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조영록 ( Young Rok Cho ),주종길 ( Jong Kil Joo ),김휘곤 ( Hwi Gon Kim ),나용진 ( Yong Jin Na ),이규섭 ( Kyu Sup Lee ) 대한산부인과학회 2009 Obstetrics & Gynecology Science Vol.52 No.3
Objective: To investigate the effects of leptin on in vitro development of mouse embryos. Methods: Female C57BL mice, aged 8 to 15 weeks, were superovulated with IP injection of 5 IU of PMSG followed by 5 IU hCG at 48 hours later. And then the mice were mated with male mice. The next morning, one-cell embryos were collected and cultured in media added with various concentrations (0, 5, 50, 500 ng/mL) of leptin for 4 days. In addition, to determine whether the sensitivity to leptin varied at different stages of development, embryos at 2- or 4-cell stage were treated with the same concentrations of leptin and cultured up to blastocyst stage. The total cell number of blastocyst was assessed and the expression of leptin receptor was examined in all stages of development by immnuofluorescence. Results: The rate of blastocyst formation from one-cell embryos significantly increased at culture media that leptin was added at 50 ng/mL concentration, whereas decreased at 500 ng/mL concentration compared to the control (P<0.05). The development rate of embryos, from 2-cell stage, was similar to the rate from 1-cell stage. However, the addition of leptin to culture media in 4-cell embryos had no significant effects on embryo development compared to the control. In addition, the dose-dependent stimulatory or inhibitory effect of leptin on embryo development was weakened at 2-cell and 4-cell embryo stages compared one-cell embryo stage. The total cell number of blastocyst also significantly increased at 50 ng/mL of leptin, but decreased at 500 ng/mL. Leptin receptor was expressed in all stages from one-cell embryos to blastocyst. The intensity of Ob-Rb immnuostaining was mainly stronger in one- or two-cell embryos, decreased with advancing development stages, and increased again in blastocyst. Conclusion: This study shows that addition of leptin to embryo culture media affects embryo development in a dose-dependent and developmental stage-dependent manner. The effects of leptin seems to be associated with the expression pattern of leptin receptor at different stages of development.
이상숙,배지연,강유나,조영록,김시남,박남조,김선영,김정희,Lee, Sang-Sook,Bae, Ji-Yeon,Kang, Yu-Na,Cho, Young-Rok,Kim, Si-Nam,Park, Nam-Jo,Kim, Seun-Young,Kim, Jung-Hi 대한세포병리학회 1996 대한세포병리학회지 Vol.7 No.2
Abnormalities of p53 gene are common in lung cancers and are associated with immunologically detectable p53 protein. p53 immunoreactivity is uncommon in normal cells but is frequently seen in neoplasia. Therefore, assessment of p53 expression may assist in the cytological diagnosis of malignancy. The usefulness of p53 immunostaining as a marker of malignancy in the cytological analysis of bronchial brush specimens from the patients with lung cancers was investigated in this study. A total of 71 bronchial brush samples submitted for cytologic diagnosis were immunostained with D07, a monoclonal antibody to recombinant p53 protein. Resultant p53 data were correlated with cytologic diagnosis and clinical information. Of the 17 smears with a benign cytodiagnosis, all were p53 negative. Of the 40 cases with a malignant cytodiagnosis (histologically confirmed), 35 were p53 positive and 5 were negative. Of the 14 cases that were cytologically suspicious but nondiagnostic for malignancy, 11 were p53 positive, 9 of which were subsequently proved to be malignant by histologic examination, and the remaining 2 cases were tuberculosis clinically. Forty four of 51 histologically confirmed lung carcinomas were p53 positive, including 25 of 28 squamous cell carcinomas, 13 of 17 small cell carcinomas, 3 of 3 adenocarcinomas, and 3 of 3 large cell undifferentiated carcinomas. These results suggest that p53 immunostaining could be of value as a marker of malignancy in the cytologic examination of bronchial brush specimens. Furthermore, we have shown the possible clinical utility of p53 immunostaining in cytopathological diagnosis, that is, as a valuable adjunct to morphological assessment in the analysis of cytopathologically suspicious cases.
방광암 환자의 요세포 검사에서 p53 단백 발현의 의의
이상숙,배지연,강유나,조영록,박남조,김선영,김정희,Lee, Sang-Sook,Bae, Ji-Yeon,Kang, Yu-Na,Cho, Young-Rok,Park, Nam-Jo,Kim, Seun-Young,Kim, Jung-Hi 대한세포병리학회 1996 대한세포병리학회지 Vol.7 No.2
Although bladder cancers are very common, little is known about their molecular pathogenesis. It is known that p53 alteration is found in about 60% of muscle-invasive bladder cancer, necessiating aggressive therapy and poor outcome. We examined the nuclear expression of p53 protein, using D07 monoclonal antibody in the urine samples from 31 patients with transitional cell carcinoma of the bladder to investigate the correlation of p53 overexpression with histologic grades and depth of invasion. The positive rate of p53 protein was 27% in superficial bladder tumor, but increased up to 71% in the invasive bladder carcinomas. The overexpression of p53 protein increased according to Mostofi grading system from 18% in grade I, 45% in grade II, and up to 100% in grade III. The p53 expression tended to be higher in the invasive and high grade bladder cancers than in the superficial and low grade ones(p<0.05). These results suggest that immunohistochemical analysis of the urine specimen in the bladder cancer patients could be a useful method of screening for the presence of p53 mutant protein. The mutant p53 protein expression may be an indicator of bladder cancer with more proliferative potential and/or aggressive biologic behavior.