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Updated: Jul 1, 2025

Anticancer Efficacy of Photodynamic Therapy with Lung Cancer-Targeted Nanoparticles
Published on: December 1, 2016
Adjuvant Novel Nanocarrier-Based Targeted Therapy for Lung Cancer
Kangkan Sarma1, Md Habban Akther1, Irfan Ahmad2
1School of Pharmaceutical and Population Health Informatics (SoPPHI), DIT University, Dehradun 248009, India.
Abstract:
Lung cancer has the lowest survival rate due to its late-stage diagnosis, poor prognosis, and intra-tumoral heterogeneity. These factors decrease the effectiveness of treatment. They release chemokines and cytokines from the tumor microenvironment (TME). To improve the effectiveness of treatment, researchers emphasize personalized adjuvant therapies along with conventional ones. Targeted chemotherapeutic drug delivery systems and specific pathway-blocking agents using nanocarriers are a few of them. This study explored the nanocarrier roles and strategies to improve the treatment profile's effectiveness by striving for TME. A biofunctionalized nanocarrier stimulates biosystem interaction, cellular uptake, immune system escape, and vascular changes for penetration into the TME. Inorganic metal compounds scavenge reactive oxygen species (ROS) through their photothermal effect. Stroma, hypoxia, pH, and immunity-modulating agents conjugated or modified nanocarriers co-administered with pathway-blocking or condition-modulating agents can regulate extracellular matrix (ECM), Cancer-associated fibroblasts (CAF),Tyro3, Axl, and Mertk receptors (TAM) regulation, regulatory T-cell (Treg) inhibition, and myeloid-derived suppressor cells (MDSC) inhibition. Again, biomimetic conjugation or the surface modification of nanocarriers using ligands can enhance active targeting efficacy by bypassing the TME. A carrier system with biofunctionalized inorganic metal compounds and organic compound complex-loaded drugs is convenient for NSCLC-targeted therapy.
Insights
Nanocarriers offer novel strategies to enhance lung cancer treatment by targeting the tumor microenvironment (TME). These biofunctionalized systems improve drug delivery and modulate the TME for better therapeutic outcomes.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Oncology
Background:
- Lung cancer has a low survival rate due to late diagnosis, poor prognosis, and tumor heterogeneity, limiting treatment effectiveness.
- The tumor microenvironment (TME) releases factors that impede conventional therapies.
- Personalized adjuvant therapies, including targeted drug delivery, are crucial for improving treatment outcomes.
Purpose of the Study:
- To explore the role of nanocarriers in improving lung cancer treatment effectiveness by targeting the TME.
- To investigate strategies for enhancing nanocarrier penetration and function within the TME.
- To evaluate the potential of biofunctionalized nanocarriers for personalized non-small cell lung cancer (NSCLC) therapy.
Main Methods:
- Utilizing biofunctionalized nanocarriers to enhance interaction with biological systems, cellular uptake, and immune escape.
- Employing inorganic metal compounds for reactive oxygen species (ROS) scavenging via photothermal effects.
- Conjugating or modifying nanocarriers with agents to modulate the TME, including extracellular matrix (ECM), cancer-associated fibroblasts (CAFs), TAMs, Tregs, and MDSCs.
Main Results:
- Biofunctionalized nanocarriers facilitate penetration into the TME by stimulating vascular changes and immune system escape.
- Inorganic metal compounds within nanocarriers can scavenge ROS through photothermal effects.
- Modified nanocarriers, when co-administered with other agents, can regulate key components of the TME, such as CAFs and suppress T-cells.
Conclusions:
- Nanocarriers, particularly those with biofunctionalized inorganic metal compounds and complex-loaded drugs, show promise for targeted NSCLC therapy.
- Strategies involving nanocarrier modification and conjugation enhance active targeting and TME penetration.
- Personalized nanocarrier-based approaches hold potential for overcoming treatment resistance in lung cancer.
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