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Highly Efficient Elimination of Colorectal Tumor-Initiating Cells by an EpCAM/CD3-Bispecific Antibody Engaging Human T Cells
With their resistance to genotoxic and anti-proliferative drugs and potential to grow tumors and metastases from very few cells, cancer stem or tumor-initiating cells (TICs) are a severe limitation for the treatment of cancer by conventional therapies. Here, we explored whether human T cells that ar...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2956687/ https://www.ncbi.nlm.nih.gov/pubmed/20976159 http://dx.doi.org/10.1371/journal.pone.0013474 |
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author | Herrmann, Ines Baeuerle, Patrick A. Friedrich, Matthias Murr, Alexander Filusch, Susanne Rüttinger, Dominik Majdoub, Mariam W. Sharma, Sherven Kufer, Peter Raum, Tobias Münz, Markus |
author_facet | Herrmann, Ines Baeuerle, Patrick A. Friedrich, Matthias Murr, Alexander Filusch, Susanne Rüttinger, Dominik Majdoub, Mariam W. Sharma, Sherven Kufer, Peter Raum, Tobias Münz, Markus |
author_sort | Herrmann, Ines |
collection | PubMed |
description | With their resistance to genotoxic and anti-proliferative drugs and potential to grow tumors and metastases from very few cells, cancer stem or tumor-initiating cells (TICs) are a severe limitation for the treatment of cancer by conventional therapies. Here, we explored whether human T cells that are redirected via an EpCAM/CD3-bispecific antibody called MT110 can lyse colorectal TICs and prevent tumor growth from TICs. MT110 recognizes EpCAM, a cell adhesion molecule expressed on TICs from diverse human carcinoma, which was recently shown to promote tumor growth through engagement of elements of the wnt pathway. MT110 was highly potent in mediating complete redirected lysis of KRAS-, PI3 kinase- and BRAF-mutated colorectal TICs, as demonstrated in a soft agar assay. In immunodeficient mice, MT110 prevented growth of tumors from a 5,000-fold excess of a minimally tumorigenic TIC dose. T cells engaged by MT110 may provide a potent therapeutic means to eradicate TICs and bulk tumor cells derived thereof. |
format | Text |
id | pubmed-2956687 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-29566872010-10-25 Highly Efficient Elimination of Colorectal Tumor-Initiating Cells by an EpCAM/CD3-Bispecific Antibody Engaging Human T Cells Herrmann, Ines Baeuerle, Patrick A. Friedrich, Matthias Murr, Alexander Filusch, Susanne Rüttinger, Dominik Majdoub, Mariam W. Sharma, Sherven Kufer, Peter Raum, Tobias Münz, Markus PLoS One Research Article With their resistance to genotoxic and anti-proliferative drugs and potential to grow tumors and metastases from very few cells, cancer stem or tumor-initiating cells (TICs) are a severe limitation for the treatment of cancer by conventional therapies. Here, we explored whether human T cells that are redirected via an EpCAM/CD3-bispecific antibody called MT110 can lyse colorectal TICs and prevent tumor growth from TICs. MT110 recognizes EpCAM, a cell adhesion molecule expressed on TICs from diverse human carcinoma, which was recently shown to promote tumor growth through engagement of elements of the wnt pathway. MT110 was highly potent in mediating complete redirected lysis of KRAS-, PI3 kinase- and BRAF-mutated colorectal TICs, as demonstrated in a soft agar assay. In immunodeficient mice, MT110 prevented growth of tumors from a 5,000-fold excess of a minimally tumorigenic TIC dose. T cells engaged by MT110 may provide a potent therapeutic means to eradicate TICs and bulk tumor cells derived thereof. Public Library of Science 2010-10-18 /pmc/articles/PMC2956687/ /pubmed/20976159 http://dx.doi.org/10.1371/journal.pone.0013474 Text en Herrmann et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Herrmann, Ines Baeuerle, Patrick A. Friedrich, Matthias Murr, Alexander Filusch, Susanne Rüttinger, Dominik Majdoub, Mariam W. Sharma, Sherven Kufer, Peter Raum, Tobias Münz, Markus Highly Efficient Elimination of Colorectal Tumor-Initiating Cells by an EpCAM/CD3-Bispecific Antibody Engaging Human T Cells |
title | Highly Efficient Elimination of Colorectal Tumor-Initiating Cells by an EpCAM/CD3-Bispecific Antibody Engaging Human T Cells |
title_full | Highly Efficient Elimination of Colorectal Tumor-Initiating Cells by an EpCAM/CD3-Bispecific Antibody Engaging Human T Cells |
title_fullStr | Highly Efficient Elimination of Colorectal Tumor-Initiating Cells by an EpCAM/CD3-Bispecific Antibody Engaging Human T Cells |
title_full_unstemmed | Highly Efficient Elimination of Colorectal Tumor-Initiating Cells by an EpCAM/CD3-Bispecific Antibody Engaging Human T Cells |
title_short | Highly Efficient Elimination of Colorectal Tumor-Initiating Cells by an EpCAM/CD3-Bispecific Antibody Engaging Human T Cells |
title_sort | highly efficient elimination of colorectal tumor-initiating cells by an epcam/cd3-bispecific antibody engaging human t cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2956687/ https://www.ncbi.nlm.nih.gov/pubmed/20976159 http://dx.doi.org/10.1371/journal.pone.0013474 |
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