Cargando…
Molecular analysis of circulating tumor DNA from breast cancer patients before and after surgery and following adjuvant chemotherapy
The primary aim of the present study is to provide a complex molecular profile of tumors using liquid biopsy and to monitor profile changes over time in association with surgery and administered adjuvant therapy. Our secondary aim was to compare the liquid biopsy profile with the tissue biopsy and a...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7403808/ https://www.ncbi.nlm.nih.gov/pubmed/32765873 http://dx.doi.org/10.3892/mco.2020.2096 |
_version_ | 1783567014731710464 |
---|---|
author | Zelinova, Katarina Jagelkova, Marianna Laucekova, Zuzana Bobrovska, Martina Dankova, Zuzana Grendar, Marian Dokus, Karol |
author_facet | Zelinova, Katarina Jagelkova, Marianna Laucekova, Zuzana Bobrovska, Martina Dankova, Zuzana Grendar, Marian Dokus, Karol |
author_sort | Zelinova, Katarina |
collection | PubMed |
description | The primary aim of the present study is to provide a complex molecular profile of tumors using liquid biopsy and to monitor profile changes over time in association with surgery and administered adjuvant therapy. Our secondary aim was to compare the liquid biopsy profile with the tissue biopsy and assess concordance. A total of 27 samples of circulating tumor DNA (ctDNA) collected from 9 breast cancer patients at three different time points and their matched formalin-fixed and paraffin-embedded (FFPE) samples of primary tumor were analyzed with targeted next-generation sequencing. Somatic pathogenic variants were detected before surgery in samples from 5 patients (55.6%). The most frequently mutated genes were phosphatase and tensin homolog (4/9, 44.4%) and tumor protein 53 (4/9, 44.4%). Serial sampling of ctDNA enabled the detection of more variants compared with single-time tissue primary tumor biopsy. There were 17 ctDNA variants across all samples, but only 6 FFPE variants across all patients. In addition, the concordance between ctDNA and FFPE DNA was determined in only 1 patient, and this was connected with higher variant allele frequency. The findings of the present study suggest that liquid biopsy and tissue biopsy may be used as complementary analyses to adequately capture all tumor variants. |
format | Online Article Text |
id | pubmed-7403808 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-74038082020-08-05 Molecular analysis of circulating tumor DNA from breast cancer patients before and after surgery and following adjuvant chemotherapy Zelinova, Katarina Jagelkova, Marianna Laucekova, Zuzana Bobrovska, Martina Dankova, Zuzana Grendar, Marian Dokus, Karol Mol Clin Oncol Articles The primary aim of the present study is to provide a complex molecular profile of tumors using liquid biopsy and to monitor profile changes over time in association with surgery and administered adjuvant therapy. Our secondary aim was to compare the liquid biopsy profile with the tissue biopsy and assess concordance. A total of 27 samples of circulating tumor DNA (ctDNA) collected from 9 breast cancer patients at three different time points and their matched formalin-fixed and paraffin-embedded (FFPE) samples of primary tumor were analyzed with targeted next-generation sequencing. Somatic pathogenic variants were detected before surgery in samples from 5 patients (55.6%). The most frequently mutated genes were phosphatase and tensin homolog (4/9, 44.4%) and tumor protein 53 (4/9, 44.4%). Serial sampling of ctDNA enabled the detection of more variants compared with single-time tissue primary tumor biopsy. There were 17 ctDNA variants across all samples, but only 6 FFPE variants across all patients. In addition, the concordance between ctDNA and FFPE DNA was determined in only 1 patient, and this was connected with higher variant allele frequency. The findings of the present study suggest that liquid biopsy and tissue biopsy may be used as complementary analyses to adequately capture all tumor variants. D.A. Spandidos 2020-10 2020-07-20 /pmc/articles/PMC7403808/ /pubmed/32765873 http://dx.doi.org/10.3892/mco.2020.2096 Text en Copyright: © Zelinova et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Zelinova, Katarina Jagelkova, Marianna Laucekova, Zuzana Bobrovska, Martina Dankova, Zuzana Grendar, Marian Dokus, Karol Molecular analysis of circulating tumor DNA from breast cancer patients before and after surgery and following adjuvant chemotherapy |
title | Molecular analysis of circulating tumor DNA from breast cancer patients before and after surgery and following adjuvant chemotherapy |
title_full | Molecular analysis of circulating tumor DNA from breast cancer patients before and after surgery and following adjuvant chemotherapy |
title_fullStr | Molecular analysis of circulating tumor DNA from breast cancer patients before and after surgery and following adjuvant chemotherapy |
title_full_unstemmed | Molecular analysis of circulating tumor DNA from breast cancer patients before and after surgery and following adjuvant chemotherapy |
title_short | Molecular analysis of circulating tumor DNA from breast cancer patients before and after surgery and following adjuvant chemotherapy |
title_sort | molecular analysis of circulating tumor dna from breast cancer patients before and after surgery and following adjuvant chemotherapy |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7403808/ https://www.ncbi.nlm.nih.gov/pubmed/32765873 http://dx.doi.org/10.3892/mco.2020.2096 |
work_keys_str_mv | AT zelinovakatarina molecularanalysisofcirculatingtumordnafrombreastcancerpatientsbeforeandaftersurgeryandfollowingadjuvantchemotherapy AT jagelkovamarianna molecularanalysisofcirculatingtumordnafrombreastcancerpatientsbeforeandaftersurgeryandfollowingadjuvantchemotherapy AT laucekovazuzana molecularanalysisofcirculatingtumordnafrombreastcancerpatientsbeforeandaftersurgeryandfollowingadjuvantchemotherapy AT bobrovskamartina molecularanalysisofcirculatingtumordnafrombreastcancerpatientsbeforeandaftersurgeryandfollowingadjuvantchemotherapy AT dankovazuzana molecularanalysisofcirculatingtumordnafrombreastcancerpatientsbeforeandaftersurgeryandfollowingadjuvantchemotherapy AT grendarmarian molecularanalysisofcirculatingtumordnafrombreastcancerpatientsbeforeandaftersurgeryandfollowingadjuvantchemotherapy AT dokuskarol molecularanalysisofcirculatingtumordnafrombreastcancerpatientsbeforeandaftersurgeryandfollowingadjuvantchemotherapy |