Mouse strain susceptibility to diethylnitrosamine induced hepatocarcinogenesis is cell autonomous whereas sex-susceptibility is due to the micro-environment: Analysis with C3H <-> BALB/c sexually chimeric mice

Citation
T. Tsukamoto et al., Mouse strain susceptibility to diethylnitrosamine induced hepatocarcinogenesis is cell autonomous whereas sex-susceptibility is due to the micro-environment: Analysis with C3H <-> BALB/c sexually chimeric mice, JPN J CANC, 91(7), 2000, pp. 665-673
Citations number
37
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
JAPANESE JOURNAL OF CANCER RESEARCH
ISSN journal
09105050 → ACNP
Volume
91
Issue
7
Year of publication
2000
Pages
665 - 673
Database
ISI
SICI code
0910-5050(200007)91:7<665:MSSTDI>2.0.ZU;2-2
Abstract
In man, li,er cancer is on the increase, especially in males. Sex differenc es also exist in rodent models, To elucidate the mechanisms, chimeric mice were produced by amalgamation of early embryos from high and lon hepatocarc inogen-susceptible strains, C3H and BALB/c, Tumor formation vc as initiated with 10 mg/kg of diethylnitrosamine at the ages of 7 and 14 days and mice were sacrificed at 30 and 45 weeks. The chimeras were classified into XY <- ---> XY, XY <----> XX, XX <----> XY and XX <----> XX in terms of sex chromo somes by means of polymerase chain reaction-simple sequence length polymorp hism analysis (SSLP) using Y chromosome-specific Sry primers in combination with the D3Mit21 marker. Liver lesions were analyzed histopathologically, by immunostaining using a C3H strain-specific antibody and by DNA in situ h ybridization with the Y chromosome-specific digoxigenin-labeled Y353/B prob e. Ses and strain genotyping by SSLP analysis matched histological observat ions, confirming the reliability of our system. The strain differences in l iver tumor numbers of each strain type in XY <----> XY and XY <----> XX sub types of C3H <----> BALB/c chimeras were retained well (P<0.0001 and P<0.00 1, respectively), indicating a minimum influence of the C3H or BALB/c surro unding milieu on development of individual lesions. On the other hand, sign ificant promotion of XX cell tumors was evident in phenotypically male sexu ally chimeric XY <----> XX and XX <----> XY chimeras for both C3H (P<0.02) and BALB/c (P<0.01) lesions compared to the,XX <----> XX case. The results suggest the presence of hormonal or micro-environmental factors specific fo r males, which are not caused cell-autonomously. Basic strain differences, however, are determined by intrinsic genetic factors rather than the strain -dependent micro-environment.