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年轻女性宫颈CINⅠ/Ⅱ级病变中p16InK4a和Ki67临床意义(4)
http://www.100md.com 2014年5月1日 李思琦 董颖 毕蕙 张晓明 陈锐
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     [9]Samir R, Asplund A, Tot T, et al. High-risk HPV infection and CIN grade correlates to the expression of c-myc, CD4+, FHIT, E-cadherin, Ki-67, and p16INK4a. J Low Genit Tract Dis,2011, 15(4):280-286.

    [10]Mimica M, Tomic'S, Kardum G, et al. Ki67 quantitative evaluation as a marker of cervical intraepithelial neoplasia and humanpapillomavirus infection. Int J Gynecol Cancer,2010,20(1): 116-119.

    [11]Roncaglia MT, Fregnani JH, Tacla M, et al. Characterization of p16 and E6 HPV-related proteins in uterine cervix high-grade lesions of patients treated by conization with large loop excision. Oncol Lett,2013,6(1):63-68.

    [12]Nishio S, Fujii T, Nishio H, et al. p16INK4a immunohistochemistry is a promising biomarker to predict the outcome of low grade cervical intraepithelial neoplasia: comparison study with HPV genotyping. J Gynecol Oncol, 2013,24(3): 215-221.

    [13]Koo YJ, Hahn HS, Lee IH, et al. Dual immunostaining of cervical cytology specimens with atypical squamous cells for p16/Ki-67 does not exclude the existence of a high-grade squamous intraepithelial lesion. Virchows Arch,2013,463(5): 689-696.

    [14]Carozzi F, Gillio-Tos A, Confortini M, et al. Risk of high-grade cervical intraepithelial neoplasia during follow-up in HPV-positive women according to baseline p16-INK4A results: a prospective analysis of a nested substudy of the NTCC randomised controlled trial. Lancet Oncol, 2013,14(2):168-176.

    [15]Cortecchia S, Galanti G,Sgadari C, et al. Follow-up study of patients with cervical intraepithelial neoplasia grade 1 overexpressing p16Ink4a. Int J Gynecol Cancer, 2013,23(9):1663-1669.

    (收稿日期:2013-10-29)

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