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1,25 二羟维生素D_3对乳腺癌细胞株生长及凋亡的影响 被引量:5

The effect of 1,25(OH) 2D 3 on growth and apoptosis in breast cancer cell line MCF 7
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摘要 目的 研究1 ,25 二羟维生素 D3[1 ,25( O H)2 D3] 对乳腺癌细胞株 M C F7 生长及凋亡的影响。 方法 采用四唑氮蓝比色( M T T) 法检测细胞增殖,光镜和电镜形态学观察,流式细胞仪测定细胞周期和凋亡率,末端脱氧核苷酸转移酶介导的原位酶标记( T U N E L) 法计数凋亡细胞,免疫印迹法检测bcl2 蛋白表达。 结果 10 - 7 mol/ L 的1 ,25( O H)2 D3 就可以抑制 M C F7 增生,改变细胞周期时相分布,致 G0/ G1 期阻滞,加强细胞毒性化疗药阿霉素( Adr) 的作用,促进细胞凋亡,下调bcl2 蛋白表达。 结论 1 ,25( O H)2 D3 可以作为细胞调亡诱导剂成为新一类乳腺癌激素治疗药。 Objective To study the effect of 1,25 dihydroxyvitamin D 3 [1,25(OH) 2D 3] on growth and apoptosis in breast cancer cell line MCF 7. Methods We compared cell numbers by using MTT method, analyzed cell cycle and apoptosis percentage by flow cytometric, observed cellular structure and ultrastructure, determinaed quantitatively apoptosis cells by terminal deoxynucleotidyl transferase mediated dUTP nick end labeling (TUNEL), and detected expression of bcl 2 protein by Western Blot. Results Incubation with 1,25(OH) 2D 3 10 -7 mol/L, MCF 7 cells exhibited significant growth inhibition. Flow cytometric analysis indicated cell′s G 0/G 1 arrest along with increasing apoptotic peak and percentage. The action of cytotoxic drug Adr was strengthened. Western Blot showed that 1,25(OH) 2D 3 could downregulate bcl 2 protein expression. Conclusions 1,25(OH) 2D 3 could be a new hormone for the treatment of breast cancer.
作者 张静 姚榛祥
出处 《中华外科杂志》 CAS CSCD 北大核心 1999年第8期497-499,共3页 Chinese Journal of Surgery
关键词 肿瘤细胞 乳腺癌 MCF-7 二羟维生素D3 Breast neoplasms Cholecalciferol Growth inhibitors Tumor cells,cultured
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参考文献2

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同被引文献17

  • 1刘静,赵浩亮.1,25二羟维生素D_3与5-氟尿嘧啶对乳腺癌细胞生长及凋亡的影响[J].中华实验外科杂志,2005,22(5):535-537. 被引量:8
  • 2廖智超,蔡林,余毅,廖正凯.塞来昔布抑制裸鼠乳腺癌骨转移实验研究[J].实用肿瘤杂志,2005,20(3):207-210. 被引量:1
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  • 4Segersten U, Holm P K, Bjorklund P , et al. 25-Hydroxyvitamin D3 lalpha-hydroxylase expression in breast cancer and use of non-lalpha-bydroxylated vitamin D analogue [ J ]. Breast Cancer Research, 2005,5(7) :980 -6.
  • 5Sugimoto T, Bartholomeusz C, Tari A M, et al. Adenovirus type 5 E1A-induced apoptosis in COX-2-overexpressing breast cancer cells [ J ]. Breast Cancer Res,2007,9 (4) :41 - 3.
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