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Updated: Apr 22, 2026

Tissue Engineering of Tumor Stromal Microenvironment with Application to Cancer Cell Invasion
Published on: March 18, 2014
Emerging role of tissue lectins as microenvironmental effectors in tumors and wounds
Karel Smetana1, Pavol Szabo1, Peter Gal2
1Charles University, 1st Faculty of Medicine, Institute of Anatomy, Prague, Czech Republic.
Abstract:
Detailed comparative analysis of at first sight not related process cascades is a means toward this aim: to trace common effector mechanisms and hereby eventually inspire innovative routes for therapeutic management. Following this concept, promotion of tumor progression by stroma, especially cancer-associated fibroblasts and smooth muscle actin-positive myofibroblasts, and beneficial activity of respective cells in wound healing have helped to delineate the involvement of endogenous lectins of the family of galectins. In addition to initiating conversion of fibroblasts to myofibroblasts, galectin-1 instructs the cells to produce a structurally complex extracellular matrix. This bioscaffold is useful for keratinocyte culture, also apparently operative in ameliorating wound healing. These functional aspects encourage to study in detail how lectin-(glycan) counterreceptor display is orchestrated. Such insights are assumed to have potential to contribute to rationally manipulate stem/precursor cells as resource in regenerative medicine.
Insights
Comparing tumor progression and wound healing revealed galectins
Area of Science:
- Biochemistry
- Cell Biology
- Oncology
- Regenerative Medicine
Background:
- Stromal cells, including cancer-associated fibroblasts and myofibroblasts, significantly influence tumor progression.
- These same cell types play a beneficial role in wound healing processes.
- Endogenous lectins, specifically galectins, are implicated in both tumor promotion and wound repair.
Purpose of the Study:
- To investigate the common effector mechanisms underlying seemingly unrelated biological processes like tumor progression and wound healing.
- To elucidate the specific role of galectins in mediating these processes.
- To explore the potential of galectin-related insights for therapeutic strategies and regenerative medicine.
Main Methods:
- Comparative analysis of distinct biological process cascades (tumor progression vs. wound healing).
- Focus on the involvement and function of endogenous galectins and their counterreceptors.
- Investigation of galectin-1's role in fibroblast-to-myofibroblast conversion and extracellular matrix production.
Main Results:
- Galectins, particularly galectin-1, are identified as key mediators linking stromal cell activity in tumor progression and wound healing.
- Galectin-1 induces fibroblasts to differentiate into myofibroblasts and produce a complex extracellular matrix.
- This galectin-induced matrix shows potential utility in keratinocyte culture and wound healing amelioration.
Conclusions:
- Understanding galectin-mediated lectin-glycan interactions is crucial for deciphering their roles in disease and repair.
- Insights into these mechanisms may enable rational manipulation of stem/precursor cells for regenerative medicine applications.
- This research highlights a novel therapeutic avenue targeting galectin pathways for cancer and wound management.
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