Results 1 to 10 of about 12,335 (206)

B7–H3 regulates osteoclast differentiation via type I interferon-dependent IDO induction [PDF]

open access: yesCell Death and Disease, 2021
While their function, as immune checkpoint molecules, is well known, B7-family proteins also function as regulatory molecules in bone remodeling. B7–H3 is a receptor ligand of the B7 family that functions primarily as a negative immune checkpoint.
Younseo Oh   +6 more
doaj   +2 more sources

Expression of the costimulatory molecule B7-H3 is associated with prolonged survival in human pancreatic cancer [PDF]

open access: yesBMC Cancer, 2009
Background Costimulatory signaling has been implicated as a potential regulator of antitumor immunity in various human cancers. In contrast to the negative prognostic value of aberrant B7-H1 expression by pancreatic cancer cells, the role of B7-H3 is ...
Kleeff Jörg   +7 more
doaj   +4 more sources

B7-H3 is widely expressed in soft tissue sarcomas [PDF]

open access: yesBMC Cancer
Purpose Targeted therapy development in soft tissue sarcoma (STS) has been burdened by the heterogeneity of this group of rare tumors. B7 homolog 3 protein (B7-H3) is a molecule in the same family as programmed death-ligand 1 (PD-L1).
Meghan M. Lynch   +13 more
doaj   +4 more sources

Design and Preclinical Validation of an Anti-B7-H3-Specific Radiotracer: A Non-Invasive Imaging Tool to Guide B7-H3-Targeted Therapies [PDF]

open access: yesPharmaceuticals
Background: B7-H3, an immunoregulatory protein of the B7 family, has been associated with both anti-cancer immunity and tumor promotion, with its expression commonly correlated with poor prognosis.
Cyprine Neba Funeh   +5 more
doaj   +2 more sources

B7-H3 nanobody-based CAR T cells control multiple myeloma growth, while dual BCMA/B7-H3 CAR T cells overcome antigen escape [PDF]

open access: yesJournal of Hematology & Oncology
Background CAR T cell therapy targeting BCMA has shown remarkable efficacy in multiple myeloma (MM), but relapses occur due to T cell exhaustion and the emergence of BCMA-negative subpopulations.
Arne Van der Vreken   +21 more
doaj   +2 more sources

Research progress of B7-H3 in malignant tumors. [PDF]

open access: yesFront Immunol
B7 homolog 3 (B7-H3, also known as CD276) is a novel member of the B7 immune protein family. There is a marked difference in the expression and distribution of B7-H3 protein and mRNA between normal and tumor tissues, with widespread expression in tumor ...
Zhao S, Zhang H, Shang G.
europepmc   +3 more sources

Non-immune functions of B7-H3: bridging tumor cells and the tumor vasculature [PDF]

open access: yesFrontiers in Oncology
B7-H3 (CD276), an immune checkpoint molecule, is overexpressed in various types of cancer and their tumor vasculature, demonstrating significant associations with adverse clinical outcomes.
Shuo Wu   +4 more
doaj   +3 more sources

High B7-H3 protein expression in Medulloblastoma is associated with metastasis and unfavorable patient outcomes [PDF]

open access: yesDiagnostic Pathology
Background Medulloblastoma (MB) is the most common malignant brain tumor in children. Although the 5-year survival rate is approximately 70–80%, the current standard treatment results in severe and long-term side effects.
Patrícia Fontão   +8 more
doaj   +2 more sources

Gastric carcinomas with stromal b7-h3 expression have lower intratumoural cd8+ t cell density [PDF]

open access: yes, 2021
Publisher Copyright: © 2021 by the authors. Licensee MDPI, Basel, Switzerland.CD8+ T cells are the main effector cells of anti-cancer immune response that can be regulated by various costimulatory and coinhibitory molecules, including members of the B7 ...
Behrens, Hans Michael   +4 more
core   +1 more source

Immune Checkpoint B7-H3 Is a Therapeutic Vulnerability in Prostate Cancer Harboring Pten and TP53 Deficiencies [PDF]

open access: yes, 2023
Checkpoint immunotherapy has yielded meaningful responses across many cancers but has shown modest efficacy in advanced prostate cancer. B7 homolog 3 protein (B7-H3/CD276) is an immune checkpoint molecule and has emerged as a promising therapeutic target.
Aparicio, Ana   +13 more
core   +2 more sources

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