期刊文献+

趋化因子配体18在乳腺癌组织中的表达与预后分析

CCL18 expression and its association with prognosis in breast cancer
下载PDF
导出
摘要 目的探讨趋化因子配体18在乳腺癌组织中的表达及其与乳腺癌患者预后的关系。方法入组病例的疾病诊断均以我院病理诊断为准并且均为女性患者,其中共有94例乳腺癌患者的组织标本,47例良性乳腺疾病患者的组织标本,对照组组织标本为良性乳腺病病灶周边的正常乳腺组织,共27例。采用免疫组化Envision方法,对标本检测CCL18、ER、PR、Her-2以及Ki-67等的表达。并对乳腺癌患者进行随访。结果在对照组、良性乳腺病组均未发现CCL18表达,在乳腺癌患者组中,CCL18的阳性表达率为67.02%(63/94);乳腺癌组CCL18的阳性表达率较对照组及良性乳腺疾病组显著升高(P<0.05)。在表达CCL18的63例乳腺癌患者中,CCL18的表达水平与肿瘤大小、淋巴结转移数目、临床分期,乳腺癌的分子类型以及ER、PR、Her-2的表达均有密切联系(P<0.05)。CCL18阳性乳腺癌患者的无病生存期(DFS)、总生存期(OS)均较CCL18阴性的乳腺癌患者的差(P<0.05)。结论 CCL18与乳腺癌的生物学特性密切相关,乳腺癌的一个重要的生物学指标,并且与乳腺患者的预后密切相关,可作为判断乳腺癌预后的一个重要参考指标进行研究。 Objective To research the expression of CCL18 in breast cancer and its association with prognosis of breast cancer. Methods Ninety-four tissue samples from patients with breast cancer were collected,and 47 tissue samples with benign breast diseases were also collected. The control group contained 27 samples,which were collected from tissues aside the benign breast disease leisions.All of the cases were female..Envision immunohistochemical method was used to examine CL18, ER, PR, Her-2 and Ki67. All of the patients with breast cancer were followed-up for a mean of 39 months. Results Among patients with benign breast diseases and the control group, CCL18 was not found..While in the 94 patients with breast cancer,CCL18 was found in 63 cases, positive ratio was 67.02%,and CCL18 was significantly up-regulated in breast cancer samples as compared with benign tumors or normal breast tissues(P〈0.05).Moreover,the expression level of CCL18 was different according to the size of tumors,the number of metastasized lymph node,tumor stage,subtype of breast cancer, ER, PR, Her-2, and all of the differences were significant(P〈0.05). High CCL18 expression was associated with poor disease-free survival and overall survival(both P〈0.05).Conclusion CCL18 showed high expression in breast cancer,wirch was associated with poor prognosis and may serve as an independent prognostic marker for investigating breast cancer.
出处 《岭南现代临床外科》 2015年第6期664-667,共4页 Lingnan Modern Clinics in Surgery
基金 国家自然科学基金资助项目(编号:81202111) 广州市医药卫生科技项目(编号20151A011074)
关键词 乳腺肿瘤 趋化因子配体18 CCL18 抗原 Breast cancer Chemokine CC-motif ligand 18 CCL18 Antigen
  • 相关文献

参考文献19

  • 1Shao ZM, Nguyen M, Barsky SH. Human breast carcinoma desmoplasia in PDGF initiated[J]. Oncogene, 2000, 19(38): 4337-4345.
  • 2Kalluri R, Zeibsberg M. Fibrobasts in cancer[J]. Nat Rev Cancer, 2006, 6 (5): 392-401.
  • 3Orimo A, Weinberg RA. Stromal fibroblasts in cancer: a novel tumor -promoting cell type[J]. Cell Cycle, 2006, 5 (15): 1597-160l.
  • 4Allinen M, Beroukhim R, Cai L, et al Molecular characterization of the tumor microenvironment :in breast cancer[J] . Cancer Cell, 2004, 6(1): 17-32.
  • 5Woo SU, BaeJW, Kim CH, et al. A significant correlation between nuclear CXCR4 expression and axillary lymph node metastasis in hormonal receptor negative breast cancer[J]. Ann Surg Oncol , 2008,15(1): 281-285.
  • 6Struyf S, Schutyser E, Gouwy M, et al. PARC/CCL18 is a plasma CC chemokine with increased levels in childhood acute lymphoblastic leukemia[.I]. AmJ Pathol, 2003, 163 (5): 2065-2075.
  • 7JunYang,Zheng-PingXu,YunHuang,HopeE.Hamrick,PenelopeJ.Duerksen-Hughes,Ying-NianYu.ATM and ATR:Sensing DNA damage[J].World Journal of Gastroenterology,2004,10(2):155-160. 被引量:29
  • 8Schutyser E, Struyf S, Proost P, et al Identification of biologically active chemokine isoforms ascetic fluid and elevated levels of CCLl8/pulmonary and activation-regulated chemokine in ovarian carcinoma[J].J Bioi Chern, 2002, 277(27): 24584- 24593.
  • 9ChenJQ, Yao YY, Gong C, et al. CCLl8 from Tumor-associated macrophages promotes breast cancer metastasis via PITPNM3[J]. Cancer Cell, 2011, 19 (4): 541-555.
  • 10Graves DT,Jiang Y. Chemokines, a family of chemotactic cytokines[J]. Crit Rev Oral Bioi Med, 1995, 6 (2): 109- 118.

二级参考文献110

  • 1Plumb MA, Smith GC, Cunniffe SM, Jackson SP, O'Neill P. DNAPK activation by ionizing radiation-induced DNA single-strand breaks. Int J Radiat Biol 1999; 75:553-561.
  • 2Jackson SP. DNA-dependent protein kinase. Int J Biochem Cell Biol 1997; 29:935-938.
  • 3Gately DP, Hittle JC, Chan GK, Yen TJ. Characterization of ATM expression, localization, and associated DNA-dependent protein kinase activity. Mol Blol Cell 1998; 9:2361-2374.
  • 4Pandita TK, Lieberman HB, Lim DS, Dhar S, Zheng W, Taya Y,Kastan MB. Ionizing radiation activates the ATM kinase throughout the cell cycle. Oncoygene 2000; 19:1386-1391.
  • 5Andegeko Y, Moyal L, Mittelman L, Tsarfaty I, Shiloh Y, Rotman G. Nuclear retention of ATM at sites of DNA double strand breaks. J Biol Chem 2001; 276:38224-38230.
  • 6Wright JA, Keegan KS, Herendeen DR, Bentley NJ, Carr AM,Hoekstra MF, Concannon P. Protein kinase mutants of human ATR increase sensitivity to UV and ionizing radiation and abrogate cell cycle checkpoint control. Proc Natl Acad Sci U S A 1998;95:7445-7450.
  • 7Hekmat-Nejad M, You Z, Yee MC, Newport JW, Cimprich KA.Xenopus ATR is a replication-dependent chromatm-binding protein required for the DNA replication checkpoint. Curr Biol 2000;10:1565-1573.
  • 8Wahl GM, Carr AM. The evolution of diverse biological responses to DNA damage: insights from yeast and p53. Nature Cell Biol 2001; 3:E227-E286.
  • 9Suzuki K, Kodama S, Watanabe M. Recruitment of ATM protein to double strand DNA irradiated with ionizing radiation. J Biol Chem 1999; 274:25571-25575.
  • 10Smith GC, Cary RB, Lakin ND, Harm BC, Teo SH, Chen DJ, Jackson SP. Purification and DNA binding properties of the ataxiatelangiectasia gene product ATM. Proc Natl Acad Sci U S A 1999;96:11134-11139.

共引文献32

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