Gupta A K, Galoforo S S, Berns C M, Martinez A A, Corry P M, Guan K L, Lee Y J
Department of Radiation Oncology, William Beaumont Hospital, Michigan, Royal Oak 48073, USA.
Cell Prolif. 1996 Dec;29(12):655-63. doi: 10.1111/j.1365-2184.1996.tb00979.x.
We investigated the effect of elevated levels of protein kinase C alpha (PKC alpha) on cell proliferation in human breast carcinoma cells (MCF-7). MCF-7 cells transfected with either the pSV2M(2)6 vector without the insert (MCF-7/Vector) or containing a full length cDNA encoding PKC alpha (MCF-7/PKC alpha) were compared. MCF-7/PKC alpha cells were found to have an increased proliferative rate with a doubling time of 15 h as compared to 42 h for MCF-7/Vector cells. Flow cytometry illustrated a greater percentage of MCF-7/PKC alpha cells in the S phase of the cell cycle. Western and Northern blot analyses demonstrated an increase in extracellular regulated protein kinase 2 (ERK2) gene expression in MCF-7/PKC alpha cells but no alteration of this gene expression in MCF-7/Vector cells. These results suggested that the elevated level of ERK2 which is also known as mitogen activated protein kinase is probably involved in the increase in MCF-7/PKC alpha cell proliferation.
我们研究了蛋白激酶Cα(PKCα)水平升高对人乳腺癌细胞(MCF-7)增殖的影响。比较了用无插入片段的pSV2M(2)6载体(MCF-7/载体)或含有编码PKCα的全长cDNA的载体转染的MCF-7细胞(MCF-7/PKCα)。发现MCF-7/PKCα细胞的增殖速率增加,倍增时间为15小时,而MCF-7/载体细胞为42小时。流式细胞术显示细胞周期S期的MCF-7/PKCα细胞百分比更高。蛋白质印迹和Northern印迹分析表明,MCF-7/PKCα细胞中细胞外调节蛋白激酶2(ERK2)基因表达增加,而MCF-7/载体细胞中该基因表达无变化。这些结果表明,也称为丝裂原活化蛋白激酶的ERK2水平升高可能与MCF-7/PKCα细胞增殖增加有关。