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The impact of non-genetic heterogeneity on cancer cell death

Journal

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/10409238.2017.1412395

Keywords

Cell death; heterogeneity; apoptosis; cancer; single-cell

Funding

  1. National Science Foundation [DGE-1656518]
  2. NIH [4R00CA166517, 1R01GM122923]
  3. Damon Runyon Cancer Research Foundation
  4. NATIONAL CANCER INSTITUTE [R00CA166517, T32CA009302] Funding Source: NIH RePORTER
  5. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM122923] Funding Source: NIH RePORTER

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The goal of cancer chemotherapy is to induce homogeneous cell death within the population of targeted cancer cells. However, no two cells are exactly alike at the molecular level, and sensitivity to drug-induced cell death, therefore, varies within a population. Genetic alterations can contribute to this variability and lead to selection for drug resistant clones. However, there is a growing appreciation for the role of non-genetic variation in producing drug-tolerant cellular states that exhibit reduced sensitivity to cell death for extended periods of time, from hours to weeks. These cellular states may result from individual variation in epigenetics, gene expression, metabolism, and other processes that impact drug mechanism of action or the execution of cell death. Such population-level non-genetic heterogeneity may contribute to treatment failure and provide a cellular substrate for the emergence of genetic alterations that confer frank drug resistance.

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