子宫颈细胞学的未来分子方面

K. Astbury, C.M. Martin, M. Ring, L. Pilkington, N. Bolger, O.M. Sheils, J.J. O’Leary
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引用次数: 6

摘要

宫颈癌是一种可以预防的疾病,仍然是全世界妇女中第二大常见的恶性肿瘤。目前的筛查方案依赖于巴氏涂片检查,据报道其假阴性率为15-50%。宫颈细胞学自动化的进步导致了细胞保存技术的改进和整体高质量的细胞材料,适合于分子分析。目前的重点主要是使用分子生物标志物作为现有筛选程序的辅助手段。这些生物标志物包括人乳头瘤病毒(HPV)和宿主细胞调节分子、小染色体维持蛋白、Cdc6(一种细胞分裂周期蛋白)和p16(INK4A)肿瘤抑制蛋白。微阵列技术的发展及其在宫颈癌研究中的应用极大地扩展了已知参与宫颈癌的差异调控基因的列表。这将有助于揭示HPV感染和发育不良进展的发病机制,并最终改善宫颈上皮内瘤变和宫颈癌的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Future molecular aspects of cervical cytology

Cervical cancer, a potentially preventable disease, remains the second most common malignancy in women worldwide. Current screening protocols rely on the Pap smear test, which has a reported false-negative rate of 15–50%. Advances in automation of cervical cytology have resulted in improved cell preservation techniques and overall high-quality cellular material that is suitable for molecular analysis. The current focus is primarily on the use of molecular biomarkers as adjuncts to existing screening procedures. These biomarkers include human papillomavirus (HPV) and the host cell regulatory molecules, minichromosome maintenance proteins, Cdc6 (a cell division cycle protein) and p16(INK4A) tumour suppressor protein. Developments in micro-array technology and its application to the study of cervical cancer have greatly expanded the list of differentially regulated genes known to be involved in cervical cancer. This will help to unravel the pathogenesis of HPV infection and dysplastic progression, and ultimately improve treatment of cervical intra-epithelial neoplasia and cervical cancer.

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