AI Article Synopsis

  • Following effective tumor therapy, some cancer cells can enter a dormant state, which may lead to tumor recurrence and poorer patient outcomes.
  • Research shows that redox mechanisms play a crucial role in the dormancy cycle, influencing how cancer cells enter dormancy, maintain it, and potentially relapse into active disease.
  • Various strategies aimed at manipulating redox signaling to target dormant cancer cells are being explored in early clinical trials, but the specific molecular pathways involved in redox control of these cells are still not well understood and require more investigation.

Article Abstract

Following efficient tumor therapy, some cancer cells may survive through a dormancy process, contributing to tumor recurrence and worse outcomes. Dormancy is considered a process where most cancer cells in a tumor cell population are quiescent with no, or only slow, proliferation. Recent advances indicate that redox mechanisms control the dormant cancer cell life cycle, including dormancy entrance, long-term dormancy, and metastatic relapse. This regulatory network is orchestrated mainly through redox modification on key regulators or global change of reactive oxygen species (ROS) levels in dormant cancer cells. Encouragingly, several strategies targeting redox signaling, including sleeping, awaking, or killing dormant cancer cells are currently under early clinical evaluation. However, the molecular mechanisms underlying redox control of the dormant cancer cell cycle are poorly understood and need further exploration. In this review, we discuss the underlying molecular basis of redox signaling in the cell life cycle of dormant cancer and the potential redox-based targeting strategies for eliminating dormant cancer cells.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8535080PMC
http://dx.doi.org/10.3390/cells10102707DOI Listing

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