Results 251 to 260 of about 463,193 (304)

Spatial remodeling of the tumor immune microenvironment in hepatocellular carcinoma with cirrhosis driven by Treg-CD8⁺T cell crosstalk via the SPP1-ITGA4 axis. [PDF]

open access: yesTransl Oncol
Xue D   +14 more
europepmc   +1 more source

Engineered Microfluidic Organoid Systems: New Paradigms for Menopause Mechanism Research and Personalized Medicine

open access: yesAdvanced Materials Technologies, EarlyView.
This review explores the integration of microfluidic technology with organoid systems as an innovative platform for studying menopausea complex multi‐organ condition. By enabling precise simulation of inter‐organ communication and hormone responses, microfluidic organoids offer a physiologically relevant model for investigating menopausal syndrome and ...
Qianyi Zhang   +4 more
wiley   +1 more source

Tumor immune microenvironment and immune phenotypes in PD-L1-tested canine urothelial carcinoma. [PDF]

open access: yesBMC Vet Res
Muscatello LV   +11 more
europepmc   +1 more source

TLR8 agonists remodel the tumor immune microenvironment through PF4-dependent T cell recruitment and ancillary mechanisms. [PDF]

open access: yesCancer Immunol Immunother
Zhou Q   +8 more
europepmc   +1 more source

Single-cell atlas of the tumor immune microenvironment across syngeneic murine models. [PDF]

open access: yesFront Immunol
Wang J   +6 more
europepmc   +1 more source

The Tumor Microenvironment Reprograms Immune Cells

Cellular Reprogramming, 2022
Tumor tissue comprises a highly complex network of diverse cell types. The tumor microenvironment (TME) can be mainly subdivided into cancer cells and stromal cell compartments, the latter include different types of immune cells, fibroblasts, endothelial cells, and pericytes.
Handi Cao   +3 more
openaire   +2 more sources

Tumor Microenvironment and Immune Escape

Surgical Oncology Clinics of North America, 2007
This article describes the multiple escape mechanisms used by tumor cells to avoid T-cell-mediated recognition and destruction. The discussion focuses on escape mechanisms that may result from changes at the level of TA-specific cytotoxic T lymphocytes and tumor cells in the tumor microenvironment.
Soldano, Ferrone, Theresa L, Whiteside
openaire   +2 more sources

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