Andea Aleodor A, Patel Raj, Ponnazhagan Selvarangan, Isayeva Tatyana, Kumar Sanjay, Siegal Gene P
Department of Pathology, University of Michigan, Ann Arbor, MI, USA;
Rom J Morphol Embryol. 2014;55(3 Suppl):1057-62.
Merkel cell carcinoma (MCC) is a rare, but highly aggressive primary cutaneous malignancy, showing neuroendocrine differentiation. In 2008, a novel member of the polyomavirus family, named Merkel cell polyomavirus (MCPyV) was identified in the genome of MCC tumors raising the possibility of an involvement in its pathogenesis. Due to the rarity of this tumor and current pathology practices, the most readily available tissue is archival formalin-fixed, paraffin-embedded (FFPE) material. In this study, we evaluated the presence of MCPyV in FFPE tissue and correlated its presence with tumor progression. Representative FFPE specimens from 18 tumors belonging to 14 patients with a diagnosis of MCC spanning the period from 2003 to 2008 were retrieved. Following DNA extraction, we performed PCR amplification and sequencing with four different MCPyV-specific primer pairs mapping within the T antigen and VP1 region. Overall, we detected MCPyV amplicons in 8/18 (44.4%) analyzed tumors from 7/14 (50%) cases. Two-year survival rate and median survival for the MCPyV-positive MCCs were 48% and 22.5 months, respectively and for the negative ones 69% and 51.3 months, respectively; however, the difference did not reach statistical significance (p=0.8). There was no significant correlation between the presence of the virus and the stage at presentation; however, tumors in the head and neck area had a lower frequency of viral positivity compared to those arising in the extremities suggesting a MCPyV-independent oncogenetic pathway perhaps, dependent on UV exposure, in a subset of these cases.
默克尔细胞癌(MCC)是一种罕见但侵袭性很强的原发性皮肤恶性肿瘤,具有神经内分泌分化特征。2008年,在MCC肿瘤基因组中发现了多瘤病毒家族的一个新成员,称为默克尔细胞多瘤病毒(MCPyV),这增加了其参与肿瘤发病机制的可能性。由于这种肿瘤罕见且当前病理实践中,最容易获得的组织是存档的福尔马林固定、石蜡包埋(FFPE)材料。在本研究中,我们评估了FFPE组织中MCPyV的存在情况,并将其存在与肿瘤进展相关联。检索了2003年至2008年期间14例诊断为MCC的患者的18个肿瘤的代表性FFPE标本。DNA提取后,我们使用在T抗原和VP1区域内定位的四对不同的MCPyV特异性引物对进行PCR扩增和测序。总体而言,我们在14例(50%)病例中的18个分析肿瘤中的8个(44.4%)中检测到MCPyV扩增子。MCPyV阳性MCC的两年生存率和中位生存期分别为48%和22.5个月,阴性者分别为69%和51.3个月;然而,差异未达到统计学意义(p = 0.8)。病毒的存在与就诊时的分期之间没有显著相关性;然而,与四肢发生的肿瘤相比,头颈部区域的肿瘤病毒阳性频率较低,这表明在这些病例的一个亚组中,可能存在一条不依赖MCPyV的致癌途径,也许依赖于紫外线暴露。