TUMOR MARKERS IN RATS WITH RENAL TUMOR INDUCED BY N-ETHYL-N-HYDROXYETHYLNITROSAMINE

Renal carcinomas were induced by N-ethyl-N-hydroxyethylnitrosamine (EHEN) followed by trisodium nitrilotriacetate monohydrate (NTA) in Wistar rats. In these rats, various parameters which are clinically used as tumor markers were examined. Renal tumors developed in 6 (37.5%) of 16 rats treated with...

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Published inJournal of Toxicologic Pathology Vol. 3; no. 2; pp. 239 - 243
Main Authors Okajima, Eigoro, Yamaguchi, Hisako, Kitahori, Yoshiteru, Hiasa, Yoshio, Matsuki, Hisashi, Hirao, Yoshihiko, Uemura, Hirotsugu, Samma, Shoji, Ozono, Seiichiro, Kitagawa, Hisayo, Tabata, Shoichi
Format Journal Article
LanguageEnglish
Published Tokyo JAPANESE SOCIETY OF TOXICOLOGIC PATHOLOGY 1990
Japan Science and Technology Agency
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ISSN0914-9198
1881-915X
1347-7404
DOI10.1293/tox.3.239

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Summary:Renal carcinomas were induced by N-ethyl-N-hydroxyethylnitrosamine (EHEN) followed by trisodium nitrilotriacetate monohydrate (NTA) in Wistar rats. In these rats, various parameters which are clinically used as tumor markers were examined. Renal tumors developed in 6 (37.5%) of 16 rats treated with EHEN alone and in 14 (82.4%) of 17 rats treated with EHEN and subsequently with NTA. When various parameters were compared between these two groups and the control group, RBC, Hb Al-P, LDH, BUN, Cr, and Ca in the former two groups differed significantly from those values of the untreated controls. In the EHEN-treated rats (Group 1 and 2), erythropoietin (EP) was higher in the tumor-bearing group than in the tumor-free group (p<0.025), although no other significant difference was observed. As compared to the untreated controls, tumor-bearing rats showed significant elevation in RBC (p<0.005). Cr (p<0.005), and EP (p<0.05) and significant reduction in Hb (p<0.005). Al-P (p<0.005), and LDH (p<0.05). Therefore, the significant difference in RBC, Hb, Al-P, LDH, and Cr seems to be attributable to the effect of EHEN and NTA. These results suggest that EP is specifically elevated in rats with renal tumor.
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ISSN:0914-9198
1881-915X
1347-7404
DOI:10.1293/tox.3.239