Expression of a disintegrin and metalloprotease (ADAM and ADAMTS) enzymes in human non-small-cell lung carcinomas (NSCLC)

被引:80
作者
Rocks, N
Paulissen, G
Calvo, FQ
Polette, M
Gueders, M
Munaut, C
Foidart, JM
Noel, A
Birembaut, P
Cataldo, D [1 ]
机构
[1] Univ Liege, Lab Pneumol, B-4000 Liege, Belgium
[2] Univ Liege, Lab Tumor & Dev Biol, CBIG, B-4000 Liege, Belgium
[3] CHU Liege, B-4000 Liege, Belgium
[4] CHU Reims, INSERM, U514, Lab Pol Bouin,Hop Maison Blanche, Reims, France
[5] CHU Sart Tilman, B-4000 Liege, Belgium
关键词
ADAM; ADAMTS; lung; proteinases; VEGF;
D O I
10.1038/sj.bjc.6602990
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A Disintegrin and Metalloprotease ( ADAM) are transmembrane proteases displaying multiple functions. ADAM with ThromboSpondin-like motifs ( ADAMTS) are secreted proteases characterised by thrombospondin ( TS) motifs in their C-terminal domain. The aim of this work was to evaluate the expression pattern of ADAMs and ADAMTS in non small cell lung carcinomas ( NSCLC) and to investigate the possible correlation between their expression and cancer progression. Reverse transcriptase polymerase chain reaction ( RT-PCR), Western blot and immunohistochemical analyses were performed on NSCLC samples and corresponding nondiseased tissue fragments. Among the ADAMs evaluated ( ADAM-8, -9, -10, -12, -15, -17, ADAMTS-1, TS-2 and TS-12), a modulation of ADAM-12 and ADAMTS-1 mRNA expression was observed. Amounts of ADAM-12 mRNA transcripts were increased in tumour tissues as compared to the corresponding controls. In sharp contrast, ADAMTS-1 mRNA levels were significantly lower in tumour tissues when compared to corresponding nondiseased lung. These results were corroborated at the protein level by Western blot and immunohistochemistry. A positive correlation was observed between the mRNA levels of ADAM-12 and those of two vascular endothelial growth factor ( VEGF)-A isoforms ( VEGF-A165 and VEGF-A121). Taken together, these results providing evidence for an overexpression of ADAM-12 and a lower expression of ADAMTS-1 in non-small-cell lung cancer suggest that these proteases play different functions in cancer progression.
引用
收藏
页码:724 / 730
页数:7
相关论文
共 39 条
[1]   Cardiac hypertrophy is inhibited by antagonism of ADAM12 processing of HB-EGF: Metalloproteinase inhibitors as a new therapy [J].
Asakura, M ;
Kitakaze, M ;
Takashima, S ;
Liao, Y ;
Ishikura, F ;
Yoshinaka, T ;
Ohmoto, H ;
Node, K ;
Yoshino, K ;
Ishiguro, H ;
Asanuma, H ;
Sanada, S ;
Matsumura, Y ;
Takeda, H ;
Beppu, S ;
Tada, M ;
Hori, M ;
Higashiyama, S .
NATURE MEDICINE, 2002, 8 (01) :35-40
[2]   A metalloproteinase disintegrin that releases tumour-necrosis factor-alpha from cells [J].
Black, RA ;
Rauch, CT ;
Kozlosky, CJ ;
Peschon, JJ ;
Slack, JL ;
Wolfson, MF ;
Castner, BJ ;
Stocking, KL ;
Reddy, P ;
Srinivasan, S ;
Nelson, N ;
Boiani, N ;
Schooley, KA ;
Gerhart, M ;
Davis, R ;
Fitzner, JN ;
Johnson, RS ;
Paxton, RJ ;
March, CJ ;
Cerretti, DP .
NATURE, 1997, 385 (6618) :729-733
[3]   INVASIVE AND METASTATIC POTENTIAL OF A V-HA-RAS-TRANSFORMED HUMAN BRONCHIAL EPITHELIAL-CELL LINE [J].
BONFIL, RD ;
REDDEL, RR ;
URA, H ;
REICH, R ;
FRIDMAN, R ;
HARRIS, CC ;
KLEINSZANTO, AJP .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1989, 81 (08) :587-594
[4]   Cloning, expression analysis, and structural characterization of seven novel human ADAMTSs, a family of metalloproteinases with disintegrin and thrombospondin-1 domains [J].
Cal, S ;
Obaya, AJ ;
Llamazares, M ;
Garabaya, C ;
Quesada, V ;
López-Otín, C .
GENE, 2002, 283 (1-2) :49-62
[5]   Matrix metalloproteinase-9 deficiency impairs cellular infiltration and bronchial hyperresponsiveness during allergen-induced airway inflammation [J].
Cataldo, DD ;
Tournoy, KG ;
Vermaelen, K ;
Munaut, C ;
Foidart, JM ;
Louis, R ;
Noël, A ;
Pauwels, RA .
AMERICAN JOURNAL OF PATHOLOGY, 2002, 161 (02) :491-498
[6]   METH-2 silencing and promoter hypermethylation in NSCLC [J].
Dunn, JR ;
Panutsopulos, D ;
Shaw, MW ;
Heighway, J ;
Dormer, R ;
Salmo, EN ;
Watson, SG ;
Field, JK ;
Liloglou, T .
BRITISH JOURNAL OF CANCER, 2004, 91 (06) :1149-1154
[7]   New functions for the matrix metalloproteinases in cancer progression [J].
Egeblad, M ;
Werb, Z .
NATURE REVIEWS CANCER, 2002, 2 (03) :161-174
[8]   A novel, secreted form of human ADAM 12 (meltrin α) provokes myogenesis in vivo [J].
Gilpin, BJ ;
Loechel, F ;
Mattei, MG ;
Engvall, E ;
Albrechtsen, R ;
Wewer, UM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (01) :157-166
[9]  
Hajitou A, 2001, CANCER RES, V61, P3450
[10]   Metalloproteinases and their inhibitors in tumor angiogenesis [J].
Handsley, MM ;
Edwards, DR .
INTERNATIONAL JOURNAL OF CANCER, 2005, 115 (06) :849-860