Cargando…
Integrated Workflow for the Label-Free Isolation and Genomic Analysis of Single Circulating Tumor Cells in Pancreatic Cancer
As pancreatic cancer is the third deadliest cancer in the U.S., the ability to study genetic alterations is necessary to provide further insight into potentially targetable regions for cancer treatment. Circulating tumor cells (CTCs) represent an especially aggressive subset of cancer cells, capable...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9316651/ https://www.ncbi.nlm.nih.gov/pubmed/35887203 http://dx.doi.org/10.3390/ijms23147852 |
_version_ | 1784754867606126592 |
---|---|
author | Rupp, Brittany Owen, Sarah Ball, Harrison Smith, Kaylee Judith Gunchick, Valerie Keller, Evan T. Sahai, Vaibhav Nagrath, Sunitha |
author_facet | Rupp, Brittany Owen, Sarah Ball, Harrison Smith, Kaylee Judith Gunchick, Valerie Keller, Evan T. Sahai, Vaibhav Nagrath, Sunitha |
author_sort | Rupp, Brittany |
collection | PubMed |
description | As pancreatic cancer is the third deadliest cancer in the U.S., the ability to study genetic alterations is necessary to provide further insight into potentially targetable regions for cancer treatment. Circulating tumor cells (CTCs) represent an especially aggressive subset of cancer cells, capable of causing metastasis and progressing the disease. Here, we present the Labyrinth–DEPArray pipeline for the isolation and analysis of single CTCs. Established cell lines, patient-derived CTC cell lines and freshly isolated CTCs were recovered and sequenced to reveal single-cell copy number variations (CNVs). The resulting CNV profiles of established cell lines showed concordance with previously reported data and highlight several gains and losses of cancer-related genes such as FGFR3 and GNAS. The novel sequencing of patient-derived CTC cell lines showed gains in chromosome 8q, 10q and 17q across both CTC cell lines. The pipeline was used to process and isolate single cells from a metastatic pancreatic cancer patient revealing a gain of chromosome 1q and a loss of chromosome 5q. Overall, the Labyrinth-DEPArray pipeline offers a validated workflow combining the benefits of antigen-free CTC isolation with single cell genomic analysis. |
format | Online Article Text |
id | pubmed-9316651 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-93166512022-07-27 Integrated Workflow for the Label-Free Isolation and Genomic Analysis of Single Circulating Tumor Cells in Pancreatic Cancer Rupp, Brittany Owen, Sarah Ball, Harrison Smith, Kaylee Judith Gunchick, Valerie Keller, Evan T. Sahai, Vaibhav Nagrath, Sunitha Int J Mol Sci Article As pancreatic cancer is the third deadliest cancer in the U.S., the ability to study genetic alterations is necessary to provide further insight into potentially targetable regions for cancer treatment. Circulating tumor cells (CTCs) represent an especially aggressive subset of cancer cells, capable of causing metastasis and progressing the disease. Here, we present the Labyrinth–DEPArray pipeline for the isolation and analysis of single CTCs. Established cell lines, patient-derived CTC cell lines and freshly isolated CTCs were recovered and sequenced to reveal single-cell copy number variations (CNVs). The resulting CNV profiles of established cell lines showed concordance with previously reported data and highlight several gains and losses of cancer-related genes such as FGFR3 and GNAS. The novel sequencing of patient-derived CTC cell lines showed gains in chromosome 8q, 10q and 17q across both CTC cell lines. The pipeline was used to process and isolate single cells from a metastatic pancreatic cancer patient revealing a gain of chromosome 1q and a loss of chromosome 5q. Overall, the Labyrinth-DEPArray pipeline offers a validated workflow combining the benefits of antigen-free CTC isolation with single cell genomic analysis. MDPI 2022-07-16 /pmc/articles/PMC9316651/ /pubmed/35887203 http://dx.doi.org/10.3390/ijms23147852 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Rupp, Brittany Owen, Sarah Ball, Harrison Smith, Kaylee Judith Gunchick, Valerie Keller, Evan T. Sahai, Vaibhav Nagrath, Sunitha Integrated Workflow for the Label-Free Isolation and Genomic Analysis of Single Circulating Tumor Cells in Pancreatic Cancer |
title | Integrated Workflow for the Label-Free Isolation and Genomic Analysis of Single Circulating Tumor Cells in Pancreatic Cancer |
title_full | Integrated Workflow for the Label-Free Isolation and Genomic Analysis of Single Circulating Tumor Cells in Pancreatic Cancer |
title_fullStr | Integrated Workflow for the Label-Free Isolation and Genomic Analysis of Single Circulating Tumor Cells in Pancreatic Cancer |
title_full_unstemmed | Integrated Workflow for the Label-Free Isolation and Genomic Analysis of Single Circulating Tumor Cells in Pancreatic Cancer |
title_short | Integrated Workflow for the Label-Free Isolation and Genomic Analysis of Single Circulating Tumor Cells in Pancreatic Cancer |
title_sort | integrated workflow for the label-free isolation and genomic analysis of single circulating tumor cells in pancreatic cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9316651/ https://www.ncbi.nlm.nih.gov/pubmed/35887203 http://dx.doi.org/10.3390/ijms23147852 |
work_keys_str_mv | AT ruppbrittany integratedworkflowforthelabelfreeisolationandgenomicanalysisofsinglecirculatingtumorcellsinpancreaticcancer AT owensarah integratedworkflowforthelabelfreeisolationandgenomicanalysisofsinglecirculatingtumorcellsinpancreaticcancer AT ballharrison integratedworkflowforthelabelfreeisolationandgenomicanalysisofsinglecirculatingtumorcellsinpancreaticcancer AT smithkayleejudith integratedworkflowforthelabelfreeisolationandgenomicanalysisofsinglecirculatingtumorcellsinpancreaticcancer AT gunchickvalerie integratedworkflowforthelabelfreeisolationandgenomicanalysisofsinglecirculatingtumorcellsinpancreaticcancer AT kellerevant integratedworkflowforthelabelfreeisolationandgenomicanalysisofsinglecirculatingtumorcellsinpancreaticcancer AT sahaivaibhav integratedworkflowforthelabelfreeisolationandgenomicanalysisofsinglecirculatingtumorcellsinpancreaticcancer AT nagrathsunitha integratedworkflowforthelabelfreeisolationandgenomicanalysisofsinglecirculatingtumorcellsinpancreaticcancer |