TY - JOUR T1 - Oral Carcinogenesis Is not Achieved in Different Carcinogen-treated PAI-1 Transgenic and Wild-type Mouse Models JF - In Vivo JO - In Vivo SP - 1001 LP - 1005 VL - 26 IS - 6 AU - DIMITRIS AVGOUSTIDIS AU - THEMISTOKLIS NISYRIOS AU - EMEKA NKENKE AU - ROGER LIJNEN AU - VASSILIS RAGOS AU - DESPINA PERREA AU - ISMINI DONTA AU - APOSTOLIA VAENA AU - CHRISTOS YAPIJAKIS AU - ELEFTHERIOS VAIRAKTARIS Y1 - 2012/11/01 UR - http://iv.iiarjournals.org/content/26/6/1001.abstract N2 - Aim: In an effort to assess the role of plasminogen activator inhibitor-1 (PAI-1) in oral squamous cancer development and progression, two different carcinogen treatment protocols were conducted. Materials and Methods: Protocol I included mice from a PAI-1 transgenic (Tg) breed (n=56) and their wild-type (WT) counterparts (n=56), divided into one control group and two main experimental groups, treated with 7,12-dimethylbenz[a]anthracene (DMBA) for 8 and 16 weeks, respectively. Protocol II included the same number and types of animals and groups, which were similarly treated with 4-Nitroquinoline 1-oxide (4-NQO) in drinking water. Two drugs that affect plasma PAI-1 levels, enalapril and pravastatin, were administered to certain subgroups of animals in both protocols. Results: None of the animals developed macroscopically-visible oral cancer lesions. Eleven animals under Protocol I and 52 animals under Protocol II died. Skin lesions were noted only in DMBA-treated animals (n=9). Almost all animals administered with 4-NQO developed alopecia and lost weight, while two of them developed stomach tumours, and one female mouse developed a large ovarian cyst. Conclusion: Transgenic mice may respond differently when used in well-established carcinogen models and oral carcinogenesis is hard to achieve in these rodents. ER -