Mackintosh L J, de Koning M N C, Quint W G V, Ter Schegget J, Morgan I M, Herd R M, Campo M S
Division of Pathological Sciences, Institute of Comparative Medicine, University of Glasgow, Glasgow, UK.
Br J Dermatol. 2009 Jul;161(1):56-62. doi: 10.1111/j.1365-2133.2009.09146.x. Epub 2009 Mar 30.
Nonmelanoma skin cancer (NMSC) has been linked to cutaneous human papillomaviruses of the genus beta (betaPV).
We sought to assess the presence of betaPV in NMSC biopsies from a group of Scottish skin cancer patients, both immunocompetent (IC) patients and immunosuppressed (IS) organ transplant recipients.
One hundred and twenty-one paraffin-embedded skin tumours (27 actinic keratosis, 41 intraepidermal carcinoma, 53 squamous cell carcinoma) and 11 normal skin samples were analysed for the presence of betaPV by a polymerase chain reaction-reverse hybridization assay designed to detect the presence of the 25 known betaPV genotypes.
In IC patients, betaPV was detected in 30 of 59 (51%) tumours and two of 11 (18%) normal skin samples (P = 0.046). In IS patients, betaPV was found in 27 of 62 (44%) tumours; no normal skin samples were available for comparison. The most frequently found genotypes were HPV-24, HPV-15 and HPV-38. Of those tumours infected with betaPV, 28 of 57 (49%) were infected with more than one genotype (range 2-8). Tumours from IS patients were from a younger age group (mean age 57.4 years) than IC patients (mean age 73.8 years). Multiple infections were more common in tumours from IC patients (21 of 30; 70%) compared with those from IS patients (seven of 27; 26%) (P < 0.001). In the IC group, age did not appear to influence the distribution of single and multiple infections whereas in IS patients the proportion of multiple infections to single infections increased with age. There were no multiple infections in normal skin.
A wide spectrum of betaPV types was detected in our samples. Further characterization of betaPV in vivo is needed in order to determine the mechanisms by which the virus contributes to cutaneous carcinogenesis.
非黑色素瘤皮肤癌(NMSC)已与β属皮肤人乳头瘤病毒(betaPV)相关联。
我们试图评估一组苏格兰皮肤癌患者(包括免疫功能正常(IC)患者和免疫抑制(IS)器官移植受者)的NMSC活检样本中betaPV的存在情况。
采用聚合酶链反应-反向杂交分析法,检测121个石蜡包埋的皮肤肿瘤(27个光化性角化病、41个表皮内癌、53个鳞状细胞癌)和11个正常皮肤样本中25种已知betaPV基因型的存在情况。
在IC患者中,59个肿瘤中有30个(51%)检测到betaPV,11个正常皮肤样本中有2个(18%)检测到(P = 0.046)。在IS患者中,62个肿瘤中有27个(44%)检测到betaPV;无正常皮肤样本可供比较。最常发现的基因型是HPV-24、HPV-15和HPV-38。在感染betaPV的肿瘤中,57个中有28个(49%)感染了不止一种基因型(范围为2 - 8种)。IS患者的肿瘤来自较年轻的年龄组(平均年龄57.4岁),而IC患者的肿瘤平均年龄为73.8岁。与IS患者的肿瘤(27个中的7个;26%)相比,IC患者肿瘤中的多重感染更常见(30个中的21个;70%)(P < 0.001)。在IC组中,年龄似乎不影响单一感染和多重感染的分布,而在IS患者中,多重感染与单一感染的比例随年龄增加。正常皮肤中未发现多重感染。
我们的样本中检测到多种betaPV类型。为了确定病毒促进皮肤癌发生的机制,需要对体内的betaPV进行进一步表征。