Yanhua Liu’s research while affiliated with Ningxia Medical University and other places

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Publications (61)


Photothermal-magnetic driven post-targeting retention and cascade therapy of “biomimetic glue”-based nanoreactor for cancer theranostics by bystander-like killing
  • Article

April 2025

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1 Read

Chemical Engineering Journal

Zihan Liu

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Ting Yang

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Jiale Miao

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[...]

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Yanhua Liu




Fig. 1 -Schematic diagram of albumin nanoparticles bi-directionally manipulated ferroptosis in tumor and CD8 + T cells for TNBC therapy.
Fig. 2 -(A) ESI-MS spectrum of LA-Cys. (B) Receptor as cartoon and ligand as stick. (C) Albumin and Hemin interaction. Hydrogen bonds to L185 (3.3 ˚ A), R186 (3.0 ˚ A), E425 (2.8 ˚ A), Pi-Alkyl: R114, L115, R117, I142 and I523 residues, Van der waals: V116, H146, P149, G189, K190, Q459 and E520. (D) Albumin and LA-Cys interaction. Van der waals: R117, P118, M123, A126, F134, K137, E141, I142, H146, Y161, L182, G189, and K190, carbon hydrogen bond: R186. (E) Albumin and SSO interaction. The R432 residue of albumin forms hydrogen bonds with both the amide (3.3 ˚ A) and ester (2.5) carbonyl groups of SSO, van der waals: K190, A194, R197, E400, E425, N429, S435, K436 and Q459 Schematic diagrams of particle size distribution of (F) LHS NPs and (G) LH NPs. (H) SEM-EDS image of LHS NPs. Scale bar: 100 nm. (I) TEM image of LHS NPs. Scale bar: 100 nm. (J) MB degradation induced by the Fenton reaction of LHS NPs at different pH (7.4, 6.5 and 5.0).
Fig. 3 -(A) Fluorescent images of Ce6 internalization in 4T1 cells with free Ce6 and Ce6-labeled LHS NPs treatments for different incubation times. Scale bar: 20 μm. (B) Fe 2 + , (C) GSH, and (D) MDA content in 4T1 cells incubated with different treatments ( * P < 0.05, * * P < 0.01). (E) Fluorescent images of intracellular ROS generation with different treatments. Scale bar: 200 μm.
Fig. 4 -(A) In vitro cytotoxicity profiles of 4T1 cells against different treatments for 72 h incubation. (B and C) In vitro cell apoptosis induction analyzed by flow cytometry and quantification of different treatments against 4T1 cells ( * P < 0.05, * * P < 0.01). (D) Flow cytometry analysis and (E) quantification of free fatty acid uptake by M2-TAMs with free SSO and LHS NPs treatments ( * P < 0.05, * * P < 0.01). (F) CLSM observation of the lipid peroxidation of CD8 + T cells with different treatments. Scale bar: 20 μm. (G) CRT exposure on the 4T1 cell membrane after different treatments. Scale bar: 20 μm.
Fig. 5 -(A) In vivo and ex vivo imaging of 4T1 tumor-mice after treated with free DiR and DiR-labeled LHS NPs at different time points. (B) Schematic diagram of the treatment process. (C) Relative tumor volume changes over time, (D) tumor weight changes ( * p < 0.05, * * p < 0.01, n = 6), (E) Kaplan-Meier survival profiles, and (F) photographs of mice tumors following various treatments.

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Albumin nanoassembly bi-directionally manipulated ferroptosis in tumor and CD8+ T cells for triple-negative breast cancer therapy
  • Article
  • Full-text available

October 2024

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3 Reads

Asian Journal of Pharmaceutical Sciences

Download

Dual depletion of myeloid-derived suppressor cells and tumor cells with self-assembled gemcitabine-celecoxib nano-twin drug for cancer chemoimmunotherapy

June 2024

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14 Reads

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9 Citations

Myeloid-derived suppressor cells (MDSCs) have played a significant role in facilitating tumor immune escape and inducing an immunosuppressive tumor microenvironment. Eliminating MDSCs and tumor cells remains a major challenge in cancer immunotherapy. A novel approach has been developed using gemcitabine-celecoxib twin drug-based nano-assembled carrier-free nanoparticles (GEM-CXB NPs) for dual depletion of MDSCs and tumor cells in breast cancer chemoimmunotherapy. The GEM-CXB NPs exhibit prolonged blood circulation, leading to the preferential accumulation and co-release of GEM and CXB in tumors. This promotes synergistic chemotherapeutic activity by the proliferation inhibition and apoptosis induction against 4T1 tumor cells. In addition, it enhances tumor immunogenicity by immunogenic cell death induction and MDSC-induced immunosuppression alleviation through the depletion of MDSCs. These mechanisms synergistically activate the antitumor immune function of cytotoxic T cells and natural killer cells, inhibit the proliferation of regulatory T cells, and promote the M2 to M1 phenotype repolarization of tumor-associated macrophages, considerably enhancing the overall antitumor and anti-metastasis efficacy in BALB/c mice bearing 4T1 tumors. The simplified engineering of GEM-CXB NPs, with their dual depletion strategy targeting immunosuppressive cells and tumor cells, represents an advanced concept in cancer chemoimmunotherapy. Graphical Abstract


Hybrid nano-stimulator for specific amplification of oxidative stress and precise tumor treatment

June 2024

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9 Reads

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2 Citations

Journal of Drug Targeting

Background: The use of reactive oxygen species (ROS) to target cancer cells has become a hot topic in tumor therapy. Purpose: Although ROS has strong cytotoxicity against tumor cells, the key issue currently is how to generate a large amount of ROS within tumor cells. Methods: Organic/inorganic hybrid nanoreactor materials combine the advantages of organic and inorganic components and can amplify cancer treatment by increasing targeting and material self-action. The multifunctional organic / inorganic hybrid nanoreactor is helpful to overcome the shortcomings of current reactive oxygen species in cancer treatment. It can realize the combination of in situ dynamic therapy and immunotherapy strategies, and has a synergistic anti-tumor effect. Results: This paper reviews the research progress of organic/inorganic hybrid nanoreactor materials using tumor components to amplify reactive oxygen species for cancer treatment. The article reviews the tumor treatment strategies of nanohybrids from the perspectives of cancer cells, immune cells, tumor microenvironment, as well as 3D printing and electrospinning techniques, which are different from traditional nanomaterial technologies, and will arouse interest among scientists in tumor therapy and nanomedicine.


Nanomedicine targeted anti-inflammatory therapy to deal with the "crux" of rheumatoid arthritis

February 2024

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7 Reads

Journal of Drug Targeting

Rheumatoid arthritis is a chronic and complex autoimmune disease that is marked by an inflammatory response, synovial hyperplasia, vascularisation, fascial formation, cartilage and bone destruction, which can lead to joint deformity and even loss of function, ultimately affecting a person's health and quality of life. Although the pathogenesis of RA is unclear, growing evidence suggests that inflammation-associated cells infiltrate joints, causing tissue damage, inflammation and pain. This disruption in the balance between host tolerance and immune homeostasis the progression of RA. Existing drug therapy and surgical treatments for RA are unable to completely cure the disease or reverse its accelerated progression. Therefore, the design and development of an appropriate and effective drug delivery system will substantially improve the therapeutic effect. In this review, by describing the inflammatory microenvironment of rheumatoid arthritis and the associated inflammatory cells, the progress of targeting strategies and applications of nanotechnology in the disease is summarised, which will be helpful in providing new ideas for the subsequent treatment of rheumatoid arthritis.


Nano-medicine therapy reprogramming metabolic network of tumor microenvironment: new opportunity for cancer therapies

January 2024

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12 Reads

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4 Citations

Journal of Drug Targeting

Metabolic heterogeneity is one of the characteristics of tumour cells. In order to adapt to the tumour microenvironment of hypoxia, acidity and nutritional deficiency, tumour cells have undergone extensive metabolic reprogramming. Metabolites involved in tumour cell metabolism are also very different from normal cells, such as a large number of lactate and adenosine. Metabolites play an important role in regulating the whole tumour microenvironment. Taking metabolites as the target, it aims to change the metabolic pattern of tumour cells again, destroy the energy balance it maintains, activate the immune system, and finally kill tumour cells. In this paper, the regulatory effects of metabolites such as lactate, glutamine, arginine, tryptophan, fatty acids and adenosine were reviewed, and the related targeting strategies of nano-medicines were summarised, and the future therapeutic strategies of nano-drugs were discussed. The abnormality of tumour metabolites caused by tumour metabolic remodelling not only changes the energy and material supply of tumour, but also participates in the regulation of tumour-related signal pathways, which plays an important role in the survival, proliferation, invasion and metastasis of tumour cells. Regulating the availability of local metabolites is a new aspect that affects tumour progress. (The graphical abstract is by Figdraw).



Citations (47)


... MDSCs promote tumor immune evasion primarily by secreting factors such as IL-10 and TGF-β and interacting with T cells and other immune cells, posing a significant challenge in cancer immunotherapy. The development of carrier-free nanoparticles, like gemcitabine-celecoxib nanoparticles (GEM-CXB NP), provides novel approaches for chemoimmunotherapy in BC [45]. Therefore, therapeutic strategies targeting MDSC signaling pathways remain a focal point for future research. ...

Reference:

A Systematic Review of Immune Cell Roles in Breast Cancer Immunotherapy
Dual depletion of myeloid-derived suppressor cells and tumor cells with self-assembled gemcitabine-celecoxib nano-twin drug for cancer chemoimmunotherapy

... Another significant alteration in exhausted CD8 + T cells is the disruption of amino acid metabolism. The availability of key amino acids, such as glutamine, arginine, and tryptophan, is limited inside the TME 72 . Decreased uptake and utilization of these amino acids hinders the synthesis of nucleotides and polyamines critical for T cell function 73,74 . ...

Nano-medicine therapy reprogramming metabolic network of tumor microenvironment: new opportunity for cancer therapies
  • Citing Article
  • January 2024

Journal of Drug Targeting

... These exosomes can be loaded with immune adjuvants to enhance tumor immunogenicity and improve immunotherapeutic outcomes . A key advantage of nanomedicine in personalized immunotherapy is its ability to overcome tumor heterogeneity, a significant challenge in achieving consistent treatment responses across patient populations [72][73][74]. Nanoparticles can be engineered to carry multiple therapeutic agents simultaneously, allowing for combinational delivery that targets various tumor pathways. For example, dendrimers have been explored as nanocarriers for siRNA, monoclonal antibodies, and chemotherapeutics, providing a multifaceted approach to disrupt tumor growth and induce an immune response . ...

Recent Advancements in Nanomedicine Based Lipid Metabolism for Tumor lmmunotherapy
  • Citing Article
  • November 2023

Journal of Drug Targeting

... Others authors employed pH-induced release, such as Cao et al. (2023). By complexing CXB with Poly-L-arginine arranged in micelles, it was expected that the acidic environment of the tumor microenvironment would promote the drug release and subsequent inhibition of the COX-2 related immunosuppressive profile [89]. ...

Tumor Microenvironment Sequential Drug/Gene Delivery Nanosystem for Realizing Multistage Boosting of Cancer-Immunity Cycle on Cancer Immunotherapy
  • Citing Article
  • November 2023

ACS Applied Materials & Interfaces

... PVP, lecithin, and PEG 400). A prolonged pain relief was reported with all MLX nanosuspensions compared to the control (MLX in solution) in a hind paw incision rat model, which is a common pain in vivo model for RA [32,33]. IV/infusion administration of NCs entails invasiveness and pain at the injection site that hamper therapeutic adherence, requiring a health care facility for the therapeutic follow-up. ...

In vivo behaviors of meloxicam nanocrystals by intravenous administration are not significantly affected by stabilizers
  • Citing Article
  • March 2023

Journal of Drug Delivery Science and Technology

... However, numerous challenges can be encountered, including protein adsorption, the influence of physical forces, and rapid clearance, which can obstruct effective biodistribution and drug delivery under normal physiological conditions [57,58]. The goal of developing nanoparticles is to overcome the deficiency of traditional drug delivery systems by eliminating diverse biological obstacles across patient groups and disorders [59,60]. The formulations for pH-dependent drug release use polymers whose characteristics change in response to local pH levels; while preserving stable drug loading at non-target tissues, they also provide target-specific drug release. ...

Programmed pH-responsive core-shell nanoparticles for precisely targeted therapy of ulcerative colitis
  • Citing Article
  • January 2023

Nanoscale

... Notably, HSA fusion technology has led to the development of various long-acting protein drugs now approved for treating diseases such as type II diabetes and hemophilia [8]. Additionally, HSA serves as a universal target for various antibody drugs, effectively extending their half-life in vivo by binding to HSA [9,10]. Therefore, HSA is not only an approved drug carrier but is Si-Yuan Hu and Wen Lin contributed equally to this work. ...

Bioinspired Nanocomplexes Comprising Phenolic Acid Derivative and Human Serum Albumin for Cancer Therapy
  • Citing Article
  • December 2022

Nano Letters

... Liquideliquid phase separation (LLPS) refers to the phenomenon that homogeneous solution divides into two liquid phases with the process of molecular self-assembly, one rich and one poor in solute (Fraccia & Zanchetta, 2021;Huang et al., 2023Huang et al., , 2024Xu et al., 2021;Zhao et al., 2023). Particles with various micro/nano structures can be generated by reasonably adjusting process parameters of LLPS Wang et al., 2022). ...

Liquid–liquid phase separation drug aggregate: Merit for oral delivery of amorphous solid dispersions
  • Citing Article
  • January 2023

Journal of Controlled Release

... A number of studies have shown that interventions that target certain cells involved in liver fibrosis can slow down or even reverse the progression of liver fibrosis and can significantly reduce the development of severe chronic liver disease. [5][6][7] Liver fibrosis is currently being treated by protecting normal liver cells, 8 inhibiting hepatic stellate cells (HSCs) activation, 9 decreasing extracellular matrix synthesis and secretion, 10 and reducing liver inflammation. Interferons (INF; INF-γ), 11 anti-HBV nucleotides and their analogues, 12 endothelin receptor A antagonists, 13,14 angiotensin receptor blockers, and extracts of natural products such as colchicine 15 and silymarin 16 are commonly used in the treatment of liver fibrosis, with some success. ...

Collagenase-I decorated co-delivery micelles potentiate extracellular matrix degradation and hepatic stellate cell targeting for liver fibrosis therapy
  • Citing Article
  • September 2022

Acta Biomaterialia

... Artesunate (ART) is a natural small molecule compound that shows promising potential in post-transplant immunotherapy [4]. Previous research has indicated that ART regulates inflammasome activity by inhibiting the Toll-like receptor-4 (TLR-4) signaling pathway, suppresses inflammation-related signaling pathways, and promotes the polarization of macrophages to the M2 phenotype [5,6]. Mycophenolate mofetil (MMF) acts on lymphocyte proliferation, reducing T cell proliferation and activation, and modulating the Type 1 CD4 + T cells (Th1)/Type 2 CD4 + T cells (Th2) balance. ...

An ROS-responsive artesunate prodrug nanosystem co-delivers dexamethasone for rheumatoid arthritis treatment through the HIF-1α/NF-κB cascade regulation of ROS scavenging and macrophage repolarization
  • Citing Article
  • August 2022

Acta Biomaterialia