SEQUENTIAL ALTERATION OF PROTOONCOGENE EXPRESSION IN LIVER, SPLEEN, KIDNEY AND BRAIN OF MICE SUBJECTED TO WHOLE-BODY IRRADIATION

Citation
Y. Ogawa et al., SEQUENTIAL ALTERATION OF PROTOONCOGENE EXPRESSION IN LIVER, SPLEEN, KIDNEY AND BRAIN OF MICE SUBJECTED TO WHOLE-BODY IRRADIATION, Oncology, 53(5), 1996, pp. 412-416
Citations number
8
Categorie Soggetti
Oncology
Journal title
ISSN journal
00302414
Volume
53
Issue
5
Year of publication
1996
Pages
412 - 416
Database
ISI
SICI code
0030-2414(1996)53:5<412:SAOPEI>2.0.ZU;2-T
Abstract
Reverse transcription polymerase chain reaction (RT-PCR) was performed to evaluate the sequential alteration of proto-oncogene mRNA expressi on in liver, spleen, kidney and brain of mice after whole body irradia tion (WBI). The mRNAs investigated in this study were Fas, c-fos, c-my c. bcl-2, and p53, and glyceraldehyde-3-phosphate dehydrogenase mRNA w as employed as internal control. C3H/He mice aged 9-10 weeks were expo sed to WBI of 7 Gy using a cobalt-60 teletherapy unit, without anesthe sia, and sacrificed before and 0.1, 0.5, 1, 2, 3, 6, 12, 24, 48 and 96 h after irradiation. Their liver, spleen, kidney and brain were taken and immediately stored in liquid nitrogen until ready for RT-PCR. Eac h specimen was homogenized to extract RNA for conventional RT-PCR. The liver of mice administered 7 Gy of WBI revealed no significant change s in the expression of each of the mRNAs examined. In the spleen, c-fo s mRNA expression decreased at 2 h following irradiation, and increase d remarkably thereafter. In the kidney, no significant change in the e xpression of each mRNA was shown. In the brain c-fos mRNA expression d ecreased 1-24 h after irradiation, and showed a recovery thereafter. T he remarkable differences in the sequential changes of c-fos mRNA expr ession following irradiation between each organ revealed by the presen t experiment may be an important aid in determining the tissue-specifi c radiosensitivity to ionizing radiation. Further investigations are, however, needed to clarify the signal transduction mechanisms which ar e mediated by the expression of these proto-oncogenes in each tissue f ollowing irradiation.