期刊文献+

趋化因子SDF-1及其受体对卵巢癌细胞增殖及迁移的影响 被引量:6

Effects of chemokine stromal cell- derived factor-1 and its receptor CXCR4 on the proliferation and migration of ovarian cancer cells
下载PDF
导出
摘要 目的:探讨趋化因子受体CXCR4在人卵巢癌细胞中的表达及SDF-1/CXCR4系统与卵巢癌细胞恶性表现的关系。方法:采用RT-PCR检测卵巢癌细胞系SW626中CXCR4的表达,MTT法检测SW626细胞增殖能力的变化,通过体外微孔隔离室板(Transwell)检测SDF-1对SW626细胞迁移及CXCR4的封闭对其迁移的影响。结果:CXCR4mRNA在SW626细胞呈阳性表达,抗CXCR4单克隆抗体(20μg/mL)对SW626细胞增殖有明显的抑制作用(P<0.05),SDF-1可促进SW626细胞的迁移,CXCR4的封闭能抑制SDF-1对SW626迁移的这种促进作用(P<0.05)。结论:SDF-1及其受体CXCR4的相互作用可能在卵巢癌细胞增殖和迁移中发挥着重要作用,干扰SDF-1/CXCR4的相互作用可能成为治疗卵巢癌的一个有意义的靶点和策略。 Objective To investigate the expression of CXCR4 in human ovarian cancer cells and the relationship between SDF-1/CXCR4 system and the malignity of ovarian cancer ceils, Methods Expression of CXCR4 mRNA in ovarian cancer cell llne SW626 was detected by reverse transcriptase-polymerase chain reaction (RT-PCR); the proliferation of SW626 cells was identified by MTT method; Transweil was used to analyze the migration of SW626 cells in presence of SDF-1 or when CXCR4 was blocked by anti-CXCR4 McAh. Results CXCR4 mRNA was expressed in SW626 ceils; anti-CXCR4 McAh (20 μg/mL) inhibited the proliferation of SW626 cells( P 〈 0. 05); SDF-1 induced the migration of SW626 cells, which could he effectively blocked by anti-CXCR4 McAh( P 〈 0.05), Conclusion SDF-1 and CXCR4 may play an important role in the proliferation and migration of ovarian cancer cells, and interfering the interaction of SDF-1 and CXCR4 can he a meaningful therapeutic target and strategy.
出处 《实用医学杂志》 CAS 2006年第22期2580-2582,共3页 The Journal of Practical Medicine
基金 湖北省卫生厅科研基金资助项目(编号:JX1A07)
关键词 卵巢肿瘤 趋化因子类 受体 SDF-1 CXCR4 Ovarian neoplasms Chemotactic factors Receptor SDF-1 CXCR4
  • 相关文献

参考文献10

  • 1ZLOTNIK A, YOSHIE O. Chemokine: a new classification system and their role in immunity [J]. Immunity,2000, 12(2) : 121 - 127.
  • 2NAGASAWA T, HIROTA S, TACHIBANA K, et al. Defects of B-cell lymphopoiesis and bone-marrow myelopoiesis in mice lacking the CXC chemokine PBSF/ SDF-1[J] . Nature, 1996, 382(6592): 635-638.
  • 3MULLER A, HOMEY B, SOTO H, et al. Involvement of chemokine receptors in breast cancer metastasis [J] . Nature, 2001, 410(6824) :50 - 56.
  • 4LIBURA J, DRUKALA J, MAJKA M, et al. CXCR4-SDF-1 signaling is active in rhabdomyosarcoma cells and regulates,locomotion, chemotaxis, and adhesion [J]. Blood, 2002, 100(7):2597 - 2606.
  • 5SCHRADER A J, LECHNER O, TEMPLIN M, et al. CXCR4/CXCL12 expression and signalling in kidney cancer [J]. Br J Cancer,2002, 86(8) : 1250 - 1256.
  • 6SEHGAL A, RICKS S, BOYNTON A L, et al. Molecular characterization of CXCR.4: a potential brain tumor-associated gene[J]. J Surg Oncol, 1998, 69(4) :239 - 248.
  • 7BERTOLINI F, DELL' AGNOLA C, MANCUSO P, et al. CXCR4 neutralization, a novel therapeutic approach for non-Hodgkin's lymphoma [J]. Cancer Res, 2002, 62 (11): 3106-3112.
  • 8SCOTTON C J, WILSON J L, MILLIKEN D, et al. Epithelial cancer cell migration : a role for chemokine receptors [ J] ? Cancer Res, 2001,61(13) :4961 -4965.
  • 9SCOTTON C J, WILSON J L, SCOTT K, et al. Multiple actions of the chemoklne CXCL12 on epithelial tumor cells in human ovarian cancer [J]. Cancer Res, 2002, 62(20) :5930 - 5938.
  • 10PHILLIPS R J, BURDICK M D, LUTZ M, et al. The stromal derived factor-1/CXCL12-CXC chemokine receptor 4 biological axis in non-small cell lung cancer metastases [J] . Am J Respir Crit Care Med, 2003, 167(12) : 1676 - 1686.

同被引文献44

引证文献6

二级引证文献11

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