Chen Z, Sager R
Division of Cancer Genetics, Dana-Farber Cancer Institute, Boston MA 02115, USA.
Mol Med. 1995 Jan;1(2):153-60.
Tissue factor (TF) is a glycoprotein which binds factor VIIa. The TF-VIIa complex serves as a potent initiator of the coagulation pathways. TF, an immediate early gene, may also play a role in cell growth. Expression of TF was correlated with some types of cancers.
Normal, immortalized, and tumor human mammary epithelial cells were used in the experiments. The differential display (DD) technique was used to identify genes differentially expressed in the cells. TF expression patterns were examined by Northern blot analysis, immunofluorescence staining of cultured cells, and immunohistochemical staining in human cryostat sections.
In a 5-way display, an amplified polymerase chain reaction (PCR) product was found in normal and immortalized human mammary epithelial cells but not in the breast cancer cells. The PCR fragment was cloned and sequenced. The result showed that the fragment was identical to human tissue factor. Northern blot analysis showed that expression level of tissue factor mRNA remained high in growing, quiescent, and senescent normal mammary epithelial cells. Immunofluorescence staining also confirmed tissue factor expression pattern in the cell lines tested. Immunohistochemical staining showed that tissue factor was expressed in the normal luminal and myoepithelial cells of some ducts but not others. No staining was observed in invasive carcinoma cells. However, myoepithelial cell staining was seen in some residual ductal structures in invasive tumors.
This study shows the use of DD to reveal the loss of TF expression pattern in human breast cancer cell lines. Immunohistochemical staining results showed breast carcinoma cells expressed little TF, if any, suggesting that TF is not required for breast tumor cell invasion. The results also indicated that TF expression was independent of the proliferation status of the expressing cells. The expression pattern of TF may be a meaningful marker in the development of breast cancer.
组织因子(TF)是一种能与VIIa因子结合的糖蛋白。TF-VIIa复合物是凝血途径的强效启动剂。TF作为一种即刻早期基因,可能在细胞生长中也发挥作用。TF的表达与某些类型的癌症相关。
实验使用了正常、永生化及肿瘤性人乳腺上皮细胞。采用差异显示(DD)技术来鉴定细胞中差异表达的基因。通过Northern印迹分析、培养细胞的免疫荧光染色以及人冰冻切片的免疫组织化学染色来检测TF的表达模式。
在一次五路显示中,在正常和永生化人乳腺上皮细胞中发现了一个扩增的聚合酶链反应(PCR)产物,而在乳腺癌细胞中未发现。对该PCR片段进行了克隆和测序。结果显示该片段与人类组织因子相同。Northern印迹分析表明,组织因子mRNA的表达水平在生长、静止和衰老的正常乳腺上皮细胞中均保持较高。免疫荧光染色也证实了所检测细胞系中的组织因子表达模式。免疫组织化学染色显示,组织因子在一些导管的正常管腔和肌上皮细胞中表达,但在其他导管中不表达。在浸润性癌细胞中未观察到染色。然而,在浸润性肿瘤的一些残留导管结构中可见肌上皮细胞染色。
本研究表明利用差异显示技术揭示了人乳腺癌细胞系中TF表达模式的缺失。免疫组织化学染色结果显示乳腺癌细胞极少表达TF,即便有表达也微乎其微,这表明TF并非乳腺肿瘤细胞侵袭所必需。结果还表明TF的表达与表达细胞的增殖状态无关。TF的表达模式可能是乳腺癌发生发展中有意义的标志物。