Berg K, Luksiene Z, Moan J, Ma L
Institute for Cancer Research, Department of Biophysics, Montebello, Oslo, Norway.
Radiat Res. 1995 Jun;142(3):340-6.
The response of human colon adenocarcinoma cells of the line WiDr to the combined treatment of ionizing radiation and photosensitization by 5-aminolevulinic acid-induced protoporphyrin IX was assessed by a colony-forming assay. A dose of X rays inactivating approximately 50% of the cells was used. Seventy to 85% of the cells accumulated in S and G2 + M phase 12-24 h after such a treatment as measured by flow cytometry, while the distribution of cells in the phases of the cell cycle approached that of untreated cells 48 h after X-ray treatment. Cellular photosensitization was developed by endogenous synthesis of protoporphyrin IX (PPIX) from the precursor 5-aminolevulinic acid (5-ALA). This was performed by treating the cells with 1 mM 5-ALA for 4 h in a serum-free medium. The endogenous synthesis of PPIX increased with time after the cells had been subcultured, i.e. the ability of the cells to synthesize PPIX increased 1.5-2-fold within 48 h of incubation. This was not due to effects of trypsin on the cells. Photochemotherapy with 5-ALA was given 0-48 h after X rays. The combined cytotoxic effect was analyzed by an isobologram after correction of the survival curves for microcolony formation and differences in intracellular concentration of PPIX. The results indicate that 5-ALA PCT given 0-4 h after X rays acts slightly antagonistically while 5-ALA PCT given 12-48 h after X rays acts slightly synergistically.
通过集落形成试验评估了WiDr人结肠腺癌细胞系对电离辐射与5-氨基乙酰丙酸诱导的原卟啉IX光致敏联合治疗的反应。使用能使约50%的细胞失活的X射线剂量。通过流式细胞术检测发现,在这种治疗后12 - 24小时,70%至85%的细胞积聚在S期和G2 + M期,而在X射线治疗48小时后,细胞周期各阶段的分布接近未处理细胞。细胞光致敏是通过从前体5-氨基乙酰丙酸(5-ALA)内源性合成原卟啉IX(PPIX)来实现的。这是通过在无血清培养基中用1 mM 5-ALA处理细胞4小时来完成的。细胞传代培养后,PPIX的内源性合成随时间增加,即细胞合成PPIX的能力在孵育48小时内增加了1.5 - 2倍。这并非胰蛋白酶对细胞作用的结果。在X射线照射后0 - 48小时给予5-ALA光化学疗法。在对微集落形成的存活曲线和细胞内PPIX浓度差异进行校正后,通过等效线图分析联合细胞毒性作用。结果表明,在X射线照射后0 - 4小时给予5-ALA光化学疗法有轻微拮抗作用,而在X射线照射后12 - 48小时给予5-ALA光化学疗法有轻微协同作用。