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首页> 外文期刊>International Journal of Cancer =: Journal International du Cancer >Chromosomal profiles of high-grade cervical intraepithelial neoplasia relate to duration of preceding high-risk human papillomavirus infection
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Chromosomal profiles of high-grade cervical intraepithelial neoplasia relate to duration of preceding high-risk human papillomavirus infection

机译:高度宫颈上皮内瘤变的染色体特征与先前高危型人乳头瘤病毒感染的持续时间有关

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摘要

High-grade cervical intraepithelial neoplasia (CIN2/3) represents a heterogeneous disease both with respect to clinical behavior and chromosomal aberrations detected. We hypothesized that the extent of chromosomal aberrations reflects the duration of their existence. Chromosomal profiles were determined of CIN3 of women with a known 5-year history of high-risk human papillomavirus virus (hrHPV) infection, in which duration of prior hrHPV infection was considered a proxy for duration of CIN3 existence. Eleven women had a <5 year preceding hrHPV infection (CIN3<5yrPHI) and 24 had a PHI lasting ≤yen;5 years (CIN3≤yen;5yrPHI). For comparison, six CIN3 adjacent to squamous cell carcinomas (CIN3-SCC), the corresponding SCCs, and six CIN1 were included. Unsupervised hierarchical clustering analysis of the chromosomal profiles revealed two clusters. One was characterized by a low number of chromosomal aberrations and included all CIN1, 81.8% of CIN3<5yrPHI and 33.3% of CIN3≤yen;5yrPHI. Samples in the second cluster, displaying multiple aberrations, included 18.2% of CIN3<5yrPHI, 66.7% CIN3≤yen;5yrPHI, all except one CIN3-SCC and all SCCs. The number of genomic aberrations increased according to lesion grade and also with longer duration of PHI. The increase in aberrations in CIN3≤yen;5yrPHI compared to <5yrPHI was highly significant (p = 0.001), suggesting that CIN3≤yen;5yrPHI represent more severe lesions. In conclusion, longer duration of preceding hrHPV infection is associated with an increased number of chromosomal aberrations. Hence, CIN3 with a longer duration of existence are likely more prone to have an increased short-term risk of cervical cancer.
机译:就临床行为和检测到的染色体畸变而言,高级宫颈上皮内瘤变(CIN2 / 3)代表了一种异质性疾病。我们假设染色体畸变的程度反映了其存在的持续时间。确定具有高危人类乳头瘤病毒(hrHPV)感染5年病史的女性CIN3的染色体概况,其中先前hrHPV感染的持续时间被视为CIN3存在持续时间的代表。 11名女性hrHPV感染前<5年(CIN3 <5yrPHI),24名PHI持续≤yen; 5年(CIN3≤yen; 5yrPHI)。为了进行比较,包括与鳞状细胞癌相邻的六个CIN3(CIN3-SCC),相应的SCC和六个CIN1。染色体图谱的无监督分层聚类分析显示了两个聚类。一个以低的染色体畸变为特征,包括所有CIN1,CIN3 <5yrPHI的81.8%和CIN3≤yen; 5yrPHI的33.3%。在第二个群集中,显示多个像差的样本包括18.2%的CIN3 <5yrPHI,66.7%CIN3≤yen; 5yrPHI,除了一个CIN3-SCC和所有SCC以外。基因组畸变的数目根据病变等级增加,并且随着PHI持续时间的延长而增加。与<5yrPHI相比,CIN3≤yen; 5yrPHI的像差增加非常显着(p = 0.001),表明CIN3≤yen; 5yrPHI代表了更严重的病变。总之,以前的hrHPV感染持续时间越长,染色体畸变的数量越多。因此,存在时间更长的CIN3可能更容易增加子宫颈癌的短期风险。

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