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Expression data from graft infiltrating macrophages treated with mTORi-HDL nanobiologics
Inducing graft acceptance without chronic immunosuppression remains an elusive goal in organ transplantation. Recent data demonstrate that non-self recognition by graft infiltrating macrophages initiates transplant rejection. Using an experimental transplantation mouse model, we isolated graft-infil...
ORGANISM(S): Mus musculus 
2018-10-31 | GSE119370 | GEO
Targeting the PI3K-AKT-mTOR pathway is a promising therapeutic strategy for breast cancer treatment. However, low response rates and the development of acquired resistance to PI3K-AKT-mTOR inhibitors remain major challenges for successful patient treatment. Here, we show that MYC activation is a cen...
ORGANISM(S): Mus musculus (Mouse) 
2023-05-02 | PXD041927 | Pride
Single-cell multiome uncovers differences in glycogen metabolism underlying species-specific speed of development [mTORi]
Targeting MYC sensitizes pancreatic cancer cells to MTOR inhibition
Chronic lung allograft dysfunction (CLAD) is characterized by fibrotic graft remodeling and limits long-term survival after pulmonary transplantation. Despite clinical evidence that myeloid cells drive conditions that increase the risk of CLAD development, contemporary immunosuppression primarily ta...
ORGANISM(S): Mus musculus 
2026-06-29 | GSE314602 | GEO
Nucleolin aptamer N6L reprograms the translational machinery and acts synergistically with mTORi to inhibit pancreatic cancer proliferation
Introduction: Glioma-associated microglia/macrophages (GAM) constitute the predominant immune cell population in glioblastoma (GB). Both GB cells and GAM exhibit upregulated mTOR signaling. This study aimed to investigate the effects of pharmacological mTOR inhibition (mTORi) specifically on GAM.Mat...
ORGANISM(S): Homo sapiens 
2025-07-28 | GSE242829 | GEO
Acquired resistance to mammalian target of rapamycin inhibitors (mTORi) severely limits their clinical efficacy in triple-negative breast cancer (TNBC), a subtype devoid of targeted therapeutic options. To model acquired resistance, we established two mTORi-resistant TNBC cell lines, MDA-MB-231/DREV...
ORGANISM(S): Homo sapiens 
2026-03-06 | GSE309057 | GEO
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