Mancini W R, Stetson P L, Lawrence T S, Wagner J G, Greenberg H S, Ensminger W D
College of Pharmacy, Department of Pharmacology, University of Michigan Medical School, Ann Arbor 48109.
Cancer Res. 1991 Feb 1;51(3):870-4.
Human glioma-derived cell lines were found to vary in their ability to incorporate the radiosensitizer 5-bromo-2'-deoxyuridine (BrdUrd) into DNA after one cell doubling. The U-251 cell line was the best incorporator of BrdUrd, whereas U-118 and D-54 demonstrated poor incorporation with respective C50 (BrdUrd concentration required for 50% of the maximum amount of BrdUrd incorporation into DNA) values of 2.8- and 6-fold greater than that of U-251 (P less than 0.001). Modulation of radiosensitizer uptake into DNA could be achieved using the thymidylate synthase inhibitors 5-fluorouracil or 5-fluoro-2'-deoxyuridine (FdUrd). Incorporation into U-251 cells increased only slightly in the presence of the fluoropyrimidines. The BrdUrd concentration required for 50% of the maximum amount of BrdUrd incorporation into DNA changed (P less than 0.001) from 1.8 +/- 0.11 microM (SD) in the absence of a modulator to 1.1 +/- 0.09 or 1.1 +/- 0.16 microM in the presence of 10 microM 5-fluorouracil or 5 nM FdUrd, respectively. The D-54 cell line, which was the worst incorporator of BrdUrd, was found to have an extensive amount of BrdUrd into DNA following biomodulation. The C50 in the absence of modulation was 7.3 +/- 1.3 microM, which was reduced (P less than 0.001) to 0.62 +/- 0.04 and 0.32 +/- 0.13 microM, respectively, in the presence of 10 microM 5-fluorouracil and 5 nM FdUrd. This represents a 12- to 22-fold reduction in the concentration of radiosensitizer required to achieve the same level of BrdUrd incorporation into DNA. Furthermore, this enhancement of BrdUrd DNA incorporation seen in the presence of the fluoropyrimidines is observed at clinically achievable concentrations. The degree of radiosensitization was solely dependent upon the amount of BrdUrd incorporated into DNA. D-54 cells grown in the presence of 0.18 microM BrdUrd plus 5 nM FdUrd or 2.8 microM BrdUrd alone yielded a similar level of BrdUrd incorporation into DNA and radiosensitization, though a 15-fold lower BrdUrd concentration was used in the presence of FdUrd. The combined use of a radiosensitizer with a fluoropyrimidine may overcome poor incorporation of BrdUrd into DNA that may exist among resistant subpopulations of cells within malignant glioma.
研究发现,人胶质瘤衍生细胞系在经过一次细胞倍增后,将放射增敏剂5-溴-2'-脱氧尿苷(BrdUrd)掺入DNA的能力存在差异。U-251细胞系是BrdUrd的最佳掺入者,而U-118和D-54的掺入能力较差,其各自的C50(使BrdUrd掺入DNA的最大量达到50%所需的BrdUrd浓度)值比U-251分别高2.8倍和6倍(P小于0.001)。使用胸苷酸合成酶抑制剂5-氟尿嘧啶或5-氟-2'-脱氧尿苷(FdUrd)可实现对放射增敏剂摄取进入DNA的调节。在氟嘧啶存在的情况下,U-251细胞中的掺入量仅略有增加。使BrdUrd掺入DNA的最大量达到50%所需的BrdUrd浓度发生了变化(P小于0.001),从无调节剂时的1.8±0.11微摩尔/升(标准差)分别变为在存在10微摩尔/升5-氟尿嘧啶或5纳摩尔/升FdUrd时的1.1±0.0当存在10微摩尔/升5-氟尿嘧啶和5纳摩尔/升FdUrd时,D-54细胞系是BrdUrd最差的掺入者,在生物调节后发现其有大量BrdUrd掺入DNA。无调节时的C50为7.3±1.3微摩尔/升,在存在10微摩尔/升5-氟尿嘧啶和5纳摩尔/升FdUrd时分别降至0.62±0.04和0.32±0.13微摩尔/升。这意味着在达到相同水平的BrdUrd掺入DNA时,所需放射增敏剂的浓度降低了12至22倍。此外,在氟嘧啶存在下观察到的BrdUrd掺入DNA的这种增强在临床可达到的浓度下即可实现。放射增敏程度仅取决于掺入DNA中的BrdUrd量。在存在0.18微摩尔/升BrdUrd加5纳摩尔/升FdUrd或仅2.8微摩尔/升BrdUrd的情况下培养的D-54细胞,产生了相似水平得BrdUrd掺入DNA和放射增敏效果,尽管在存在FdUrd时使用的BrdUrd浓度低15倍。放射增敏剂与氟嘧啶的联合使用可能克服恶性胶质瘤内耐药细胞亚群中可能存在的BrdUrd掺入DNA能力差的问题。 09或1.1±0.16微摩尔/升。D-54细胞系是BrdUrd最差的掺入者,在生物调节后发现其有大量BrdUrd掺入DNA。无调节时其C50为7.3±1.3微摩尔/升,在存在10微摩尔/升5-氟尿嘧啶和5纳摩尔/升FdUrd时分别降至0.62±0.04和0.32±0.13微摩尔/升。这意味着在达到相同水平的BrdUrd掺入DNA时,所需放射增敏剂浓度降低了12至22倍。此外,在氟嘧啶存在下观察到的BrdUrd掺入DNA的这种增强在临床可达到的浓度下即可实现。放射增敏程度仅取决于掺入DNA中的BrdUrd量。在存在0.18微摩尔/升BrdUrd加5纳摩尔/升FdUrd或仅2.8微摩尔/升BrdUrd的情况下培养的D-54细胞,产生了相似水平的BrdUrd掺入DNA和放射增敏效果,尽管在存在FdUrd时使用的BrdUrd浓度低15倍。放射增敏剂与氟嘧啶的联合使用可能克服恶性胶质瘤内耐药细胞亚群中可能存在的BrdUrd掺入DNA能力差的问题。