Viel A, Maestro R, Toffoli G, Grion G, Boiocchi M
Division of Experimental Oncology 1, Centro di Riferimento Oncologico, Aviano.
J Cancer Res Clin Oncol. 1990;116(3):288-94. doi: 10.1007/BF01612905.
The transcriptional activity of the c-myc proto-oncogene was examined in 25 primary human colorectal carcinomas and their corresponding normal mucosae. The purpose was to determine whether the elevated levels of c-myc expression, frequently detected in this type of tumor, might be the consequence of alterations in the cell growth rate or the effect of a real transcriptional deregulation of the gene. In about 44% of the tumors the elevated c-myc expression was consequent to the enhanced growth rate of the neoplastic tissue, as estimated by the expression of the S-phase-specific histone H3 gene. In the other 56%, c-myc overexpression did not entirely depend on the proliferative activity of the neoplastic population. In this latter group, c-myc deregulation did not reside in structural modifications of the putative regulatory regions of the gene. Therefore, c-myc overexpression, at least in a subset of colorectal cancer, seems to be consequent to alterations in transregulative phenomena exerted on the c-myc gene by other genetic loci.
在25例原发性人类结肠直肠癌及其相应的正常黏膜中检测了c-myc原癌基因的转录活性。目的是确定在这类肿瘤中经常检测到的c-myc表达水平升高,是否可能是细胞生长速率改变的结果,或者是该基因真正转录失调的影响。通过S期特异性组蛋白H3基因的表达估计,约44%的肿瘤中c-myc表达升高是由于肿瘤组织生长速率增强所致。在另外56%的肿瘤中,c-myc过表达并不完全依赖于肿瘤细胞群体的增殖活性。在后一组中,c-myc失调并不存在于该基因假定调控区域的结构修饰中。因此,至少在一部分结肠癌中,c-myc过表达似乎是其他基因位点对c-myc基因施加的反式调节现象改变的结果。