Breast cancer is a highly prevalent malignant tumor among women worldwide,and its clinical treatment faces significant challenges,such as high postoperative recurrence rates,high metas-tasis rates,and therapeutic resistance.Studies indicate that monocyte-derived immune cells play a critical role in promoting breast cancer progression by establishing an immunosuppressive tumor microenviron-ment and pre-metastatic niche.Monocytic myeloid-derived suppressor cells,tumor-associated macro-phages,and monocyte-derived dendritic cells secrete various cytokines,including interleukins,colony-stimulating factors,tumor necrosis factor,chemokines C-C motif chemokine ligand/C-X-C motif chemo-kine ligand(CCL/CXCL),and growth factors,which activate multiple signaling pathways and promote the development of breast cancer and its metastasis to such organs as bones,lungs,brains and livers through mechanisms involving CCL/CXCL-mediated recruitment,angiogenesis induction,and immune evasion.Therefore,targeting the regulation of monocyte-derived immune cells and their secreted cyto-kines may become a crucial therapeutic approach to breast cancer.This review summarizes the mech-anisms by which monocyte-derived immune cells and their cytokines contribute to the development and metastasis of breast cancer by exploring.It further explores therapeutic strategies targeting these cells and cytokines,such as modulating phenotypic transformation,reprogramming cellular metabolism,and regulating cytokine expression levels.

Obesity usually exacerbates the immunosuppressive tumor microenvironment (ITME), hindering CD8⁺ T cell infiltration and function, which further represents a significant barrier to the efficacy of immunotherapy. Herein, a multifunctional liposomal system (CR-Lip) for encapsulating celastrol (CEL) was utilized to remodel obesity-related ITME and improve cancer immunotherapy, wherein Ginsenoside Rg3 (Rg3) was detected interspersed in the phospholipid bilayer and its glycosyl exposed on the surface of the liposome. CR-Lip had a relatively uniform size (116.5 nm), facilitating favorable tumor tissue accumulation through the interaction between Rg3 and glucose transporter 1 overexpressed in obese tumor cells. Upon reaching the tumor region, CR-Lip was found to induce the immunogenic cell death (ICD) of HFD tumor cells. Notably, the level of PHD3 in HFD tumor cells was effectively boosted by CR-Lip to effectively block metabolic reprogramming and increase the availability of major free fatty acids fuel sources. In vivo, experiments studies revealed that the easy-obtained nano platform stimulated enhanced the production of various cytokines in tumor tissues, DC maturation, CD8⁺ T-cell infiltration, and synergistic anticancer therapeutic potency with aPD-1 (tumor inhibition rate = 82.1%) towards obesity-related melanoma. Consequently, this study presented an efficacious approach to tumor immunotherapy in obese mice by encompassing tumor eradication, inducing ICD, and reprogramming metabolism. Furthermore, it offered a unique insight into a valuable attempt at the immunotherapy of obesity-associated related tumors.

Breast cancer is a highly prevalent malignant tumor among women worldwide,and its clinical treatment faces significant challenges,such as high postoperative recurrence rates,high metas-tasis rates,and therapeutic resistance.Studies indicate that monocyte-derived immune cells play a critical role in promoting breast cancer progression by establishing an immunosuppressive tumor microenviron-ment and pre-metastatic niche.Monocytic myeloid-derived suppressor cells,tumor-associated macro-phages,and monocyte-derived dendritic cells secrete various cytokines,including interleukins,colony-stimulating factors,tumor necrosis factor,chemokines C-C motif chemokine ligand/C-X-C motif chemo-kine ligand(CCL/CXCL),and growth factors,which activate multiple signaling pathways and promote the development of breast cancer and its metastasis to such organs as bones,lungs,brains and livers through mechanisms involving CCL/CXCL-mediated recruitment,angiogenesis induction,and immune evasion.Therefore,targeting the regulation of monocyte-derived immune cells and their secreted cyto-kines may become a crucial therapeutic approach to breast cancer.This review summarizes the mech-anisms by which monocyte-derived immune cells and their cytokines contribute to the development and metastasis of breast cancer by exploring.It further explores therapeutic strategies targeting these cells and cytokines,such as modulating phenotypic transformation,reprogramming cellular metabolism,and regulating cytokine expression levels.

A method for the simultaneous determination of 34 pesticides in sunflower oil, soybean oil and corn oil was developed. The samples were extracted and purified by a modified QuEChERS method, and then the supernatant was analyzed by on-line gel permeation chromatography-gas chromatography-mass spectrometry ( GPC-GC-MS ) . The linear range was from 0 . 01 to 0 . 2 mg/L with a good correlation coefficients ( r≥0. 9913). The average recoveries of 31 pesticides (except p,p′-DDE, p,p′-DDD, p,p′-DDT. For detail, please reference to section 3 . 6 ) ranged from 70 . 3% to 115 . 4%, 69 . 5% to 112 . 6% and 70 . 2% to 116 . 1%spiked at 0. 05 μg/g and 0. 1 μg/g with the relative standard deviations (RSDs, n=6) less than 13. 3%, 13. 5% and 12. 1% in sunflower oil, soybean oil and corn oil samples, respectively. The LODs of this method ranged from 0. 0692 to 2. 28, 0. 0559 to 2. 01 and 0. 0584 to 2. 14μg/kg (S/N=3) in sunflower oil, soybean oil and corn oil samples respectively. The convenient operation and versatility of this method are suitable for the fast screening and detection of 34 pesticide residues in sunflower oil, soybean oil and corn oil.

Objective To observe the effects of global ischemia-reperfusion on inhibitory synaptic function in hippocampal CAl region of adult rats.Methods Animals were randomly divided into three groups: sham-operation group(SH),ischemia-reperfusion 3 day(IR-3) and 7 day group(IR-7).Global ischemic episode was achieved by 4-vessel occlusion.Evoked inhibitory postsynaptic currents(eIPSCs) were recorded from CA1 pyramidal cells in hippocampal slices using whole-cell voltage-clamp.Results The eIPSCs amplitudes generated by lower stimulus intensities were significantly decreased in both IR-3 and IR-7 rats as compared with SH rats.Moreover,the rise time of eIPSCs in IR-7 group was significantly decreased as compared with SH group(P