Serous borderline ovarian tumors (SBOTs) behave between benign cystadenomas and
carcinomas, and the effective detection and clinical management of SBOTs remain clinical
challenges. Because it is difficult to isolate and enrich borderline tumor cells, a
borderline animal model is in need. 7,12-dimethylbenz[a]anthracene (DMBA) is capable of
inducing the initiation, promotion, and progression of serous ovarian tumors. This study
aims to investigate the proper dosage and induction time of DMBA for rat models of SBOTs,
and explore their morphological features demonstrated by magnetic resonance (MR) imaging
and molecular genetic characteristics. Rats were randomly divided into six groups (1 mg/70
D, 2 mg/70 D, 3 mg/70 D, 2 mg/50 D, 2 mg/90 D, and 2 mg/110 D). The 3 mg/70 D group
induced the most SBOTs (50.0%, 12/24). The micropapillary projections were shown on MR
imaging, which was the characteristic of SBOTs. The Cyclin D1 characterizing an early
pathogenetic event strongly expressed in induced serous benign tumors (SBTs). The
immunoreactivity staining scores of P53 expression significantly increased from SBTs,
SBOTs to serous ovarian carcinomas (SCAs), which elucidate that P53 might be a promising
biomarker to grade serous ovarian tumors. Based on morphological and molecular genetic
similarities, this rodent SBOT model was suitable for investigating the pathogenesis of
serous ovarian tumors and developing an early detection strategy.