monitoring-cancer-cell-invasion-and-t-cell-cytotoxicity-in-3d-culture

Monitoring Cancer Cell Invasion and T-Cell Cytotoxicity in 3D Culture

Significant progress has been made in treating cancer with immunotherapy, although a large number of cancers remain resistant to treatment. A limited ...

Georgetown University

Base excision repair (BER) is one of the most frequently used cellular DNA repair mechanisms and modulates many human pathophysiological conditions related to DNA damage. Through live cell and  reconstitution experiments, we have discovered a major sub-pathway of conventional long-patch BER that involves formation of a 9-nucleotide gap 5' to the lesion. This new sub-pathway is mediated by RECQ1 DNA helicase and ERCC1-XPF endonuclease in cooperation with PARP1 poly(ADP-ribose) polymerase and RPA The novel gap formation step is employed during repair of a variety of DNA lesions, including oxidative and alkylation damage. Moreover, RECQ1 regulates PARP1 auto-(ADP-ribosyl)ation and the choice between long-patch and single-nucleotide BER, thereby modulating cellular sensitivity to DNA damage. Based on these results, we propose a revised model of long-patch BER and a new key regulation point for pathway choice in BER.

Sharon Camacho

Lombardi Comprehensive Cancer Center,
Department of Oncology,
Lombardi Comprehensive Cancer Center, Department of Oncology

Georgetown University

Monitoring Cancer Cell Invasion and T-Cell Cytotoxicity in 3D Culture

Sharon Camacho

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Georgetown University

Monitoring Cancer Cell Invasion and T-Cell Cytotoxicity in 3D Culture

Lombardi Comprehensive Cancer Center,
Department of Oncology,
Lombardi Comprehensive Cancer Center, Department of Oncology