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A Mouse Model to Investigate the Role of Cancer-Associated Fibroblasts in Tumor Growth
Published on: December 22, 2020
Drug targeting to myofibroblasts: Implications for fibrosis and cancer
Saleh Yazdani1, Ruchi Bansal1, Jai Prakash2
1Targeted Therapeutics Division, Department of Biomaterials, Science and Technology, MIRA Institute for Biomedical Technology and Technical Medicine, University of Twente, Enschede, The Netherlands.
Abstract:
Myofibroblasts are the key players in extracellular matrix remodeling, a core phenomenon in numerous devastating fibrotic diseases. Not only in organ fibrosis, but also the pivotal role of myofibroblasts in tumor progression, invasion and metastasis has recently been highlighted. Myofibroblast targeting has gained tremendous attention in order to inhibit the progression of incurable fibrotic diseases, or to limit the myofibroblast-induced tumor progression and metastasis. In this review, we outline the origin of myofibroblasts, their general characteristics and functions during fibrosis progression in three major organs: liver, kidneys and lungs as well as in cancer. We will then discuss the state-of-the art drug targeting technologies to myofibroblasts in context of the above-mentioned organs and tumor microenvironment. The overall objective of this review is therefore to advance our understanding in drug targeting to myofibroblasts, and concurrently identify opportunities and challenges for designing new strategies to develop novel diagnostics and therapeutics against fibrosis and cancer.
Insights
Myofibroblasts drive fibrosis and cancer progression. Targeting these cells offers new therapeutic strategies for incurable fibrotic diseases and cancer, addressing key challenges in drug development.
Area of Science:
- Cell Biology
- Pathology
- Pharmacology
Background:
- Myofibroblasts are crucial for extracellular matrix remodeling in fibrotic diseases.
- Myofibroblasts also play a significant role in tumor progression, invasion, and metastasis.
- Targeting myofibroblasts is a promising strategy for treating fibrotic diseases and cancer.
Purpose of the Study:
- To review the origin, characteristics, and functions of myofibroblasts in liver, kidney, and lung fibrosis, as well as in cancer.
- To discuss current drug targeting technologies for myofibroblasts in fibrotic organs and the tumor microenvironment.
- To identify opportunities and challenges for developing novel diagnostics and therapeutics against fibrosis and cancer by targeting myofibroblasts.
Main Methods:
- Literature review of myofibroblast biology and therapeutic targeting strategies.
- Analysis of myofibroblast roles in organ fibrosis (liver, kidneys, lungs) and cancer.
- Evaluation of state-of-the-art drug targeting technologies.
Main Results:
- Myofibroblasts are central to extracellular matrix remodeling in fibrotic diseases and contribute to cancer progression.
- Diverse origins and functions of myofibroblasts across different organs and cancer types.
- Current drug targeting technologies show potential but face challenges in efficacy and specificity.
Conclusions:
- Understanding myofibroblast biology is key to developing effective anti-fibrotic and anti-cancer therapies.
- Advanced drug targeting strategies are needed to overcome challenges in myofibroblast-specific therapies.
- Further research is essential for novel diagnostics and therapeutics targeting myofibroblasts in fibrosis and cancer.
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