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1.
Contraception ; 38(6): 641-57, 1988 Dec.
Article in English | MEDLINE | ID: mdl-3146463

ABSTRACT

A large scale, phased investigation of NORPLANT contraceptive systems was conducted in the People's Republic of China. The first phase comprehended 1,200 women in four cities. Expanded trials included 11,918 women at 12 major centers and at sub-centers by 31 May 1987. At that date 4,676 NORPLANT capsule subjects and 1,089 rod subjects had completed one year of use, 1,381 capsule acceptors had completed two years as had 197 rod users. Gross pregnancy rates were less than 0.1 per 100 for each implant type both at one and at two years. Continuation rates were 94 per 100 for each implant type at one year, and were 82.0 and 83.6 per 100 among users of NORPLANT capsule and rod implants, respectively, at two years. Disruption of menstrual function was the dominant reason for termination, but mean hemoglobin levels increased in each of the nine centers reporting values at admission and at one year. First year gross cumulative termination rates for medical reasons were 1.2 to 1.3 per 100, reaching 3.8 and 5.6 per 100 for capsule and rod implants, respectively, at two years. Microdose contraception with these levonorgestrel-releasing implants appears to be a highly acceptable and effective modality suitable for Chinese women. NORPLANT implants are now approved by the national drug regulatory agency for general use in China.


Subject(s)
Drug Evaluation, Preclinical/methods , Norgestrel/standards , Adolescent , Adult , Cardiovascular System/physiopathology , China , Contraceptive Agents, Female/adverse effects , Contraceptive Agents, Female/standards , Drug Implants , Female , Humans , Levonorgestrel , Menstruation Disturbances , Norgestrel/adverse effects , Platelet Count , Pregnancy
2.
Exp Oncol ; 28(3): 235-40, 2006 Sep.
Article in English | MEDLINE | ID: mdl-17080019

ABSTRACT

AIM: To investigate the role of human papillomavirus (HPV) HPV16/18 E6 oncogene in the carcinogenesis of esophageal cell carcinoma (ESCC). MATERIALS AND METHODS: Tissue microarray (TMA) block was constructed from 60 cases of paraffin-embedded ESCC tissues and pair-matched controls (adjacent normal epithelium). Immunohistochemistry (IHC) methods were applied to detect the expression of HPV16/18 E6, p53, p21(WAF1), MDM2, Ki67 and cyclin D1 proteins on TMA slides. In situ hybridization (ISH) targeting HPV gene was also used. RESULTS: In ESCC samples, 18.3% (11/60) were revealed HPV16/18 E6 positive by IHC, while 40.0% (24/60) HPV positive by ISH; HPV16/18 E6 expression was significantly higher than that of control samples. In ESCC samples, the expressions of p53, p21(WAF1), Cyclin D1, MDM2 and Ki67 were recorded in 60.0% (36/60), 40.0% (24/60), 51.7% (31/60), 65.0% (39/60) and 88.3% (53/60) cases respectively, In ESCC samples, p53, MDM2 and Ki67 expression correlated with the HPV16/18 E6 expression (p less, similar 0.01), p21(WAF1) expression - with these of MDM2 and cyclin D1 (p less, similar 0.01) whilst expression of Ki67 - with ESCC grade (p less, similar 0.01). CONCLUSION: HPV might be one of etiological factor of esophageal carcinoma in Shantou, China. p53, MDM2 proteins may play important roles in the pathogenesis of HPV-associated ESCC.


Subject(s)
Carcinoma, Squamous Cell/virology , DNA-Binding Proteins/metabolism , Esophageal Neoplasms/virology , Oncogene Proteins, Viral/metabolism , Repressor Proteins/metabolism , Adult , Aged , Carcinoma, Squamous Cell/chemistry , Carcinoma, Squamous Cell/metabolism , Cyclin D , Cyclin-Dependent Kinase Inhibitor p21/analysis , Cyclin-Dependent Kinase Inhibitor p21/metabolism , Cyclins/analysis , Cyclins/metabolism , DNA-Binding Proteins/analysis , DNA-Binding Proteins/genetics , Esophageal Neoplasms/chemistry , Esophageal Neoplasms/metabolism , Female , Humans , Immunohistochemistry , In Situ Hybridization , Ki-67 Antigen/analysis , Ki-67 Antigen/metabolism , Male , Middle Aged , Oncogene Proteins, Viral/analysis , Oncogene Proteins, Viral/genetics , Proto-Oncogene Proteins c-mdm2/analysis , Proto-Oncogene Proteins c-mdm2/metabolism , Repressor Proteins/analysis , Repressor Proteins/genetics , Tissue Array Analysis , Tumor Suppressor Protein p53/analysis , Tumor Suppressor Protein p53/metabolism
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