Sato K, Nishi T, Takeshima H, Kochi M, Kuratsu J, Masuko N, Sugimoto Y, Yamada Y, Ushio Y
Department of Neurosurgery, Kumamoto University School of Medicine, Honjo, Kumamoto, Japan.
Int J Oncol. 1999 Mar;14(3):417-24. doi: 10.3892/ijo.14.3.417.
p120 is a nucleolar proliferating antigen which is expressed in tumor cells but not normal resting cells. The expression and localization of p120 in human gliomas were studied by Northern blot analysis, Western blot analysis and immunohistochemistry. All five of the glioma cell lines and all of the glioma specimens we investigated expressed p120 at both the mRNA and protein levels. p120 expression was not detected in adjacent brain tissues. A ribozyme vector was constructed to cleave the first GUC sequence in the coding region of p120 mRNA. This p120 ribozyme vector was transfected into the glioma cell line SF188, which expresses p120. The reduced p120 expression of the transfectant at both the mRNA and protein levels was confirmed. An MTT assay indicated that the transfected cells grew more slowly than control cells. These results indicate that i) p120 has an important role in the proliferation of gliomas, and ii) the ribozyme against p120 mRNA can suppress glioma cell growth.
p120是一种核仁增殖抗原,在肿瘤细胞中表达,但在正常静息细胞中不表达。通过Northern印迹分析、Western印迹分析和免疫组织化学研究了p120在人胶质瘤中的表达和定位。我们研究的所有五种胶质瘤细胞系和所有胶质瘤标本在mRNA和蛋白质水平均表达p120。在相邻脑组织中未检测到p120表达。构建了一种核酶载体以切割p120 mRNA编码区的第一个GUC序列。将该p120核酶载体转染到表达p120的胶质瘤细胞系SF188中。证实转染子在mRNA和蛋白质水平上p120表达均降低。MTT分析表明,转染细胞比对照细胞生长更慢。这些结果表明:i)p120在胶质瘤增殖中起重要作用;ii)针对p120 mRNA的核酶可抑制胶质瘤细胞生长。