Assessment of somatic mutations in urine and plasma of Wilms tumor patients

被引:11
作者
Kerekes Miguez, Ana Carolina [1 ]
de Figueiredo Barros, Bruna D. [1 ]
de Souza, Jorge E. S. [2 ]
Costa, Cecilia Maria L. [3 ]
Cunha, Isabela Werneck [4 ]
Barbosa, Paula Nicole Vieira P. [5 ]
Apezzato, Maria Lucia P. [6 ]
de Souza, Sandro J. [2 ,7 ,8 ]
Carraro, Dirce Maria [1 ,8 ]
机构
[1] AC Camargo Canc Ctr, Lab Genom & Mol Biol, Int Res Ctr CIPE, Sao Paulo, Brazil
[2] Univ Fed Rio Grande do Norte, Digital Metropolis Inst, Bioinformat Multidisciplinary Environm, Natal, RN, Brazil
[3] AC Camargo Canc Ctr, Pediat Dept, Sao Paulo, Brazil
[4] AC Camargo Canc Ctr, Anat Pathol Dept, Sao Paulo, Brazil
[5] AC Camargo Canc Ctr, Imaging Dept, Sao Paulo, Brazil
[6] AC Camargo Canc Ctr, Pediat Surg Dept, Sao Paulo, Brazil
[7] Univ Fed Rio Grande do Norte, Brain Inst, Natal, RN, Brazil
[8] Natl Inst Sci & Technol Oncogen & Therapeut Innov, Sao Paulo, Brazil
来源
CANCER MEDICINE | 2020年 / 9卷 / 16期
关键词
cancer genetics; liquid biopsy; pediatric cancer; Wilms tumor; GENETIC-HETEROGENEITY; CANCER-PATIENTS; BETA-CATENIN; DNA; LANDSCAPE; ORIGIN;
D O I
10.1002/cam4.3236
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Tumor DNA has been detected in body fluids of cancer patients. Somatic tumor mutations are being used as biomarkers in body fluids to monitor chemotherapy response as a minimally invasive tool. In this study, we evaluated the potential of tracking somatic mutations in free DNA of plasma and urine collected from Wilms tumor (WT) patients for monitoring treatment response. Wilms tumor is a pediatric renal tumor resulting from cell differentiation errors during nephrogenesis. Its mutational repertoire is not completely defined. Thus, for identifying somatic mutations from tumor tissue DNA, we screened matched tumor/leukocyte DNAs using either a panel containing 16 WT-associated genes or whole-exome sequencing (WES). The identified somatic tumor mutations were tracked in urine and plasma DNA collected before, during and after treatment. At least one somatic mutation was identified in five out of six WT tissue samples analyzed. Somatic mutations were detected in body fluids before treatment in all five patients (three patients in urine, three in plasma, and one in both body fluids). In all patients, a decrease of the variant allele fraction of somatic mutations was observed in body fluids during neoadjuvant chemotherapy. Interestingly, the persistence of somatic mutations in body fluids was in accordance with clinical parameters. For one patient who progressed to death, it persisted in high levels in serial body fluid samples during treatment. For three patients without disease progression, somatic mutations were not consistently detected in samples throughout monitoring. For one patient with bilateral disease, a somatic mutation was detected at low levels with no support of clinical manifestation. Our results demonstrated the potential of tracking somatic mutations in urine and plasma DNA as a minimally invasive tool for monitoring WT patients. Additional investigation is needed to check the clinical value of insistent somatic mutations in body fluids.
引用
收藏
页码:5948 / 5959
页数:12
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