Expression and gene polymorphisms of the chemokine CXCL5 in colorectal cancer patients

被引:3
作者
Dimberg, Jan
Dienus, Olaf
Lofgren, Sture
Hugander, Anders
Wagsater, Dick
机构
[1] Univ Coll Hlth Sci, Dept Nat Sci & Biomed, SE-55111 Jonkoping, Sweden
[2] Ryhov Cty Hosp, Dept Clin Microbiol, Jonkoping, Sweden
[3] Ryhov Cty Hosp, Dept Surg, Jonkoping, Sweden
[4] Karolinska Inst, King Gustaf V Res Inst, Dept Med, Atherosclerosis Res Unit, Stockholm, Sweden
关键词
CXCL5; polymorphism; tissue level; colorectal cancer; IL-1; beta; ACTIVATING PEPTIDE ENA-78; INTESTINAL-MUCOSA; ANGIOGENESIS; INTERLEUKIN-8; INFLAMMATION; CARCINOMA; DISEASE; COLON; ALPHA;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Several studies indicate that chemokines play important roles in colorectal mucosal immunity by recruiting leukocytes into and out of the lamina propria adjacent to the epithelium. The chemokine CXCL5 which is expressed by epithelial cells within colorectal mucosa is a chemoattractant for neutrophils and has been implicated in Crohn's disease and ulcerative colitis. In addition, CXCL5 is one chemokine which promote angiogenesis related to cancer. The objective of this study was to determine by ELISA assay whether CXCL5 protein level is altered in colorectal cancer (CRC) tissues (n=80) compared with paired normal mucosa. Furthermore, the plasma CXCL5 levels from CRC patients (n=62) compared with controls (n=71) were also examined. Using a TaqMan system we screened for -156G -> C and +398G -> A CXCL5 gene variants in CRC patients (n=228) and a control group (n=231) to assess the role of CXCL5 genotype in CRC. The analyses showed that CXCL5 protein level in colorectal tumours was significantly (P < 0.0001) higher than in normal tissue and was lower in plasma in CRC patients compared with controls (P=0.026). Immunohistochemistry revealed CXCL5 immunoreactivity mainly in epithelial cells of the colorectal carcinoma and in normal epithelial cells. Furthermore, patients who were -156C carriers had higher CXCL5 protein concentration compared with -156G carriers in normal tissue (P=0.027) and CXCL5 protein levels in cancerous tissue tended to be higher for the patient -156C carriers (P=0.059). To our knowledge this is the first report on the influence of CXCL5 gene variants and their relation to expression of CXCL5 protein in human CRC.
引用
收藏
页码:97 / 102
页数:6
相关论文
共 21 条
[1]   Two polymorphisms in the epithelial cell-derived neutrophil-activating peptide (ENA-78) gene [J].
Amoli, MM ;
Larijani, B ;
Thomson, W ;
Ollier, WER ;
Gonzalez-Gay, MA .
DISEASE MARKERS, 2005, 21 (02) :75-77
[2]   Epithelial-neutrophil activating peptide (ENA-78) is an important angiogenic factor in non-small cell lung cancer [J].
Arenberg, DA ;
Keane, MP ;
DiGiovine, B ;
Kunkel, SL ;
Morris, SB ;
Xue, YY ;
Burdick, MD ;
Glass, MC ;
Iannettoni, MD ;
Strieter, RM .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (03) :465-472
[3]  
Baier PK, 2005, ANTICANCER RES, V25, P3581
[4]   Chemokine biology in cancer [J].
Balkwill, F .
SEMINARS IN IMMUNOLOGY, 2003, 15 (01) :49-55
[5]   Inflammation and cancer: back to Virchow? [J].
Balkwill, F ;
Mantovani, A .
LANCET, 2001, 357 (9255) :539-545
[6]   Inflammation and cancer [J].
Coussens, LM ;
Werb, Z .
NATURE, 2002, 420 (6917) :860-867
[7]   Immunobiology of epithelial chemokines in the intestinal mucosa [J].
Dwinell, MB ;
Johanesen, PA ;
Smith, JM .
SURGERY, 2003, 133 (06) :601-607
[8]   Enterocytes are the primary source of the chemokine ENA-78 in normal colon and ulcerative colitis [J].
Keates, S ;
Keates, AC ;
Mizoguchi, E ;
Bhan, A ;
Kelly, CP .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1997, 273 (01) :G75-G82
[9]   Chemokines regulate lymphocyte homing to the intestinal mucosa [J].
Luster, AD .
GASTROENTEROLOGY, 2001, 120 (01) :291-294
[10]   Intra-tumoral interleukin-6 down-regulation system and genetic mutations of tumor suppressor genes in colorectal carcinoma [J].
Miki, C ;
Tonouchi, H ;
Wakuda, R ;
Hatada, T ;
Inoue, Y ;
Minato, E ;
Kobayashi, M ;
Kusunoki, M .
CANCER, 2002, 94 (05) :1584-1592