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人肺癌细胞中生长因子的自泌循环和癌基因表达
Gene expressiou of growth factors, growth factor receptor and oncogenes in human lung cancer cell lines
【摘要】 用Northern核酸杂交技术对4个人肺癌细胞系进行了表皮生长因子(EGF)、转化生长因子α(TGFα)以及表皮生长因子受体(EGFR)的基因表达研究,发现这些肺癌细胞系中均有EGF和TGF_α的基因表达,3/4中亦有EGFR的基因表达。这些癌细胞系中自泌的生长因子作用于自身的EGF受体形成的自泌循环,不断刺激其自身的增殖,这可能是癌细胞无休止生长的主要原因之一。Northern核酸杂交结果还表明:在这4个肺癌细胞系中,无c-myc癌基因表达的细胞系中有大量的EGF和TGFα的基因表达。用EGL抗EGF和抗EGFR抗体处理这些人肺癌细胞系,抗EGF和抗EGFR抗体在一定程度上可抑制其增殖,这也说明这些癌细胞中生长因子自泌环路的存在。
【Abstract】 ene expression of growth factors including epidermal growth factor (EGF),transforming growth factor α(TGFα),epidermal growth factor receptor(EGFR),oncogenes such as c-myc,N-ras,c-erbB2 and tumor suppressor gene P53 were studied in 4 human lung cancer cell lines using Northern blot tech-nique. Among these cell lines were 2 adenocarcinoma cell lines, one large cell carcinoma cell line and one small cell carcinoma cell line. Expression of EGF and TGFα mRNAs were found in all 4 cell lines and E-FGR mRNA was seen in 3 out of 4 cell lines. Among these cell lines, 2 cell lines with weaker expression of EGF and TGFα,expressed c-myc mRNA. Another 2 cell lines had no c-myc but expressed large amounts of EGF and TGFα mRNA. No expression of N-ras,c-erbB2 and p53 were found in these cell lines. The results indicate the presence of autocrine loop of growth factors in these cancer cells. The au-tostimulation of growth factors may be the main cause for the uncontrolled growth of cancer cells. After treating the cancer cells with EGF anti-EGF and anti-EGFR antibodies, EGF was found to exert a mild stimulating effect on the growth of one cell line, but no effect on the other cell lines. Anti-EGF and anti-EGFR antibodies inhibited the cell growth on all cell lines. These results provided further evidence for the presence of autocrine loop of growth factors in these lung cancer cell lines.
【Key words】 Lung neoplasms Transforming growth factor alpha Receptors; epidermal growth factor-Urogastrone;
- 【文献出处】 中华病理学杂志 ,CHINESE JOURNAL OF PATHOLOGY , 编辑部邮箱 ,1995年01期
- 【分类号】R734.2
- 【被引频次】18
- 【下载频次】62