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1.
Chinese Journal of Pathology ; (12): 33-38, 2012.
Article in Chinese | WPRIM | ID: wpr-242002

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the expression and promoter methylation status of p73 gene in ovarian epithelial tumors and their clinicopathological correlations.</p><p><b>METHODS</b>Tissue microarrays (TMA) consisting of 68 ovarian cancers, 37 ovarian borderline tumors and 21 ovarian benign tumors were constructed. p73 expression was detected by immunohistochemistry (EnVision method). Fresh-frozen tissue samples from 13 cases of ovarian carcinomas and 5 cases of borderline tumors were evaluated for the presence of p73 promoter methylation using bisulfite sequencing.</p><p><b>RESULTS</b>Overall, 92.6% (63/68) ovarian carcinomas expressed p73, with a mean value of 32% (percentage of p73 positive cells in the tumor). The mean value of p73 expression rate (40%) in serous carcinoma (26/26) was higher than those of other cancer types (P = 0.006). The mean value of p73 expression rate (40%) in type II ovarian carcinoma was significantly higher than that in type I ovarian carcinoma (24%, P = 0.010). The expression of p73 was not associated with FIGO stage and histological grade (both P > 0.05). The mean values of p73 expression in ovarian borderline tumor (30/37) and benign tumor (12/21) were 16% and 15%, respectively. Of the two groups, the mean value of p73 expression rate in serous type was higher than that in mucous type (P = 0.003, P = 0.026). Ovarian carcinomas had a higher level of p73 expression than borderline tumors and benign tumors (both P < 0.05), while that between ovarian borderline tumors and benign tumors had no statistical difference (P > 0.05). Among serous tumors (49/53), the mean value of p73 expression in the carcinoma group (26/26) was significantly higher than those in the borderline tumor group (12/14) and benign tumor group (11/13; P = 0.024 and P = 0.002, respectively), while that between borderline tumor group and benign tumor group had no statistical difference (P = 0.428). Among mucous tumors (15/27), the mean value of p73 expression in carcinoma group (6/7) was higher than that in benign tumor group (1/8; P = 0.032). No statistical difference of p73 expression was seen between the carcinoma group and ovarian borderline tumor group (8/12) and between the borderline tumor group and benign tumor group (P = 0.234, P = 0.201, respectively). p73 promotor methylation was found in 8 of 13 cases of carcinomas but at different methylation levels with a mean value of 8.0%. Two of 5 ovarian borderline tumors showed detectable p73 promotor methylation with a mean value of 9.0%. Compared with the borderline tumors, ovarian carcinomas showed a similar p73 methylation level (P > 0.05). The p73 methylation level in ovarian carcinomas was not associated with histological type, pathogenetic type, histological grade and FIGO stage (all P > 0.05).</p><p><b>CONCLUSIONS</b>Most of ovarian epithelial tumors express p73 protein with mean values higher in ovarian carcinomas than those in the borderline and benign tumors. Ovarian serous carcinomas have the highest expression level of p73. A simple linear correlation does not exist between the promoter methylation and protein expression of p73.</p>


Subject(s)
Adult , Aged , Female , Humans , Middle Aged , Young Adult , Cystadenocarcinoma, Mucinous , Metabolism , Pathology , Cystadenocarcinoma, Serous , Metabolism , Pathology , Cystadenofibroma , Metabolism , Pathology , Cystadenoma, Mucinous , Metabolism , Pathology , Cystadenoma, Serous , Metabolism , Pathology , DNA Methylation , DNA-Binding Proteins , Metabolism , Gene Expression Regulation, Neoplastic , Immunohistochemistry , Neoplasm Grading , Neoplasm Staging , Neoplasms, Glandular and Epithelial , Metabolism , Pathology , Nuclear Proteins , Metabolism , Oligonucleotide Array Sequence Analysis , Ovarian Neoplasms , Metabolism , Pathology , Promoter Regions, Genetic , Tumor Protein p73 , Tumor Suppressor Proteins , Metabolism
2.
Chinese Journal of Pathology ; (12): 694-697, 2011.
Article in Chinese | WPRIM | ID: wpr-358262

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the role of p57 and p53 immunohistochemistry in the differential diagnosis of hydropic abortion, partial hydatidiform mole and complete hydatidiform mole.</p><p><b>METHODS</b>Immunohistochemical stains (EnVision method) for p57 and p53 were performed in tissue samples of normal placenta chorionic villi (n=10), abortion chorionic villi (n=12), partial hydatidiform (n=23) and complete hydatidiform moles (n=20).</p><p><b>RESULTS</b>The expression of p57 was predominantly localized in the nuclei of villous cytotrophoblasts and stromal cells. The positive rates of p57 in normal placenta, hydropic abortion and partial hydatidiform mole were 10/10, 12/12, and 100% (23/23), respectively, with no significant difference among the groups (P>0.05). However, none of the complete hydatidiform moles analyzed exhibited p57 positivity in cytotrophoblasts and stromal cells. There was a significant difference between partial and complete hydatidiform moles (P<0.05). The expression of p53 was observed in the nuclei of cytotrophoblastic cells and intermediate trophoblasts. No p53 expression was seen in normal placenta and only 1 of 12 hydropic abortion showed p53 positivity. The positive rates of p53 expression in partial and complete hydatidiform mole were 60.9% (14/23) and 85.0% (17/20) respectively. It was significantly higher in partial hydatidiform mole than that in hydropic abortion. A significant difference was also found between partial and complete hydatidiform moles (P<0.05).</p><p><b>CONCLUSIONS</b>Our findings confirm that p57 immunohistochemistry assists the differential diagnosis of complete hydatidiform mole from partial hydatidiform mole. Expression of p53 may be helpful in distinguishing partial hydatidiform mole from hydropic abortion.</p>


Subject(s)
Female , Humans , Pregnancy , Abortion, Spontaneous , Diagnosis , Metabolism , Pathology , Cyclin-Dependent Kinase Inhibitor p57 , Metabolism , Diagnosis, Differential , Hydatidiform Mole , Diagnosis , Metabolism , Pathology , Immunohistochemistry , Stromal Cells , Metabolism , Trophoblasts , Metabolism , Tumor Suppressor Protein p53 , Metabolism , Uterine Neoplasms , Diagnosis , Metabolism , Pathology
3.
Chinese Journal of Pathology ; (12): 747-751, 2010.
Article in Chinese | WPRIM | ID: wpr-295119

ABSTRACT

<p><b>OBJECTIVE</b>to investigate the expression of folate receptor(FR)α in ovarian epithelial tumors and its clinopathological significance.</p><p><b>METHODS</b>tissue microarrays (TMAs) were constructed from 86 epithelial ovarian cancers and 29 borderline ovarian tumors, followed by the FRα expression evaluation by immunohistochemistry. FRα mRNA expression was investigated by quantitative real-time PCR using fresh-frozen tissues from 40 cases of ovarian carcinoma and 14 cases of borderline tumor. FRα expression levels in ovarian tumors were also analyzed in correlation with tumor morphology, pathogenesis and FIGO stage.</p><p><b>RESULTS</b>FRα expression was detected in 40 of 86 (46.5%) of ovarian cancers, with the highest rate of expression observed in serous carcinomas (62.7%, 32/51) compared with that of the other cancer types (P = 0.000). Depending on pathogenesis type, FRα expressions in type II ovarian carcinomas were significantly higher than those in type I ovarian carcinomas (P = 0.001). Ovarian carcinomas had a tendency to express higher FRα than the borderline tumors (46.5% vs 27.6%), although statistically not significant (P = 0.074). FRα expressions in ovarian carcinomas showed no correlation with the FIGO stage (P = 0.498). However, real-time PCR showed that FRα mRNA levels were significantly higher in ovarian carcinomas compared with that of the borderline tumors (P = 0.000) and also higher in serous ovarian borderline tumors compared with mucinous type (P = 0.007).</p><p><b>CONCLUSION</b>higher level of FRα expression occurs frequently in ovarian epithelial tumors, especially in carcinomas and ovarian serous tumors.</p>


Subject(s)
Adult , Aged , Female , Humans , Middle Aged , Young Adult , Adenocarcinoma, Clear Cell , Metabolism , Pathology , Adenocarcinoma, Mucinous , Metabolism , Pathology , Carcinoma, Endometrioid , Metabolism , Pathology , Cystadenocarcinoma, Serous , Metabolism , Pathology , Cystadenoma, Mucinous , Metabolism , Pathology , Cystadenoma, Serous , Metabolism , Pathology , Folate Receptor 1 , Genetics , Metabolism , Gene Expression Regulation, Neoplastic , Ovarian Neoplasms , Metabolism , Pathology , RNA, Messenger , Metabolism
4.
Chinese Journal of Applied Physiology ; (6): 105-110, 2005.
Article in Chinese | WPRIM | ID: wpr-287086

ABSTRACT

<p><b>AIM</b>To establish the culturing of cortical, hippocampal and sympathetic ganglia neurons derived from neonatal rats and the whole-cell recording techniques of potassium and sodium currents in cultured neurons.</p><p><b>METHODS</b>Cortex, hippocampus and sympathetic ganglion were isolated from neonatal rats (1-3 days) and digested by trypsin (0.125%). The neurons were cultured in polylysine covered petri dish (O35 mm) with DEME medium(high glucose) for seven days for electrophysiological experiments.</p><p><b>RESULTS</b>The neurons cultured by this method were in good conditions and could be sealed easily in whole-cell recording. I(Na), I(A), and I(K) could be recorded respectively in cultured neurons by different recording paradigms in Ca2+ -free extracellular solution.</p><p><b>CONCLUSION</b>It is a practicable and economical method for electrophysiological study of nervous system.</p>


Subject(s)
Animals , Rats , Calcium Channels , Physiology , Cells, Cultured , Cerebral Cortex , Physiology , Ganglia, Sympathetic , Cell Biology , Physiology , Hippocampus , Physiology , Membrane Potentials , Physiology , Patch-Clamp Techniques , Potassium Channels , Physiology , Rats, Wistar , Sodium Channels , Physiology
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