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作 者:冷静[1] 彭韬[1] 徐秉栋[1] 印虹[1] 陆培新 王能进 张松平 张瑞菊
机构地区:[1]南京医科大学病理教研室,210029 [2]启东市肝癌研究所
出 处:《江苏医药》1998年第6期387-389,共3页Jiangsu Medical Journal
基 金:江苏省自然科学基金
摘 要:以点杂交和原位杂交法检测了34例启东地区原发性肝癌手术切除标本N-ras、c-myc基因的表达水平和定位。点杂交结果显示:N-ras、c-myc的检出率分别为647%(22/34)和23.5%(8/34)。前期的实验表明此34例标本HBV-DNA的检出率为588%(20/34),Southernblot实验结果未见病毒DNA的整合。N-ras、c-myc阳性标本中HBV-DNA的检出率分别为54.5%(12/22)和75%(6/8),两者之间无差异,P>0.05。原位杂交结果显示:肝癌癌组织中N-ras、c-myc基因的表达水平并没有明显增高,相反,肿瘤周围肝组织中的表达水平增高并主要位于慢性肝炎、肝硬变中的再生肝细胞中,阳性细胞呈灶性及成片分布,不伴有毛玻璃样改变(HE染色)。结论:虽然N-ras、c-myc与肝癌的发生密切相关,肝癌患者中常见其表达水平增高,但这很可能只是一种肝细胞损伤后再生时的细胞增殖性调控的表现,此种N-ras、c-myc的高表达是否直接导致肝癌发生,癌基因是否为突变型,有待进一步研究、此外,本实验中c-myc基因相对于N-ras基因的低检出率可能与c-mycMRNA极短的半衰期有关。34 cases of primary liver carcinoma from Qitung city, a high liver cancer risk region in China, hadbeen examined by dot and in situ hybridization tests for studying the expression and location of N-ras and c-myconcogenes. Dot hybridization test showed that the positive expressions of N-ras and c-myc were 64.7% (22/34)and 23. 5% (8/34) respectively. Besides, HBV-DNA was found in 58. 8% (20/34) of these cases and 12 out of 22(54.5 % ) in N-ras positive cases, 6 out of 8(75%) in c-myc positive cases, the difference was insignificant (P>0. 05). No HBV-DNA was found integrated into hepatic genome by Southern blot hybridization by out previousstudy. In situ hybridization tests showed indistinct expressions of N-ras and c-myc in cancerous region and over-expressive level in cancer-surrounding tissues especia1ly the proliferous hepatocytes of chronic hePatitis and cirrho-sis. The positive cells were in spotty and focal distribution without 'ground glass' changes (by HE stain). Wesupposed that although there were great relations between over-expression of N-ras,c-myc oncogenes and primaryliver carcinoma, it is possible that it was.simply a phenomenon associated with the proliferative gene control whenpost-injury regeneration initiated- It is still unknown if these over-expressive genes were mutated- In addition, thelower positive rate of c-myc expression as compared to that of N-ras in our experiment was probably due to the ex-tremely short half-life time of c-myc mRNA.
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