美国食品和药物管理局批准的分子测试用于确定导致宫颈癌的人乳头瘤病毒(hpv)感染

A. Cali, Rukiye Aslan, C. Çelik, A. Alim
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摘要

人乳头瘤病毒(HPV)是一种非包膜性传播病毒,具有二十面体对称和双链环状DNA。其基因组约8kb大小,编码早期基因(E1-8)和两个晚期结构衣壳基因(L1和L2)。在参与病毒发病的基因中,常见的有L1、E6、E7基因。E6和E7病毒基因在细胞凋亡抑制、病毒传播、鳞状上皮内病变(SIL)的发展、细胞永生化、肿瘤转化和侵袭性癌症中发挥重要作用。宫颈癌和HPV感染之间的关系的证明增加了人们对这一主题的兴趣,并对宫颈癌高危人群(HR-HPV)中的一些HPV基因型进行了分类。已经开发了许多商业分子测试,用于识别HPV基因型,涉及不同的方法。美国食品和药物管理局(FDA)批准的HPV分子检测包括Hybrid Capture®2 (HC2)、Cervista™、cobas®、Aptima®和BD Onclarity™。本文回顾了五种fda批准的检测方法、局限性和共性。HC2和Cervista测试使用非基于pcr的信号扩增方法,而cobas®和BD Onclarity™测试使用基于pcr的靶扩增方法。另一方面,Aptima®检测使用mRNA转录介导扩增(TMA)方法。每一种用于HPV诊断和随访的方法都有其优点和缺点。这些HPV分子检测具有很高的敏感性和特异性。它们也比细胞学方法更加自动化和可重复。除了这些优点之外,也有一些限制。由于这些限制,分子检测并不比细胞学检测更完美。这种情况表明,这些测试不应单独用于评估HPV感染和癌症鉴定。相反,HPV检测结果应与细胞学或活检结果相关。
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FDA-APPROVED MOLECULAR TESTS USED TO DEFINE HUMAN PAPILLOMAVIRUS (HPV) INFECTIONS WHICH CAUSE CERVIX CANCER
Human papillomavirus (HPV) is a non-enveloped, commonly sexually transmitted virus with icosahedral symmetry and double-stranded circular DNA. Its genome, which is about 8 kb in size, encodes early genes (E1-8) and two late structural capsid genes (L1 and L2). Among the genes that play a role in viral pathogenesis, L1, E6, and E7 genes frequently exist. The E6 and E7 viral genes have a significant role in apoptosis inhibition, viral spread, development of squamous intraepithelial lesion (SIL), cell immortalization, neoplastic transformation, and invasive cancer. Demonstration of the relationship between cervical cancer and HPV infections has led to increased interest in this subject and the classification of some HPV genotypes in the high-risk group (HR-HPV) for cervical cancer. Numerous commercial molecular tests have been developed for the identification of HPV genotypes involving different approaches. HPV molecular tests approved by the US Food and Drug Administration (FDA) include Hybrid Capture® 2 (HC2), Cervista™, cobas®, Aptima®, and BD Onclarity™. This article reviews the methodologies, limitations, and commonalities of five FDA-approved tests. The HC2 and Cervista™ tests use non-PCR-based signal amplification methods, while the cobas® and BD Onclarity™ tests use PCR-based target amplification methods. On the other hand, the Aptima® test uses the mRNA transcriptional mediated amplification (TMA) method. Each of these methods used in the diagnosis and follow-up of HPV has its strengths and weaknesses. These HPV molecular tests have high sensitivity and specificity. They are also more automated and repeatable than cytological methods. In addition to these advantages, there are also several limitations. Because of these limitations, molecular tests are no more perfect than cytological tests. This situation shows that these tests should not be used alone in the evaluation of HPV infections and cancer identification. On the contrary, HPV test results should be correlated with cytology or biopsy findings.
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