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机构地区:[1]第四军医大学唐都医院病理科,第四军医大学唐都病理学教研室,大连军医学校病理学教研室
出 处:《中国组织化学与细胞化学杂志》1995年第2期129-133,231,共6页Chinese Journal of Histochemistry and Cytochemistry
基 金:国家自然科学基金;军队"八五"医疗卫生科研(青年)基金
摘 要:为了明确N-ras、c-myc癌基因在人肝细胞癌(HCC)中的表达及其形态学分布,我们对38例石蜡包埋的HCC(其中33例带有癌周肝组织)标本进行了原位核酸杂交和免疫组化研究。结果表明,HCC及癌周肝组织中N-ras表达阳性率分别为42%和39%;c-mycmRNA阳性表达率分别为47%和36%;c-myc蛋白阳性率分别为53%和39%。HCC与癌周肝之间N-ras、c-mycmRNA及c-myc蛋白表达水平无显著差别;c-mycmRNA及蛋白阳性强度也无显著差别,其形态学分布基本一致,主要集中于癌细胞和癌周肝中的部分高度增生结节;N-ras表达增强主要见于癌细胞、癌周肝中的高度增生结节、小细胞性不典型增生及少部分肝小多角细胞。它们与HBxAg表达之间无明确的对应关系。上述结果显示,HCC中N-ras、c-myc表达都显著增强,它们可能是人HCC发生中较晚期的事件,而N-ras表达增强早于c-myc癌基因活化。An in situ hibridization and immunohistochemical study was made on the expressions ofN-ras,c-myc oncogene as well as their histologic distribution in 38 cases of human hepatocellular carcinoma(HCC)tissue in which Thirty-three cases were with pericancerous livertissues. esults shosed N-ras mRNA hibridization signals were found in 42% of HCCs and39% of the pericancerous liver tissues and C-myc mRNA positive signals was foind in 47%ofHCCs and 36% of the pericancerous tissues C-myc protein immunoreactive products were observed in 53% of HCCs and 39% of the pericancerous tissues. No significant difference wasfound between the expression levels of N-ras mRNA,c-myc mRNA and C-myc protein inHCCs and in the pericancerous liver tissues. Moreover,good correlation was found betweentheexpressions of C-myc mRNA and protein and their histologic distribution both in HCCsand in the pericancerous liver tissues. C-myc mRNA and protein was localized mainly in thecancer cells and hyperplastic nodules in the pericancerous liver tissues. Hyperexpression ofN-ras mRNA, c-myc mrNA was observed maninly in the cancer cells and the hyperlpasticnodules, small-cell dyplasia as well as a small number of small polygonal liver cells in thepericancerous tissues. No definite correlation was found between the expressions of N-ras orc-myc mRNA and HBxAg.These results demonstrated that expressions of N-ras and c-mycincreased significantly in HCC compared with normal liver.It is suggested that N-ras and c-myc hyperexpression may he rather late events, compared with IGF Ⅱ gene reactivation, inthe course human hepatocarcion-genesis, The hyperexpression of N-ras may be earlier thanthat of c-myc.
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