首页> 外文期刊>World Journal of Gastroenterology >Early apoptosis and cell death induced by ATX-S10Na (Ⅱ)-mediated photodynamic therapy are Bax- and p53-dependent in human colon cancer cells
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Early apoptosis and cell death induced by ATX-S10Na (Ⅱ)-mediated photodynamic therapy are Bax- and p53-dependent in human colon cancer cells

机译:ATX-S10Na(Ⅱ)介导的光动力疗法诱导的早期凋亡和细胞死亡在人结肠癌细胞中是Bax和p53依赖性的

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AIM: To investigate the roles of Bax and p53 proteins in photosensitivity of human colon cancer cells by using lysosome-localizing photosensitizer, ATX-S10Na (Ⅱ). METHODS: HCT116 human colon cancer cells and Bax-null or p53-null isogenic derivatives were irradiated with a diode laser. Early apoptosis and cell death in response to photodynamic therapy were determined by MTT assays, annexin V assays, transmission electron microscopy assays, caspase assays and western blotting. RESULTS: Induction of early apoptosis and cell death was Bax- and p53-dependent. Bax and p53 were required for caspase-dependent apoptosis. The levels of anti-apoptotic Bcl-2 family proteins, Bcl-2 and Bcl-XL, were decreased in Bax- and p53-independent manner. CONCLUSION: Our results indicate that early apoptosis and cell death of human colon cancer cells induced by photodynamic therapy with lysosome-localizing photosensitizer ATX-S10Na (Ⅱ) are mediated by p53-Bax network and low levels of Bcl-2 and Bcl-XL proteins. Our results might help in formulating new therapeutic approaches in photodynamic therapy.
机译:目的:利用溶酶体定位光敏剂ATX-S10Na(Ⅱ)研究Bax和p53蛋白在人结肠癌细胞光敏中的作用。方法:用二极管激光器辐照HCT116人结肠癌细胞和Bax-null或p53-null同基因衍生物。通过MTT测定法,膜联蛋白V测定法,透射电子显微镜测定法,胱天蛋白酶测定法和蛋白质印迹法确定对光动力疗法的响应的早期凋亡和细胞死亡。结果:早期凋亡和细胞死亡的诱导是依赖Bax和p53的。 Bax和p53是caspase依赖性凋亡所必需的。抗凋亡的Bcl-2家族蛋白Bcl-2和Bcl-XL的水平以Bax和p53独立的方式降低。结论:溶酶体定位光敏剂ATX-S10Na(Ⅱ)光动力学治疗诱导人结肠癌细胞的早期凋亡和细胞死亡是由p53-Bax网络和低水平的Bcl-2和Bcl-XL蛋白介导的。 。我们的结果可能有助于制定光动力疗法的新治疗方法。

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