Polyploidy in Cancer: Causal Mechanisms, Cancer-Specific Consequences, and Emerging Treatments

Author:

Conway Patrick J.12ORCID,Dao Jonathan13ORCID,Kovalskyy Dmytro4ORCID,Mahadevan Daruka125ORCID,Dray Eloise35ORCID

Affiliation:

1. 1Mays Cancer Center, University of Texas Health San Antonio, San Antonio, Texas.

2. 2Department of Molecular Immunology & Microbiology, University of Texas Health San Antonio, San Antonio, Texas.

3. 3Long School of Medicine, University of Texas Health San Antonio, San Antonio, Texas.

4. 4Greehey Children's Cancer Research Institute, University of Texas Health San Antonio, San Antonio, Texas.

5. 5Department of Biochemistry and Structural Biology, University of Texas Health San Antonio, San Antonio, Texas.

Abstract

Abstract Drug resistance is the major determinant for metastatic disease and fatalities, across all cancers. Depending on the tissue of origin and the therapeutic course, a variety of biological mechanisms can support and sustain drug resistance. Although genetic mutations and gene silencing through epigenetic mechanisms are major culprits in targeted therapy, drug efflux and polyploidization are more global mechanisms that prevail in a broad range of pathologies, in response to a variety of treatments. There is an unmet need to identify patients at risk for polyploidy, understand the mechanisms underlying polyploidization, and to develop strategies to predict, limit, and reverse polyploidy thus enhancing efficacy of standard-of-care therapy that improve better outcomes. This literature review provides an overview of polyploidy in cancer and offers perspective on patient monitoring and actionable therapy.

Funder

National Cancer Institute

Publisher

American Association for Cancer Research (AACR)

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