Based on China National Standard of Soil Engineering Classification (GB/T 50145-2007) and the Unified Soil Classification System of American Society for Testing Materials (ASTM D-2478), two kinds of soil laboratory en...Based on China National Standard of Soil Engineering Classification (GB/T 50145-2007) and the Unified Soil Classification System of American Society for Testing Materials (ASTM D-2478), two kinds of soil laboratory engineering classification methods were discussed and analyzed from the aspects of the definition in particle fraction, classification of soil type and evaluation standard for soil gradation. There is a same limit of fine grains fraction in the two standards, and there are three main types of soil in GB/T 50145-2007 and two in ASTM D-2487. Different evaluation standards of gradation are put forward for gravels and sands in ASTM D-2487. Same criteria of A line, B line and controlling value of plastic index are in the plasticity chart of both standards.展开更多
Objective This study aims to investigate the effects of the long noncoding RNA(lncRNA)DRAIC on the proliferation,apoptosis,and radiosensitivity of hepatocellular carcinoma(HCC)cells and the molecular mechanisms involv...Objective This study aims to investigate the effects of the long noncoding RNA(lncRNA)DRAIC on the proliferation,apoptosis,and radiosensitivity of hepatocellular carcinoma(HCC)cells and the molecular mechanisms involved.Methods Cancer tissues and their corresponding adjacent tissues from 30 patients with HCC were collected,and the expression levels of DRAIC and miR-223-3p were detected via RT-q PCR.DRAIC interference and miR-223-3p overexpression vectors were transfected into HepG2 cells.In addition,DRAIC and miR-223-3p interference vectors were co-transfected into HepG2 cells.The constructed cells were irradiated at 4 Gy.Cell colony formation assay,MTT assay,and flow cytometry were performed to detect the radiosensitivity,proliferation inhibition rate,and apoptosis rate of HepG2 cells,respectively.Dual luciferase reporter gene assay was performed to detect the targeted regulation of DRAIC on miR-223-3p expression.Results The expression level of DRAIC in HCC tissues was higher than that in paracancer tissues,whereas the expression level of miR-223-3p was lower in HCC tissues than that in paracancer tissues(P<0.05).Inhibition of DRAIC expression or overexpression of miR-223-3p increased the proliferation inhibition and apoptosis rates of HepG2 cells(P<0.05).After irradiation,cell survival fraction decreased and cell proliferation inhibition and apoptosis rates increased(P<0.05).DRAIC targeted the regulation of miR-223-3p expression,and interference of miR-223-3p expression reversed the effects of inhibiting DRAIC expression on the proliferation,apoptosis,and radiosensitivity of HepG2 cells.Conclusion Inhibition of DRAIC expression can inhibit the proliferation of HepG2 cells,promote cell apoptosis,and enhance the radiosensitivity of cells via upregulation of miR-223-3p.展开更多
基金Supported by Projects of National Natural Science Foundation of China ( Nos. 40902077,41111120084,41172236)
文摘Based on China National Standard of Soil Engineering Classification (GB/T 50145-2007) and the Unified Soil Classification System of American Society for Testing Materials (ASTM D-2478), two kinds of soil laboratory engineering classification methods were discussed and analyzed from the aspects of the definition in particle fraction, classification of soil type and evaluation standard for soil gradation. There is a same limit of fine grains fraction in the two standards, and there are three main types of soil in GB/T 50145-2007 and two in ASTM D-2487. Different evaluation standards of gradation are put forward for gravels and sands in ASTM D-2487. Same criteria of A line, B line and controlling value of plastic index are in the plasticity chart of both standards.
文摘Objective This study aims to investigate the effects of the long noncoding RNA(lncRNA)DRAIC on the proliferation,apoptosis,and radiosensitivity of hepatocellular carcinoma(HCC)cells and the molecular mechanisms involved.Methods Cancer tissues and their corresponding adjacent tissues from 30 patients with HCC were collected,and the expression levels of DRAIC and miR-223-3p were detected via RT-q PCR.DRAIC interference and miR-223-3p overexpression vectors were transfected into HepG2 cells.In addition,DRAIC and miR-223-3p interference vectors were co-transfected into HepG2 cells.The constructed cells were irradiated at 4 Gy.Cell colony formation assay,MTT assay,and flow cytometry were performed to detect the radiosensitivity,proliferation inhibition rate,and apoptosis rate of HepG2 cells,respectively.Dual luciferase reporter gene assay was performed to detect the targeted regulation of DRAIC on miR-223-3p expression.Results The expression level of DRAIC in HCC tissues was higher than that in paracancer tissues,whereas the expression level of miR-223-3p was lower in HCC tissues than that in paracancer tissues(P<0.05).Inhibition of DRAIC expression or overexpression of miR-223-3p increased the proliferation inhibition and apoptosis rates of HepG2 cells(P<0.05).After irradiation,cell survival fraction decreased and cell proliferation inhibition and apoptosis rates increased(P<0.05).DRAIC targeted the regulation of miR-223-3p expression,and interference of miR-223-3p expression reversed the effects of inhibiting DRAIC expression on the proliferation,apoptosis,and radiosensitivity of HepG2 cells.Conclusion Inhibition of DRAIC expression can inhibit the proliferation of HepG2 cells,promote cell apoptosis,and enhance the radiosensitivity of cells via upregulation of miR-223-3p.
