miR-96-5p-mediated Inhibition of CD47 contributes to pancreatic tumor regression via activating both innate and adaptive anti-tumor immunity
Year: 2025
Type: article
Abstract: Blocking immune checkpoints has become a viable immunotherapy option for cancer. CD47, an anti-phagocytic molecule, engages with SIRPα on macrophages to transmit a “don’t eat me” signal, facilitating immunoevasion. This research examined the molecular pathways influenced by miR-96-5p in pancreatic ductal adenocarcinoma (PDAC) and evaluates its clinical and biological significance. Utilizing bioinformatics, Western blot, luciferase reporter assays and RNA fluorescence in situ hybridization, results revealed that miR-96-5p directly targeted and inversely regulated CD47 expression, indicating patient survival in PDAC. Further investigation into the effects of miR-96-5p on PDAC was conducted through co-culture phagocytosis, antigen presentation, and T cell activation experiments, and mouse PDAC models. The results demonstrated that specifically re-establishing miR-96-5p expression in PDAC cells significantly repressed PDAC tumorigenesis and reprogramed the immunosuppressive microenvironment by diminishing CD47 protein abundance. This modulation encouraged the shift of tumor-associated macrophages (TAMs) into pro-phagocytic M1-like phenotypes via exosomal transfer of miR-96-5p and boosted T cell activation within both peripheral and tumor immune microenvironments. Mechanistically, experiments based on the ovalbumin (OVA) antigen system revealed that the phagocytic function of miR-96-5p enhanced the presentation of tumor antigens to T cells, resulting in more effective activation of antigen-specific T cells, instead of miR-96-5p directly activating T cells. The findings verify that miR-96-5p serves as an effective tumor suppressor, reducing tumor burden by triggering both innate and adaptive anti-tumor immune responses, offering a promising avenue for PDAC immunotherapy improvement.
Source: Cell Communication and Signaling
Authors: Shoufang Tong, Shushan Hua, Yunling Wu, Xingxing Xiao, Yeqing Leng, Yubin Wang, Yubin Wang, Mengfan Sun, Jin Li, Xiping Ou, Wenfeng Zhao, Liping Wang, Yingwei Wang, Yingwei Wang, Shuhua Tan
Language: English
Subfield: Immunology
Field: Immunology and Microbiology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $3,390
OpenAlex ID: W4417027655
