Extracellular vesicle-mediated crosstalk in tumor microenvironment dominates tumor fate DOI

Xinyu Dou,

Chunyu Feng, Ji Li

et al.

Trends in Cell Biology, Journal Year: 2024, Volume and Issue: unknown

Published: Sept. 1, 2024

Language: Английский

Advanced Polymeric Nanoparticles for Cancer Immunotherapy: Materials Engineering, Immunotherapeutic Mechanism and Clinical Translation DOI Open Access

Wencong Jia,

Ye Wu, Yujie Xie

et al.

Advanced Materials, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 10, 2025

Abstract Cancer immunotherapy, which leverages immune system components to treat malignancies, has emerged as a cornerstone of contemporary therapeutic strategies. Yet, critical concerns about the efficacy and safety cancer immunotherapies remain formidable. Nanotechnology, especially polymeric nanoparticles (PNPs), offers unparalleled flexibility in manipulation‐from chemical composition physical properties precision control nanoassemblies. PNPs provide an optimal platform amplify potency minimize systematic toxicity broad spectrum immunotherapeutic modalities. In this comprehensive review, basics polymer chemistry, state‐of‐the‐art designs from physicochemical standpoint for encompassing vaccines, situ vaccination, adoptive T‐cell therapies, tumor‐infiltrating cell‐targeted antibodies, cytokine therapies are delineated. Each immunotherapy necessitates distinctively tailored design strategies nanoplatforms. The extensive applications PNPs, investigation their mechanisms action enhanced particularly focused on. profiles clinical research progress discussed. Additionally, forthcoming developments emergent trends nano‐immunotherapeutics poised transform treatment paradigms into clinics explored.

Language: Английский

Citations

5

FGF-based drug discovery: advances and challenges DOI
Gaozhi Chen, Lingfeng Chen, Xiaokun Li

et al.

Nature Reviews Drug Discovery, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 28, 2025

Language: Английский

Citations

4

A KIF20A-based thermosensitive hydrogel vaccine effectively potentiates immune checkpoint blockade therapy for hepatocellular carcinoma DOI Creative Commons

Xingyang Zhao,

Feichao Xuan,

Zirong Li

et al.

npj Vaccines, Journal Year: 2025, Volume and Issue: 10(1)

Published: Jan. 3, 2025

Language: Английский

Citations

2

Co-activating STING-TLR9 pathways promotes radiotherapy-induced cancer vaccination DOI
Yuling Sun, Liang Liu,

Huilan He

et al.

Journal of Controlled Release, Journal Year: 2025, Volume and Issue: 379, P. 327 - 343

Published: Jan. 14, 2025

Language: Английский

Citations

1

Integrin‐Targeted, Activatable Nanophototherapeutics for Immune Modulation: Enhancing Photoimmunotherapy Efficacy in Prostate Cancer Through Macrophage Reprogramming DOI Creative Commons
Cheng Zhang, Xiaolan Yin,

Lei Hao

et al.

Aggregate, Journal Year: 2025, Volume and Issue: unknown

Published: Feb. 2, 2025

ABSTRACT Prostate cancer is an epithelial malignancy with a high incidence among elderly men. Photochemistry‐based dye photodrugs (known as photosensitizers) offer promising clinical approach for treating tumors. These agents work by inducing immunogenic cell death (ICD), which activates antitumor immune response. This favored owing to its minimal invasiveness, low toxicity, and efficiency. However, the immunosuppressive microenvironment of characteristics “cold” tumors significantly restricts efficacy photodrugs. Developing advanced nanocarrier system deliver agonists efficient drug delivery tumor lesion sites reshape crucial in practice. Therefore, this study, we designed integrin‐targeted, activatable nano photodrug co‐assembly agonist (RPST@IMQ) enhancing photoimmunotherapy prostate via reprogramming tumor‐associated macrophages. The active‐targeted nanosystem enhanced dosage at site through systemic administration. High doses glutathione cleaved disulfide bonds RPST@IMQ, releasing imiquimod (IMQ). Under photoirradiation, generated significant singlet oxygen eliminate cells, thereby ICD activate responses. Simultaneously, released IMQ reprograms M2‐type macrophages (TAMs) into M1‐type TAMs tumor‐killing capabilities, converting “hot” conversion enhances therapeutic against primary distant vivo. study offers new insights development innovative, smart, enhance anticancer outcomes.

Language: Английский

Citations

1

A Biomimetic Autophagosomes‐Based Nanovaccine Boosts Anticancer Immunity DOI
Liping Qu,

Guanhong Cui,

Yinping Sun

et al.

Advanced Materials, Journal Year: 2024, Volume and Issue: unknown

Published: Aug. 28, 2024

Personalized cancer vaccines based on tumor cell lysates offer promise for immunotherapy yet fail to elicit a robust therapeutic effect due the weak immunogenicity of antigens. Autophagosomes, obtained from pleural effusions and ascites patients, have been identified as abundant reservoirs neoantigens that exhibit heightened immunogenicity. However, their potential personalized constrained by suboptimal lymphatic-targeting performances challenges in antigen-presenting endocytosis. Here,a reinforced biomimetic autophagosome-based (BAPs) nanovaccine generated precisely amalgamating autophagosome-derived two types adjuvants capable targeting lymph nodes is developed potently antitumor immunity. The redox-responsive BAPs facilitate cytosolic vaccine opening within cells, thereby exposing antigens stimulate strong immune response. evoke broad-spectrum T-cell responses, culminating effective eradication 71.4% established tumors. Notably, vaccination triggers enduring responses confer protection, with 100% mice shielded against rechallenge significant reduction incidence 87.5%. Furthermore, synergize checkpoint blockade therapy inhibit growth poorly immunogenic breast model. approach presents powerful formula high versatility immunotherapy.

Language: Английский

Citations

5

DNA Nanostructures‐Based In Situ Cancer Vaccines: Mechanisms and Applications DOI Open Access
Bingyu Lin, Yanfei Liu, Qi‐Wen Chen

et al.

Small Methods, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 22, 2025

Abstract Current tumor vaccines suffer from inadequate immune responsive due to the insufficient release of antigens, low infiltration, and immunosuppressive microenvironment. DNA nanostructures with their ability precisely engineer, controlled release, biocompatibility, capability augment immunogenicity microenvironment, have gained significant attention for potential revolutionize vaccine designing. This review summarizes various applications in construction situ cancer vaccines, which can generate tumor‐associated antigens directly damaged tumors immune‐stimulation. The mechanisms components are listed, specific strategies constructing using explored underlying action elucidated. immunogenic cell death (ICD) induced by chemotherapeutic agents, photothermal therapy (PTT), photodynamic (PDT), radiation (RT) related building systematically summarized. different immunotherapy elaborated, exerts precise, long‐lasting, robust responses. current challenges future prospectives proposed. provides a holistic understanding evolving role development.

Language: Английский

Citations

0

In situ vaccine “seeds” for enhancing cancer immunotherapy by exploiting apoptosis-associated morphological changes DOI
Binghua Wang,

Rong Guo,

Fujun Qiu

et al.

Journal of Controlled Release, Journal Year: 2025, Volume and Issue: 379, P. 757 - 767

Published: Jan. 25, 2025

Language: Английский

Citations

0

Subcellular Organelle Targeting as a Novel Approach to Combat Tumor Metastasis DOI Creative Commons
Zefan Liu, Yang Liu, Xin Kang

et al.

Pharmaceutics, Journal Year: 2025, Volume and Issue: 17(2), P. 198 - 198

Published: Feb. 5, 2025

Tumor metastasis, the spread of cancer cells from primary site to distant organs, remains a formidable challenge in oncology. Central this process is involvement subcellular organelles, which undergo significant functional and structural changes during metastasis. Targeting these specific organelles offers promising avenue for enhanced drug delivery metastasis therapeutic efficacy. This precision increases potency reduces potential off-target effects. Moreover, by understanding role each organelle treatments can be designed disrupt metastatic at multiple stages, cell migration establishment secondary tumors. review delves deeply into tumor processes their connection with organelles. In order target biomembranes, cell-penetrating peptides, localization signal aptamers, small molecules, various other strategies have been developed. review, we will elucidate targeting look forward prospects domain.

Language: Английский

Citations

0

CD44-targeting and ZIF-8-gated gold nanocage for programmed breast cancer therapy through Pt-induced immunogenic cell death DOI
Xin Li, Fei Xiong, Xudong Cao

et al.

Chinese Chemical Letters, Journal Year: 2025, Volume and Issue: unknown, P. 110970 - 110970

Published: Feb. 1, 2025

Language: Английский

Citations

0