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Related Concept Videos

Targeted Cancer Therapies02:57

Targeted Cancer Therapies

The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
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Site-targeted drug delivery systems enhance therapeutic efficacy while minimizing systemic toxicity and treatment costs. Unlike conventional methods, these systems ensure precise drug delivery, improving bioavailability and reducing side effects. Targeted drug delivery is classified into three levels. First-order targeting directs drugs to the capillary beds of specific organs or tissues. Second-order targets specific cell types, such as tumor cells, using receptor-mediated interactions.
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Related Experiment Video

Updated: Jun 8, 2026

Uptake of New Lipid-coated Nanoparticles Containing Falcarindiol by Human Mesenchymal Stem Cells
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Liposomes targeting tumour stromal cells.

Sylvia A Kuijpers1, Maria J Coimbra, Gert Storm

  • 1Division of Pharmaceutics, Department of Pharmaceutical Sciences, Utrecht Institute for Pharmaceutical Sciences, Faculty of Science, Utrecht University, Utrecht, The Netherlands.

Molecular Membrane Biology
|October 14, 2010
PubMed
Summary

Liposomes enhance cancer therapy by delivering drugs to tumor cells, minimizing side effects. Emerging strategies target tumor stromal cells to inhibit cancer growth and metastasis.

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Area of Science:

  • Oncology
  • Nanotechnology
  • Drug Delivery

Background:

  • Liposomes are clinically used for targeted delivery of cytostatic agents in cancer therapy, widening the therapeutic window by minimizing toxicity to healthy tissues.
  • Cancer therapy is increasingly focusing on tumor stromal cells, which promote tumor growth, invasion, and metastasis through chronic pro-inflammatory and pro-angiogenic signaling.
  • Tumor microenvironment modulation by cancer cells creates a pro-tumorigenic state, necessitating novel therapeutic approaches targeting these stromal components.

Purpose of the Study:

  • To review emerging liposomal formulations targeting key stromal cell types involved in tumor progression.
  • To discuss promising, yet untargeted, stromal cell populations in cancer therapy.
  • To highlight the shift from stromal cell depletion to modulating their activity towards an anti-tumor phenotype.

Main Methods:

  • Review of current literature on liposomal drug delivery systems in cancer therapy.
  • Analysis of studies focusing on targeting tumor microenvironment and stromal cells.
  • Identification of novel stromal cell targets and therapeutic strategies.

Main Results:

  • Liposomal formulations have been developed to target specific stromal cells contributing to tumor growth.
  • Many potential stromal cell targets remain underexplored in current research.
  • Existing strategies often focus on depleting stromal cells rather than reprogramming them.

Conclusions:

  • Future cancer therapy requires liposomal formulations that target specific stromal cells to modulate the tumor microenvironment.
  • Developing drugs that suppress pro-tumorigenic signals while preserving anti-tumor activities is crucial.
  • Optimizing liposomal strategies to reprogram stromal cells represents a significant challenge and opportunity for improved cancer treatment.