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Immune co-culture cell microarray – a feasible tool for high-throughput functional investigation of lymphocyte–cancer interactions
Omics analyses often result in dozens to hundreds of potential targets, requiring validation for their biological relevance. Current high-throughput functional investigation methods are frequently labor-intensive, expensive, and display low reproducibility. The Immune Co-Culture Cell Microarray (ICC...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7194292/ https://www.ncbi.nlm.nih.gov/pubmed/32373399 http://dx.doi.org/10.1080/2162402X.2020.1741267 |
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author | Baruch, Erez Nissim Ortenberg, Rona Avivi, Camila Anafi, Liat Dick-Necula, Daniela Stossel, Chani Moshkovits, Yonatan Itzhaki, Orit Besser, Michal Judith Schachter, Jacob Barshack, Iris Markel, Gal |
author_facet | Baruch, Erez Nissim Ortenberg, Rona Avivi, Camila Anafi, Liat Dick-Necula, Daniela Stossel, Chani Moshkovits, Yonatan Itzhaki, Orit Besser, Michal Judith Schachter, Jacob Barshack, Iris Markel, Gal |
author_sort | Baruch, Erez Nissim |
collection | PubMed |
description | Omics analyses often result in dozens to hundreds of potential targets, requiring validation for their biological relevance. Current high-throughput functional investigation methods are frequently labor-intensive, expensive, and display low reproducibility. The Immune Co-Culture Cell Microarray (ICCM) is a formalin-fixed paraffin-embedded cell block microarray based on co-cultures of patient-derived tumor-infiltrating lymphocytes and their autologous melanoma cells. Each ICCM slide represents the same experiment and can be stained using standard immunohistochemistry and immunofluorescence techniques. Functional dynamics assessment of both proteins and microRNAs using ICCM stained slides demonstrated similar findings to flow cytometry assays and to previously published patient-derived biopsy reports. |
format | Online Article Text |
id | pubmed-7194292 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-71942922020-05-05 Immune co-culture cell microarray – a feasible tool for high-throughput functional investigation of lymphocyte–cancer interactions Baruch, Erez Nissim Ortenberg, Rona Avivi, Camila Anafi, Liat Dick-Necula, Daniela Stossel, Chani Moshkovits, Yonatan Itzhaki, Orit Besser, Michal Judith Schachter, Jacob Barshack, Iris Markel, Gal Oncoimmunology Original Research Omics analyses often result in dozens to hundreds of potential targets, requiring validation for their biological relevance. Current high-throughput functional investigation methods are frequently labor-intensive, expensive, and display low reproducibility. The Immune Co-Culture Cell Microarray (ICCM) is a formalin-fixed paraffin-embedded cell block microarray based on co-cultures of patient-derived tumor-infiltrating lymphocytes and their autologous melanoma cells. Each ICCM slide represents the same experiment and can be stained using standard immunohistochemistry and immunofluorescence techniques. Functional dynamics assessment of both proteins and microRNAs using ICCM stained slides demonstrated similar findings to flow cytometry assays and to previously published patient-derived biopsy reports. Taylor & Francis 2020-03-25 /pmc/articles/PMC7194292/ /pubmed/32373399 http://dx.doi.org/10.1080/2162402X.2020.1741267 Text en © 2020 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Baruch, Erez Nissim Ortenberg, Rona Avivi, Camila Anafi, Liat Dick-Necula, Daniela Stossel, Chani Moshkovits, Yonatan Itzhaki, Orit Besser, Michal Judith Schachter, Jacob Barshack, Iris Markel, Gal Immune co-culture cell microarray – a feasible tool for high-throughput functional investigation of lymphocyte–cancer interactions |
title | Immune co-culture cell microarray – a feasible tool for high-throughput functional investigation of lymphocyte–cancer interactions |
title_full | Immune co-culture cell microarray – a feasible tool for high-throughput functional investigation of lymphocyte–cancer interactions |
title_fullStr | Immune co-culture cell microarray – a feasible tool for high-throughput functional investigation of lymphocyte–cancer interactions |
title_full_unstemmed | Immune co-culture cell microarray – a feasible tool for high-throughput functional investigation of lymphocyte–cancer interactions |
title_short | Immune co-culture cell microarray – a feasible tool for high-throughput functional investigation of lymphocyte–cancer interactions |
title_sort | immune co-culture cell microarray – a feasible tool for high-throughput functional investigation of lymphocyte–cancer interactions |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7194292/ https://www.ncbi.nlm.nih.gov/pubmed/32373399 http://dx.doi.org/10.1080/2162402X.2020.1741267 |
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