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作 者:郑颂国[1] 殷莲华[1] 许良中[1] 叶明[1] 吕彪[1] 朱振东[1]
机构地区:[1]上海医科大学肿瘤医院病理研究室,浙江省台州医院病理科
出 处:《上海医科大学学报》1996年第1期7-9,共3页Journal of Fudan University(Medical Science)
基 金:国家教育委员会博士点基金
摘 要:研究SRS鼠白血病/淋巴瘤克隆株(包括SRS─82亲系和SAC─ⅡB2、SAC─ⅡC3克隆株)癌基因和癌基因蛋白的表达,筛选此克隆株的癌基因表达谱型,为SRS淋巴瘤株的实验性反义核酸治疗提供目标。用ABC免疫组织化学方法筛选SRS─82亲系和SAC─ⅡB2、SAC─ⅡC3克隆株癌基因表达诺型。在SRS克隆株中呈强表达的有c─fos和c─myc。c─jun、ras─p21和c─erbB─2呈中度表达,P53和bcl─2则不表达。同时用CD4和CD8细胞表面标记进研究,发现SRS克隆株属于原始干细胞。结果提示:癌基因谱型的建立对SRS淋巴瘤克隆株的实验性反义核酸治疗具有相当重要的作用,c─fos和c─myc可能是反义核酸治疗最好的癌基因靶。PURPOSE The studies of oncogenes expression in a SRS─82 mouse Lymphoma cell line and SAC─ⅡB2,SAC─ⅡC3 clones have been less reported.We must establish a oncogene spectrum for finishing the experimental antisense treatment to SRS lymphoma.METHODS:SRS─82 mouse lymphoma cell line and SAC─ⅡB2,SAC─ⅡC3 clones were obtained from the Department of Pathophysiology,Shanghai Medical University.ABC immunohistochemical method was used.RESULTS Strong staining was found for c─fos and c─myc,medium staining for c─jun,ras─p21 and c─erbB─2,and negative reactions for P53 and bcl─2 in SRS─82 cell line and its clones,Cell surface marks(CD4 and CD8) of these two clones and their parent cell line were negative,all of them belong to primary stem cell origin.CONCLUSIONS Establishments of oncogene spectrum play an important role in the experimental antisense treatment in SRS lymphoma,and c─fos and c─myc were the best targets for the antisense treatment.
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