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Radiation-enhanced therapeutic targeting of galectin-1 enriched malignant stroma in triple negative breast cancer

Currently there are no FDA approved targeted therapies for Triple Negative Breast Cancer (TNBC). Ongoing clinical trials for TNBC have focused primarily on targeting the epithelial cancer cells. However, targeted delivery of cytotoxic payloads to the non-transformed tumor associated-endothelium can...

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Autores principales: Upreti, Meenakshi, Jyoti, Amar, Johnson, Sara E., Swindell, Elden P., Napier, Dana, Sethi, Pallavi, Chan, Ryan, Feddock, Jonathan M., Weiss, Heidi L., O'Halloran, Thomas V., Mark Evers, B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5173078/
https://www.ncbi.nlm.nih.gov/pubmed/27223428
http://dx.doi.org/10.18632/oncotarget.9490
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author Upreti, Meenakshi
Jyoti, Amar
Johnson, Sara E.
Swindell, Elden P.
Napier, Dana
Sethi, Pallavi
Chan, Ryan
Feddock, Jonathan M.
Weiss, Heidi L.
O'Halloran, Thomas V.
Mark Evers, B.
author_facet Upreti, Meenakshi
Jyoti, Amar
Johnson, Sara E.
Swindell, Elden P.
Napier, Dana
Sethi, Pallavi
Chan, Ryan
Feddock, Jonathan M.
Weiss, Heidi L.
O'Halloran, Thomas V.
Mark Evers, B.
author_sort Upreti, Meenakshi
collection PubMed
description Currently there are no FDA approved targeted therapies for Triple Negative Breast Cancer (TNBC). Ongoing clinical trials for TNBC have focused primarily on targeting the epithelial cancer cells. However, targeted delivery of cytotoxic payloads to the non-transformed tumor associated-endothelium can prove to be an alternate approach that is currently unexplored. The present study is supported by recent findings on elevated expression of stromal galectin-1 in clinical samples of TNBC and our ongoing findings on stromal targeting of radiation induced galectin-1 by the anginex-conjugated arsenic-cisplatin loaded liposomes using a novel murine tumor model. We demonstrate inhibition of tumor growth and metastasis in response to the multimodal nanotherapeutic strategy using a TNBC model with orthotopic tumors originating from 3D tumor tissue analogs (TTA) comprised of tumor cells, endothelial cells and fibroblasts. The ‘rigorous’ combined treatment regimen of radiation and targeted liposomes is also shown to be well tolerated. More importantly, the results presented provide a means to exploit clinically relevant radiation dose for concurrent receptor mediated enhanced delivery of chemotherapy while limiting overall toxicity. The proposed study is significant as it falls in line with developing combinatorial therapeutic approaches for stroma-directed tumor targeting using tumor models that have an appropriate representation of the TNBC microenvironment.
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spelling pubmed-51730782016-12-23 Radiation-enhanced therapeutic targeting of galectin-1 enriched malignant stroma in triple negative breast cancer Upreti, Meenakshi Jyoti, Amar Johnson, Sara E. Swindell, Elden P. Napier, Dana Sethi, Pallavi Chan, Ryan Feddock, Jonathan M. Weiss, Heidi L. O'Halloran, Thomas V. Mark Evers, B. Oncotarget Research Paper Currently there are no FDA approved targeted therapies for Triple Negative Breast Cancer (TNBC). Ongoing clinical trials for TNBC have focused primarily on targeting the epithelial cancer cells. However, targeted delivery of cytotoxic payloads to the non-transformed tumor associated-endothelium can prove to be an alternate approach that is currently unexplored. The present study is supported by recent findings on elevated expression of stromal galectin-1 in clinical samples of TNBC and our ongoing findings on stromal targeting of radiation induced galectin-1 by the anginex-conjugated arsenic-cisplatin loaded liposomes using a novel murine tumor model. We demonstrate inhibition of tumor growth and metastasis in response to the multimodal nanotherapeutic strategy using a TNBC model with orthotopic tumors originating from 3D tumor tissue analogs (TTA) comprised of tumor cells, endothelial cells and fibroblasts. The ‘rigorous’ combined treatment regimen of radiation and targeted liposomes is also shown to be well tolerated. More importantly, the results presented provide a means to exploit clinically relevant radiation dose for concurrent receptor mediated enhanced delivery of chemotherapy while limiting overall toxicity. The proposed study is significant as it falls in line with developing combinatorial therapeutic approaches for stroma-directed tumor targeting using tumor models that have an appropriate representation of the TNBC microenvironment. Impact Journals LLC 2016-05-19 /pmc/articles/PMC5173078/ /pubmed/27223428 http://dx.doi.org/10.18632/oncotarget.9490 Text en Copyright: © 2016 Upreti et al. http://creativecommons.org/licenses/by/2.5/ 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 credited.
spellingShingle Research Paper
Upreti, Meenakshi
Jyoti, Amar
Johnson, Sara E.
Swindell, Elden P.
Napier, Dana
Sethi, Pallavi
Chan, Ryan
Feddock, Jonathan M.
Weiss, Heidi L.
O'Halloran, Thomas V.
Mark Evers, B.
Radiation-enhanced therapeutic targeting of galectin-1 enriched malignant stroma in triple negative breast cancer
title Radiation-enhanced therapeutic targeting of galectin-1 enriched malignant stroma in triple negative breast cancer
title_full Radiation-enhanced therapeutic targeting of galectin-1 enriched malignant stroma in triple negative breast cancer
title_fullStr Radiation-enhanced therapeutic targeting of galectin-1 enriched malignant stroma in triple negative breast cancer
title_full_unstemmed Radiation-enhanced therapeutic targeting of galectin-1 enriched malignant stroma in triple negative breast cancer
title_short Radiation-enhanced therapeutic targeting of galectin-1 enriched malignant stroma in triple negative breast cancer
title_sort radiation-enhanced therapeutic targeting of galectin-1 enriched malignant stroma in triple negative breast cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5173078/
https://www.ncbi.nlm.nih.gov/pubmed/27223428
http://dx.doi.org/10.18632/oncotarget.9490
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