期刊文献+

趋化因子CXCL12及其受体CXCR4在子宫内膜癌组织中的表达及其临床意义 被引量:4

Expression and clinical significance of chemokine CXCL12 and receptor CXCR4 in endometrial carcinoma
原文传递
导出
摘要 目的检测趋化因子CXCL12及其受体CXCR4在子宫内膜癌组织中的表达水平,探讨其与子宫内膜癌患者的临床病理特征和预后的关系。方法采用组织芯片技术和免疫组化方法检测子宫内膜癌组织中CXCL12、CXCR4表达水平,并分析它们与FIGO分期、细胞分化程度、淋巴结转移、病理类型及年龄等临床病理特征及总生存率的关系。结果子宫内膜癌组织中CXCL12、CXCR4的表达水平均显著高于正常子宫内膜组,且二者在子宫内膜癌组的上调表达呈正相关。CXCR4的表达与子宫内膜癌细胞分化程度呈正相关(P<0.05)。CXCL12、CXCR4均不影响子宫内膜癌患者的生存率(P>0.05)。结论 CXCL12和CXCR4可能在子宫内膜癌的发生、发展中发挥生物学作用。 Objective To observe the translations of chemokine CXCL12 and its receptor CXCR4 in endometrial carcino- ma, and to evaluate their significance in clinical pathologic features and prognosis of endometrial carcinoma. Methods We examined the translations of CXCL12 and CXCR4 in human endometrial carcinoma tissue and normal endometrial tis- sue by tissue chip technique and immunochemical staining. Then we analyzed the relationship between the expression of CXCL12, CXCR4 and FIGO stage, the grade of differentiation, metastasis of lymph nodes, type of pathology, age and prognosis of patient from endometrial carcinoma. Results The chemokine pair CXCL12/CXCR4 was translated in nor- mal endometrial tissue. The expression of CXCL12 and CXCR4 increased in endometrial carcinoma significantly, and their up-regulation correlated positively with each other. The expression of CXCR4 correlated significantly with histological grade of endometrial carcinoma, but patients with CXCL12 or CXCR4 expression had similar overall survival with those without them. Conclusion The interactions between CXCL12 and CXCR4 may play important roles in the evolution and progression of endometrial carcinoma.
出处 《中国实用妇科与产科杂志》 CAS CSCD 北大核心 2013年第8期653-656,共4页 Chinese Journal of Practical Gynecology and Obstetrics
基金 国家自然科学基金青年基金(30700763) 山东省优秀中青年科学家科研奖励基金(BS2009SW002)
关键词 子宫内膜肿瘤 趋化因子CXCL12 受体 CXCR4 endometrial neoplasms chemokine CXCL12 receptors, CXCR4
  • 相关文献

参考文献8

  • 1Maroni P, Bendinelli P, Matteucci E, et al. HGF induces CX- CR4 and CXCL12-mediated tumor invasion through Etsl and NF- kappaB[J]. Carcinogenesis, 2007, 28(2): 267-279.
  • 2Muller A, Homey B, Soto H, et al. Involvement of chemokine receptors in breast cancer metastasis [ J ]. Nature, 2001, 410 (6824) : 50-56.
  • 3Kryczek I, Wei S, Keller E, et al. Stroma-derived factor( SDF- 1/CXCL12) and human tumor pathogenesis [ J]. Am J Physiol Cell Physiol , 2007, 292 (3) : C987-C995.
  • 4Kitaya K, Nakayama T, Daikoku N, et al. Spatial and temporal Expression of ligands for CXCR3 and CXCR4 in human endome- trium[J]. J Clin Endocrinol, 2004, 89(5): 2470-2476.
  • 5Dominguez F, Galan A, Martin JJ, et al. Hormonal and embry- onic regulation of chemokin receptors CXCR1, CXCR4, CCR5 and CCR2B in the human endometfium and the human blastocyst [J]. Mol Hum Reprod, 2003, 9(4) : 189-198.
  • 6Mizokami Y, Kajiyama H, Shibata K, et al. Stromal cell-de- rived factor-lalpha induced cell proliferation and its possible reg- ulation by CD26/dipeptidyl peptidase IV in Endometrial adeno- carcinoma[J]. Int J Cancer, 2004, 110(5) : 652-659.
  • 7Laguri C, Arenzana-Seisdedos F, Lortat-Jacob H. Relationships between glycosaminoglycan and receptor binding sites in chemo- kines-the CXCL12 example [ J ]. Carbohydr Res, 2008, 343 (12) : 2018-2023.
  • 8Hartmann TN, Grabovsky V, Pasvolsky R, et al. A cmsstalk be- tween intracellular CXCR7 and CXCR4 involved in rapid CX- CL12-tiggered integrin activation but not in chemokine-triggcred motility of human T lymphocytes and CD34 +cells [ J ]. J Leukoc Biol,2008, 84(4) : 1130-1140.

同被引文献26

  • 1肖琳,唐良萏.肝细胞生长因子及其受体在子宫内膜癌组织中的表达及其意义[J].重庆医科大学学报,2004,29(6):789-791. 被引量:4
  • 2王玉萍,楚天骄,党秋红,雷冬梅,郝志伟.乳腺癌中肝细胞生长因子及其受体C-Met和血管内皮生长因子表达的意义[J].实用诊断与治疗杂志,2006,20(5):336-338. 被引量:11
  • 3吴鸣,郎景和.子宫内膜癌的热点问题[J].癌症进展,2006,4(1):7-12. 被引量:11
  • 4Shetty S, Velusamy T, Idell S, et al. Regulation of urokinase receptor ex- pression by p53 :novel role in stabilization of uPAR Mrna. Mol Cell Biol, 2012,27:5607-5618.
  • 5Smith HW, Marshall CJ. Regulation of cell signaling by uPAR. Nat Rev Nol Cell Biol,2010,11:23-36.
  • 6Mlonas I, Jeschke U, Shabsni N, et al. Normal and malignant human en- dometrium express immunohistochemically estrogen receptor alpha ( ER- alpha), estrogen receptor(PR). Anticancer Res ,2005,25 : 1679-1686.
  • 7Nose N, Uramoto H, Iwata T, et al. Expression of estrogen receptor beta predicts a clinical response and longer progression-free survival after treatment with EGFRTKI for adenoearcinoma of the lung. Lung Cancer, 2011,71:350-355.
  • 8Sien W, Kobel M, Longaere TA, et al. Hormone-receptor expression and ovarian cancer survival, an Ovarian Tumor Tissue Analysis consortium study. Lancet Oneol, 2013,14 : 853-862.
  • 9Akrish S, Ben-Izhak O, Peled M. P27/SKP-2 histoehemieal profile is relevant to malignant salibary gland tumors (MST)histogenesis and tumor grade. Head Neck Patho1,2012,6 : 157-165.
  • 10Guo T, Li B, Gu C. Expression of hPEBP4 negatively correlates with es- trogen and progesterone receptors in endometrial eareinoma. J BUON, 2013.18:465-470.

引证文献4

二级引证文献22

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