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新型多瘤病毒(MCPyV)不会影响 MCC 的临床病程。

The new polyomavirus (MCPyV) does not affect the clinical course in MCCs.

机构信息

Department for Cranio- and Maxillofacial Surgery, Heinrich-Heine-University, Düsseldorf, Germany.

出版信息

Int J Oral Maxillofac Surg. 2010 Nov;39(11):1086-90. doi: 10.1016/j.ijom.2010.06.024. Epub 2010 Aug 3.

Abstract

Since 2008, a new polyomavirus (MCPyV) in Merkel cell carcinomas (MCC) has been described, but little is known about its impact on the clinical course. The purpose of this study was to determine the presence of MCPyV in a large sample and to correlate the results with the clinical course of the disease. 59 samples from 44 patients were analysed for the presence of MCPyV using the primers LT3, VP1 and LT1. The clinical records of these patients were evaluated and correlated with the presence of MCPyV. 58% of specimens were positive for MCPyV. Of these, LT3 was positive in 53%, VP1 in 37% and LT1 in 10%. 57% of primary tumours and 53% of metastases were positive for LT3; the numbers for VP1 and LT1 were lower. There was no correlation between the detection of MCPyV in the primary tumour and the appearance of metastases. The survival time was statistically independent from the presence of MCPyV. There is a striking occurrence of MCPyV in MCC, but whether it affects the clinical course remains unclear.

摘要

自 2008 年以来,一种新的多瘤病毒(MCPyV)已在 Merkel 细胞癌(MCC)中被描述,但人们对其对临床病程的影响知之甚少。本研究的目的是确定在大量样本中是否存在 MCPyV,并将结果与疾病的临床病程相关联。使用 LT3、VP1 和 LT1 引物分析了来自 44 名患者的 59 个样本中 MCPyV 的存在情况。评估了这些患者的临床记录,并将其与 MCPyV 的存在相关联。58%的标本呈 MCPyV 阳性。其中,LT3 阳性率为 53%,VP1 阳性率为 37%,LT1 阳性率为 10%。57%的原发肿瘤和 53%的转移灶 LT3 阳性;VP1 和 LT1 的阳性率较低。原发肿瘤中 MCPyV 的检测与转移灶的出现之间无相关性。生存时间与 MCPyV 的存在无关。MCC 中 MCPyV 的发生率显著,但它是否影响临床病程尚不清楚。

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