Chumakova Olga V, Liopo Anton V, Evers B Mark, Esenaliev Rinat O
Center for Biomedical Engineering, The University of Texas Medical Branch, Galveston, TX 77555-0456, USA.
Ultrasound Med Biol. 2006 May;32(5):751-8. doi: 10.1016/j.ultrasmedbio.2006.01.011.
The aim of this study was to analyze cell viability and expression of apoptotic-related signaling proteins in MCF-7 breast cancer cells induced by combinations of ultrasound, the anticancer drug 5-fluorouracil (5-FU) and the ultrasound contrast agent Optison. MCF-7 cells were treated with 5-FU and sonicated at the frequency of 3.0 MHz and intensity of 3.0 W/cm2 for 1 min in the presence of Optison. The cells were analyzed for lactate dehydrogenase (LDH) release (a measure of cytotoxicity) and cell proliferation (by MTT assays). The LDH/MTT ratio was used for assessment of cell death. Expression of the apoptotic-related proteins, Bax and p27kip1, as well as phosphorylated forms of ERK and Akt proteins was assessed by Western blot analysis. We demonstrate that, immediately after treatment, cell death was most dependent on Optison; however, 24 h after treatment, cell death was more dependent on 5-FU. Ultrasound duty cycle increased cell death associated with either Optison or 5-FU. Furthermore, we show that treatment with 5-FU and ultrasound increased the levels of the Bax and p27kip1 proteins, but the addition of Optison appears to suppress apoptotic protein expression.
本研究旨在分析超声、抗癌药物5-氟尿嘧啶(5-FU)和超声造影剂Optison联合作用诱导MCF-7乳腺癌细胞的细胞活力及凋亡相关信号蛋白的表达。在Optison存在的情况下,用5-FU处理MCF-7细胞,并以3.0 MHz的频率和3.0 W/cm2的强度超声处理1分钟。分析细胞的乳酸脱氢酶(LDH)释放(细胞毒性的一种测量指标)和细胞增殖(通过MTT测定)。LDH/MTT比值用于评估细胞死亡。通过蛋白质印迹分析评估凋亡相关蛋白Bax和p27kip1以及ERK和Akt蛋白磷酸化形式的表达。我们证明,处理后立即,细胞死亡最依赖于Optison;然而,处理后24小时,细胞死亡更依赖于5-FU。超声占空比增加了与Optison或5-FU相关的细胞死亡。此外,我们表明,用5-FU和超声处理会增加Bax和p27kip1蛋白的水平,但添加Optison似乎会抑制凋亡蛋白的表达。