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

被引:18
|
作者
Kim, Sungsik [1 ,4 ]
Kim, Soochi [3 ,5 ]
Kim, Jinhyun [1 ]
Kim, Boyun [6 ]
Kim, Se Ik [7 ]
Kim, Min A. [8 ]
Kwon, Sunghoon [1 ,2 ,3 ]
Song, Yong Sang [5 ,7 ,9 ,10 ]
机构
[1] Seoul Natl Univ, Dept Elect & Comp Engn, Seoul 08826, South Korea
[2] Seoul Natl Univ, Inst Entrepreneurial BioConvergence, Seoul 08826, South Korea
[3] Seoul Natl Univ Hosp, Biomed Res Inst, Seoul 03080, South Korea
[4] Seoul Natl Univ, Interdisciplinary Program Bioengn, Seoul 08826, South Korea
[5] Seoul Natl Univ, Canc Res Inst, Coll Med, Seoul 03080, South Korea
[6] Univ Texas Hlth Sci Ctr Houston, Dept Anesthesiol, McGovern Med Sch, Houston, TX 77030 USA
[7] Seoul Natl Univ, Dept Obstet & Gynecol, Coll Med, Seoul 03080, South Korea
[8] Seoul Natl Univ, Dept Pathol, Coll Med, Seoul 03080, South Korea
[9] Seoul Natl Univ, Interdisciplinary Program Canc Biol, Coll Med, Seoul 03080, South Korea
[10] Seoul Natl Univ, Biomodulat Dept Agr Biotechnol, Seoul 03080, South Korea
来源
SCIENTIFIC REPORTS | 2018年 / 8卷
关键词
GRADE SEROUS CARCINOMA; TRANSCOELOMIC METASTASIS; SOMATIC MUTATION; CANCER-CELLS; OVARIAN; HETEROGENEITY; EPIDEMIOLOGY; PATTERNS; BREAST; TP53;
D O I
10.1038/s41598-018-31097-y
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
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.
引用
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页数:11
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