Cargando…
A melt-electrowritten filter for capture and culture of circulating colon cancer cells
Metastasis is the major cause of death in cancer patients accounting for about 90% of the mortality. The detection and analysis of the hallmark of metastasis, circulating tumor cells (CTCs), have significant impact in cancer biology and clinical practice. However, the scarcity of CTCs in blood, part...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7256632/ https://www.ncbi.nlm.nih.gov/pubmed/32490373 http://dx.doi.org/10.1016/j.mtbio.2020.100052 |
_version_ | 1783539954612174848 |
---|---|
author | Jørgensen, M.L. Müller, C. Sikkersoq, M. Nadzieja, M. Zhang, Z. Su, Y. Just, J. Garm Spindler, K.-L. Chen, M. |
author_facet | Jørgensen, M.L. Müller, C. Sikkersoq, M. Nadzieja, M. Zhang, Z. Su, Y. Just, J. Garm Spindler, K.-L. Chen, M. |
author_sort | Jørgensen, M.L. |
collection | PubMed |
description | Metastasis is the major cause of death in cancer patients accounting for about 90% of the mortality. The detection and analysis of the hallmark of metastasis, circulating tumor cells (CTCs), have significant impact in cancer biology and clinical practice. However, the scarcity of CTCs in blood, particularly in that of colorectal cancer patients, is a serious bottleneck in the development of CTC-based precision medicine. Herein, the melt electrowriting (MEW) technology was used for reproductive fabrication of a biocompatible antibody-presenting polycaprolactone filter with tailored porous structure. It is demonstrated, for the first time, that such filter can be used not only to catch cancer cells spiked in whole blood but also to culture the cancer cells directly on site. Specifically, HT29 colon cancer cells can be captured with an efficiency of 85%, and when spiked into 4 mL of whole blood, 47% were captured on one Ø12mm filter. Furthermore, repeated capture and culture experiments have shown that as few as 20 HT29 colon cancer cells spiked into 4 mL of whole blood can be captured on the filter and within 2 weeks be expanded on site to become tumor bodies that are visible to the untrained eye. This filter allows for downstream analysis, such as flow cytometry, immunocytochemistry, Western blotting, and rt-qPCR. This technology represents a simple and cost-effective platform that potentially enables fast and efficient culture of rare CTCs from patients’ blood. This provides non-invasive alternatives for solid biopsy tumor materials for treatment screening, with great potential to realize precision medicine for cancer treatment. |
format | Online Article Text |
id | pubmed-7256632 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-72566322020-06-01 A melt-electrowritten filter for capture and culture of circulating colon cancer cells Jørgensen, M.L. Müller, C. Sikkersoq, M. Nadzieja, M. Zhang, Z. Su, Y. Just, J. Garm Spindler, K.-L. Chen, M. Mater Today Bio Full Length Article Metastasis is the major cause of death in cancer patients accounting for about 90% of the mortality. The detection and analysis of the hallmark of metastasis, circulating tumor cells (CTCs), have significant impact in cancer biology and clinical practice. However, the scarcity of CTCs in blood, particularly in that of colorectal cancer patients, is a serious bottleneck in the development of CTC-based precision medicine. Herein, the melt electrowriting (MEW) technology was used for reproductive fabrication of a biocompatible antibody-presenting polycaprolactone filter with tailored porous structure. It is demonstrated, for the first time, that such filter can be used not only to catch cancer cells spiked in whole blood but also to culture the cancer cells directly on site. Specifically, HT29 colon cancer cells can be captured with an efficiency of 85%, and when spiked into 4 mL of whole blood, 47% were captured on one Ø12mm filter. Furthermore, repeated capture and culture experiments have shown that as few as 20 HT29 colon cancer cells spiked into 4 mL of whole blood can be captured on the filter and within 2 weeks be expanded on site to become tumor bodies that are visible to the untrained eye. This filter allows for downstream analysis, such as flow cytometry, immunocytochemistry, Western blotting, and rt-qPCR. This technology represents a simple and cost-effective platform that potentially enables fast and efficient culture of rare CTCs from patients’ blood. This provides non-invasive alternatives for solid biopsy tumor materials for treatment screening, with great potential to realize precision medicine for cancer treatment. Elsevier 2020-05-01 /pmc/articles/PMC7256632/ /pubmed/32490373 http://dx.doi.org/10.1016/j.mtbio.2020.100052 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Full Length Article Jørgensen, M.L. Müller, C. Sikkersoq, M. Nadzieja, M. Zhang, Z. Su, Y. Just, J. Garm Spindler, K.-L. Chen, M. A melt-electrowritten filter for capture and culture of circulating colon cancer cells |
title | A melt-electrowritten filter for capture and culture of circulating colon cancer cells |
title_full | A melt-electrowritten filter for capture and culture of circulating colon cancer cells |
title_fullStr | A melt-electrowritten filter for capture and culture of circulating colon cancer cells |
title_full_unstemmed | A melt-electrowritten filter for capture and culture of circulating colon cancer cells |
title_short | A melt-electrowritten filter for capture and culture of circulating colon cancer cells |
title_sort | melt-electrowritten filter for capture and culture of circulating colon cancer cells |
topic | Full Length Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7256632/ https://www.ncbi.nlm.nih.gov/pubmed/32490373 http://dx.doi.org/10.1016/j.mtbio.2020.100052 |
work_keys_str_mv | AT jørgensenml ameltelectrowrittenfilterforcaptureandcultureofcirculatingcoloncancercells AT mullerc ameltelectrowrittenfilterforcaptureandcultureofcirculatingcoloncancercells AT sikkersoqm ameltelectrowrittenfilterforcaptureandcultureofcirculatingcoloncancercells AT nadziejam ameltelectrowrittenfilterforcaptureandcultureofcirculatingcoloncancercells AT zhangz ameltelectrowrittenfilterforcaptureandcultureofcirculatingcoloncancercells AT suy ameltelectrowrittenfilterforcaptureandcultureofcirculatingcoloncancercells AT justj ameltelectrowrittenfilterforcaptureandcultureofcirculatingcoloncancercells AT garmspindlerkl ameltelectrowrittenfilterforcaptureandcultureofcirculatingcoloncancercells AT chenm ameltelectrowrittenfilterforcaptureandcultureofcirculatingcoloncancercells AT jørgensenml meltelectrowrittenfilterforcaptureandcultureofcirculatingcoloncancercells AT mullerc meltelectrowrittenfilterforcaptureandcultureofcirculatingcoloncancercells AT sikkersoqm meltelectrowrittenfilterforcaptureandcultureofcirculatingcoloncancercells AT nadziejam meltelectrowrittenfilterforcaptureandcultureofcirculatingcoloncancercells AT zhangz meltelectrowrittenfilterforcaptureandcultureofcirculatingcoloncancercells AT suy meltelectrowrittenfilterforcaptureandcultureofcirculatingcoloncancercells AT justj meltelectrowrittenfilterforcaptureandcultureofcirculatingcoloncancercells AT garmspindlerkl meltelectrowrittenfilterforcaptureandcultureofcirculatingcoloncancercells AT chenm meltelectrowrittenfilterforcaptureandcultureofcirculatingcoloncancercells |