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首页> 外文期刊>Journal of Veterinary Science >Hematoporphyrin monomethyl ether combined with He-Ne laser irradiation-induced apoptosis in canine breast cancer cells through the mitochondrial pathway
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Hematoporphyrin monomethyl ether combined with He-Ne laser irradiation-induced apoptosis in canine breast cancer cells through the mitochondrial pathway

机译:血卟啉单甲醚与He-Ne激光辐照通过线粒体途径诱导犬乳腺癌细胞凋亡

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摘要

Hematoporphyrin monomethyl ether (HMME) combined with He-Ne laser irradiation is a novel and promising photodynamic therapy (PDT)-induced apoptosis that can be applied in vitro on canine breast cancer cells. However, the exact pathway responsible for HMME-PDT in canine breast cancer cells remains unknown. CHMm cells morphology and apoptosis were analyzed using optical microscope, terminal deoxynucleotidyl transferase dUTP nick end labeling fluorescein staining and DNA ladder assays. Apoptotic pathway was further confirmed by Real-time-polymerase chain reaction and Western blotting assays. Our results showed that HMME-PDT induced significant changes in cell morphology, such as formation of cytoplasmic vacuoles and the gradual rounding of cells coupled with decreased size and detachment. DNA fragmentation and cell death was shown to occur in a time-dependent manner. Furthermore, HMME-PDT increased the activities of caspase-9 and caspase-3, and released cytochrome c from mitochondria into the cytoplasm. HMME-PDT also significantly increased both mRNA and protein levels of Bax and decreased P53 gene expression in a time-dependent manner, while the mRNA and protein expression of Bcl-2 were repressed. These alterations suggest that HMME-PDT induced CHMin cell apoptosis via the mitochondrial apoptosis pathway and had anti-canine breast cancer effects in vitro.
机译:血卟啉单甲醚(HMME)与He-Ne激光照射相结合是一种新颖且有希望的光动力疗法(PDT)诱导的细胞凋亡,可在体外应用于犬乳腺癌细胞。但是,犬乳腺癌细胞中负责HMME-PDT的确切途径仍然未知。使用光学显微镜,末端脱氧核苷酸转移酶dUTP缺口末端标记荧光素染色和DNA阶梯分析法分析CHMm细胞的形态和凋亡。实时聚合酶链反应和蛋白质印迹分析进一步证实了细胞凋亡途径。我们的结果表明,HMME-PDT诱导了细胞形态的显着变化,例如细胞质液泡的形成和逐渐变圆的细胞,以及尺寸和脱离的减小。 DNA片段化和细胞死亡显示出时间依赖性。此外,HMME-PDT增加了caspase-9和caspase-3的活性,并将细胞色素c从线粒体释放到细胞质中。 HMME-PDT还以时间依赖性方式显着增加Bax的mRNA和蛋白水平,并降低P53基因表达,而Bcl-2的mRNA和蛋白表达受到抑制。这些改变表明,HMME-PDT通过线粒体凋亡途径诱导CHMin细胞凋亡,并在体外具有抗犬乳腺癌的作用。

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