Additional characterization of these endpoint tumors showed a highly significant reduction in the percentage of ductal tumor lesions in EMyc:PARP2 –/– compared with EMyc:PARP2 +/+ mice (8.7 versus 38.7%) ( Fig. 2E ).
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PARP2 deficiency impairs pancreatic cancer progression by promoting genomic instability and antitumor immunity.
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