Targeting dormant micrometastases: rationale, evidence to date and clinical implications.

Ther Adv Med Oncol

Department of Pharmaceutical Sciences, College of Pharmacy, Oklahoma University Health Sciences Center, Oklahoma City, OK, USA.

Published: March 2016

AI Article Synopsis

  • Cancer survival rates have only improved slightly over the years primarily because research has focused on primary tumors rather than disseminated dormant cancer cells, which contribute to recurrence.
  • The paper highlights the need to better understand how these dormant cells work in order to find effective treatments and discusses potential drugs currently available or in clinical trials aimed at preventing metastasis.
  • It also presents new research from the authors' labs that demonstrates a successful screening method for targeting these dormant cancer cells, suggesting that addressing micrometastatic cells is achievable.

Article Abstract

In spite of decades of research, cancer survival has increased only modestly. This is because most research is based on models of primary tumors. Slow recognition has begun that disseminated, dormant cancer cells (micrometastatic cells) that are generally resistant to chemotherapy are the culprits in recurrence, and until these are targeted effectively we can expect only slow progress in increasing overall survival from cancer. This paper reviews efforts to understand the mechanisms by which cancer cells can become dormant, and thereby identify potential targets and drugs either on the market or in clinical trials that purport to prevent metastasis. This review targets the most recent literature because several excellent reviews have covered the literature from more than two years ago. The paper also describes recent work in the authors' laboratories to develop a screening-based approach that does not require understanding of mechanisms of action or the molecular target. Success of this approach shows that targeting micrometastatic cells is definitely feasible.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4753353PMC
http://dx.doi.org/10.1177/1758834015624277DOI Listing

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