Evidence map›Paper›PMID 30143682›Full record

ArticleScientific reports2018

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

Sungsik Kim, Soochi Kim, Jinhyun Kim, Boyun Kim, Se Ik Kim, Min A Kim, Sunghoon Kwon, Yong Sang Song

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 31% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 22 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 5 countries.

Sungsik KimDepartment of Electrical and Computer Engineering, Seoul National University, Seoul, 08826, Republic of Korea.
Soochi KimSeoul National University Hospital Biomedical Research Institute, Seoul National University Hospital, Seoul, 03080, Republic of Korea.
Jinhyun KimDepartment of Electrical and Computer Engineering, Seoul National University, Seoul, 08826, Republic of Korea.
Boyun KimDepartment of Anesthesiology, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX, USA.ORCID 0000-0002-4973-6647
Se Ik KimDepartment of Obstetrics and Gynecology, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea.ORCID 0000-0002-9790-6735
Min A KimDepartment of Pathology, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea.
Sunghoon KwonDepartment of Electrical and Computer Engineering, Seoul National University, Seoul, 08826, Republic of Korea. skwon@snu.ac.kr.
Yong Sang SongCancer Research Institute, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea. yssong@snu.ac.kr.
Seoul National University · KRThe University of Texas Health Science Center at Houston · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

AdultAscitesCarcinoma, Ovarian EpithelialDNA Copy Number VariationsExome SequencingFemaleGene FrequencyGenome, HumanGenomicsHumansPhylogenyPolymorphism, Single NucleotideSpheroids, Cellular

Identifiers

PMID30143682
PMCPMC6109089
OpenAlexW2888198404

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.