TY - JOUR
T1 - Radiation-enhanced therapeutic targeting of galectin-1 enriched malignant stroma in triple negative breast cancer
AU - Upreti, Meenakshi
AU - Jyoti, Amar
AU - Johnson, Sara E.
AU - Swindell, Elden P.
AU - Napier, Dana
AU - Sethi, Pallavi
AU - Chan, Ryan
AU - Feddock, Jonathan M.
AU - Weiss, Heidi L.
AU - O'Halloran, Thomas V.
AU - Evers, B. Mark
PY - 2016/7/5
Y1 - 2016/7/5
N2 - 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.
AB - 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.
KW - TNBC tumor model
KW - galectin-1
KW - stromal-targeting
KW - triple negative breast cancer
KW - tumor tissue analog (TTA)
UR - http://www.scopus.com/inward/record.url?scp=85027849264&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85027849264&partnerID=8YFLogxK
U2 - 10.18632/oncotarget.9490
DO - 10.18632/oncotarget.9490
M3 - Article
C2 - 27223428
AN - SCOPUS:85027849264
SN - 1949-2553
VL - 7
SP - 41559
EP - 41574
JO - Oncotarget
JF - Oncotarget
IS - 27
ER -