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作 者:李如冰[1] 吴强[1] 徐素娟[1] 冯炎[2,3] 罗厚蔚
机构地区:[1]复旦大学生理及生物物理学系 [2]上海医科大学肿瘤医院 [3]中国药科大学植物化学系
出 处:《辐射研究与辐射工艺学报》1998年第1期29-33,共5页Journal of Radiation Research and Radiation Processing
基 金:国家自然科学基金
摘 要:利用体外细胞集落形成法研究二氢丹参酮Ⅰ对肿瘤细胞放射敏感性的影响。实验表明,二氢丹参酮Ⅰ对人肝癌细胞株(QGY7703)和人肺腺癌细胞株(SPCA1)有较强的细胞毒作用,半致死剂量LD50分别为8.86μmol/L和7.73μmol/L。该药物与X射线联合作用能增强细胞对射线的敏感性,1μmol/L的二氢丹参酮Ⅰ作用于有氧细胞1h后照射,对QGY7703细胞和SPCA1细胞的增敏比(SER)分别为1.42和1.62;QGY7703细胞和SPCA1细胞的氧增比(OER)分别为2.08和3.03。1μmol/L的二氢丹参酮Ⅰ在乏氧状态下对这两种细胞亦有放射增敏作用,QGY7703细胞的SER仍为1.42,而SPCA1细胞的SER增大为1.96。在分次照射实验中,1μmol/L的二氢丹参酮Ⅰ能完全抑制这两种细胞的亚致死性损伤修复(SLDR)。In the experiments, the radiosensitization of dihydrotanshinone Ⅰ on human hepatocelluar carcinoma cells QGY 7703 and lung adenocarcinoma cells SPC A 1 was studied through in vitro colony formation method. The results showed that dihytanshinone Ⅰ has cytotoxity to the two kinds of cells and the LD 50 was 7.73μmol/L and 8.86μmol/L, respectively. The compound enhanced the radiation effect. Under aerobic condition the SER (sensitizing ehnancement ratio) of the compound was 1.42 for QGY 7703 cells and 1.62 for SPC A 1 cells at the concentration of 1μmol/L. The OER (Oxygen enhancemen tratio) for QGY 7703 cells and SPC A 1 cells was 2.08 and 3.03, respectively. Under hypoxic condition dihydrotanshinone Ⅰ also had radiosensitivity for the two kinds of cells, and the SER of SPC A 1 cells increased to 1.96 while the SER of QGY 7703 kept 1.42. In split dose radiation experiment, dihydrotanshinone Ⅰ could inhibit SLDR (sublethal damage repair) obviously at the concentration of 1μmol/L.
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