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Endovascular image-guided sampling of tumor-draining veins provides an enriched source of oncological biomarkers
INTRODUCTION: Circulating tumor-derived biomarkers can potentially impact cancer management throughout the continuum of care. This small exploratory study aimed to assess the relative levels of such biomarkers in the tumor-draining vascular beds in patients with solid tumors compared to levels in th...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10064007/ https://www.ncbi.nlm.nih.gov/pubmed/37007151 http://dx.doi.org/10.3389/fonc.2023.916196 |
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author | Tamrazi, Anobel Sundaresan, Srividya Gulati, Aishwarya Tan, Frederick J. Wadhwa, Vibhor Bartlett, Bjarne R. Diaz, Luis A. Jr. |
author_facet | Tamrazi, Anobel Sundaresan, Srividya Gulati, Aishwarya Tan, Frederick J. Wadhwa, Vibhor Bartlett, Bjarne R. Diaz, Luis A. Jr. |
author_sort | Tamrazi, Anobel |
collection | PubMed |
description | INTRODUCTION: Circulating tumor-derived biomarkers can potentially impact cancer management throughout the continuum of care. This small exploratory study aimed to assess the relative levels of such biomarkers in the tumor-draining vascular beds in patients with solid tumors compared to levels in their peripheral veins. METHODS: Using an endovascular image-guided approach, we obtained blood samples from peripheral veins and other vascular compartments–including the most proximal venous drainage from solid tumors–from a set of nine oncology patients with various primary and metastatic malignancies. We then interrogated these samples for a panel of oncological biomarkers, including circulating tumor cells (CTCs), exosome-derived microRNAs (miRNAs), circulating tumor DNA (ctDNA) mutations, and certain cancer-related proteins/biochemical markers. RESULTS: We found substantially higher levels of CTCs, certain miRNAs, and specific ctDNA mutations in samples from vascular beds closer to the tumor compared with those from peripheral veins and also noted that some of these signals were altered by treatment procedures. DISCUSSION: Our results indicate that tumor-proximal venous samples are highly enriched for some oncological biomarkers and may allow for more robust molecular analysis than peripheral vein samples. |
format | Online Article Text |
id | pubmed-10064007 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100640072023-04-01 Endovascular image-guided sampling of tumor-draining veins provides an enriched source of oncological biomarkers Tamrazi, Anobel Sundaresan, Srividya Gulati, Aishwarya Tan, Frederick J. Wadhwa, Vibhor Bartlett, Bjarne R. Diaz, Luis A. Jr. Front Oncol Oncology INTRODUCTION: Circulating tumor-derived biomarkers can potentially impact cancer management throughout the continuum of care. This small exploratory study aimed to assess the relative levels of such biomarkers in the tumor-draining vascular beds in patients with solid tumors compared to levels in their peripheral veins. METHODS: Using an endovascular image-guided approach, we obtained blood samples from peripheral veins and other vascular compartments–including the most proximal venous drainage from solid tumors–from a set of nine oncology patients with various primary and metastatic malignancies. We then interrogated these samples for a panel of oncological biomarkers, including circulating tumor cells (CTCs), exosome-derived microRNAs (miRNAs), circulating tumor DNA (ctDNA) mutations, and certain cancer-related proteins/biochemical markers. RESULTS: We found substantially higher levels of CTCs, certain miRNAs, and specific ctDNA mutations in samples from vascular beds closer to the tumor compared with those from peripheral veins and also noted that some of these signals were altered by treatment procedures. DISCUSSION: Our results indicate that tumor-proximal venous samples are highly enriched for some oncological biomarkers and may allow for more robust molecular analysis than peripheral vein samples. Frontiers Media S.A. 2023-03-17 /pmc/articles/PMC10064007/ /pubmed/37007151 http://dx.doi.org/10.3389/fonc.2023.916196 Text en Copyright © 2023 Tamrazi, Sundaresan, Gulati, Tan, Wadhwa, Bartlett and Diaz https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Tamrazi, Anobel Sundaresan, Srividya Gulati, Aishwarya Tan, Frederick J. Wadhwa, Vibhor Bartlett, Bjarne R. Diaz, Luis A. Jr. Endovascular image-guided sampling of tumor-draining veins provides an enriched source of oncological biomarkers |
title | Endovascular image-guided sampling of tumor-draining veins provides an enriched source of oncological biomarkers |
title_full | Endovascular image-guided sampling of tumor-draining veins provides an enriched source of oncological biomarkers |
title_fullStr | Endovascular image-guided sampling of tumor-draining veins provides an enriched source of oncological biomarkers |
title_full_unstemmed | Endovascular image-guided sampling of tumor-draining veins provides an enriched source of oncological biomarkers |
title_short | Endovascular image-guided sampling of tumor-draining veins provides an enriched source of oncological biomarkers |
title_sort | endovascular image-guided sampling of tumor-draining veins provides an enriched source of oncological biomarkers |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10064007/ https://www.ncbi.nlm.nih.gov/pubmed/37007151 http://dx.doi.org/10.3389/fonc.2023.916196 |
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