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Circulating tumor cell and cell-free RNA capture and expression analysis identify platelet-associated genes in metastatic lung cancer

BACKGROUND: Circulating tumor cells (CTC) and plasma cell-free RNA (cfRNA) can serve as biomarkers for prognosis and treatment response in lung cancer. One barrier to the selected or routine use of CTCs and plasma cfRNA in precision oncology is the limited quantity of both, and CTCs are only seen in...

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Autores principales: Beck, Tim N., Boumber, Yanis A., Aggarwal, Charu, Pei, Jianming, Thrash-Bingham, Catherine, Fittipaldi, Patricia, Vlasenkova, Ramillya, Rao, Chandra, Borghaei, Hossein, Cristofanilli, Massimo, Mehra, Ranee, Serebriiskii, Ilya, Alpaugh, R. Katherine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6582501/
https://www.ncbi.nlm.nih.gov/pubmed/31215484
http://dx.doi.org/10.1186/s12885-019-5795-x
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author Beck, Tim N.
Boumber, Yanis A.
Aggarwal, Charu
Pei, Jianming
Thrash-Bingham, Catherine
Fittipaldi, Patricia
Vlasenkova, Ramillya
Rao, Chandra
Borghaei, Hossein
Cristofanilli, Massimo
Mehra, Ranee
Serebriiskii, Ilya
Alpaugh, R. Katherine
author_facet Beck, Tim N.
Boumber, Yanis A.
Aggarwal, Charu
Pei, Jianming
Thrash-Bingham, Catherine
Fittipaldi, Patricia
Vlasenkova, Ramillya
Rao, Chandra
Borghaei, Hossein
Cristofanilli, Massimo
Mehra, Ranee
Serebriiskii, Ilya
Alpaugh, R. Katherine
author_sort Beck, Tim N.
collection PubMed
description BACKGROUND: Circulating tumor cells (CTC) and plasma cell-free RNA (cfRNA) can serve as biomarkers for prognosis and treatment response in lung cancer. One barrier to the selected or routine use of CTCs and plasma cfRNA in precision oncology is the limited quantity of both, and CTCs are only seen in metastatic disease. As capture of CTCs and plasma cfRNA presents an opportunity to monitor and assess malignancies without invasive procedures, we compared two methods for CTC capture and identification, and profiled mRNA from CTCs and plasma cfRNA to identify potential tumor-associated biomarkers. METHODS: Peripheral blood was collected from ten patients with small cell lung cancer (SCLC), ten patients with non-small cell lung cancer (NSCLC) and four healthy volunteers. Two methods were used for CTC capture: the standard epithelial cell adhesion molecule (EpCam) CellSearch kit (unicapture) and EpCAM plus HER2, EGFR and MUC-1 specific combined ferrofluid capture (quadcapture). For the quadcapture, anti-cytokeratin 7 (CK7) was additionally used to assist in CTC identification. NanoString analysis was performed on plasma cfRNA and on mRNA from combined ferrofluid isolated CTCs. Expression data was analyzed using STRING and Reactome. RESULTS: Unicapture detected CTCs in 40% of NSCLC and 60% of SCLC; whereas, quadcapture/CK7 identified CTCs in 20% of NSCLC and 80% of SCLC. Bioinformatic analysis of NanoString data identified high expression of a platelet factor 4 (PF4)-related group of transcripts. CONCLUSIONS: Quadcapture ferrofluid reagent did not significantly improve CTC capture efficacy. NanoString analysis based on CTC and plasma cfRNA data highlighted an intriguing PF-4-centric network in patients with metastatic lung cancer. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-019-5795-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-65825012019-06-26 Circulating tumor cell and cell-free RNA capture and expression analysis identify platelet-associated genes in metastatic lung cancer Beck, Tim N. Boumber, Yanis A. Aggarwal, Charu Pei, Jianming Thrash-Bingham, Catherine Fittipaldi, Patricia Vlasenkova, Ramillya Rao, Chandra Borghaei, Hossein Cristofanilli, Massimo Mehra, Ranee Serebriiskii, Ilya Alpaugh, R. Katherine BMC Cancer Research Article BACKGROUND: Circulating tumor cells (CTC) and plasma cell-free RNA (cfRNA) can serve as biomarkers for prognosis and treatment response in lung cancer. One barrier to the selected or routine use of CTCs and plasma cfRNA in precision oncology is the limited quantity of both, and CTCs are only seen in metastatic disease. As capture of CTCs and plasma cfRNA presents an opportunity to monitor and assess malignancies without invasive procedures, we compared two methods for CTC capture and identification, and profiled mRNA from CTCs and plasma cfRNA to identify potential tumor-associated biomarkers. METHODS: Peripheral blood was collected from ten patients with small cell lung cancer (SCLC), ten patients with non-small cell lung cancer (NSCLC) and four healthy volunteers. Two methods were used for CTC capture: the standard epithelial cell adhesion molecule (EpCam) CellSearch kit (unicapture) and EpCAM plus HER2, EGFR and MUC-1 specific combined ferrofluid capture (quadcapture). For the quadcapture, anti-cytokeratin 7 (CK7) was additionally used to assist in CTC identification. NanoString analysis was performed on plasma cfRNA and on mRNA from combined ferrofluid isolated CTCs. Expression data was analyzed using STRING and Reactome. RESULTS: Unicapture detected CTCs in 40% of NSCLC and 60% of SCLC; whereas, quadcapture/CK7 identified CTCs in 20% of NSCLC and 80% of SCLC. Bioinformatic analysis of NanoString data identified high expression of a platelet factor 4 (PF4)-related group of transcripts. CONCLUSIONS: Quadcapture ferrofluid reagent did not significantly improve CTC capture efficacy. NanoString analysis based on CTC and plasma cfRNA data highlighted an intriguing PF-4-centric network in patients with metastatic lung cancer. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-019-5795-x) contains supplementary material, which is available to authorized users. BioMed Central 2019-06-19 /pmc/articles/PMC6582501/ /pubmed/31215484 http://dx.doi.org/10.1186/s12885-019-5795-x Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Beck, Tim N.
Boumber, Yanis A.
Aggarwal, Charu
Pei, Jianming
Thrash-Bingham, Catherine
Fittipaldi, Patricia
Vlasenkova, Ramillya
Rao, Chandra
Borghaei, Hossein
Cristofanilli, Massimo
Mehra, Ranee
Serebriiskii, Ilya
Alpaugh, R. Katherine
Circulating tumor cell and cell-free RNA capture and expression analysis identify platelet-associated genes in metastatic lung cancer
title Circulating tumor cell and cell-free RNA capture and expression analysis identify platelet-associated genes in metastatic lung cancer
title_full Circulating tumor cell and cell-free RNA capture and expression analysis identify platelet-associated genes in metastatic lung cancer
title_fullStr Circulating tumor cell and cell-free RNA capture and expression analysis identify platelet-associated genes in metastatic lung cancer
title_full_unstemmed Circulating tumor cell and cell-free RNA capture and expression analysis identify platelet-associated genes in metastatic lung cancer
title_short Circulating tumor cell and cell-free RNA capture and expression analysis identify platelet-associated genes in metastatic lung cancer
title_sort circulating tumor cell and cell-free rna capture and expression analysis identify platelet-associated genes in metastatic lung cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6582501/
https://www.ncbi.nlm.nih.gov/pubmed/31215484
http://dx.doi.org/10.1186/s12885-019-5795-x
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