Effective capture of circulating tumor cells from an S180-bearing mouse model using electrically charged magnetic nanoparticles

Abstract Background Technology enabling the separation of rare circulating tumor cells (CTCs) provides the potential to enhance our knowledge of cancer metastasis and improve the care of cancer patients. Modern detection approaches commonly depend on tumor antigens or the physical size of CTCs. Howe...

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Main Authors: Zhiming Li, Jun Ruan, Xuan Zhuang
Format: Article
Language:English
Published: BMC 2019-05-01
Series:Journal of Nanobiotechnology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12951-019-0491-1
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spelling doaj-91fb10d4a675413c8a17f8e5383f917f2020-11-25T02:01:33ZengBMCJournal of Nanobiotechnology1477-31552019-05-011711910.1186/s12951-019-0491-1Effective capture of circulating tumor cells from an S180-bearing mouse model using electrically charged magnetic nanoparticlesZhiming Li0Jun Ruan1Xuan Zhuang2Institue of Reproductive Health, Tongji Medical College, Huazhong University of Science and TechnologyCollege of Life Sciences, Central China Normal UniversityDepartment of Urology, The First Affiliated Hospital of Xiamen UniversityAbstract Background Technology enabling the separation of rare circulating tumor cells (CTCs) provides the potential to enhance our knowledge of cancer metastasis and improve the care of cancer patients. Modern detection approaches commonly depend on tumor antigens or the physical size of CTCs. However, few studies report the detection of CTCs by the electrical differences between cancer cells and normal cells. Results In this study, we report a procedure for capturing CTCs from blood samples using electrically charged superparamagnetic nanoparticles (NPs). We found that only positively charged NPs attached to cancer cells, while negatively charged NPs did not. The capture method with positively charged NPs offered a sensitivity of down to 4 CTCs in 1 mL blood samples and achieved a superior capture yield (> 70%) for a high number of CTCs in blood samples (103–106 cells/mL). Following an in vitro evaluation, S180-bearing mice were employed as an in vivo model to assess the specificity and sensitivity of the capture procedure. The number of CTCs in blood from tumor-bearing mice was significantly higher than that in blood from healthy controls (on average, 75.8 ± 16.4 vs. zero CTCs/100 μL of blood, p < 0.0001), suggesting the high sensitivity and specificity of our method. Conclusions Positively charged NPs combined with an in vivo tumor model demonstrated that CTCs can be distinguished and isolated from other blood cells based on their electrical properties.http://link.springer.com/article/10.1186/s12951-019-0491-1Circulating tumor cellsCell surface chargeS180-bearing mouseNanoparticles
collection DOAJ
language English
format Article
sources DOAJ
author Zhiming Li
Jun Ruan
Xuan Zhuang
spellingShingle Zhiming Li
Jun Ruan
Xuan Zhuang
Effective capture of circulating tumor cells from an S180-bearing mouse model using electrically charged magnetic nanoparticles
Journal of Nanobiotechnology
Circulating tumor cells
Cell surface charge
S180-bearing mouse
Nanoparticles
author_facet Zhiming Li
Jun Ruan
Xuan Zhuang
author_sort Zhiming Li
title Effective capture of circulating tumor cells from an S180-bearing mouse model using electrically charged magnetic nanoparticles
title_short Effective capture of circulating tumor cells from an S180-bearing mouse model using electrically charged magnetic nanoparticles
title_full Effective capture of circulating tumor cells from an S180-bearing mouse model using electrically charged magnetic nanoparticles
title_fullStr Effective capture of circulating tumor cells from an S180-bearing mouse model using electrically charged magnetic nanoparticles
title_full_unstemmed Effective capture of circulating tumor cells from an S180-bearing mouse model using electrically charged magnetic nanoparticles
title_sort effective capture of circulating tumor cells from an s180-bearing mouse model using electrically charged magnetic nanoparticles
publisher BMC
series Journal of Nanobiotechnology
issn 1477-3155
publishDate 2019-05-01
description Abstract Background Technology enabling the separation of rare circulating tumor cells (CTCs) provides the potential to enhance our knowledge of cancer metastasis and improve the care of cancer patients. Modern detection approaches commonly depend on tumor antigens or the physical size of CTCs. However, few studies report the detection of CTCs by the electrical differences between cancer cells and normal cells. Results In this study, we report a procedure for capturing CTCs from blood samples using electrically charged superparamagnetic nanoparticles (NPs). We found that only positively charged NPs attached to cancer cells, while negatively charged NPs did not. The capture method with positively charged NPs offered a sensitivity of down to 4 CTCs in 1 mL blood samples and achieved a superior capture yield (> 70%) for a high number of CTCs in blood samples (103–106 cells/mL). Following an in vitro evaluation, S180-bearing mice were employed as an in vivo model to assess the specificity and sensitivity of the capture procedure. The number of CTCs in blood from tumor-bearing mice was significantly higher than that in blood from healthy controls (on average, 75.8 ± 16.4 vs. zero CTCs/100 μL of blood, p < 0.0001), suggesting the high sensitivity and specificity of our method. Conclusions Positively charged NPs combined with an in vivo tumor model demonstrated that CTCs can be distinguished and isolated from other blood cells based on their electrical properties.
topic Circulating tumor cells
Cell surface charge
S180-bearing mouse
Nanoparticles
url http://link.springer.com/article/10.1186/s12951-019-0491-1
work_keys_str_mv AT zhimingli effectivecaptureofcirculatingtumorcellsfromans180bearingmousemodelusingelectricallychargedmagneticnanoparticles
AT junruan effectivecaptureofcirculatingtumorcellsfromans180bearingmousemodelusingelectricallychargedmagneticnanoparticles
AT xuanzhuang effectivecaptureofcirculatingtumorcellsfromans180bearingmousemodelusingelectricallychargedmagneticnanoparticles
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