Adaptive DNA amplification of synthetic gene circuit opens a way to overcome cancer chemoresistance

Author:

Wan Yiming12ORCID,Mu Quanhua3ORCID,Krzysztoń Rafał12ORCID,Cohen Joseph12,Coraci Damiano12,Helenek Christopher12ORCID,Tompkins Christopher4,Lin Annie12,Farquhar Kevin12,Cross Erin4,Wang Jiguang3ORCID,Balázsi Gábor125ORCID

Affiliation:

1. Department of Biomedical Engineering, Stony Brook University, Stony Brook, NY 11794

2. The Louis and Beatrice Laufer Center for Physical and Quantitative Biology, Stony Brook University, Stony Brook, NY 11794

3. Department of Chemical and Biological Engineering, Division of Life Science, State Key Laboratory of Molecular Neuroscience, The Hong Kong University of Science and Technology, Hong Kong Special Administrative Region 999077, China

4. KromaTid, Inc., Longmont, CO 80501

5. Stony Brook Cancer Center, Stony Brook University, Stony Brook, NY 11794

Abstract

Drug resistance continues to impede the success of cancer treatments, creating a need for experimental model systems that are broad, yet simple, to allow the identification of mechanisms and novel countermeasures applicable to many cancer types. To address these needs, we investigated a set of engineered mammalian cell lines with synthetic gene circuits integrated into their genome that evolved resistance to Puromycin. We identified DNA amplification as the mechanism underlying drug resistance in 4 out of 6 replicate populations. Triplex-forming oligonucleotide (TFO) treatment combined with Puromycin could efficiently suppress the growth of cell populations with DNA amplification. Similar observations in human cancer cell lines suggest that TFOs could be broadly applicable to mitigate drug resistance, one of the major difficulties in treating cancer.

Funder

HHS | National Institutes of Health

SUNY | SBU | Laufer Center for Physical and Quantitative Biology, Stony Brook University

Stony Brook Cancer Center

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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