Evaluating Tumor Evolution via Genomic Profiling of Individual Tumor Spheroids in a Malignant Ascites

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作者
Sungsik Kim
Soochi Kim
Jinhyun Kim
Boyun Kim
Se Ik Kim
Min A. Kim
Sunghoon Kwon
Yong Sang Song
机构
[1] Seoul National University,Department of Electrical and Computer Engineering
[2] Seoul National University,Institutes of Entrepreneurial BioConvergence
[3] Seoul National University Hospital Biomedical Research Institute,Interdisciplinary Program for Bioengineering
[4] Seoul National University Hospital,Cancer Research Institute
[5] Seoul National University,Department of Anesthesiology, McGovern Medical School
[6] Seoul National University College of Medicine,Department of Obstetrics and Gynecology
[7] The University of Texas Health Science Center at Houston,Department of Pathology
[8] Seoul National University College of Medicine,Interdisciplinary Program in Cancer Biology
[9] Seoul National University College of Medicine,Biomodulation Department of Agricultural Biotechnology
[10] Seoul National University College of Medicine,undefined
[11] Seoul National University,undefined
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Tumor Spheroids; Malignant Ascites; Single Nucleotide Variants (SNVs); Copy Number Alterations (CNAs); Epithelial Ovarian Cancer;
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摘要
Epithelial ovarian cancer (EOC) is a silent but mostly lethal gynecologic malignancy. Most patients present with malignant ascites and peritoneal seeding at diagnosis. In the present study, we used a laser-aided isolation technique to investigate the clonal relationship between the primary tumor and tumor spheroids found in the malignant ascites of an EOC patient. Somatic alteration profiles of ovarian cancer-related genes were determined for eight spatially separated samples from primary ovarian tumor tissues and ten tumor spheroids from the malignant ascites using next-generation sequencing. We observed high levels of intra-tumor heterogeneity (ITH) in copy number alterations (CNAs) and single-nucleotide variants (SNVs) in the primary tumor and the tumor spheroids. As a result, we discovered that tumor cells in the primary tissues and the ascites were genetically different lineages. We categorized the CNAs and SNVs into clonal and subclonal alterations according to their distribution among the samples. Also, we identified focal amplifications and deletions in the analyzed samples. For SNVs, a total of 171 somatic mutations were observed, among which 66 were clonal mutations present in both the primary tumor and the ascites, and 61 and 44 of the SNVs were subclonal mutations present in only the primary tumor or the ascites, respectively. Based on the somatic alteration profiles, we constructed phylogenetic trees and inferred the evolutionary history of tumor cells in the patient. The phylogenetic trees constructed using the CNAs and SNVs showed that two branches of the tumor cells diverged early from an ancestral tumor clone during an early metastasis step in the peritoneal cavity. Our data support the monophyletic spread of tumor spheroids in malignant ascites.
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