Han E K, Sgambato A, Jiang W, Zhang Y J, Santella R M, Doki Y, Cacace A M, Schieren I, Weinstein I B
Columbia-Presbyterian Cancer Center, Columbia University, College of Physicians and Surgeons, New York, New York 10032.
Oncogene. 1995 Mar 2;10(5):953-61.
Amplification and/or increased expression of cyclin D1 occurs in an appreciable fraction of primary human breast carcinomas and several other types of human cancer. In addition, overexpression of cyclin D1 in rodent fibroblasts enhances growth and malignant transformation. The present study demonstrates that the extent of amplification and expression of cyclin D1 varies widely amongst a series of cell lines established from normal human mammary epithelium or human breast carcinomas. The HBL-100 mammary epithelial cell line did not display amplification or increased expression of cyclin D1. We used retrovirus-mediated transduction to obtain derivatives of this cell line that stably expressed relatively high levels of an exogenous cyclin D1 cDNA. These derivatives displayed an increased doubling time, decreased saturation density, decreased cloning efficiency, decreased anchorage-independent growth, an increased fraction of cells in the S-phase, and decreased tumorigenicity. Thus, increased expression of cyclin D1 in this cell line markedly inhibits rather than enhances growth, which may be due to the prolongation of S-phase.
细胞周期蛋白D1的扩增和/或表达增加在相当一部分原发性人类乳腺癌和其他几种类型的人类癌症中出现。此外,细胞周期蛋白D1在啮齿动物成纤维细胞中的过表达会增强生长和恶性转化。本研究表明,细胞周期蛋白D1的扩增和表达程度在一系列从正常人乳腺上皮或人类乳腺癌建立的细胞系中差异很大。HBL-100乳腺上皮细胞系未显示细胞周期蛋白D1的扩增或表达增加。我们使用逆转录病毒介导的转导来获得该细胞系的衍生物,这些衍生物稳定表达相对高水平的外源性细胞周期蛋白D1 cDNA。这些衍生物表现出倍增时间增加、饱和密度降低、克隆效率降低、非贴壁依赖性生长降低、S期细胞比例增加以及致瘤性降低。因此,该细胞系中细胞周期蛋白D1表达的增加显著抑制而非增强生长,这可能是由于S期延长所致。