ESTRO 2023 - Abstract Book

S696

Monday 15 May 2023

ESTRO 2023

PD-0826 Radiosensitization by DNA Damage response inhibitors correlates with Replication stress & HR scores W. Waissi 1 , S. Rebus 2 , R. Carruthers 3 , M. Jackson 4 , L. McGarry 5 , S. Dreyer 2 , D. Chang 2 , A. Chalmers 2 1 School of Cancer Sciences, Wolfson Wohl Cancer Research Centre, University of Glasgow, Glasgow, United Kingdom; 2 School of Cancer Sciences, Wolfson Wohl Cancer Research Centre, University of Glasgow, Glasgow, United Kingdom; 3 School of Cancer Sciences Wolfson Wohl Cancer Research Centre, University of Glasgow, Wohl Cancer Research Centre, University of Glasgow, Glasgow, United Kingdom; 4 School of Cancer Sciences Wolfson, Wohl Cancer Research Centre, University of Glasgow, Glasgow, United Kingdom; 5 Cancer Research UK, Beatson Institute, Glasgow, United Kingdom Purpose or Objective Pancreatic ductal adenocarcinoma (PDAC) is a devastating disease with 5-year overall survival of 9% for all stages. A key determinant of cellular radiosensitivity is the capacity to repair lethal DNA double-strand breaks (DSBs) that are induced by ionizing radiation. Targeting proteins involved in the DNA damage response (DDR) is therefore a promising therapeutic strategy, but predictive biomarkers are required to maximise clinical benefit. We conducted an in vitro study to determine the extent to which clinically relevant inhibitors of key DDR proteins (ATR, PARP and ATM) radiosensitized a panel of PDAC cell lines. We then looked for molecular alterations that associated with the magnitude of radiosensitization across the panel. Materials and Methods Eight patient derived PDAC cell lines were treated with small molecule inhibitors of ATR (AZD6738 : 20nM - 1 µ M), PARP (olaparib : 20nM - 1 µ M) or ATM (AZD1390: 1nM - 100nM) alone and in combination with radiation (0 to 6 Gy). Responses were evaluated by proliferation (8 cell lines) and clonogenic assays (7 cell lines). Sensitizer enhancement ratios (SERs) were calculated from mean inactivation doses, which were determined by integration of the LQ equation. Previously obtained genomic and transcriptomic data were then interrogated to identify possible biomarkers of radiosensitization. Transcriptomic replication stress (RS) scores were generated by totaling the score of GO Terms involved in DDR and cell cycle control (sig.score function from R package genefu). Three DDR deficiency scores derived from whole genome sequencing data were also assessed (BRCA signature, Structural Variant, HRDetect). Results The ATM inhibitor AZD1390 had no single agent activity but was a potent radiosensitizer at low concentrations and in all cell lines ( 5nM, SER 1.30-1.83; Fig.1). SER value for AZD1390 correlated with RS score as a continuous variable (p=0.01; Fig. 2). In contrast, the radiosensitizing effects of olaparib and AZD6738 were dependent on drug concentration and cell line. Cell lines harbouring homologous recombination deficiency (BRCA signature) and high RS score were radiosenstized by olaparib (SER :1.75 vs 1.09, p=0.01). and ATRi (SER : 1.35 vs 1.05) respectively (Fig. 2).

Figure 1 : Survival curves showing radiosensitization of 7 patient derived PDAC cell lines with ATRi(green), ATMi(Blue), PARPi(Red)