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SKOV3卵巢癌细胞中雌激素对LRP16的调控作用及其影响 被引量:4

E2 regulation on LRP16 and its action in ovarian cancer cell lines
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摘要 目的:研究雌激素受体ER阳性的卵巢癌细胞系中,E2对LRP16的调控作用以及LRP16对细胞增殖的影响。方法:Northern Blot、Western Blot方法分别检测RNA、蛋白表达水平;生长曲线测定过表达或抑表达LRP16对SKOV3细胞生长特性的影响。结果:雌激素敏感的BG-1细胞系中,E2正调控LRP16的表达;而不同浓度雌激素处理雌激素不敏感SKOV3细胞,LRP16蛋白的表达下降,而ICI182780对其作用相反;LRP16对SKOV3细胞的生长、增殖有微弱的调节作用。结论:在雌激素不敏感的SKOV3细胞系中,E2对LRP16的调节作用及LRP16发挥的生长调节作用与雌激素敏感的BG-1卵巢癌细胞系及乳腺癌体外研究结果不同。提示雌激素不敏感浆液性卵巢癌中E2对LRP16的调控可能存在新的机制,可能用来解释部分卵巢癌对内分泌治疗敏感性不同的原因。 Objective:To investigate the regulation of estradiol (E2) on LRP16 and its effect of LRP16 on ERalpha( + ) ovarian cancer cell line. Methods:Northern Blot and Western Blot examined the expression of LRP16 RNA and protein. The growth trait of cells transfected with LRP16 or LRP16 - siRNA was examined by growth curves. Results: In estrogen- sensitive BG- 1 cells, E2 upregulated LRP16 expression. However in estrogen- insensitive SKOV3 cell line treated with different amount of E2, estrogen decrease LRP16 expression ,ICI182 780 played inversely. LRP16 had slightly effect on the growth and proliferation of SKOV3 cell line. Conclusion:In estrogen -insenstive SKOV3 cell lines ,the regulation of E2 on LRP16 and the function of LRP16 on the growth of SKOV3 were different from the results in BG - 1 ovarian cancer cell line and breast cancer in vitro. It's hinted that in estrogen - insensitive serous ovarian cancer new mechanism may exist on E2 regulation to LRP16, which may explain the insensitivity of certain ovarian cancer patients to endocrine therapy.
出处 《现代肿瘤医学》 CAS 2010年第1期4-8,共5页 Journal of Modern Oncology
基金 国家自然科学基金项目(编号:30670809 30870969)
关键词 卵巢肿瘤 雌激素受体 基因 LRP16 细胞增殖 基因表达调控 ovarian neoplasms estrogen receptor alpha genes LRP16 proliferasion gene expression regulation
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  • 1张成岗,袁守军,邓美玉,李林,汤仲明,贺福初.一种对斑点和条带信号进行半定量图像分析的简便方法[J].中国体视学与图像分析,2001,6(3):167-170. 被引量:13
  • 2韩为东,李琦,赵亚力,母义明,李雪,宋海静,陆祖谦.小干扰RNA抑制LRP16基因表达限制了MCF-7乳腺癌细胞增殖[J].中国生物化学与分子生物学报,2005,21(1):113-119. 被引量:22
  • 3韩为东,赵亚力,李琦,母义明,李雪,宋海静,陆祖谦.INHIBITION OF PROLIFERATION OF HUMAN BREAST CANCER MCF-7 CELLS BY SMALL INTERFERENCE RNA AGAINST LRP16 GENE[J].Chinese Journal of Cancer Research,2004,16(4):239-245. 被引量:1
  • 4廖代祥,韩为东,赵亚力,蒲永东,母义明,罗成华,李向红.LRP16基因在乳腺癌组织中的表达及其临床意义[J].癌症,2006,25(7):866-870. 被引量:21
  • 5Safe S. Transcriptional activation of genes by 17 beta estradiol through estrogen receptor-Sp1 interactions[J]. Vitam Horm,2001,62 : 231-252.
  • 6Klinge CM. Estrogen receptor interaction with estrogen response elements[J]. Nucleic Acids Res, 2001, 29( 14 ) : 2905-2919.
  • 7Qin C, Singh P, Safe S. Transcriptional activation of insulin-like growth factor-binding protein-4 by 17beta-estradiol in MCF-7 cells: role of estrogen receptor-Spl complexes. Endocrinology, 1999, 140:2501-2508
  • 8HanWD, MuY M, Lu X C, LiXJ, Yu L, Song H J, Li M, Lu J M, Zhao Y L, Pan C Y. Up-regulation of LRP16 mRNA by 17αestradiol through activation of estrogen receptor α (ERα), but not estrogen receptor β(ERβ), and promotes human breast Cancer MCF-7cell pro
  • 9Mu Y-M, Yanase T, Nishi Y, Takayanagi R, Goto K, Nawata H.Combined treatment with specific ligands for PPARγ: RXR nuclear receptor system markedly inhibits the expression of cytochrome P450arom in human granulosa cancer cells. Mol Cell Endocrinol, 2001,
  • 10Porter W, Wang F, Wang W, Duan R, Safe S. Role of estrogen receptor/Spl complexes in estrogen-induced heat shock protein 27 gene expression. Mol Endocrinol, 1996,10:1371 - 1378

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