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1.
Chinese Journal of Experimental and Clinical Virology ; (6): 298-300, 2011.
Artigo em Chinês | WPRIM | ID: wpr-246259

RESUMO

<p><b>OBJECTIVE</b>To study the relationship between thinprep cytologic test and the types of human papilloma virus (HPV) infection in cervical precancerous lesion screening.</p><p><b>METHODS</b>To perform high-risk HPV types test in 1375 samples. Choose 256 positive samples to take thinprep cytologic test (TCT) and directed biopsies under colposcopy. Adopting two-channels real time PCR to genotype and quantify eight high risk HPV DNA (high risk types: HPV 16, 18, 45, 31; intermediate risk types: HPV 33, 52, 58, 67).</p><p><b>RESULTS</b>There are 256 positive samples in High risk HPV DNA test (18.62%). WNL rate for TCT is 16.41% (42/256), ASCUS and above rate for TCT is 83.59% (214/256). There is no statistically significant difference in the viral loads of HPV infection rate between the TCT negative patients and positive patients (P > 0.5). Positive correspondence rate for TCT and biopsy are 92.86% (39/42), 81.36% (48/59), 85.19% (23/27) and 9/10.</p><p><b>CONCLUSION</b>High-risk HPV types checking combined with TCT and biopsy can raise positive rate significantly. It should be used as a reliable method for early diagnosis in cervical cancer and CIN screening.</p>


Assuntos
Feminino , Humanos , Alphapapillomavirus , Classificação , Genética , Citodiagnóstico , Métodos , Detecção Precoce de Câncer , Métodos , Infecções por Papillomavirus , Diagnóstico , Patologia , Virologia , Neoplasias do Colo do Útero , Diagnóstico , Patologia , Virologia
2.
China Biotechnology ; (12)2006.
Artigo em Chinês | WPRIM | ID: wpr-686255

RESUMO

In order to further study mouse embryonic stem cells(ES cells),lentiviral vector PLL-IRES-Nanog-Neo was constructed.Mouse ES cells overexpressed nanog by mediation of lentiviral were cultured on mouse fetal fibroblast feeders after 2 weeks under G418 media and examined according to gowth characteristics. Results were showed that 918 bp nanog fragments were expressed in mouse ES cells mediated by lentiviral vector PLL-IRES-Nanog-Neo,mouse nanog-ES cells were taken on mass-like image and positve with alkaline phosphatase staining and Oct4 and SSEA1 immunocytochemistry under no LIF condition in the media. It is concluded that mouse ES cells Elevated nanog gene expression by mediation of lentiviral were constucted and cultured.

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