Newswise — STONY BROOK, NY, June 24,, 2019 -- A significant problem when treating cancer patients remains drug resistance, which often causes chemotherapy treatments to ultimately fail. Scientists in recent years have hypothesized that cell-cell differences, also known as cell heterogeneity, aides the emergence of drug resistance. Previous studies suggest that these effects depend on drug levels. To date this theory has not been experimentally tested. Now a new study published online in Nature Communications has tested this theory and yielded findings that may provide a path to reduce chemotherapy resistance.

Led by Gábor Balázsi, PhD, the Henry Laufer Associate Professor in Stony Brook University’s Laufer Center and Department of Biomedical Engineering, the research team engineered mammalian cell lines to test how chemotherapy drug resistance evolves in the context of cell-cell differences. The researchers developed a model system of two otherwise identical cell lines, except that synthetic gene circuits caused one of the cell lines to have higher heterogeneity. This enabled Balázsi and colleagues to mimic the evolution of drug resistance in the laboratory.

“After evolving these cells at various drug concentrations, we observed that heterogeneity does help the evolution of drug resistance at high drug concentrations, however, heterogeneity hinders drug resistance at low drug levels,” summarized Balázsi.

The researchers also discovered cells that are dormant, which neither grow nor die (called ‘persister’ cells) appear necessary for the evolution of drug resistance at high drug levels.

Their findings suggest that by combining current chemotherapy treatments with future methods that alter tumor heterogeneity, or by targeting persister cells, clinicians may be able to improve therapeutic efficiency by minimizing drug resistance.

“As we further advance this research, we may be able to evolve patients’ tumor cells in the laboratory as a powerful way to screen and optimize treatments,” projects Balázsi.

The National Institute of Health (NIH) has funded Balázsi’s drug resistance research for more than five years. The research for this paper was funded by the NIH’s National Institute of General Medical Sciences (NIGMS) MIRA grant, and the Laufer Center.


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