期刊文献+

雌激素对人乳腺癌细胞系基质细胞衍化因子-1影响的观察 被引量:6

Effects of estrogen on the expression of SDF-1 in human breast cancer cell lines
原文传递
导出
摘要 目的:探讨雌激素对基质细胞衍化因子-1(SDF-1)的影响。方法:选取乳腺癌细胞系MCF-7和MDA-MB-231为研究对象,分成对照组、雌激素组和雌激素+雌激素受体阻断组,分别加入不同生理浓度的17-β雌二醇作用一定时间以及同一浓度17-β雌二醇作用不同时间点,用酶联免疫吸附实验(ELISA)方法测定培养液中SDF-1的浓度,半定量逆转录聚合酶链反应(RT-PCR)法检测细胞SDF-1 mRNA的表达。结果:MDA-MB-231细胞系加与未加雌激素,均未检测到SDF-1的分泌。而MCF-7细胞基础培养液中可检测到SDF-1分泌。不同生理浓度的17-β雌二醇均可增加MCF-7细胞SDF-1的分泌水平。当加入1×10-7mol/L的生理高浓度17-β雌二醇时,细胞分泌SDF-1水平在2 h达到高峰,是对照组的6倍〔(1 823.17±325.18)ρg/mLvs(307.23±5.42)ρg/mL,F=201.02,P<0.01〕,该作用可被雌激素受体拮抗剂(ICI182,780)消除。此外,SDF-1mRNA的表达水平与测得的SDF-1蛋白水平相一致。结论:在某些乳腺癌细胞系,生理浓度的雌激素可促进SDF-1的分泌,而这种作用主要是通过雌激素受体来实现。雌激素可通过SDF-1来影响乳腺癌的生物学特性。 OBJECTIVE: To investigate the effect of estrogen on the biological characteristics of breast cancer cells through SDF-1. METHODS:Two breast cancer cell lines(MCF-7 and MDA- MB-231) were used for tests, which were divided into control group, estrogen group and estrogen plus estrogen receptor blocker group. 17-β estradiol of different physiological concentrations was applied to the cultured cells in the three groups at a setted of time. The SDF-1 level in culture medium was measured by enzyme linked immunosorbent assay (ELISA) and the expression of SDF-1 mRNA was examined using semi-quantitative reverse transcription-polymerase chain reaction (RT-PCR) technique. RESULTS:SDF-1 protein was not detected in MDA-MB-231 cell line with or without estrogen, however, SDF-1 protein could be detected in MCF-7 cell line, and the level of SDF-1 increased with the application of 17-β estradiol applied to the cells. When adding 1 × 10^-7 mol/L of physiological concentration of 17-β estradiol to the culture cells for 2 h, the SDF-1 levels reached a peak, which was 6 times than the control group [(1 823. 17±325. 18) ρg/mL vs (307. 23± 5. 42)ρg/mL, F=201. 02, P〈0. 01]. Furthermore, the secretion of SDF-1 increased by estradiol could be eliminated by a pure estrogen receptor antagonist (ICI182, 780). In addition, SDF-1 mRNA expression level was also changed in a similar way as SDF-1 protein. CONCLUSIONS:In some breast cancer cell lines, physiological concentrations of estrogen can increase the secretion of SDF-1, and this effect is mainly achieved through estrogen combined with its recep tor. Estrogen can affect the biological behaviour of breast cancer cells by SDF-1.
出处 《中华肿瘤防治杂志》 CAS 2011年第7期502-505,共4页 Chinese Journal of Cancer Prevention and Treatment
基金 北京市留学人员科技活动择优资助项目(20050906)
关键词 乳腺肿瘤 17-Β雌二醇 MCF-7 MDA—MB-231 基质细胞衍生因子-1 Breast neoplasms, 17-β estrodial, MCF-7, MDA-MB-231, SDF-1
  • 相关文献

参考文献14

  • 1Muller A, Homey B,Soto H, et al. Involvement of chemokine receptors in breast cancer metastasis[J]. Nature, 2001, 410 (6824) :50-56.
  • 2KangH,Mansel R,Jiang W G. Genetic manipulation of stromal cell derived factor-l attests the pivmal role ot the autoerine SDF- 1-CXCR4 pathway in the aggressiveness of breast cancer cells [J]. Int J Oncol2005,26(5):1429 1434.
  • 3Rossouw J E.Anderson G L,Prentice R L,et al. Risks and benefits of estrogen plus progestin in healthy postmenopausal women: principal results from the women's health initiative ran domized controlled trial[J]. JAMA,2002,288(3):321-333.
  • 4Yamaguchi Y. Microenvironmental regulation of estrogen signals in breast caneer[J]. Breast Cancer,2007,14(2),175-181.
  • 5HarringtonW R.Kim SH,FunkCC,et al. Estrogendendrimer conjugates that preferentially activate extranuclear, nongenomic versus genomic pathways of estrogen action[J]. Mol Endocrinol,2006,20(3) :491 502.
  • 6张锋良,康骅.雌激素通过SDF-1/CXCR4信号通路对乳腺癌的影响[J].国际外科学杂志,2009,36(1):51-54. 被引量:3
  • 7Kang H,WatkinsG,Parr C.et al. Stromalcellderived factor l: its influence on invasiveness and migration of breast cancer cells in vitro,and its association with prognosis and survival in human breast cancer[J]. Breast Cancer Res,2005,7(4):402-410.
  • 8HallJ M,Korach K S. Stromal cell derived factor 1,a novel tar get of estrogen receptor action, mediates the mitogenic effects of estradiol in ovarian and breast cancer cells[J].Mol Endocrinol, 2003,17(5) :792-803.
  • 9Levin E R. Integration of the extranuclear and nuclear actions of estrogen[J]. Mol Endocrinol, 2005,19(8) : 1951-1959.
  • 10Pedram A,Razandi M,Levin E R. Nature of functional estrogen receptors at the plasma membrane[J]. Mol Endocrinol,2006,20 (9) : 1996-2009.

二级参考文献25

  • 1康骅,Robert EMansel,Wen G Jiang.基质细胞衍化因子-1的表达及其与乳腺癌患者预后的关系[J].中国普外基础与临床杂志,2005,12(5):483-487. 被引量:7
  • 2Sengupta K, Banerjee S, Saxena N, et al. Estradiol-induced vascular endothelial growth factor-A expression in breast tumor cells is biphasic and regulated by estrogen receptor-alpha dependent pathway [J].lnt J Oncol, 2003, 22(3) :609~14.
  • 3Beral V, Million Women Study Collaborators. Breast cancer and hor-mone-replacement therapy in the Million Women Study [ J ]. Lancet, 2003, 362 (9382) :419-427.
  • 4Stender JD, Frasor J, Komm B, et al. Estrogen regulated gene networks in human breast cancer ceils : involvement of E2 in the regulation of cell proliferation [ J ]. Mol Endocrinol, 2007, 21 ( 9 ) :2112- 2123.
  • 5Yao J, Li Y, Chang M, et al. Catechol estrogen 4 - hydroxyequile nin is a substrate and an inhibitor of eatechol - 0 - rnethyltrans ferase [J]. Chem Res Toxicol. 2003, 16(5) : 668-675.
  • 6Vendrell JA, Magnino F, Danis E, et al. Estrogen regulation in human breast cancer cells of new downstream gene targets involved in estrogen metabolism, cell proliferation and cell transformation [ J ]. J Mol Endocrinol, 2004, 32(2) :397-414.
  • 7Hayashi S, Yamaguchi Y. Basic research for hormone-sensitivity of breast cancer[J]. Breast Cancer, 2006, 13 (2) :123-128.
  • 8Zhao YL, Han WD, Li Q, et al. Mechanism of transcriptional regulation of LRP16 gene expression by 17-estradiol in MCF-7 human breast cancer cells[J]. J Mol Endoc, 2005, 34 ( 1 ) : 77-89.
  • 9Levin ER. Bidirectional signaling between the estrogen receptor and the epidermal growth factor receptor[ J]. Mol Endocrinol, 2003, 17 (3) :309-317.
  • 10Kang H, Mansel R, Jiang WG. Genetic manipulation of stromal cell-derived factor-1 attests the pivotal role of the autocrine SDF-1- CXCR4 pathway in the aggressiveness of breast cancer cells[ J]. Int J Oncol, 2005, 26(5) :1429-1434.

共引文献2

同被引文献100

  • 1卞爱菊.巡回护士在腹腔镜手术中的护理配合[J].河南外科学杂志,2010,16(6):109-110. 被引量:11
  • 2陈伟财,何劲松,王敏,吴恢升,王先明.老年乳腺癌患者新辅助内分泌治疗的临床应用[J].中国癌症杂志,2011,21(5):359-362. 被引量:23
  • 3Hendrayani SF, A1-Khalaf HH, Aboussekhra A. Curcurnin trig- gers pl6-dependent senescence in active breast cancer-associated fibroblasts and suppresses their paracrine procarcinogenic effects ~J~. Neoplasia, 2013, 15(6): 631-640.
  • 4Kang H, Mansel RE, Jiang WG. Genetic manipulation of stromal cell-derived factor-1 attests the pivotal role of the autocdne SDF-1- CXCR4 pathway in the aggressiveness of breast cancer cells [J]. Int J Oncol, 2005, 26(5): 1429-1434.
  • 5Kang H, Watkins G, Douglas-Jones A, et al. The elevated level of CXCR4 is correlated with nodal metastasis of human breast cancer [J~. Breast, 2005, 14(5): 360-367.
  • 6Naito S, von Eschenbach AC, Giavazzi R, et al. Growth and metastasis of tumor ceils isolated from a human renal cell carci- noma implanted into different organs of nude mice [ J ]. Cancer R.es, 1986, 46(8): 4109-4115.
  • 7Mao Y, Keller ET, Garfield DH, et al. Stromal cells in tumor microenvironment and breast cancer [J]. Cancer Metastasis Rev, 2013, 32(1-2): 303-315.
  • 8Sadlonova A, Bowe DB, Novak Z, et al. Identification of mole- cular distinctions between normal breast-associated fibroblasts and breast cancer-associated fibroblasts [ J]. Cancer Microenviron, 2009, 2(1): 9-21.
  • 9Woo SU, Bae JW, Kim CH, et al. A significant correlation bet- ween nuclear CXCR4 expression and axillary lymph node metas- tasis in hormonal receptor negative breast cancer [J]. Ann Surg Oncol, 2008, 15(1): 281-285.
  • 10Liang Z, Brooks J, Willard M, et al. CXCR4/CXCL12 axis pro- motes VEGF-mediated tumor angiogenesis through Akt signaling pathway [J]. Biochem Biophys Res Commun, 2007, 359(3): 716-722.

引证文献6

二级引证文献38

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