Zappacosta Roberta, Colasante Antonella, Viola Patrizia, D'Antuono Tommaso, Lattanzio Giuseppe, Capanna Serena, Gatta Daniela Maria Pia, Rosini Sandra
Cytopathology Unit, Experimental and Clinical Sciences Department, "G. d'Annunzio" University of Chieti-Pescara, Via dei Vestini, 66100 Chieti, Italy.
Surgical Pathology Unit, "SS Annunziata" Hospital, ASL2 Abruzzo, Chieti, Italy.
Biomed Res Int. 2013;2013:453606. doi: 10.1155/2013/453606. Epub 2013 Nov 24.
Although HPV-DNA test and E6/E7 mRNA analyses remain the current standard for the confirmation of human papillomavirus (HPV) infections in cytological specimens, no universally adopted techniques exist for the detection of HPV in formalin-fixed paraffin-embedded samples. Particularly, in routine laboratories, molecular assays are still time-consuming and would require a high level of expertise. In this study, we investigated the possible use of a novel HPV tyramide-based chromogenic in situ hybridization (CISH) technology to locate HPV on tissue specimens. Then, we evaluate the potential usefulness of p16(INK4a)/Ki-67 double stain on histological samples, to identify cervical cells expressing HPV E6/E7 oncogenes. In our series, CISH showed a clear signal in 95.2% of the specimens and reached a sensitivity of 86.5%. CISH positivity always matched with HPV-DNA positivity, while 100% of cases with punctated signal joined with cervical intraepithelial neoplasia grade 2 or worse (CIN2+). p16/Ki67 immunohistochemistry gave an interpretable result in 100% of the cases. The use of dual stain significantly increased the agreement between pathologists, which reached 100%. Concordance between dual stain and E6/E7 mRNA test was 89%. In our series, both CISH and p16(INK4a)/Ki67 dual stain demonstrated high grade of performances. In particular, CISH would help to distinguish episomal from integrated HPV, in order to allow conclusions regarding the prognosis of the lesion, while p16(INK4a)/Ki67 dual stain approach would confer a high level of standardization to the diagnostic procedure.
尽管HPV-DNA检测和E6/E7 mRNA分析仍是目前用于确认细胞学标本中人乳头瘤病毒(HPV)感染的标准方法,但对于福尔马林固定石蜡包埋样本中的HPV检测,尚无普遍采用的技术。特别是在常规实验室中,分子检测仍然耗时,且需要高水平的专业知识。在本研究中,我们调查了一种基于酪胺的新型HPV显色原位杂交(CISH)技术在组织标本上定位HPV的可能性。然后,我们评估了p16(INK4a)/Ki-67双重染色在组织学样本上的潜在用途,以识别表达HPV E6/E7癌基因的宫颈细胞。在我们的系列研究中,CISH在95.2%的标本中显示出清晰的信号,灵敏度达到86.5%。CISH阳性始终与HPV-DNA阳性匹配,而100%点状信号的病例伴有2级或更高级别的宫颈上皮内瘤变(CIN2+)。p16/Ki67免疫组化在100%的病例中给出了可解释的结果。双重染色的使用显著提高了病理学家之间的一致性,达到了100%。双重染色与E6/E7 mRNA检测的一致性为89%。在我们的系列研究中,CISH和p16(INK4a)/Ki67双重染色均表现出较高的性能。特别是,CISH有助于区分游离型HPV和整合型HPV,以便对病变的预后得出结论,而p16(INK4a)/Ki67双重染色方法将使诊断程序具有高度的标准化。