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Dormant cancer cells accumulate high protoporphyrin IX levels and are sensitive to 5-aminolevulinic acid-based photodynamic therapy

机译:休眠癌细胞积聚高原卟啉IX水平并对基于5-氨基乙酰丙酸的光动力疗法敏感

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摘要

Photodynamic therapy (PDT) and diagnosis (PDD) using 5-aminolevulinic acid (ALA) to drive the production of an intracellular photosensitizer, protoporphyrin IX (PpIX), are in common clinical use. However, the tendency to accumulate PpIX is not well understood. Patients with cancer can develop recurrent metastatic disease with latency periods. This pause can be explained by cancer dormancy. Here we created uniformly sized PC-3 prostate cancer spheroids using a 3D culture plate (EZSPHERE). We demonstrated that cancer cells exhibited dormancy in a cell density-dependent manner not only in spheroids but also in 2D culture. Dormant cancer cells accumulated high PpIX levels and were sensitive to ALA-PDT. In dormant cancer cells, transporter expressions of PEPT1, ALA importer, and ABCB6, an intermediate porphyrin transporter, were upregulated and that of ABCG2, a PpIX exporter, was downregulated. PpIX accumulation and ALA-PDT cytotoxicity were enhanced by G0/G1-phase arrestors in non-dormant cancer cells. Our results demonstrate that ALA-PDT would be an effective approach for dormant cancer cells and can be enhanced by combining with a cell-growth inhibitor.
机译:使用5-氨基乙酰丙酸(ALA)来驱动细胞内光敏剂原卟啉IX(PpIX)的生产的光动力疗法(PDT)和诊断(PDD)在临床上很常见。但是,积累PpIX的趋势还没有被很好地理解。癌症患者可能会出现潜伏期复发的转移性疾病。这种停顿可以用癌症休眠来解释。在这里,我们使用3D培养板(EZSPHERE)创建了大小一致的PC-3前列腺癌球体。我们证明癌细胞不仅以球体形式而且以2D培养方式均以细胞密度依赖性方式表现出休眠。休眠癌细胞积累高PpIX水平,并对ALA-PDT敏感。在休眠的癌细胞中,上调了PEPT1,ALA导入物和中间卟啉转运蛋白ABCB6的转运蛋白表达,而下调了PpIX出口蛋白ABCG2的转运蛋白表达。在非休眠癌细胞中,G0 / G1期阻滞剂增强了PpIX的积累和ALA-PDT的细胞毒性。我们的结果表明,ALA-PDT将是休眠细胞的有效方法,并且可以通过与细胞生长抑制剂结合来增强。

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