Head and neck cancer of unknown primary: unveiling primary tumor sites through machine learning on DNA methylation profiles.

IF 4.8 2区 医学 Q1 GENETICS & HEREDITY
Leonhard Stark, Atsuko Kasajima, Fabian Stögbauer, Benedikt Schmidl, Jakob Rinecker, Katharina Holzmann, Sarah Färber, Nicole Pfarr, Katja Steiger, Barbara Wollenberg, Jürgen Ruland, Christof Winter, Markus Wirth
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Abstract

Background: The unknown tissue of origin in head and neck cancer of unknown primary (hnCUP) leads to invasive diagnostic procedures and unspecific and potentially inefficient treatment options for patients. The most common histologic subtype, squamous cell carcinoma, can stem from various tumor primary sites, including the oral cavity, oropharynx, larynx, head and neck skin, lungs, and esophagus. DNA methylation profiles are highly tissue-specific and have been successfully used to classify tissue origin. We therefore developed a support vector machine (SVM) classifier trained with publicly available DNA methylation profiles of commonly cervically metastasizing squamous cell carcinomas (n = 1103) in order to identify the primary tissue of origin of our own cohort of squamous cell hnCUP patient's samples (n = 28). Methylation analysis was performed with Infinium MethylationEPIC v1.0 BeadChip by Illumina.

Results: The SVM algorithm achieved the highest overall accuracy of tested classifiers, with 87%. Squamous cell hnCUP samples on DNA methylation level resembled squamous cell carcinomas commonly metastasizing into cervical lymph nodes. The most frequently predicted cancer localization was the oral cavity in 11 cases (39%), followed by the oropharynx and larynx (both 7, 25%), skin (2, 7%), and esophagus (1, 4%). These frequencies concord with the expected distribution of lymph node metastases in epidemiological studies.

Conclusions: On DNA methylation level, hnCUP is comparable to primary tumor tissue cancer types that commonly metastasize to cervical lymph nodes. Our SVM-based classifier can accurately predict these cancers' tissues of origin and could significantly reduce the invasiveness of hnCUP diagnostics and enable a more precise therapy after clinical validation.

原发灶不明的头颈部癌症:通过对 DNA 甲基化图谱的机器学习揭示原发肿瘤部位。
背景:原发部位不明的头颈部癌症(hnCUP)的原发组织不明,导致诊断程序繁琐,患者无法选择特异性治疗方案,而且治疗效果可能不佳。最常见的组织学亚型--鳞状细胞癌可能来自不同的肿瘤原发部位,包括口腔、口咽、喉、头颈部皮肤、肺和食道。DNA 甲基化图谱具有高度的组织特异性,已成功用于组织来源的分类。因此,我们开发了一种支持向量机(SVM)分类器,该分类器利用公开的常见颈部转移鳞状细胞癌(n = 1103)DNA甲基化图谱进行训练,以确定我们自己的鳞状细胞hnCUP患者样本群(n = 28)的原发组织。甲基化分析是通过 Illumina 的 Infinium MethylationEPIC v1.0 BeadChip 进行的:结果:在测试的分类器中,SVM 算法的总体准确率最高,达到 87%。鳞状细胞 hnCUP 样本的 DNA 甲基化水平与通常转移到宫颈淋巴结的鳞状细胞癌相似。最常预测的癌症部位是口腔(11 例,占 39%),其次是口咽和喉部(均为 7 例,占 25%)、皮肤(2 例,占 7%)和食道(1 例,占 4%)。这些频率与流行病学研究中预期的淋巴结转移分布一致:结论:在DNA甲基化水平上,hnCUP与常转移至宫颈淋巴结的原发肿瘤组织癌症类型相当。我们基于 SVM 的分类器能准确预测这些癌症的原发组织,可大大降低 hnCUP 诊断的侵入性,并在临床验证后提供更精确的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
自引率
5.30%
发文量
150
期刊介绍: Clinical Epigenetics, the official journal of the Clinical Epigenetics Society, is an open access, peer-reviewed journal that encompasses all aspects of epigenetic principles and mechanisms in relation to human disease, diagnosis and therapy. Clinical trials and research in disease model organisms are particularly welcome.
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