Zhang H L, Wu B Q, Zhang W G
Department of Pathology, Beijing Medical University.
Zhonghua Zhong Liu Za Zhi. 1994 Nov;16(6):403-6.
The expression level of 67-KD LN-R mRNA was observed in high-metastatic PG tumor cells and low-metastatic PAa tumor cells based on the cDNA fragments of 67-KD LN-R amplified by PCR technique and the specific cDNA probe prepared by random primer labeling method. Results showed that the transcripts were homologous in size, about 1.7kb, in PG and PAa tumor cells. The 67-KD LN-R mRNA level was higher in PG than that in PAa tumor cells, and gene amplification was also more marked in PG tumor cells. After treated with 67-KD LN-R monoclonioal antibody (50, 100 and 400 micrograms/ml) for 48 hours, LN-R mRNA of PG tumor cells decreased significantly. It is suggested that 67-KD LN-R may play important roles in metastatic processes of PG tumor cells.
基于PCR技术扩增的67-KD LN-R cDNA片段和随机引物标记法制备的特异性cDNA探针,观察67-KD LN-R mRNA在高转移性PG肿瘤细胞和低转移性PAa肿瘤细胞中的表达水平。结果显示,PG和PAa肿瘤细胞中的转录本大小同源,约为1.7kb。PG肿瘤细胞中的67-KD LN-R mRNA水平高于PAa肿瘤细胞,并且PG肿瘤细胞中的基因扩增也更明显。用67-KD LN-R单克隆抗体(50、100和400微克/毫升)处理48小时后,PG肿瘤细胞的LN-R mRNA显著下降。提示67-KD LN-R可能在PG肿瘤细胞的转移过程中起重要作用。