AIM： To explore the correlation between the expressions of gastrin （GAS）, somatostatin （SS） and cyclin, cyclin- dependent kinase （CDK） in colorectal cancer, and to detect the specific regulatory sites where gas...AIM： To explore the correlation between the expressions of gastrin （GAS）, somatostatin （SS） and cyclin, cyclin- dependent kinase （CDK） in colorectal cancer, and to detect the specific regulatory sites where gastrointestinal hormone regulates cell proliferati6n. METHODS： Seventy-nine resected large intestine carcinomatous specimens were randomly selected. Immunohistochemical staining for GAS, SS, cyclin D1, cyclin E, cyclin A, cyclin B1, CDK2 and CDK4 was performed according to the standard streptavidinbiotin-peroxidase （S-P） method. According to the semiquantitative integral evaluation, SS and GAS were divided into high, middle and low groups. Cyclin D1, cyclin E, cyclin A, cydin B1, CDK2, CDK4 expressions in the three GAS and SS groups were assessed. RESULTS： The positive expression rate of cyclin D1 was significantly higher in high （78.6%, 11/14） and middle GAS groups （73.9%, 17/23） than in low GAS group （45.2%, 19/42） （P〈0.05, X^2 high vs low = 4.691; P〈0.05, X^2 middle vs low = 4.945）. The positive expression rate of cyclin A was significantly higher in high （100%, 14/14） and middle GAS groups （82.6%, 19/23） than in low GAS group （54.8%, 23/42） （P〈0.01, X2high vs low = 9.586; P〈0.05, X^2 middle vs low = 5.040）. The positive expression rate of CDK2 was significantly higher in high （92.9%, 13/14） and middle GAS groups （87.0%, 20/23） than in low GAS group （50.0%, 21142） （P〈0.01, X^2 high vs low = 8.086; P〈0.01,X^2 middle low = 8.715）. The positive expression rate of CDK4 was significantly higher in high （78.6%, 11/14）and middle GAS groups （78.3%, 18/23） than in low GAS group （42.9%, 18/42） （P〈0.05, X^2 high vs low= 5.364; P〈0.01, X^2 middle vs low = 7.539）. The positive expression rate of cyclin E was prominently higher in low SS group （53.3%, 24/45） than in high （9.1%, 1/11） and middle （21.7%, 5/23） SS groups （P〈0.05, X^2 high vs low = 5.325; P〈0.05, X^2 middle vs low = 6.212）. The positive expression rate of CDK2 was significantly higher in low SS group （77.8%, 35/45） than in high SS group （27.3%, 3/11） （P〈0.01, X^2 high vs low = 8.151）. There was a significant positive correlation between the integral ratio of GAS to SS and the semi-quantitative integral of cyclin D1, cyclin E, cyclin A, CDK2, CDK4 （P〈0.05, 0% = 0.252; P〈0.01, E^rs = 0.387; P〈0.01,A^rs = 0.466; P〈0.01, K2^rs = 0.519; P〈0.01, K4^rs = 0.434）. CONCLUSION： The regulation and control of gastrin, SS in colorectal cancer cell growth may be directly related to the abnormal expressions of cyclins D1, A, E, and CDK2, CDK4. The regulatory site of GAS in the cell cycle of colorectal carcinoma may be at the G2, S and G2 phases. The regulatory site of SS may be at the entrance of S phase.展开更多
AIM： To investigate the in vivo effect of beta-casomorphin-7on the regulation of gastric somatostatin and gastrin messenger RNA in rat gastric mucosa.METHODS： Somatostatin and gastrin mRNA were quantified by RT-PCR ...AIM： To investigate the in vivo effect of beta-casomorphin-7on the regulation of gastric somatostatin and gastrin messenger RNA in rat gastric mucosa.METHODS： Somatostatin and gastrin mRNA were quantified by RT-PCR and in situ hybridization （ISH）in 24 rats. The rats were divided into three treatment groups： basal diet ＋ physiological saline （n = 8）, basal diet ＋ beta-casomorphin-7 （7.5 × 10^-7 mol） （n = 8）,and basal diet ＋ poly-Gly-7 （containing equal mol of N with 7.5 × 10^-7 mol beta-casomorphin-7） （n = 8）.After oral administration for 30 days, rats were killed by exsanguinations.RESULTS： After intra-gastric administration of betacasomorphin-7 for 30 d, gastrin mRNA increased by 52.8% （P 〈 0.05, n = 8）, and somatostatin mRNA levels decreased by 30.7% compared with the controls （P 〈0.01, n = 8）. No significant differences in the expression of the two genes were observed in the poly-Gly-treated group, although gastrin mRNA expression was elevated by 35.6% as against the control group （P = 0.15, n =8）. The long-term oral administration of a casomorphin solution significantly decreased the even gray of D-cells,but did not lower the number of D-cells both in the antrum and fundus. Interestingly, the number of G-cells increased in the antrum and fundus, but its average density was augmented only in the antrum.CONCLUSION： Beta-casomorphin-7 is capable of modulating gene expression of the regulatory peptides from G and D cells. Data from in situ hybridization studies indicate that beta-casomorphin-7 affects gastrin gene expression indirectly by means of the paracrine action of somatostatin, and depends on its intrinsic molecular function.展开更多
AIM: To explore the correlation between expression of somatostatin (SS), gastrin (GAS) and cell apoptosis regulation gene bcl-2/bax in large intestine carcinoma.METHODS: Sixty-two large intestine cancer tissue samples...AIM: To explore the correlation between expression of somatostatin (SS), gastrin (GAS) and cell apoptosis regulation gene bcl-2/bax in large intestine carcinoma.METHODS: Sixty-two large intestine cancer tissue samples were randomly and retrospectively selected from patients with large intestine carcinoma. Immunohistochemical staining for bcl-2, bax, GAS, SS was performed according to the standard streptavidin-biotin-peroxidase (S-P) method.According to the semi-quantitative integral evaluation, SS and GAS were divided into three groups as follows. Scores1-3 were defined as the low expression group, 4-8 as the intermediate expression group, 9-16 as the high expression group. Bax and bcl-2 protein expressions in different GAS and SS expression groups of large intestine carcinoma were assessed.RESULTS: The positive expression rate of bax had a prominent difference between SS and GAS high, intermediate and low expression groups (P＜0.05, x2ss = 9.246; P＜0.05,x2GAS = 6.981). The positive expression rate of bax in SS high (80.0%, 8/10) and intermediate (76.5%, 13/17)expression groups was higher than that in low expression group (40.0%, 14/35) (P＜0.05, x2high vs low = 5.242; P＜0.05,x2middle vs low = 6.097). The positive expression rate of bax in GAS high expression group (27.3%, 3/8) was lower than that in low expression group (69.4%, 25/36) (P＜0.05,x2 = 4.594). However, bax expression in GAS intermediate expression group (46.7%, 7/15) was lower than that in low expression group, but not statistically significant. The positive expression rate of bcl-2 had a prominent difference between SS and GAS high, intermediate and low expression groups (P＜0.05, x2ss = 7.178; P＜0.05, x2GAS = 13.831). The positive expression rate of bcl-2 in GAS high (90.9%, 10/11)and intermediate (86.7%, 13/15) expression groups was higher than that in low expression group (44.4%, 16/36)(P＜0.05,x2high vs low = 5.600; P＜0.05, x2 middle vs low = 7.695).However, the positive expression rate of bcl-2 in SS high (40.0%, 4/10) and intermediate (47.1%, 8/9) expression groups was lower than that in low expression group (77.1%, 27/35)(P＜0.05, x2 high vs low = 4.710; P＜0.05, x2 middle vs low = 4.706).There was a significant positive correlation between the integral ratio of GAS to SS and the integral of bcl-2 (P＜0.01,r=0.340). However, there was a negative correlation between the integral ratio of GAS to the SS and bax the integral of (P＜0.05, r = -0.299).CONCLUSION: The regulation and control of gastrin,somatostatin in cell apoptosis of large intestine carcinoma may be directly related to the abnormal expression of bcl-2, bax.展开更多
基金Supported by the Natural Science Foundation of Anhui Province,No.03043704
文摘AIM： To explore the correlation between the expressions of gastrin （GAS）, somatostatin （SS） and cyclin, cyclin- dependent kinase （CDK） in colorectal cancer, and to detect the specific regulatory sites where gastrointestinal hormone regulates cell proliferati6n. METHODS： Seventy-nine resected large intestine carcinomatous specimens were randomly selected. Immunohistochemical staining for GAS, SS, cyclin D1, cyclin E, cyclin A, cyclin B1, CDK2 and CDK4 was performed according to the standard streptavidinbiotin-peroxidase （S-P） method. According to the semiquantitative integral evaluation, SS and GAS were divided into high, middle and low groups. Cyclin D1, cyclin E, cyclin A, cydin B1, CDK2, CDK4 expressions in the three GAS and SS groups were assessed. RESULTS： The positive expression rate of cyclin D1 was significantly higher in high （78.6%, 11/14） and middle GAS groups （73.9%, 17/23） than in low GAS group （45.2%, 19/42） （P〈0.05, X^2 high vs low = 4.691; P〈0.05, X^2 middle vs low = 4.945）. The positive expression rate of cyclin A was significantly higher in high （100%, 14/14） and middle GAS groups （82.6%, 19/23） than in low GAS group （54.8%, 23/42） （P〈0.01, X2high vs low = 9.586; P〈0.05, X^2 middle vs low = 5.040）. The positive expression rate of CDK2 was significantly higher in high （92.9%, 13/14） and middle GAS groups （87.0%, 20/23） than in low GAS group （50.0%, 21142） （P〈0.01, X^2 high vs low = 8.086; P〈0.01,X^2 middle low = 8.715）. The positive expression rate of CDK4 was significantly higher in high （78.6%, 11/14）and middle GAS groups （78.3%, 18/23） than in low GAS group （42.9%, 18/42） （P〈0.05, X^2 high vs low= 5.364; P〈0.01, X^2 middle vs low = 7.539）. The positive expression rate of cyclin E was prominently higher in low SS group （53.3%, 24/45） than in high （9.1%, 1/11） and middle （21.7%, 5/23） SS groups （P〈0.05, X^2 high vs low = 5.325; P〈0.05, X^2 middle vs low = 6.212）. The positive expression rate of CDK2 was significantly higher in low SS group （77.8%, 35/45） than in high SS group （27.3%, 3/11） （P〈0.01, X^2 high vs low = 8.151）. There was a significant positive correlation between the integral ratio of GAS to SS and the semi-quantitative integral of cyclin D1, cyclin E, cyclin A, CDK2, CDK4 （P〈0.05, 0% = 0.252; P〈0.01, E^rs = 0.387; P〈0.01,A^rs = 0.466; P〈0.01, K2^rs = 0.519; P〈0.01, K4^rs = 0.434）. CONCLUSION： The regulation and control of gastrin, SS in colorectal cancer cell growth may be directly related to the abnormal expressions of cyclins D1, A, E, and CDK2, CDK4. The regulatory site of GAS in the cell cycle of colorectal carcinoma may be at the G2, S and G2 phases. The regulatory site of SS may be at the entrance of S phase.
基金Supported by the National Natural Science Foundation of China, No. 39770540
文摘AIM： To investigate the in vivo effect of beta-casomorphin-7on the regulation of gastric somatostatin and gastrin messenger RNA in rat gastric mucosa.METHODS： Somatostatin and gastrin mRNA were quantified by RT-PCR and in situ hybridization （ISH）in 24 rats. The rats were divided into three treatment groups： basal diet ＋ physiological saline （n = 8）, basal diet ＋ beta-casomorphin-7 （7.5 × 10^-7 mol） （n = 8）,and basal diet ＋ poly-Gly-7 （containing equal mol of N with 7.5 × 10^-7 mol beta-casomorphin-7） （n = 8）.After oral administration for 30 days, rats were killed by exsanguinations.RESULTS： After intra-gastric administration of betacasomorphin-7 for 30 d, gastrin mRNA increased by 52.8% （P 〈 0.05, n = 8）, and somatostatin mRNA levels decreased by 30.7% compared with the controls （P 〈0.01, n = 8）. No significant differences in the expression of the two genes were observed in the poly-Gly-treated group, although gastrin mRNA expression was elevated by 35.6% as against the control group （P = 0.15, n =8）. The long-term oral administration of a casomorphin solution significantly decreased the even gray of D-cells,but did not lower the number of D-cells both in the antrum and fundus. Interestingly, the number of G-cells increased in the antrum and fundus, but its average density was augmented only in the antrum.CONCLUSION： Beta-casomorphin-7 is capable of modulating gene expression of the regulatory peptides from G and D cells. Data from in situ hybridization studies indicate that beta-casomorphin-7 affects gastrin gene expression indirectly by means of the paracrine action of somatostatin, and depends on its intrinsic molecular function.
基金Supported by National Natural Science Foundation of China, No.39270769, Natural Science Foundation of Anhui Province, No.03043704, Natural Science Foundation of Education Bureau of Anhui Province, No.2002kj307
文摘AIM: To explore the correlation between expression of somatostatin (SS), gastrin (GAS) and cell apoptosis regulation gene bcl-2/bax in large intestine carcinoma.METHODS: Sixty-two large intestine cancer tissue samples were randomly and retrospectively selected from patients with large intestine carcinoma. Immunohistochemical staining for bcl-2, bax, GAS, SS was performed according to the standard streptavidin-biotin-peroxidase (S-P) method.According to the semi-quantitative integral evaluation, SS and GAS were divided into three groups as follows. Scores1-3 were defined as the low expression group, 4-8 as the intermediate expression group, 9-16 as the high expression group. Bax and bcl-2 protein expressions in different GAS and SS expression groups of large intestine carcinoma were assessed.RESULTS: The positive expression rate of bax had a prominent difference between SS and GAS high, intermediate and low expression groups (P＜0.05, x2ss = 9.246; P＜0.05,x2GAS = 6.981). The positive expression rate of bax in SS high (80.0%, 8/10) and intermediate (76.5%, 13/17)expression groups was higher than that in low expression group (40.0%, 14/35) (P＜0.05, x2high vs low = 5.242; P＜0.05,x2middle vs low = 6.097). The positive expression rate of bax in GAS high expression group (27.3%, 3/8) was lower than that in low expression group (69.4%, 25/36) (P＜0.05,x2 = 4.594). However, bax expression in GAS intermediate expression group (46.7%, 7/15) was lower than that in low expression group, but not statistically significant. The positive expression rate of bcl-2 had a prominent difference between SS and GAS high, intermediate and low expression groups (P＜0.05, x2ss = 7.178; P＜0.05, x2GAS = 13.831). The positive expression rate of bcl-2 in GAS high (90.9%, 10/11)and intermediate (86.7%, 13/15) expression groups was higher than that in low expression group (44.4%, 16/36)(P＜0.05,x2high vs low = 5.600; P＜0.05, x2 middle vs low = 7.695).However, the positive expression rate of bcl-2 in SS high (40.0%, 4/10) and intermediate (47.1%, 8/9) expression groups was lower than that in low expression group (77.1%, 27/35)(P＜0.05, x2 high vs low = 4.710; P＜0.05, x2 middle vs low = 4.706).There was a significant positive correlation between the integral ratio of GAS to SS and the integral of bcl-2 (P＜0.01,r=0.340). However, there was a negative correlation between the integral ratio of GAS to the SS and bax the integral of (P＜0.05, r = -0.299).CONCLUSION: The regulation and control of gastrin,somatostatin in cell apoptosis of large intestine carcinoma may be directly related to the abnormal expression of bcl-2, bax.
