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Dual‐Isolation and Profiling of Circulating Tumor Cells and Cancer Exosomes from Blood Samples with Melanoma Using Immunoaffinity‐Based Microfluidic Interfaces

Melanoma is among the most aggressive cancers, and its rate of incidence continues to grow. Early detection of melanoma has been hampered due to the lack of promising markers for testing. Recent advances in liquid biopsy have proposed noninvasive alternatives for cancer diagnosis and monitoring. Cir...

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Autores principales: Kang, Yoon‐Tae, Hadlock, Thomas, Lo, Ting‐Wen, Purcell, Emma, Mutukuri, Anusha, Fouladdel, Shamileh, Raguera, Monica De Silva, Fairbairn, Heather, Murlidhar, Vasudha, Durham, Alison, McLean, Scott A., Nagrath, Sunitha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7539202/
https://www.ncbi.nlm.nih.gov/pubmed/33042766
http://dx.doi.org/10.1002/advs.202001581
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author Kang, Yoon‐Tae
Hadlock, Thomas
Lo, Ting‐Wen
Purcell, Emma
Mutukuri, Anusha
Fouladdel, Shamileh
Raguera, Monica De Silva
Fairbairn, Heather
Murlidhar, Vasudha
Durham, Alison
McLean, Scott A.
Nagrath, Sunitha
author_facet Kang, Yoon‐Tae
Hadlock, Thomas
Lo, Ting‐Wen
Purcell, Emma
Mutukuri, Anusha
Fouladdel, Shamileh
Raguera, Monica De Silva
Fairbairn, Heather
Murlidhar, Vasudha
Durham, Alison
McLean, Scott A.
Nagrath, Sunitha
author_sort Kang, Yoon‐Tae
collection PubMed
description Melanoma is among the most aggressive cancers, and its rate of incidence continues to grow. Early detection of melanoma has been hampered due to the lack of promising markers for testing. Recent advances in liquid biopsy have proposed noninvasive alternatives for cancer diagnosis and monitoring. Circulating tumor cells (CTCs) and cancer‐exosomes are gaining influence as promising biomarkers because of their cancer‐associated molecular markers and signatures. However, technologies that offer the dual‐isolation of CTCs and exosomes using a single sample have not been thoroughly developed. The dual‐utilization OncoBean (DUO) device is conjugated with melanoma specific antibodies, MCAM and MCSP, enabling simultaneous CTC and exosome isolations. Using blood samples from patients, CTCs and exosomes are specifically isolated from a single sample and then undergo molecular profiling for comprehensive study. Melanoma patients have 0–17CTCs mL(−1) and 299 µg exosomal protein mL(−1) while healthy donors display fewer than 2CTCs and 75.6 µg of exosomes mL(−1), respectively. It is also demonstrated that both markers express melanoma‐associated genes using multiplex qRT‐PCR to test for expression pattern of a 96 gene panel. The dual isolation and molecular characterization will allow for further research into melanoma to identify viable markers for disease progression and treatment efficacy.
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spelling pubmed-75392022020-10-09 Dual‐Isolation and Profiling of Circulating Tumor Cells and Cancer Exosomes from Blood Samples with Melanoma Using Immunoaffinity‐Based Microfluidic Interfaces Kang, Yoon‐Tae Hadlock, Thomas Lo, Ting‐Wen Purcell, Emma Mutukuri, Anusha Fouladdel, Shamileh Raguera, Monica De Silva Fairbairn, Heather Murlidhar, Vasudha Durham, Alison McLean, Scott A. Nagrath, Sunitha Adv Sci (Weinh) Full Papers Melanoma is among the most aggressive cancers, and its rate of incidence continues to grow. Early detection of melanoma has been hampered due to the lack of promising markers for testing. Recent advances in liquid biopsy have proposed noninvasive alternatives for cancer diagnosis and monitoring. Circulating tumor cells (CTCs) and cancer‐exosomes are gaining influence as promising biomarkers because of their cancer‐associated molecular markers and signatures. However, technologies that offer the dual‐isolation of CTCs and exosomes using a single sample have not been thoroughly developed. The dual‐utilization OncoBean (DUO) device is conjugated with melanoma specific antibodies, MCAM and MCSP, enabling simultaneous CTC and exosome isolations. Using blood samples from patients, CTCs and exosomes are specifically isolated from a single sample and then undergo molecular profiling for comprehensive study. Melanoma patients have 0–17CTCs mL(−1) and 299 µg exosomal protein mL(−1) while healthy donors display fewer than 2CTCs and 75.6 µg of exosomes mL(−1), respectively. It is also demonstrated that both markers express melanoma‐associated genes using multiplex qRT‐PCR to test for expression pattern of a 96 gene panel. The dual isolation and molecular characterization will allow for further research into melanoma to identify viable markers for disease progression and treatment efficacy. John Wiley and Sons Inc. 2020-08-19 /pmc/articles/PMC7539202/ /pubmed/33042766 http://dx.doi.org/10.1002/advs.202001581 Text en © 2020 The Authors. Published by Wiley‐VCH GmbH This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Kang, Yoon‐Tae
Hadlock, Thomas
Lo, Ting‐Wen
Purcell, Emma
Mutukuri, Anusha
Fouladdel, Shamileh
Raguera, Monica De Silva
Fairbairn, Heather
Murlidhar, Vasudha
Durham, Alison
McLean, Scott A.
Nagrath, Sunitha
Dual‐Isolation and Profiling of Circulating Tumor Cells and Cancer Exosomes from Blood Samples with Melanoma Using Immunoaffinity‐Based Microfluidic Interfaces
title Dual‐Isolation and Profiling of Circulating Tumor Cells and Cancer Exosomes from Blood Samples with Melanoma Using Immunoaffinity‐Based Microfluidic Interfaces
title_full Dual‐Isolation and Profiling of Circulating Tumor Cells and Cancer Exosomes from Blood Samples with Melanoma Using Immunoaffinity‐Based Microfluidic Interfaces
title_fullStr Dual‐Isolation and Profiling of Circulating Tumor Cells and Cancer Exosomes from Blood Samples with Melanoma Using Immunoaffinity‐Based Microfluidic Interfaces
title_full_unstemmed Dual‐Isolation and Profiling of Circulating Tumor Cells and Cancer Exosomes from Blood Samples with Melanoma Using Immunoaffinity‐Based Microfluidic Interfaces
title_short Dual‐Isolation and Profiling of Circulating Tumor Cells and Cancer Exosomes from Blood Samples with Melanoma Using Immunoaffinity‐Based Microfluidic Interfaces
title_sort dual‐isolation and profiling of circulating tumor cells and cancer exosomes from blood samples with melanoma using immunoaffinity‐based microfluidic interfaces
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7539202/
https://www.ncbi.nlm.nih.gov/pubmed/33042766
http://dx.doi.org/10.1002/advs.202001581
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