Objective: To study the correlation between the expression of CyclinB1/CDK1 complex in esophageal cancer tissue and the contents of marker molecules in serum and lesion. Methods:Patients who were diagnosed with esopha...Objective: To study the correlation between the expression of CyclinB1/CDK1 complex in esophageal cancer tissue and the contents of marker molecules in serum and lesion. Methods:Patients who were diagnosed with esophageal cancer in Mianyang Central Hospital between April 2014 and December 2016 were selected as esophageal cancer group, and the esophageal cancer lesion tissue, adjacent lesion tissue and serum samples were collected;healthy volunteers who received physical examination during the same period were selected as control group and serum samples were collected. The expression of CyclinB1/CDK1 complex, tumor suppressor genes and invasion genes in esophageal cancer lesion tissue and adjacent lesion tissue as well as the levels of tumor markers in serum were detected. Results: CyclinB1, CDK1 and E2F-1 mRNA expression in esophageal cancer lesion were significantly higher than those in adjacent lesion;serum tumor markers CYFRA21-1, SCC-Ag, CD44v5 and Stathmin levels of esophageal cancer group were significantly higher than those of control group and positively correlated with CyclinB1, CDK1 and E2F-1 mRNA expression in esophageal cancer lesion, PTEN, Spink8, p21 and p18 mRNA expression in esophageal cancer lesion were significantly lower than those in adjacent lesion and negatively correlated with CyclinB1, CDK1 and E2F-1 mRNA expression in esophageal cancer lesion, and nestin, β-catenin, Snail and Vimentin mRNA expression in esophageal cancer lesion were significantly higher than those in adjacent lesion and positively correlated with CyclinB1, CDK1 and E2F-1 mRNA expression in esophageal cancer lesion. Conclusion: The high expression of CyclinB1/CDK1 complex in esophageal cancer tissue can promote the proliferation and invasion of cancer cells.展开更多
文摘Objective: To study the correlation between the expression of CyclinB1/CDK1 complex in esophageal cancer tissue and the contents of marker molecules in serum and lesion. Methods:Patients who were diagnosed with esophageal cancer in Mianyang Central Hospital between April 2014 and December 2016 were selected as esophageal cancer group, and the esophageal cancer lesion tissue, adjacent lesion tissue and serum samples were collected;healthy volunteers who received physical examination during the same period were selected as control group and serum samples were collected. The expression of CyclinB1/CDK1 complex, tumor suppressor genes and invasion genes in esophageal cancer lesion tissue and adjacent lesion tissue as well as the levels of tumor markers in serum were detected. Results: CyclinB1, CDK1 and E2F-1 mRNA expression in esophageal cancer lesion were significantly higher than those in adjacent lesion;serum tumor markers CYFRA21-1, SCC-Ag, CD44v5 and Stathmin levels of esophageal cancer group were significantly higher than those of control group and positively correlated with CyclinB1, CDK1 and E2F-1 mRNA expression in esophageal cancer lesion, PTEN, Spink8, p21 and p18 mRNA expression in esophageal cancer lesion were significantly lower than those in adjacent lesion and negatively correlated with CyclinB1, CDK1 and E2F-1 mRNA expression in esophageal cancer lesion, and nestin, β-catenin, Snail and Vimentin mRNA expression in esophageal cancer lesion were significantly higher than those in adjacent lesion and positively correlated with CyclinB1, CDK1 and E2F-1 mRNA expression in esophageal cancer lesion. Conclusion: The high expression of CyclinB1/CDK1 complex in esophageal cancer tissue can promote the proliferation and invasion of cancer cells.