Comparison between L and E gene amplification analytical methods for human papillomavirus typing / 부인종양
Journal of Gynecologic Oncology
; : 251-255, 2008.
Article
en En
| WPRIM
| ID: wpr-140247
Biblioteca responsable:
WPRO
ABSTRACT
OBJECTIVE: L and E6/E7 gene amplification analyses were compared to identify human papillomavirus (HPV) infection and verify the HPV type, with the intent to minimize HPV typing errors. METHODS: L1 gene verified HPV typing was accomplished via polymerase chain reaction (PCR) and membrane assays. Verification of HPV typing via E6/E7 genes was accomplished through nested multiplexed PCR. The results from 104 samples were compared. RESULTS: The rates of accordance and difference were 35% and 65%, respectively. For 29% of the analyses, nested multiplexed PCR was more diversified than the membrane assay. CONCLUSION: HPV can be classified into low-risk HPV and high-risk HPV groups. In parallel amplifications of the L and E genes is more efficient for accurate diagnosis in light of the different symptoms and attendant precautions of the risk groups.
Palabras clave
Texto completo:
1
Índice:
WPRIM
Asunto principal:
Amplificación de Genes
/
Reacción en Cadena de la Polimerasa
/
Luz
/
Membranas
Límite:
Humans
Idioma:
En
Revista:
Journal of Gynecologic Oncology
Año:
2008
Tipo del documento:
Article