Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Tumor Immunotherapy01:27

Tumor Immunotherapy

643
Immunotherapy is a treatment that boosts or manipulates the immune system to fight diseases, including cancer. For instance, by stimulating an immune response through vaccinations against viruses that cause cancers, like hepatitis B virus and human papillomavirus, these diseases can be prevented. Nonetheless, some cancer cells can avoid the immune system due to their rapid mutation and division. The immune response to many cancers involves three phases: elimination, equilibrium, and escape.
643

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Thulium fiber laser versus holmium:YAG laser for ureteroscopic lithotripsy: a single-center retrospective cohort study.

Frontiers in surgery·2026
Same author

Formation of Bimetallic Nanoparticles via Exsolution Using a Reducible Metal Oxide Capping Layer.

ACS nano·2026
Same author

Self-Organized Nanoplasmonic Artificial Leaf for Hot-Carrier Bioelectronic Interfaces.

Nature photonics·2026
Same author

Efficient Hybrid Mixed Ion Perovskite Photovoltaics: <i>In Situ</i> Diagnostics of the Roles of Cesium and Potassium Alkali Cation Addition.

Solar RRL·2026
Same author

Prussian blue-based nanoplatforms for programmable and synergistic antimicrobial therapy.

Chemical communications (Cambridge, England)·2026
Same author

Suppressing Phase Segregation and Improving Stability in Mixed-Halide Perovskites through Spinel Oxide-Directed Epitaxy.

Journal of the American Chemical Society·2026
Same journal

An intrinsically stretchable nanowire-based sensing patch for wearable analysis of sweat chloride ion composition.

Chemical communications (Cambridge, England)·2026
Same journal

A sterically rigid-flexible balanced NHC-Pd precatalyst for room-temperature solvent-free C-N coupling of benzocyclic amines.

Chemical communications (Cambridge, England)·2026
Same journal

Portable fluorescent conjugated microporous polymer sensor coupled with a smartphone for on-site Fe<sup>3+</sup> detection in water.

Chemical communications (Cambridge, England)·2026
Same journal

Accelerated discovery of NO<sub>3</sub>RR single-atom catalysts <i>via</i> high-throughput DFT and machine learning.

Chemical communications (Cambridge, England)·2026
Same journal

Wafer-scale robust graphene electronics under industrial processing conditions.

Chemical communications (Cambridge, England)·2026
Same journal

Subnanoscale IrW oxide anodes: breaking immiscibility for high activity and durability in water electrolysis.

Chemical communications (Cambridge, England)·2026
See all related articles

Related Experiment Video

Updated: Aug 29, 2025

Experimental Melanoma Immunotherapy Model Using Tumor Vaccination with a Hematopoietic Cytokine
09:15

Experimental Melanoma Immunotherapy Model Using Tumor Vaccination with a Hematopoietic Cytokine

Published on: February 24, 2023

3.5K

Self-assemblies with cascade effect to boost antitumor systemic immunotherapy.

Ruipeng Li1, Xiaoyu Zhao1, Yunxia Wang1

  • 1School of Chemistry and Chemical Engineering, Shanxi University, Taiyuan, 030006, P. R. China. wangyunxia@sxu.edu.cn.

Chemical Communications (Cambridge, England)
|September 8, 2022
PubMed
Summary
This summary is machine-generated.

This study introduces a novel bio-organic self-assembly that releases nitric oxide (NO) in response to tumors and light. This multi-stage approach enhances antitumor activity, offering a new strategy for treating malignant tumors.

More Related Videos

A Nonviral Approach to Generate Transient Chimeric Antigen Receptor T Cells Using mRNA for Cancer Immunotherapy
09:56

A Nonviral Approach to Generate Transient Chimeric Antigen Receptor T Cells Using mRNA for Cancer Immunotherapy

Published on: February 21, 2025

754
Enrich and Expand Rare Antigen-specific T Cells with Magnetic Nanoparticles
09:28

Enrich and Expand Rare Antigen-specific T Cells with Magnetic Nanoparticles

Published on: November 17, 2018

11.7K

Related Experiment Videos

Last Updated: Aug 29, 2025

Experimental Melanoma Immunotherapy Model Using Tumor Vaccination with a Hematopoietic Cytokine
09:15

Experimental Melanoma Immunotherapy Model Using Tumor Vaccination with a Hematopoietic Cytokine

Published on: February 24, 2023

3.5K
A Nonviral Approach to Generate Transient Chimeric Antigen Receptor T Cells Using mRNA for Cancer Immunotherapy
09:56

A Nonviral Approach to Generate Transient Chimeric Antigen Receptor T Cells Using mRNA for Cancer Immunotherapy

Published on: February 21, 2025

754
Enrich and Expand Rare Antigen-specific T Cells with Magnetic Nanoparticles
09:28

Enrich and Expand Rare Antigen-specific T Cells with Magnetic Nanoparticles

Published on: November 17, 2018

11.7K

Area of Science:

  • Biomaterials Science
  • Nanotechnology
  • Cancer Research

Background:

  • Malignant tumors present a significant therapeutic challenge due to low cure rates.
  • Developing effective strategies for targeted cancer treatment remains a critical need.
  • Existing therapies often struggle with efficacy against both primary and distant tumor sites.

Purpose of the Study:

  • To fabricate bio-organic hybrid self-assemblies with tumor-responsive and light-triggered nitric oxide (NO) release.
  • To investigate the synergistic antitumor effects of a multi-level cascade strategy.
  • To enhance the efficacy of cancer therapy against primary and distant tumors.

Main Methods:

  • Fabrication of bio-organic hybrid self-assemblies using amino acids, conjugated polymers, Fe3+, and enzymes.
  • Incorporation of tumor environment-responsive and light-triggered NO release capabilities.
  • Evaluation of a three-level cascade strategy involving starvation, NO release, and immune activation (FFPG).

Main Results:

  • The developed FFPG exhibited tumor environment-responsive and light-triggered NO release.
  • Sequential energy consumption, NO attack, and immune activation led to boosted antitumor activity.
  • Significant efficacy was observed against both primary and distant tumors.

Conclusions:

  • The FFPG demonstrates a promising approach for enhanced antitumor activity through a multi-stage cascade.
  • This strategy addresses the limitations of current cancer therapies, particularly for malignant tumors.
  • The developed self-assembly offers a potential pathway to improve the cure rate of malignant tumors.