Because many of the animal studies performed to investigate the role of PUFA metabolites in tumor growth relied on the manipulation of CYP enzyme levels and/or the exogenous application of EETs, as well as the injection of tumor cell lines, this study set out to assess the consequences of sEH deletion in a spontaneous model of breast cancer, i.e., in PyMT mice. Here, EPHX2 is linked to neoplasm.