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Distribution of circulating tumor DNA in lung cancer: analysis of the primary lung and bone marrow along with the pulmonary venous and peripheral blood
Circulating tumor DNA (ctDNA), extracted from plasma, is a non-invasive surrogate biomarker. However, the distribution of ctDNA in the body still remains to be elucidated. In this study, resected lung tumors, with simultaneous blood and bone marrow samples, were analyzed to elucidate the distributio...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601731/ https://www.ncbi.nlm.nih.gov/pubmed/28938635 http://dx.doi.org/10.18632/oncotarget.19538 |
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author | Goto, Taichiro Hirotsu, Yosuke Amemiya, Kenji Nakagomi, Takahiro Shikata, Daichi Yokoyama, Yujiro Okimoto, Kenichiro Oyama, Toshio Mochizuki, Hitoshi Omata, Masao |
author_facet | Goto, Taichiro Hirotsu, Yosuke Amemiya, Kenji Nakagomi, Takahiro Shikata, Daichi Yokoyama, Yujiro Okimoto, Kenichiro Oyama, Toshio Mochizuki, Hitoshi Omata, Masao |
author_sort | Goto, Taichiro |
collection | PubMed |
description | Circulating tumor DNA (ctDNA), extracted from plasma, is a non-invasive surrogate biomarker. However, the distribution of ctDNA in the body still remains to be elucidated. In this study, resected lung tumors, with simultaneous blood and bone marrow samples, were analyzed to elucidate the distribution of ctDNA. Rib bone marrow, pulmonary venous blood (Pul.V) and peripheral blood (Peri.B) were obtained from 30 patients. The liquid samples were divided into cell pellets and supernatant by centrifugation; a total of 212 DNA samples were subjected to massively parallel sequencing. ctDNA was detected in 5 patients. Given that the frequency of mutations in the primary tumor was considered to be 100%, those in the other specimens were as follows; Pul.V plasma 20%, Peri.B plasma 11%, and the other samples 0%. Furthermore, ctDNA reflected the predominant mutations in the primary lesion. Clinically, the presence of ctDNA was associated with significantly poorer survival. These results suggest ctDNA “spill over” into an immediate outflow tract (Pul.V), and from there is disseminated to the entire body. Thus, it can be inferred that ctDNA reflects the cancer progression and could function as a prognostic marker. |
format | Online Article Text |
id | pubmed-5601731 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-56017312017-09-21 Distribution of circulating tumor DNA in lung cancer: analysis of the primary lung and bone marrow along with the pulmonary venous and peripheral blood Goto, Taichiro Hirotsu, Yosuke Amemiya, Kenji Nakagomi, Takahiro Shikata, Daichi Yokoyama, Yujiro Okimoto, Kenichiro Oyama, Toshio Mochizuki, Hitoshi Omata, Masao Oncotarget Research Paper Circulating tumor DNA (ctDNA), extracted from plasma, is a non-invasive surrogate biomarker. However, the distribution of ctDNA in the body still remains to be elucidated. In this study, resected lung tumors, with simultaneous blood and bone marrow samples, were analyzed to elucidate the distribution of ctDNA. Rib bone marrow, pulmonary venous blood (Pul.V) and peripheral blood (Peri.B) were obtained from 30 patients. The liquid samples were divided into cell pellets and supernatant by centrifugation; a total of 212 DNA samples were subjected to massively parallel sequencing. ctDNA was detected in 5 patients. Given that the frequency of mutations in the primary tumor was considered to be 100%, those in the other specimens were as follows; Pul.V plasma 20%, Peri.B plasma 11%, and the other samples 0%. Furthermore, ctDNA reflected the predominant mutations in the primary lesion. Clinically, the presence of ctDNA was associated with significantly poorer survival. These results suggest ctDNA “spill over” into an immediate outflow tract (Pul.V), and from there is disseminated to the entire body. Thus, it can be inferred that ctDNA reflects the cancer progression and could function as a prognostic marker. Impact Journals LLC 2017-07-25 /pmc/articles/PMC5601731/ /pubmed/28938635 http://dx.doi.org/10.18632/oncotarget.19538 Text en Copyright: © 2017 Goto et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Goto, Taichiro Hirotsu, Yosuke Amemiya, Kenji Nakagomi, Takahiro Shikata, Daichi Yokoyama, Yujiro Okimoto, Kenichiro Oyama, Toshio Mochizuki, Hitoshi Omata, Masao Distribution of circulating tumor DNA in lung cancer: analysis of the primary lung and bone marrow along with the pulmonary venous and peripheral blood |
title | Distribution of circulating tumor DNA in lung cancer: analysis of the primary lung and bone marrow along with the pulmonary venous and peripheral blood |
title_full | Distribution of circulating tumor DNA in lung cancer: analysis of the primary lung and bone marrow along with the pulmonary venous and peripheral blood |
title_fullStr | Distribution of circulating tumor DNA in lung cancer: analysis of the primary lung and bone marrow along with the pulmonary venous and peripheral blood |
title_full_unstemmed | Distribution of circulating tumor DNA in lung cancer: analysis of the primary lung and bone marrow along with the pulmonary venous and peripheral blood |
title_short | Distribution of circulating tumor DNA in lung cancer: analysis of the primary lung and bone marrow along with the pulmonary venous and peripheral blood |
title_sort | distribution of circulating tumor dna in lung cancer: analysis of the primary lung and bone marrow along with the pulmonary venous and peripheral blood |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601731/ https://www.ncbi.nlm.nih.gov/pubmed/28938635 http://dx.doi.org/10.18632/oncotarget.19538 |
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