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Echographic detection of diethylnitrosamine‐induced liver tumors in rats and the effect of the intratumoral injection of an inhibitor of c‐Jun N‐terminal kinase
Author(s) -
Hanajiri Kazuyuki,
Mitsui Hiroshi,
Maruyama Toshiyuki,
Hashimoto Naoaki,
Sata Masataka,
Omata Masao
Publication year - 2009
Publication title -
journal of gastroenterology and hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.214
H-Index - 130
eISSN - 1440-1746
pISSN - 0815-9319
DOI - 10.1111/j.1440-1746.2008.05722.x
Subject(s) - proliferating cell nuclear antigen , medicine , in vivo , carcinogenesis , pathology , c jun , kinase , cell growth , cell , cancer research , immunohistochemistry , biology , cancer , biochemistry , microbiology and biotechnology , gene , transcription factor
Background and Aim: There have so far been few reports describing echographic studies of chemically‐induced carcinogenesis in rodent livers. Using echography, we observed diethylnitrosamine‐induced liver tumors in rats and examined the effect of an intratumoral injection of an inhibitor of c‐Jun N‐terminal kinase. Methods: Male Wistar rats were given 100 ppm of diethylnitrosamine for 6 weeks and their liver nodules were examined by echography weekly. The size of the nodules was measured and they were examined histologically. The effect of SP600125, an inhibitor of c‐Jun N‐terminal kinase, on the growth of rat hepatoma cell line McA‐RH7777 was tested in vitro . Thereafter, SP600125 was injected into the liver nodules under echographic guidance in vivo and the changes in the proliferating cell nuclear antigen expression and size of the nodules were examined. Results: The four distinct lobes of rat livers were clearly observed by transabdominal echography. The nodules in the livers were first detected 6 weeks after the treatment began, when they were as small as 1.6 mm in diameter. The nodules thereafter became more malignant histologically as they grew larger than 4 mm. SP600125 decreased the expression of proliferating cell nuclear antigen and the growth of McA‐RH7777 cells. After SP600125 was injected in vivo , the proliferating cell nuclear antigen level and the growth rate of the rat liver nodules all significantly decreased. Conclusions: Our results indicate that echography is quite useful for follow‐up studies of liver carcinogenesis in rats, and c‐Jun N‐terminal kinase might be another therapeutic target in liver neoplasms.