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阴茎癌中的DNA拷贝数畸变与人乳头瘤病毒状态。临床病理相关性及潜在驱动基因。

DNA Copy Number Aberrations, and Human Papillomavirus Status in Penile Carcinoma. Clinico-Pathological Correlations and Potential Driver Genes.

作者信息

La-Touche Susannah, Lemetre Christophe, Lambros Maryou, Stankiewicz Elzbieta, Ng Charlotte K Y, Weigelt Britta, Rajab Ramzi, Tinwell Brendan, Corbishley Cathy, Watkin Nick, Berney Dan, Reis-Filho Jorge S

机构信息

Bart's Cancer Institute, Centre for Molecular Oncology, Queen Mary University of London, John Vane Science Centre, Charterhouse square, London, United Kingdom.

Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, New York, United States of America.

出版信息

PLoS One. 2016 Feb 22;11(2):e0146740. doi: 10.1371/journal.pone.0146740. eCollection 2016.

Abstract

Penile squamous cell carcinoma is a rare disease, in which somatic genetic aberrations have yet to be characterized. We hypothesized that gene copy aberrations might correlate with human papillomavirus status and clinico-pathological features. We sought to determine the spectrum of gene copy number aberrations in a large series of PSCCs and to define their correlations with human papillomavirus, histopathological subtype, and tumor grade, stage and lymph node status. Seventy formalin-fixed, paraffin embedded penile squamous cell carcinomas were centrally reviewed by expert uropathologists. DNA was extracted from micro-dissected samples, subjected to PCR-based human papillomavirus assessment and genotyping (INNO-LiPA human papillomavirus Genotyping Extra Assay) and microarray-based comparative genomic hybridization using a 32K Bacterial Artificial Chromosome array platform. Sixty-four samples yielded interpretable results. Recurrent gains were observed in chromosomes 1p13.3-q44 (88%), 3p12.3-q29 (86%), 5p15.33-p11 (67%) and 8p12-q24.3 (84%). Amplifications of 5p15.33-p11 and 11p14.1-p12 were found in seven (11%) and four (6%) cases, respectively. Losses were observed in chromosomes 2q33-q37.3 (86%), 3p26.3-q11.1 (83%) and 11q12.2-q25 (81%). Although many losses and gains were similar throughout the cohort, there were small significant differences observed at specific loci, between human papillomavirus positive and negative tumors, between tumor types, and tumor grade and nodal status. These results demonstrate that despite the diversity of genetic aberrations in penile squamous cell carcinomas, there are significant correlations between the clinico-pathological data and the genetic changes that may play a role in disease natural history and progression and highlight potential driver genes, which may feature in molecular pathways for existing therapeutic agents.

摘要

阴茎鳞状细胞癌是一种罕见疾病,其体细胞遗传畸变尚未得到明确描述。我们推测基因拷贝畸变可能与人乳头瘤病毒状态及临床病理特征相关。我们试图确定大量阴茎鳞状细胞癌(PSCC)中基因拷贝数畸变的谱型,并明确其与人乳头瘤病毒、组织病理学亚型、肿瘤分级、分期及淋巴结状态的相关性。70例经福尔马林固定、石蜡包埋的阴茎鳞状细胞癌由泌尿病理专家进行集中复查。从显微切割样本中提取DNA,进行基于PCR的人乳头瘤病毒评估和基因分型(INNO-LiPA人乳头瘤病毒基因分型额外检测),并使用32K细菌人工染色体阵列平台进行基于微阵列的比较基因组杂交。64个样本产生了可解释的结果。在染色体1p13.3-q44(88%)、3p12.3-q29(86%)、5p15.33-p11(67%)和8p12-q24.3(84%)观察到反复出现的增益。5p15.33-p11和11p14.1-p12的扩增分别在7例(11%)和4例(6%)病例中发现。在染色体2q33-q37.3(86%)、3p26.3-q11.1(83%)和11q12.2-q25(81%)观察到缺失。尽管整个队列中许多缺失和增益相似,但在特定基因座、人乳头瘤病毒阳性和阴性肿瘤之间、肿瘤类型之间以及肿瘤分级和淋巴结状态之间观察到了微小的显著差异。这些结果表明,尽管阴茎鳞状细胞癌的遗传畸变具有多样性,但临床病理数据与可能在疾病自然史和进展中起作用的遗传变化之间存在显著相关性,并突出了潜在的驱动基因,这些基因可能存在于现有治疗药物的分子途径中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e998/4763861/9ad8510f4f59/pone.0146740.g001.jpg

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