4.6 Review

Targeting dormant tumor cells to prevent cancer recurrence

Journal

FEBS JOURNAL
Volume 288, Issue 21, Pages 6286-6303

Publisher

WILEY
DOI: 10.1111/febs.15626

Keywords

cancer recurrence; cell‐ cycle modulation; dormancy‐ targeting drugs; dormant cancer cells; enhanced drug delivery; therapy resistance

Funding

  1. European Research Council [648804]
  2. Doctor Josef Steiner Foundation
  3. Boehringer Ingelheim Fonds PhD Fellowship
  4. European Research Council (ERC) [648804] Funding Source: European Research Council (ERC)

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Developments in oncology have improved clinical outcomes for cancer patients, but cancer recurrence remains a major challenge, particularly involving dormant cancer cells. Current therapies are largely ineffective against dormant cancer cells, necessitating exploration of novel therapy strategies.
Over the years, developments in oncology led to significantly improved clinical outcome for cancer patients. However, cancer recurrence after initial treatment response still poses a major challenge, as it often involves more aggressive, metastatic disease. The presence of dormant cancer cells is associated with recurrence, metastasis, and poor clinical outcome, suggesting that these cells may play a crucial role in the process of disease relapse. Cancer cell dormancy typically presents as growth arrest while retaining proliferative capacity and can be induced or reversed by a wide array of cell-intrinsic and cell-extrinsic factors. Conventional therapies preferentially target fast-dividing cells, leaving dormant cancer cells largely insensitive to these treatments. In this review, we discuss the role of dormant cancer cells in cancer recurrence and highlight how novel therapy strategies based on cell-cycle modulation, modifications of existing drugs, or enhanced drug-delivery vehicles may be used to specifically target this subpopulation of tumor cells, and thereby have the potential to prevent disease recurrence.

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