort study, preoperative MetS, especially hyperglycemia, was predictive of significant gastric cancer mortality in patients with radical gastrectomy, especially for early stage of gastric cancer.
“…Even with surgical management, the prognosis of gastric cancer is still unsatisfactory, with an estimated 5-year survival rate of 20–25% in China (Hartgrink et al, 2009). Considerable efforts have been made to determine the risk factors for gastric cancer and to identify biomarkers in order to enhance screening and early detection and to better predict the clinical outcomes (Saragoni et al, 2013, Tiberio et al, 2015, Oyama et al, 2013, Hiraki et al, 2011, Lv et al, 2015). In addition to intensified screening for early detection, it is of timely and clinical importance to find novel approaches to improve the prognosis and prolong the survival of patients with gastric cancer.…”
Metabolic syndrome (MetS) has been shown to be associated with an increased risk of gastric cancer. However, the impact of MetS on gastric cancer mortality remains largely unknown. Here, we prospectively examined the prediction of preoperative MetS for gastric cancer mortality by analyzing a subset of data from the ongoing Fujian prospective investigation of cancer (FIESTA) study. This study was conducted among 3012 patients with gastric cancer who received radical gastrectomy between 2000 and 2010. The latest follow-up was completed in 2015. Blood/tissue specimens, demographic and clinicopathologic characteristics were collected at baseline. During 15-year follow-up, 1331 of 3012 patients died of gastric cancer. The median survival time (MST) of patients with MetS was 31.3 months, which was significantly shorter than that of MetS-free patients (157.1 months). The coexistence of MetS before surgery was associated with a 2.3-fold increased risk for gastric cancer mortality (P < 0.001). The multivariate-adjusted hazard ratios (HRs) were increased with invasion depth T1/T2 (HR = 2.78, P < 0.001), regional lymph node metastasis N0 (HR = 2.65, P < 0.001), positive distant metastasis (HR = 2.53, P < 0.001), TNM stage I/II (HR = 3.00, P < 0.001), intestinal type (HR = 2.96, P < 0.001), negative tumor embolus (HR = 2.34, P < 0.001), and tumor size ≤ 4.5 cm (HR = 2.49, P < 0.001). Further survival tree analysis confirmed the top splitting role of TNM stage, followed by MetS or hyperglycemia with remarkable discrimination ability. In this large cohort study, preoperative MetS, especially hyperglycemia, was predictive of significant gastric cancer mortality in patients with radical gastrectomy, especially for early stage of gastric cancer.
“…Therefore, these antibodies have a diagnostic potential, reflecting apoptosis and/or necrosis in various situations. Increased levels of caspase‐cleaved CK18 are detected in the serum of cancer patients , septic patients and patients with liver disease . In the present study, apoptosis and necrosis are investigated in patients with acute pancreatitis.…”
Plasma concentrations of M65 and the M30/M65 ratio can be useful in predicting the severity of acute pancreatitis as early as 24 h after the onset of symptoms. The rates of IL-17 early in the course of acute pancreatitis are indicative of the disease.
“…Therefore, much effort has been made to develop preliminary screening tests in easily accessible specimens. Serum cytokeratin 18, hypermethylation of Sox17 gene, S100A9/AAT in gastric fluid, proteomics approach, and serum metabolomics were reported as useful diagnostic biomarkers for gastric cancer . More recently, some studies identified miRNA‐378, miRNA‐451, miRNA‐486, and four up‐regulated GC‐associated miRNAs (miRNA‐17‐5p, miRNA‐21, miRNA‐106a, and miRNA‐106b), which also displayed higher expression levels in GC serum .…”
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