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Expression of CEACAM-1 in colorectal carcinoma and correlation with tumor angiogenesis and metastasis |
XIA Longfei1 LIU Yujun1 ZHANG Junmin1 HAN Junyi2 |
1.Department of General Surgery, Maternal and Child Health Hospital of Zhoushan City, Zhejiang Province, Zhoushan 316000, China;
2.Department of Gastrosurgery, Dongfang Hospital, Tongji University, Shanghai 200120, China |
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Abstract Objective To investigate the expression of CEACAM-1 and the correlation with the tumor angiogenesis and metastasis, and explore feasibility as a monitoring indicator for the diagnosis, treatment and prognosis in evaluating colorectal carcinoma. Methods Fifty specimens of colorectal adenomacarcinoma tissues and 50 specimens of normal colorectal tissues from January 2016 to January 2017 in the Department of General Surgery, Maternal and Child Health Hospital of Zhoushan City were collected. The expression of CEACAM-1, VEGF was detected by immunohistochemistry method, and the value of micro-vascular density (MVD) was observed. The correlation between clinicopathologic features of tumors and expression of CEACAM-1, VEGF and MVD value, as well as the correlation among the three indices was analyzed. Results The positive expression of CEACAM-1 and VEGF in colorectal carcinoma tissues were significantly higher than those in normal tissues, and the differences were highly significant (P = 0.000); MVD value in colorectal carcinoma tissues was significantly higher than that of normal tissue, and the difference was highly significant (P = 0.000); the expression of CEACAM-1, VEGF and MVD value were correlated to degree of colorectal tumor differentiation, tumor serous membrane infiltration, TNM staging, vascular infiltration, lymph node metastasis and liver metastasis (P < 0.05); MVD value of CEACAM-1 and VEGF positive expression groups was significantly higher than that of the negative group in colorectal carcinoma tissues (P < 0.01); the expression of CEACAM-1 and VEGF were positively correlated in colorectal carcinoma tissues (r = 0.483, P < 0.001). Conclusion The high expression of CEACAM-1 can induce the formation of tumor microvasculature, and is closely related to the tumor infiltration and metastasis. CEACAM-1 can be used as a potential molecular biological indicator for early diagnosis and prognosis in monitoring colorectal carcinoma.
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[1] 史刚刚,郝敬鹏,王力何,等.结直肠癌组织中血管抑制蛋白1表达的临床意义及其与血管内皮生长因子A和微血管密度的相关性[J].中华胃肠外科杂志,2015,18(3):272-276.
[2] Gebauer F,Wicklein D,Horst J,et al. Carcinoembryonic antigen-related cell adhesion molecules(CEACAM)1,5 and 6 as biomarkers in pancreatic cancer [J]. PLoS One,2014,9(11):e113023.
[3] Zhang L,Mai HM,Zheng J,et al. Propranolol inhibits angiogenesis via down-regulating the expression of vascular endothelial growth factor in hemangioma derived stem cell [J]. Int J Clin Exp Pathol,2014,7(1):48-55.
[4] 武雪亮,王立坤,薛军,等.DNA结合分化抑制蛋白1和血管内皮生长因子的表达及其与肿瘤微血管生成的相关性研究[J].中国临床药理学杂志,2016,32(5):430-436.
[5] 王子昕,盛伟伟,董明,等.结合基序蛋白6在结直肠癌组织中的表达及临床意义[J].中国实验诊断学,2017,21(5):765-768.
[6] 许良中,杨文涛.免疫组织化学反应结果的判定标准[J].中国癌症杂志,1996,6(4):229-231.
[7] Weidner N,Folkman J,Pozza F,et al. Tumor angiogenesis:a new signifincant independent prognostic indicator in early stage breast carcinoma [J]. J Nail Cancer Inst,1992, 84(9):1875-1887.
[8] 兰蓝,赵飞,蔡玥,等.中国居民2015年恶性肿瘤死亡率流行病学特征分析[J].中华流行病学杂志,2018,39(1):32-34.
[9] 詹天成,顾晋.NCCN2016V1版直肠癌诊治指南更新及其解读[J].实用肿瘤杂志,2016,31(4):291-295.
[10] 郑树,张苏展,黄彦钦.结直肠癌研究30年回顾和现状[J].实用肿瘤杂志,2016,31(1):2-5.
[11] Okegawa T,Pong RC,Li Y,et al. The role of cell adhesion molecule in cancer progression and its application in cancer therapy [J]. Acta Biochim Pol,2004,51(2):445-457.
[12] Dupuis ML,Fiori V,Soriani A,et al. The Human Antibody Fragment DIATHIS1 Specific for CEACAM-1 Enhances Natural Killer Cell Cytotoxicity Against Melanoma Cell Lines In Vitro [J]. J Immunother,2015,38(9):357-370.
[13] Lu R,Kujawski M,Pan H,et al. Tumor angiogenesis mediated by myeloid cells is negatively regulated by CEACAM-1 [J]. Cancer Res,2012,72(9):2239-2250.
[14] Zippel D,Barlev H,Ortenberg R,et al. A longitudinal study of CEACAM-1 expression in melanoma disease progression [J]. Oncol Rep,2015,33(3):1314-1318.
[15] Bennett DC,Cazet A,Charest J,et al. MPDU1 regulates CEACAM1 and cell adhesion in vitro and in vivo [J]. Glycoconj J,2018,35(3):265-274.
[16] Zheng J,Hernandez JM,Doussot A,et al. Extracellular matrix proteins and carcinoembryonic antigen-related cell adhesion molecules characterize pancreatic duct fluid exosomes in patients with pancreatic cancer [J]. HPB(Oxford),2018,20(7):597-604.
[17] 马赛,安峰,胥爱文,等.CEACAM1和VEGF在涎腺黏液表皮样癌中的表达及在血管生成中的作用[J].河北医科大学学报,2017,38(1):43-47.
[18] Paudyal B,Paudyal P,Shah D,et al. Detection of vascular endothelial growth factor in colon cancer xenografts using bevacizumab based near infrared fluorophore conjugate [J]. J Biomed Sci,2014,21(11):35-46.
[19] An Y,Liu WJ,Xue P,et al. Autophagy promotes MSC-mediated vascularization in cutaneous wound healing via regulation of VEGF secretion [J]. Cell Death Dis,2018,9(2):58-65.
[20] 吴涛,徐亮,杨志惠.结直肠癌中CEACAM1、VEGF的表达及与血管生成的关系[J].现代中西医结合杂志,2016,25(33):3666-3668. |
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