期刊文献+

姜黄素对人前列腺癌细胞放疗增敏作用的实验研究 被引量:4

Experimental study on sensibility of radiotherapy for human prostate cancer cell lines PC-3 with curcumin
下载PDF
导出
摘要 目的观察姜黄素对人前列腺癌细胞株PC-3的体外放射增敏作用,并探讨其可能机制。方法不同浓度姜黄素以及不同剂量放射治疗作用于PC-3细胞,使用MTT法检测姜黄素毒性及放疗敏感性,克隆形成实验研究姜黄素对放疗敏感性的影响。姜黄素(浓度30μmol/L)联合放疗作用PC-3细胞24 h,流式细胞术检测各组细胞的凋亡率及细胞周期分布。结果姜黄素对人前列腺癌细胞株PC-3细胞有明显抑制作用,存在剂量和时间依赖性。姜黄素可降低放疗后PC-3细胞的克隆形成率,放疗增敏作用明显。姜黄素联合放疗组诱导细胞凋亡作用增强,且可将细胞周期阻滞在辐射敏感时相G2/M期。结论姜黄素对人前列腺癌细胞株PC-3的毒性呈剂量和时间依赖性,姜黄素可提高PC-3细胞放疗敏感性,可能与其引起肿瘤细胞周期阻滞和诱导细胞凋亡有关。 【Objective】To investigate the influence of sensibility of radiotherapy for PC-3 cells with curcumin.【Methods】The Human prostate cancer cell lines PC-3 was treated with different concentrations of curcumin and different intensity radiation dose, then the MTT assay was used to evaluate the cytotoxic effects of curcumin and radio-sensitivity on PC-3 cells. Clonogenic assay was employed to observe the effects on the radio-sensitivity of the PC-3.(30 μmol/L) curcumin with radiotherapy on PC-3 cells for 24 h. The flow cytometry was utilized to observe the apoptosis of PC-3 cells induced by curcumin and the cell-cycle of PC-3 cells in response to X-ray irradiation.【Results】The curcumin could significantly inhibit the proliferation of PC-3 cells, with obvious dose-and time-dependent effects. Subtoxic dose of curcumin at 30 μmol/L could significantly reduce the clonogenic activity. Irradiation combined with curcumin resulted in cell cycle arrest at G2/M phase in PC-3 cells. 【Conclusions】Curcumin can enhance the radio-sensitivity of the human prostate cancer cell lines PC-3 in vitro. The mechanism may involve the increased apoptosis and prolonged cell cycle arrest induced by the combined treatment.
出处 《中国现代医学杂志》 CAS CSCD 北大核心 2014年第18期27-30,共4页 China Journal of Modern Medicine
关键词 姜黄素 放射治疗 凋亡 敏感性 curcumin radiotherapy apoptosis sensibility
  • 相关文献

参考文献7

  • 1刘红艳,王海燕,叶松,郭静明.姜黄素药理作用及其机制研究进展[J].中国现代医学杂志,2012,22(6):48-51. 被引量:52
  • 2龙丽,曹友德.姜黄素对乳腺癌MDA-MB-231细胞NOTCH1和NF-κB表达的影响[J].肿瘤防治研究,2010,37(2):158-161. 被引量:5
  • 3PARK C, KIM GY, KIM GD, et al. Induction of G2/M arrest and inhibition of cyclooxygenase-2 activity by curcumin in hu- man bladder cancer T24 cells[J]. Oncol Rep, 2006, 15(5): 1225- 1231.
  • 4LOTEMPIO MM, VEENA MS, STEELE HL, et al. Curcumin suppresses growth of head and neck squamous cell carcinoma[J]. Clin Cancer Res, 2005, 11(19): 6994-7002.
  • 5SIEGEL R, DESANTIS C, VIRGO K, et at. Cancer treatment and survivorship statistics[J]. Cancer J Clin, 2012, 62(4): 220-241.
  • 6HANIF R, QIAOL, SHIFF SJ, et al. Curcumin a natural plant phenolic food additive ,inhibits cell proliferation and induces cell cycle changes in colon adenocacinoma cell lines by a prostaglmldin-independent pathway[J]. J lab Clin Med, 1997, 130: 576-584.
  • 7AGGARWAL S, TAKADA Y, SINGH S, et al. Inhibition of growth and survival of human head and neck squamous cell carcinoma ceils by curcumin via modulation of nuclear factor -kappaB[J]. Int J Cancer, 2004, 111: 679-692.

二级参考文献22

  • 1Hua liang Chang-Sheng Deng Ming Zhang Jian Xia.Curcumin-attenuated trinitrobenzene sulphonic acid induces chronic colitis by inhibiting expression of cyclooxygenase-2[J].World Journal of Gastroenterology,2006,12(24):3848-3853. 被引量:8
  • 2姚运红,余健华,熊晖.姜黄素体内外对鼻咽癌的抗癌作用[J].肿瘤防治研究,2006,33(7):487-489. 被引量:8
  • 3赵慧娟,陶正贤,龙明智,谭晓,王迪斌,陶立翠.姜黄素对代谢综合征大鼠血浆TNF-α和血清sICAM-1水平的影响[J].中国康复医学杂志,2006,21(7):599-601. 被引量:11
  • 4Oswald F, Liptay S, Adler G, et al. NF-kappaB2 is a putative target gene of activated Notch-1 via RBP-Jkappa[J]. Mol Cell Bio, 1998, 18 (4) : 2077-2088.
  • 5Jang MS, Miao H, Carlesso N, et al. Notch-1 regulates cell death independently of differentiation in murine erythroleukemia cells through multiple apoptosis and cell cycle pathways [J]. J Cell Physiol,2004, 199(3) : 418-433.
  • 6Poma P, Notarbartolo M, Labbozzetta M, et al. The antitumor activities of curcumin and of its isoxazole analogue are not affected by multiple gene expression changes in an MDR model of the MCF7 breast cancer cell line: analysis of the possible molecular basis[J]. Int J Mol Med,2007 ,2(1(3): 329-335.
  • 7Ohishi K, Katayama N, Shiku H, et al. Notch signalling in hematopoiesis[J]. Semin Cell Dev Biol , 2003, 14(2) : 143- 150.
  • 8Zagouras P, Stifani S, Blaumueller CM, et al. Alteration in notch signaling in neoplastic lesions of the human cervix [J]. Proc Natl Acad Sci USA, 1995, 92(14) :6414-6418.
  • 9Niekoloff BJ, Osborne BA, Miele L. NOTCH Signaling as a therapeutic target in Cancer: a new approach to the development of cell fate modifying agents[J]. Oncogene, 2003, 22 (42) : 6598-6608.
  • 10Nair P, Somasundaram K, Krishna S. Activated Notchl inhibits p53- induced apoptosis and sustains transformation by human papillomavirus type 16 E6 and E7 oncogenes through a PI3K-PKB/Akt-dependent pathway [J]. J Virol, 2003, 77 (12): 7106-7112.

共引文献55

同被引文献55

引证文献4

二级引证文献10

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部