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人类组织中癌胚抗原家族基因表达调控的研究。

Studies on the control of gene expression of the carcinoembryonic antigen family in human tissue.

作者信息

Boucher D, Cournoyer D, Stanners C P, Fuks A

机构信息

McGill Cancer Centre, McGill University, Montreal, Quebec, Canada.

出版信息

Cancer Res. 1989 Feb 15;49(4):847-52.

PMID:2912558
Abstract

The control of expression of genes of the carcinoembryonic antigen family was investigated in 22 specimens of malignant and nonmalignant human colonic tissues. These surgical specimens included seven colonic adenocarcinomas that were compared with normal adjacent colonic mucosal tissues from the same individual. mRNA preparations from all colonic tissues expressed three bands of 3.5, 3.0, and 2.6 kilobases on Northern blots probed with carcinoembryonic antigen (CEA) complementary DNA probe while normal liver and spleen were negative. The major band of 3.0 kilobases was 6 to 10 times more intense in the colon tumor specimens than in the matched normal mucosa. However, the tumor/normal ratios of immunoreactive CEA in these pairs varied from 2- to greater than 100-fold. Furthermore, there was no direct proportionality between mRNA levels and gene product expression, suggesting that the known variations in CEA expression in human colonic tissues result from both transcriptional and posttranscriptional control mechanisms. Southern blots of DNA from these specimens did not reveal any gene rearrangements or amplifications accompanying expression. Finally, Southern blots of DNA digested with methylation-sensitive endonucleases and probed with a genomic DNA fragment upstream of CEA gene coding regions demonstrated that CEA expression is correlated with a decreased level of methylation in the 5' region of the CEA gene.

摘要

在22份人类恶性和非恶性结肠组织标本中,研究了癌胚抗原家族基因的表达调控。这些手术标本包括7例结肠腺癌,并与同一患者的正常相邻结肠黏膜组织进行比较。用癌胚抗原(CEA)互补DNA探针进行Northern印迹杂交时,所有结肠组织的mRNA制剂均显示出3.5、3.0和2.6千碱基的三条带,而正常肝脏和脾脏为阴性。3.0千碱基的主要条带在结肠肿瘤标本中的强度比匹配的正常黏膜高6至10倍。然而,这些配对中免疫反应性CEA的肿瘤/正常比值在2倍至大于100倍之间变化。此外,mRNA水平与基因产物表达之间没有直接的比例关系,这表明人类结肠组织中已知的CEA表达变化是由转录和转录后控制机制共同导致的。这些标本的DNA进行Southern印迹杂交未发现伴随表达的任何基因重排或扩增。最后,用对甲基化敏感的核酸内切酶消化DNA并用CEA基因编码区上游的基因组DNA片段进行探针杂交的Southern印迹显示,CEA表达与CEA基因5'区域甲基化水平降低相关。

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