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Tumorigenic Cell Reprogramming and Cancer Plasticity: Interplay between Signaling, Microenvironment, and Epigenetics
Vittoria Poli1, Luca Fagnocchi1, Alessio Zippo1,2,3
1Laboratory of Chromatin Biology and Epigenetics, Center for Integrative Biology (CIBIO), University of Trento, 38123 Trento, Italy.
Stem Cells International
|June 2, 2018
Summary
Cancer stem cells (CSCs) drive tumor growth and relapse due to treatment resistance. Understanding CSC plasticity and targeting these cells are key to overcoming solid tumors.
Area of Science:
- Oncology
- Cancer Biology
- Stem Cell Research
Background:
- Cancer stem cells (CSCs) are crucial for tumor propagation, resistance to therapy, and relapse.
- CSCs can arise from normal cells or through dedifferentiation of non-stem cancer cells.
- Tumor microenvironment and epigenetic changes drive CSC formation and cancer cell plasticity.
Purpose of the Study:
- To elucidate the role of cancer cell origin and CSC plasticity in solid tumor initiation and maintenance.
- To discuss signaling pathways and epigenetic mechanisms involved in CSC formation.
- To review strategies for targeting CSCs and cancer cell plasticity.
Main Methods:
- Review of current literature on cancer stem cells.
- Analysis of signaling pathways and epigenetic mechanisms.
- Synthesis of therapeutic strategies targeting CSCs.
Main Results:
- CSCs possess inherent resistance to conventional treatments, contributing to tumor recurrence.
- Cancer cell plasticity, influenced by the microenvironment and epigenetics, is vital for tumor heterogeneity.
- Specific signaling pathways and epigenetic alterations are critical for CSC maintenance.
Conclusions:
- Targeting CSCs and their plasticity is essential for effective cancer therapy.
- Understanding the origin and maintenance of CSCs offers new therapeutic avenues.
- Epigenetic reprogramming and microenvironmental factors are key regulators of CSCs.
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