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Radiotherapy, EMP and dormancy in TME: An integrated perspective on tumor microenvironments and long-term relapse
Yebin Lee1, Byeongseok Jang1, Hae-Yun Jung1
1Division of Radiation Biomedical Research, Korea Institute of Radiological and Medical Sciences, Seoul, South Korea.
Radiotherapy can cause dormant cancer cells to spread, leading to recurrence. Understanding the link between radiotherapy, epithelial-mesenchymal plasticity, and dormancy may help prevent long-term cancer relapse.
Area of Science:
- Oncology
- Cancer Biology
- Radiotherapy Research
Background:
- Radiotherapy (RT) is a cornerstone of cancer treatment, but local and distant recurrences persist.
- Dormant tumor cells, often quiescent, are implicated in post-RT relapse and metastasis.
- Epithelial-mesenchymal plasticity (EMP) is a key process enabling tumor cell dormancy and subsequent reawakening.
Purpose of the Study:
- To review the molecular interplay between radiotherapy, EMP, and metastatic dormancy.
- To explore how RT influences metastasis and the dormant state of cancer cells.
- To propose therapeutic strategies targeting RT-induced metastasis and long-term relapse.
Main Methods:
- Literature review and synthesis of current research findings.
- Analysis of molecular mechanisms linking RT, EMP, and dormancy.
- Discussion of potential therapeutic interventions.
Main Results:
- Radiotherapy may modulate metastatic processes and induce or maintain tumor cell dormancy.
- EMP is a critical mechanism for disseminated tumor cells (DTCs) to achieve and maintain dormancy after RT.
- A complex relationship exists between RT, EMP, and the establishment of metastatic dormancy.
Conclusions:
- Targeting EMP and dormancy pathways could be crucial for preventing RT-mediated metastasis.
- Developing strategies to block RT-induced dormancy and reawakening is essential for improving long-term patient outcomes.
- Further research into the molecular links between RT, EMP, and dormancy may yield novel therapeutic approaches to prevent cancer recurrence.
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