Bioinformatics Core, University of Michigan, Ann Arbor, Michigan.
Department of Pathology, University of Michigan, Ann Arbor, Michigan.
Clin Cancer Res. 2018 May 1;24(9):2214-2224. doi: 10.1158/1078-0432.CCR-17-1425. Epub 2017 Dec 4.
Recent studies have highlighted the existence of subclones in tumors. Lymph nodes are generally the first location of metastasis for most solid epithelial tumors, including colorectal cancer. We sought to understand the genetic origin of lymph node metastasis in colorectal cancer by evaluating the relationship between colorectal cancer subclones present in primary tumors and lymph nodes. A total of 33 samples from seven colorectal cancers, including two or three spatially disparate regions from each primary tumor and one to four matched lymph nodes for each tumor, underwent next-generation whole-exome DNA sequencing, Affymetrix OncoScan SNP arrays, and targeted deep confirmatory sequencing. We performed mapping between SNPs and copy number events from the primary tumor and matched lymph node samples, allowing us to profile heterogeneity and the mutational origin of lymph node metastases. The computational method PyClone was used to define subclones within each tumor. The method Clonality Inference in Tumors Using Phylogeny (CITUP) was subsequently used to infer phylogenetic relationships among subclones. We found that there was substantial heterogeneity in mutations and copy number changes among all samples from any given patient. For each patient, the primary tumor regions and matched lymph node metastases were each polyclonal, and the clonal populations differed from one lymph node to another. In some patients, the cancer cell populations in a given lymph node originated from multiple distinct regions of a tumor. Our data support a model of lymph node metastatic spread in colorectal cancer whereby metastases originate from multiple waves of seeding from the primary tumor over time. .
最近的研究强调了肿瘤中存在亚克隆的现象。淋巴结通常是大多数实体上皮肿瘤(包括结直肠癌)转移的第一站。我们通过评估原发肿瘤和淋巴结中存在的结直肠癌亚克隆之间的关系,试图了解结直肠癌淋巴结转移的遗传起源。总共对来自 7 例结直肠癌的 33 个样本进行了下一代全外显子 DNA 测序、Affymetrix OncoScan SNP 阵列和靶向深度确认测序,包括每个原发肿瘤的两个或三个空间上不同的区域以及每个肿瘤的一个到四个匹配的淋巴结。我们对来自原发肿瘤和匹配淋巴结样本的 SNP 和拷贝数事件进行了映射,从而能够对异质性和淋巴结转移的突变起源进行分析。PyClone 计算方法用于定义每个肿瘤内的亚克隆。随后使用基于系统发生的肿瘤克隆推断方法(CITUP)推断亚克隆之间的系统发生关系。我们发现,任何给定患者的所有样本中,突变和拷贝数变化都存在很大的异质性。对于每个患者,原发肿瘤区域和匹配的淋巴结转移均为多克隆,并且克隆群体彼此不同。在一些患者中,特定淋巴结中的癌细胞群体源自肿瘤的多个不同区域。我们的数据支持了结直肠癌中淋巴结转移扩散的模型,即转移是随着时间的推移,原发肿瘤中多次播种的结果。