The relationship of tryptase- and chymase-positive mast cells to angiogenesis in stage I non-small cell lung cancer

被引:64
作者
Ibaraki, T [1 ]
Muramatsu, M
Takai, S
Jin, D
Maruyama, H
Orino, T
Katsumata, T
Miyazaki, M
机构
[1] Osaka Med Coll, Dept Pharmacol, Takatsuki, Osaka 5698686, Japan
[2] Osaka Med Coll, Dept Thorac & Cardiovasc Surg, Takatsuki, Osaka 5698686, Japan
[3] Hoshigaoka Koseinenkin Hosp, Dept Pathol, Hirakata, Osaka 5738511, Japan
[4] Hoshigaoka Koseinenkin Hosp, Dept Thorac Surg, Hirakata, Osaka 5738511, Japan
关键词
angiogenesis; lung cancer; chymase; mast cells; human;
D O I
10.1016/j.ejcts.2005.06.020
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: There are two types of human mast cells, tryptase-positive mast cells (MCT) and tryptase- and chymase-positive mast cells (MCTC). Although MCT have been reported to be related to the generation of angiogenesis, little is known about the involvement of MCTC in tumor angiogenesis. In this study, to clarify the relationship between MCTC and lung cancer angiogenesis, we evaluated MCTC, MCT, and microvessel counts in normal, border, and central lung cancer regions. Methods: Tumor sections from 32 cases of adenocarcinoma and 13 cases of squamous cell carcinoma were immunostained for chymase to evaluate MCTC, tryptase to evaluate MCT, and CD34 to evaluate microvessel counts. Results: Both MCTC and MCT counts in the border lung cancer region were significantly higher than in the central region, and the MCTC and MCT counts in the central region were significantly higher than those in the normal regions. The microvessel counts in the border region were higher than those in the central region. The ratio of MCTC to MCT in the border region, but not in the central region, was significantly higher than that in the normal region. In the border region, significant correlations not only between MCT and microvessel count, but also between MCTC and microvessel count were, observed. In the central region, a significant correlation between MCTC and the microvessel count was observed, but there was no significant correlation between MCT and the microvessel count. Conclusions: These findings suggest that MCTC may be involved in the pathogenesis of angiogenesis in lung cancer. (c) 2005 Published by Elsevier B.V.
引用
收藏
页码:617 / 621
页数:5
相关论文
共 26 条
[1]   Angiotensin AT1 receptor signalling modulates reparative angiogenesis induced by limb ischaemia [J].
Emanueli, C ;
Salis, MB ;
Stacca, T ;
Pinna, A ;
Gaspa, L ;
Maddeddu, P .
BRITISH JOURNAL OF PHARMACOLOGY, 2002, 135 (01) :87-92
[2]   Dog mast cell alpha-chymase activates progelatinase B by cleaving the Phe(88)-Gln(89) and Phe(91)-Glu(92) bonds of the catalytic domain [J].
Fang, KC ;
Raymond, WW ;
Blount, JL ;
Caughey, GH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (41) :25628-25635
[3]  
FERNANDEZ LA, 1985, J LAB CLIN MED, V105, P141
[4]   Mast cell tissue inhibitor of metalloproteinase-1 is cleaved and inactivated extracellularly by α-chymase [J].
Frank, BT ;
Rossall, JC ;
Caughey, GH ;
Fang, KC .
JOURNAL OF IMMUNOLOGY, 2001, 166 (04) :2783-2792
[5]   17-allylamino-17-demethoxygeldanamycin (17-AAG) is effective in down-regulating mutated, constitutively activated KIT protein in human mast cells [J].
Fumo, G ;
Akin, C ;
Metcalfe, DD ;
Neckers, L .
BLOOD, 2004, 103 (03) :1078-1084
[6]   Synthesis, storage, and release of vascular endothelial growth factor vascular permeability factor (VEGF/VPF) by human mast cells:: Implications for the biological significance of VEGF206 [J].
Grützkau, A ;
Krüger-Krasagakes, S ;
Baumeister, H ;
Schwarz, C ;
Kögel, H ;
Welker, P ;
Lippert, U ;
Henz, BM ;
Möller, A .
MOLECULAR BIOLOGY OF THE CELL, 1998, 9 (04) :875-884
[7]   Mast cells correlate with angiogenesis and poor outcome in stage I lung adenocarcinoma [J].
Imada, A ;
Shijubo, N ;
Kojima, H ;
Abe, S .
EUROPEAN RESPIRATORY JOURNAL, 2000, 15 (06) :1087-1093
[8]   Ras and TGFβ cooperatively regulate epithelial cell plasticity and metastasis:: dissection of Ras signaling pathways [J].
Janda, E ;
Lehmann, K ;
Killisch, I ;
Jechlinger, M ;
Herzig, M ;
Downward, J ;
Beug, H ;
Grünert, S .
JOURNAL OF CELL BIOLOGY, 2002, 156 (02) :299-313
[9]   RADIOTHERAPY OF REFRACTORY BONE PAIN DUE TO SYSTEMIC MAST-CELL DISEASE [J].
JOHNSTONE, PAS ;
MICAN, JM ;
METCALFE, DD ;
DELANEY, TF .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 1994, 17 (04) :328-330
[10]   Production of fibrogenic cytokines by cord blood-derived cultured human mast cells [J].
Kanbe, N ;
Kurosawa, M ;
Nagata, H ;
Yamashita, T ;
Kurimoto, F ;
Miyachi, Y .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2000, 106 (01) :S85-S90