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PIC&RUN: An integrated assay for the detection and retrieval of single viable circulating tumor cells

Circulating tumor cells (CTCs) shed from solid tumors can serve as a minimally invasive liquid biopsy for monitoring disease progression. Because CTCs are rare and heterogeneous, their biological properties need to be investigated at the single cell level, which requires efficient ways to isolate an...

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Autores principales: Kamal, Mohamed, Saremi, Shahin, Klotz, Remi, Iriondo, Oihana, Amzaleg, Yonatan, Chairez, Yvonne, Tulpule, Varsha, Lang, Julie E., Kang, Irene, Yu, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6877641/
https://www.ncbi.nlm.nih.gov/pubmed/31767951
http://dx.doi.org/10.1038/s41598-019-53899-4
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author Kamal, Mohamed
Saremi, Shahin
Klotz, Remi
Iriondo, Oihana
Amzaleg, Yonatan
Chairez, Yvonne
Tulpule, Varsha
Lang, Julie E.
Kang, Irene
Yu, Min
author_facet Kamal, Mohamed
Saremi, Shahin
Klotz, Remi
Iriondo, Oihana
Amzaleg, Yonatan
Chairez, Yvonne
Tulpule, Varsha
Lang, Julie E.
Kang, Irene
Yu, Min
author_sort Kamal, Mohamed
collection PubMed
description Circulating tumor cells (CTCs) shed from solid tumors can serve as a minimally invasive liquid biopsy for monitoring disease progression. Because CTCs are rare and heterogeneous, their biological properties need to be investigated at the single cell level, which requires efficient ways to isolate and analyze live single CTCs. Current methods for CTC isolation and identification are either performed on fixed and stained cells or need multiple procedures to isolate pure live CTCs. Here, we used the AccuCyte-RareCyte system to develop a Protocol for Integrated Capture and Retrieval of Ultra-pure single live CTCs using Negative and positive selection (PIC&RUN). The positive selection module of PIC&RUN identifies CTCs based on detection of cancer surface markers and exclusion of immune markers. Combined with a two-step cell picking protocol to retrieve ultrapure single CTCs, the positive selection module is compatible for downstream single cell transcriptomic analysis. The negative selection module of PIC&RUN identifies CTCs based on a live cell dye and the absence of immune markers, allowing retrieval of viable CTCs that are suitable for ex vivo culture. This new assay combines the CTC capture and retrieval in one integrated platform, providing a valuable tool for downstream live CTC analyses.
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spelling pubmed-68776412019-12-05 PIC&RUN: An integrated assay for the detection and retrieval of single viable circulating tumor cells Kamal, Mohamed Saremi, Shahin Klotz, Remi Iriondo, Oihana Amzaleg, Yonatan Chairez, Yvonne Tulpule, Varsha Lang, Julie E. Kang, Irene Yu, Min Sci Rep Article Circulating tumor cells (CTCs) shed from solid tumors can serve as a minimally invasive liquid biopsy for monitoring disease progression. Because CTCs are rare and heterogeneous, their biological properties need to be investigated at the single cell level, which requires efficient ways to isolate and analyze live single CTCs. Current methods for CTC isolation and identification are either performed on fixed and stained cells or need multiple procedures to isolate pure live CTCs. Here, we used the AccuCyte-RareCyte system to develop a Protocol for Integrated Capture and Retrieval of Ultra-pure single live CTCs using Negative and positive selection (PIC&RUN). The positive selection module of PIC&RUN identifies CTCs based on detection of cancer surface markers and exclusion of immune markers. Combined with a two-step cell picking protocol to retrieve ultrapure single CTCs, the positive selection module is compatible for downstream single cell transcriptomic analysis. The negative selection module of PIC&RUN identifies CTCs based on a live cell dye and the absence of immune markers, allowing retrieval of viable CTCs that are suitable for ex vivo culture. This new assay combines the CTC capture and retrieval in one integrated platform, providing a valuable tool for downstream live CTC analyses. Nature Publishing Group UK 2019-11-25 /pmc/articles/PMC6877641/ /pubmed/31767951 http://dx.doi.org/10.1038/s41598-019-53899-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kamal, Mohamed
Saremi, Shahin
Klotz, Remi
Iriondo, Oihana
Amzaleg, Yonatan
Chairez, Yvonne
Tulpule, Varsha
Lang, Julie E.
Kang, Irene
Yu, Min
PIC&RUN: An integrated assay for the detection and retrieval of single viable circulating tumor cells
title PIC&RUN: An integrated assay for the detection and retrieval of single viable circulating tumor cells
title_full PIC&RUN: An integrated assay for the detection and retrieval of single viable circulating tumor cells
title_fullStr PIC&RUN: An integrated assay for the detection and retrieval of single viable circulating tumor cells
title_full_unstemmed PIC&RUN: An integrated assay for the detection and retrieval of single viable circulating tumor cells
title_short PIC&RUN: An integrated assay for the detection and retrieval of single viable circulating tumor cells
title_sort pic&run: an integrated assay for the detection and retrieval of single viable circulating tumor cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6877641/
https://www.ncbi.nlm.nih.gov/pubmed/31767951
http://dx.doi.org/10.1038/s41598-019-53899-4
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