Human papillomavirus in high- and low-risk areas of oesophageal squamous cell carcinoma in China.

Human papillomavirus in high- and low-risk areas of oesophageal squamous cell carcinoma in China.
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中国食管鳞状细胞癌的高风险区域中的人乳头瘤病毒。

DOI:
10.1038/sj.bjc.6603765
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发表时间:
2007-05-21
影响因子:
8.8
通讯作者:
Akiba, S
Akiba, S
中科院分区:
医学1区
文献类型:
--
作者:
Shuyama, K;Castillo, A;Aguayo, F;Sun, Q;Khan, N;Koriyama, C;Akiba, S

文献摘要

被引文献

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为了研究人乳头瘤病毒(HPV)在食管鳞状细胞癌(ESCC)发展中的潜在作用,我们使用SPF10引物进行PCR,或使用SPF10引物进行PCR,检测了从中国不同ESCC发病率的两个地区(即甘肃(n = 26)和山东(n = 33))收集的石蜡包埋的ESCC组织中HPV DNA的存在情况。 GP5+/GP6+引物结合Southern印迹杂交。 HPV基因型通过INNO-LiPA HPV基因分型试剂盒测定。甘肃的食管鳞癌发病率远高于山东的 17 例(65%),山东有 2 例 HPV 阳性(6%)。 HPV 阳性样本中分别检测到 79% 和 16% 的 HPV 基因型 16 和 18。实时 PCR 分析表明,所有 HPV-16 阳性样本中都存在整合形式的 HPV DNA,但其病毒载量估计仅为 <1-2 个拷贝细胞−1。我们无法通过免疫染色在任何 HPV-16 阳性样本中检测到 HPV 16/18 E6 蛋白表达。 p16INK4a 和 p53 表达均与 ESCC 中 HPV 的存在无关。似乎有必要进一步研究 HPV 在 ESCC 中可能的病因学作用。
To examine the potential roles of human papillomavirus (HPV) in oesophageal squamous cell carcinoma (ESCC) development, we examined the presence of HPV DNA in paraffin-embedded ESCC tissues collected from two areas with different ESCC incidence rates in China, that is, Gansu (n=26) and Shandong (n=33), using PCR with SPF10 primers, or PCR with GP5+/GP6+ primers combined with Southern blot hybridisation. HPV genotype was determined by the INNO-LiPA HPV genotyping kit. HPV DNA was detected in 17 cases (65%) in Gansu, where ESCC incidence is much higher than in Shandong, where HPV was positive in two samples (6%). HPV genotypes 16 and 18 were detected in 79 and 16% of HPV-positive samples, respectively. Real-time PCR analysis suggested the presence of integrated form of HPV DNA in all the HPV-16-positive samples, but its viral load was estimated to be only <1–2 copies cell−1. We could not detect HPV 16/18 E6 protein expression by immunostaining in any of the HPV-16-positive samples. Neither p16INK4a nor p53 expression was related to HPV presence in ESCCs. Further studies seem warranted to examine the possible aetiological roles of HPV in ESCC.