| Objective:Through test the expression of LRP1B in normal pancreatic cell and three pancreaticcancer cells, discuss LRP1B relationship with pancreatic cancer.Methods:To pancreatic cancer cell lines(ASPC-1, PANC1, BxPC3, HPDE6C7) as the researchobject, Real Time-PCR is use to assay the expression of LRP1B mRNA.Western blot is useto assay the expression of LRP1B protein. Divided into two groups:1, normal pancreaticcells and three pancreatic cancer cell expression differences;2, three pancreatic cancer cellexpression differences between comparison.Results:Real Time-QPCR result revealed the LRP1B mRNA was expressed in four cell lines,and measured2^-a delta Ct value, x±s: PANC-11.278±0.165ã€ASPC-13.244±0.485ã€BXPC-38.448±1.140ã€HPDE6C717.275±0.387; the average compared with the t test andsingle factor variance analysis; P <0.05for the difference was statistically significant.Western-blot method for the detection of LRP1B protein in three pancreatic cancer celllines expressing, according to the PANC-1ASPC-1and BXPC-3’film gray analysis,LRP1B protein in the gray value and the corresponding cells in theβ-actin gray value ratioof column data table, use x±S said:PANC-10.524±0.024ã€ASPC-10.571±0.016ã€BXPC-30.721±0.019ã€HPDE6C71.233±0.023; the mean’s compare by the t test andsingle factor variance analysis; P <0.05for the difference was statistically significant. Theprotein and mRNA of LRP1B expressed in three pancreatic cancer cells by Western-blotmethod and Real Time-QPCR method: HPDE6C7> BXPC-3> ASPC-1> PANC-1.Conclusions:1.LRP1B is a high state of expression in normal pancreatic cell, in three pancreatic cancer cells showed low expression;2.LRP1B has tumor specificity expressed in pancreatic cancer cells. |