Pientong Chamsai, Ekalaksananan Tipaya, Kongyingyoes Bunkerd, Kritpetcharat Onanong, Swadpanich Ussanee, Pengsa Prasit, Yuenyao Pissamai
Department of Microbiology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
Diagn Cytopathol. 2004 Oct;31(4):235-42. doi: 10.1002/dc.20122.
The p16INK4a protein is immunocytochemically detected in liquid-based (LB) specimens as a diagnostic marker of cervical dysplasia and neoplasia. Its up-regulation is promoted by high-risk human papillomavirus (HR-HPV) infection. We aimed to detect p16INK4a on conventional Papanicolaou (Pap) test (CPT) slides and to determine the relationship between its overexpression and HR-HPV infection. CPT and LB Pap test (LBPT) slides (165 samples of each) were examined by immunocytochemical staining for p16INK4a. After polymerase chain reaction (PCR), HPV-DNA was genotyped by dot blot hybridization. The CPT slides displayed more numerous dispersed squamous cells and LBPT slides had a clearer background. Positive p16INK4a on CPT occurred in 0% (0/30), 52.5% (21/40), 54.3% (19/35), 100% (30/30), and 100% (30/30) in normal, atypical squamous cells of undetermined significance (ASCUS), low-grade squamous intraepithelial lesions (LSILs), high-grade SILs (HSILs), and squamous cell carcinomas (SCCs) cases, respectively. LBPT slides showed comparable results but were less sensitive. HPV-DNA was detected in 86.7, 70, 45, 57.14, and 10% in SCCs, HSILs, ASCUS, LSILs, and normal cervical cells, respectively. Because HR-HPV was identified in all HPV+ samples of high-grade dysplasia (HSILs and SCCs) and all positive p16INK4a samples infected with HR-HPV, the association of p16INK4a overexpression with HR-HPV infection was confirmed. This study suggests that immunocytochemical staining of p16INK4a on CPT slides is convenient and cost-effective for cervical cancer screening by the detection of dysplastic cells infected with HR-HPV.
p16INK4a蛋白可通过免疫细胞化学方法在液基(LB)标本中检测到,作为宫颈发育异常和肿瘤形成的诊断标志物。其上调由高危型人乳头瘤病毒(HR-HPV)感染促进。我们旨在检测传统巴氏试验(CPT)玻片上的p16INK4a,并确定其过表达与HR-HPV感染之间的关系。对CPT和LB巴氏试验(LBPT)玻片(各165份样本)进行p16INK4a免疫细胞化学染色检查。聚合酶链反应(PCR)后,通过斑点杂交对HPV-DNA进行基因分型。CPT玻片上的散在鳞状细胞更多,LBPT玻片背景更清晰。CPT上p16INK4a阳性在正常、意义不明确的非典型鳞状细胞(ASCUS)、低级别鳞状上皮内病变(LSIL)、高级别鳞状上皮内病变(HSIL)和鳞状细胞癌(SCC)病例中的发生率分别为0%(0/30)、52.5%(21/40)、54.3%(19/35)、100%(30/30)和100%(30/30)。LBPT玻片显示了类似结果,但敏感性较低。HPV-DNA在SCC、HSIL、ASCUS、LSIL和正常宫颈细胞中的检出率分别为86.7%、70%、45%、57.14%和10%。由于在所有高级别发育异常(HSIL和SCC)的HPV阳性样本以及所有感染HR-HPV的p16INK4a阳性样本中均鉴定出HR-HPV,因此证实了p16INK4a过表达与HR-HPV感染之间的关联。本研究表明,通过检测感染HR-HPV的发育异常细胞,CPT玻片上p16INK4a的免疫细胞化学染色对于宫颈癌筛查既方便又具有成本效益。