Steven Seaman
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View article: ANTXR1 blockade enhances cardiac function in preclinical models of heart failure
ANTXR1 blockade enhances cardiac function in preclinical models of heart failure Open
View article: m276-SL-PBD eradicates tumors and instigates long-lasting tumor-free survival in Merkel cell carcinoma preclinical models
m276-SL-PBD eradicates tumors and instigates long-lasting tumor-free survival in Merkel cell carcinoma preclinical models Open
Merkel cell carcinoma (MCC) is a rare but aggressive neuroendocrine carcinoma, and immune checkpoint inhibitors (ICIs) are the only approved therapy; nonetheless, resistance is notable and there is a critical need for novel effective thera…
View article: Uncovering receptor-ligand interactions using a high-avidity CRISPR activation screening platform
Uncovering receptor-ligand interactions using a high-avidity CRISPR activation screening platform Open
The majority of clinically approved drugs target proteins that are secreted or cell surface bound. However, further advances in this area have been hindered by the challenging nature of receptor deorphanization, as there are still many sec…
View article: Engineering CD276/B7-H3-targeted antibody-drug conjugates with enhanced cancer-eradicating capability
Engineering CD276/B7-H3-targeted antibody-drug conjugates with enhanced cancer-eradicating capability Open
CD276/B7-H3 represents a promising target for cancer therapy based on widespread overexpression in both cancer cells and tumor-associated stroma. In previous preclinical studies, CD276 antibody-drug conjugates (ADCs) exploiting a talirine-…
View article: Figure S4 from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer
Figure S4 from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer Open
L2 CAR T cells provide a survival advantage and disrupt vessels and tumor architecture in TNBC xenografts .
View article: Figure S3 from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer
Figure S3 from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer Open
L2 2G and L2 3G CAR T cell normalization and functional testing.
View article: Figure S5 from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer
Figure S5 from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer Open
No overt toxicity detected in mice receiving TEM8 CAR T cells.
View article: Data from The B7-H3–Targeting Antibody–Drug Conjugate m276-SL-PBD Is Potently Effective Against Pediatric Cancer Preclinical Solid Tumor Models
Data from The B7-H3–Targeting Antibody–Drug Conjugate m276-SL-PBD Is Potently Effective Against Pediatric Cancer Preclinical Solid Tumor Models Open
Purpose:Patients with relapsed pediatric solid malignancies have few therapeutic options, and many of these patients die of their disease. B7-H3 is an immune checkpoint protein encoded by the CD276 gene that is overexpressed in many…
View article: Figure S5 from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer
Figure S5 from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer Open
No overt toxicity detected in mice receiving TEM8 CAR T cells.
View article: Data from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer
Data from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer Open
Triple-negative breast cancer (TNBC) is an aggressive disease lacking targeted therapy. In this study, we developed a CAR T cell–based immunotherapeutic strategy to target TEM8, a marker initially defined on endothelial cells in colon tumo…
View article: Supplementary Methods and Data from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer
Supplementary Methods and Data from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer Open
Information about methods and data that further support the claims made in this article. This includes, but is not limited to TEM8 distribution in normal tissues, CAR T cell normalization, additional control groups and CAR toxicity studies.
View article: Figure S3 from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer
Figure S3 from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer Open
L2 2G and L2 3G CAR T cell normalization and functional testing.
View article: Figure S6 from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer
Figure S6 from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer Open
Mice that received systemic administration of L2 CAR T cells have normal pathology.
View article: Supplementary Data from The B7-H3–Targeting Antibody–Drug Conjugate m276-SL-PBD Is Potently Effective Against Pediatric Cancer Preclinical Solid Tumor Models
Supplementary Data from The B7-H3–Targeting Antibody–Drug Conjugate m276-SL-PBD Is Potently Effective Against Pediatric Cancer Preclinical Solid Tumor Models Open
Supplemental Tables 1-2 and Supplemental Figures 1-10
View article: Supplementary Methods and Data from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer
Supplementary Methods and Data from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer Open
Information about methods and data that further support the claims made in this article. This includes, but is not limited to TEM8 distribution in normal tissues, CAR T cell normalization, additional control groups and CAR toxicity studies.
View article: Data from The B7-H3–Targeting Antibody–Drug Conjugate m276-SL-PBD Is Potently Effective Against Pediatric Cancer Preclinical Solid Tumor Models
Data from The B7-H3–Targeting Antibody–Drug Conjugate m276-SL-PBD Is Potently Effective Against Pediatric Cancer Preclinical Solid Tumor Models Open
Purpose:Patients with relapsed pediatric solid malignancies have few therapeutic options, and many of these patients die of their disease. B7-H3 is an immune checkpoint protein encoded by the CD276 gene that is overexpressed in many…
View article: Figure S2 from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer
Figure S2 from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer Open
L2 CAR T cells reduce mammosphere formation when compared to irrelevant CAR control cells.
View article: Figure S4 from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer
Figure S4 from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer Open
L2 CAR T cells provide a survival advantage and disrupt vessels and tumor architecture in TNBC xenografts .
View article: Figure S6 from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer
Figure S6 from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer Open
Mice that received systemic administration of L2 CAR T cells have normal pathology.
View article: Figure S1 from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer
Figure S1 from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer Open
TEM8 distribution in normal tissues
View article: Supplementary Data from The B7-H3–Targeting Antibody–Drug Conjugate m276-SL-PBD Is Potently Effective Against Pediatric Cancer Preclinical Solid Tumor Models
Supplementary Data from The B7-H3–Targeting Antibody–Drug Conjugate m276-SL-PBD Is Potently Effective Against Pediatric Cancer Preclinical Solid Tumor Models Open
Supplemental Tables 1-2 and Supplemental Figures 1-10
View article: Figure S1 from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer
Figure S1 from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer Open
TEM8 distribution in normal tissues
View article: Data from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer
Data from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer Open
Triple-negative breast cancer (TNBC) is an aggressive disease lacking targeted therapy. In this study, we developed a CAR T cell–based immunotherapeutic strategy to target TEM8, a marker initially defined on endothelial cells in colon tumo…
View article: Figure S2 from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer
Figure S2 from TEM8/ANTXR1-Specific CAR T Cells as a Targeted Therapy for Triple-Negative Breast Cancer Open
L2 CAR T cells reduce mammosphere formation when compared to irrelevant CAR control cells.
View article: Supplementary Materials and Methods, Tables 1-3, Figures 1-5 from Host-Derived Tumor Endothelial Marker 8 Promotes the Growth of Melanoma
Supplementary Materials and Methods, Tables 1-3, Figures 1-5 from Host-Derived Tumor Endothelial Marker 8 Promotes the Growth of Melanoma Open
Supplementary Materials and Methods, Tables 1-3, Figures 1-5 from Host-Derived Tumor Endothelial Marker 8 Promotes the Growth of Melanoma
View article: Supplementary Materials and Methods, Tables 1-3, Figures 1-5 from Host-Derived Tumor Endothelial Marker 8 Promotes the Growth of Melanoma
Supplementary Materials and Methods, Tables 1-3, Figures 1-5 from Host-Derived Tumor Endothelial Marker 8 Promotes the Growth of Melanoma Open
Supplementary Materials and Methods, Tables 1-3, Figures 1-5 from Host-Derived Tumor Endothelial Marker 8 Promotes the Growth of Melanoma
View article: Data from Host-Derived Tumor Endothelial Marker 8 Promotes the Growth of Melanoma
Data from Host-Derived Tumor Endothelial Marker 8 Promotes the Growth of Melanoma Open
Tumor endothelial marker 8 (TEM8) was initially identified as a gene overexpressed in the vasculature of human tumors and was subsequently identified as an anthrax toxin receptor. To assess the functional role of TEM8, we dis…
View article: Data from Host-Derived Tumor Endothelial Marker 8 Promotes the Growth of Melanoma
Data from Host-Derived Tumor Endothelial Marker 8 Promotes the Growth of Melanoma Open
Tumor endothelial marker 8 (TEM8) was initially identified as a gene overexpressed in the vasculature of human tumors and was subsequently identified as an anthrax toxin receptor. To assess the functional role of TEM8, we dis…
View article: Cancer cell survival depends on collagen uptake into tumor-associated stroma
Cancer cell survival depends on collagen uptake into tumor-associated stroma Open
View article: Cancer cell survival depends on collagen uptake into tumor-associated stroma
Cancer cell survival depends on collagen uptake into tumor-associated stroma Open
Collagen I, the most abundant protein in humans, is ubiquitous in solid tumors where it provides a rich source of exploitable metabolic fuel for cancer cells. While tumor cells were unable to exploit collagen directly, here we show they ca…