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CCL17/CCR4在胃癌组织中的表达及意义 被引量:2

Expression and clinical significance of CCL17 and CCR4 in gastric cancer
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摘要 目的研究胃癌组织中CC趋化因子17(CCL17)及CC趋化因子受体4(CCR4)的表达及临床意义。方法收集经手术病理证实的胃癌患者55例(男41例,女14例,中位年龄62岁),健康对照组20例(男13例,女7例,中位年龄为61岁),应用免疫组化方法检测CCL17、CCR4在胃癌、癌旁组织及正常胃组织中的表达,并根据显微镜视野中阳性细胞所占的比例评分阐明胃癌组织中CCL17、CCR4的表达与临床、病理参数的相关性。结果胃癌组织中CCL17和CCR4的表达强度明显高于癌旁组织和正常胃组织,癌旁组织和正常胃组织两者的表达强度无明显差异。胃癌组织中CCL17及CCR4的表达与肿瘤分期有关(P<0.05),两者均与患者年龄、性别、分化程度等无关。结论 CCL17及CCR4在胃癌发生、发展中发挥一定作用。 Objective To study the expression and clinical significance of chemokine (C-C motif) ligand 17 (CCL17) and CC chemokine receptor 4 (CCR4) in gastric cancer. Methods 55 cases of pathologically confirmed gastric cancer patients (41 cases of male, 14 cases of females, mean age of 62 years) were enrolled and 20 cases of healthy persons were chosen as the control group (13 males, 7 females, mean age of 61 years). Immunohistochemical method was used to detect the expression of CCL17 and CCR4 in gastric cancer tissues, adjacent cancer tissues as well as in normal gastric tissues; then, the correlation between the expression of CCL17 and CCR4 in gastric tissues and clinical and pathological variables were analyzed. Results The expression of CCL17 and CCR4 in gastric carcinoma tissues was significantly higher than the control gastric tissue and adjacent cancer tissues, while, the expression of both showed no significant difference between the adjacent cancer tissues and the control group. The expression of CCL17 and CCR4 was positively related to tumor TNM staging (P〈0.05), but had no correlation with age, gender and degree of differentiation. Conclusion CCL17 and CCR4 play an important role in gastric carcinogenesis and development.
出处 《中华临床医师杂志(电子版)》 CAS 2015年第14期31-34,共4页 Chinese Journal of Clinicians(Electronic Edition)
关键词 趋化因子CCL17 受体 CCR4 胃肿瘤 组织 Chcmokinc CCLI7 Receptors, CCR4 Stomach neoplasms Tissue
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  • 1张巍巍,孟欣颖,马春红,王涛,马健,周长宏.胃腺癌组织CXCL10与CXCR3的表达及意义[J].齐鲁医学杂志,2015,30(1):21-23. 被引量:3
  • 2Imai T, Yoshida T, Baba M, et al. Molecular cloning of a novel T cell-directed CC ehemokine expressed in thymus by signal sequence trap using Epstein-Ban: virus vector[J]. J Biol Chem, 1996, 271(35): 21514-21521. 被引量:1
  • 3Mishalian I, Bayuh R, Eruslanov E, et al. Neutrophils recruit regulatory T-cells into tumors via secretion of CCL17-a new mechanism of impaired antitumor immunity[J]. Int J Cancer, 2014, 135(5): 1178-1186. 被引量:1
  • 4Cowan JE, McCarthy NI, Parnell SM, et al. Differential requirement for CCR4 and CCR7 during the development of innate and adaptive al3T cells in the adult thymus[J]. J Immunol, 2014, 193(3):1204-1212. 被引量:1
  • 5Power CA, Meyer A, Nemeth K, et al. Molecular cloning and functional expression of a novel CC chemokine receptor cDNA from a human basophilic cell line[J]. J Biol Chem, 1995, 270(33): 19495-19500. 被引量:1
  • 6Ishida T, Ueda R. Immonopathogenesis of lymphoma: focus on CCR4[J]. Cancer Sci, 2011, 102(1): 44-50. 被引量:1
  • 7Yang YM, Feng AL, Zhou CJ, et al. Aberrant expression of chemokine receptor CCR4 in human gastric cancer contributes to tumor-induced immunosuppression[J]. Cancer Sci, 2011, 102(7): 1264-1271. 被引量:1
  • 8Li JY, Ou ZL, Yu SJ, et al. The chemoldue receptor CCR4 promotes tumor growth and lung metastasis in breast cancer[J]. Breast Cancer Res Treat, 2012, 131(3): 837-848. 被引量:1
  • 9Viney JM, Andrew DP, Phillips RM, et al. Distinct conformations of the chemokinc receptor CCR4 with implications for its targeting in aUergy[J]. J Inlmunol, 2014, 192(7): 3419-3427. 被引量:1
  • 10Santulli-Marotto S, Boakye K, Lacy E, et al. Engagement of two distinct binding domains on CCL17 is required for signaling through CCR4 and establishment of localized inflammatory conditions in the lung[J]. PLoS One, 2013, 8(12): e81465. 被引量:1

二级参考文献11

  • 1LUSTER A D, UNKELESS J C, RAVETCH J V. Gamma-in- terferon transcriptionally regulates an early-response gene con- taining homology to platelet proteins[J]. Nature, 1985,315 (621):672 676. 被引量:1
  • 2VERBEKE H, HANNELIEN V, GEBOES K, et al. The role of CXC chemokines in the transition of chronic inflammation to esophageal and gastric cancer [J]. Biochim Biophys Acta, 2012,1825(1) :117-129. 被引量:1
  • 3OHTANI H, YOSHIE O. Morphometric analysis of the ba lance between CXCR3- T cells and FOXP3 + regulatory T cells in lymphocyte-rich and conventional gastric cancers[J] Virchows Arch, 2010,456(6) :615-623. 被引量:1
  • 4MURAKAMI T, KAWADA K, IWAMOTO M, ct al. The role of CXCR3 and CXCR4 in colorectal cancer metastasis[J]. Int J Cancer, 2013,132(2) :276 287. 被引量:1
  • 5MA X, NORSWORTHY K, KUNDU N, et al. CXCR3 ex pression is associated with poor survival in breast cancer and promotes metastasis in a murine model[J]. Mol Cancer Ther, 2009,8(3) : 490-498. 被引量:1
  • 6WU Q, DHIR R, WELLS A. Altered CXCR3 isoform expres- sion regulates prostate cancer cell migration and invasion[J]. Mol Cancer, 2012,11:3. 被引量:1
  • 7FURUYA M, YONEYAMA T, MIYAGI E, et al. Differenti al expression patterns of CXCR3 variants and corresponding CXC ehemokines in clear cell ovarian cancers and endometrio- sis[J]. Gynecol Oncol, 2011,122(3) : 648-655. 被引量:1
  • 8段波峰,郑雏,唐梅徕,范培芝,张超杰,谢靖,李洋,雷珊珊,顾晓文,何杰.CXCR3/CXCL10在乳腺癌中的表达及临床意义[J].中国医师杂志,2011,13(10):1305-1308. 被引量:6
  • 9孟欣颖,周长宏.IP-10和CXCR3与消化系统肿瘤[J].胃肠病学和肝病学杂志,2012,21(5):488-490. 被引量:1
  • 10郝建波,张劲峰,罗波,胡全君,王佩.胃癌阴性淋巴结微转移的检测及意义[J].青岛大学医学院学报,2012,48(6):495-497. 被引量:7

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