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Regenerative therapy after cancer: what are the risks?
Vera S Donnenberg1, Ludovic Zimmerlin, Joseph Peter Rubin
1University of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania 15213, USA. donnenbergvs@upmc.edu
Regenerative tissue therapies may enhance cancer recurrence in active tumors. Dormant cancer cells are not affected, suggesting reconstruction should occur after cancer remission.
Area of Science:
- Regenerative medicine
- Oncology
- Tissue engineering
Background:
- Reconstruction after cancer surgery, particularly postmastectomy breast reconstruction, often requires tissue regeneration.
- Autologous fat transfer for breast reconstruction faces challenges with graft volume retention.
- Mesenchymal stem cells (MSCs) show potential for enhancing graft vascularization.
Purpose of the Study:
- To review the interactions between tumor cells and MSCs in regenerative conditions.
- To assess the potential risks of promoting cancer recurrence with regenerative therapies.
- To inform the timing of engineered tissue reconstruction relative to cancer treatment.
Main Methods:
- Review of coculture models examining tumor/MSC interactions.
- Analysis of animal models simulating regenerative tissue environments.
- Evaluation of evidence from case reports, cell lines, and clinical isolates.
Main Results:
- Regenerating tissue appears to promote the growth of active, high-grade tumors.
- Dormant cancer cells do not exhibit activation by wound healing and regeneration signals.
- Evidence suggests a differential effect based on tumor activity status.
Conclusions:
- Engineered tissue reconstruction involving regenerative therapies may increase the risk of recurrence for active cancers.
- Dormant cancer cells are less likely to be affected by regenerative processes.
- Tissue reconstruction should be postponed until cancer remission is definitively established.
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