Stromelysin-2 overexpression in human esophageal squamous cell carcinoma: potential clinical implications

被引:43
作者
Mathew, R
Khanna, R
Kumar, R
Mathur, M
Shukla, NK
Ralhan, R [1 ]
机构
[1] All India Inst Med Sci, Inst Rotary Canc Hosp, Dept Biochem, New Delhi 110029, India
[2] All India Inst Med Sci, Inst Rotary Canc Hosp, Dept Pathol, New Delhi 110029, India
[3] All India Inst Med Sci, Inst Rotary Canc Hosp, Surg Oncol Unit, New Delhi 110029, India
来源
CANCER DETECTION AND PREVENTION | 2002年 / 26卷 / 03期
关键词
ST-2; esophageal cancer; invasion;
D O I
10.1016/S0361-090X(02)00035-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The degradation of the extracellular matrix (ECM) is a major step in the process of tumor invasion and metastasis, mediated by matrix metalloproteinases (MMPs). Knowledge of alterations in the expression of stromelysin-2 (ST-2) or MMP-10 in human esophageal squamous cell carcinoma (ESCC) is meager. Immumohistochemical analysis of ST-2 expression was carried out in surgically resected ESCCs (50 cases) and paired distal histologically normal esophageal tissues (50 cases), correlated with clinicopathological parameters. Overexpression of ST-2 protein, in tumor cell cytoplasm and stromal elements, was observed in 37 of the 50 (74%) ESCCs localized in tumor cell cytoplasm and stromal elements. Low levels of ST-2 were observed in 8 of the 50 (16%) matched histologically normal esophageal tissues. Significant associations were observed between ST-2 overexpression and tumor size (r = 0.02, P = 0.04), local invasiveness of the tumor (r = -0.30, P = 0.002) and distant organ metastasis (r = -0.227, P = 0.02), suggestive of its involvement in development and progression of ESCCs. The data underscore the significance of ST-2 expression in context to the aggressive tumor characteristics observed in ESCCs in the Indian population, wherein extremely poor prognosis has been ascribed to extensive local invasion and metastasis. (C) 2002 International Society for Preventive Oncology. Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:222 / 228
页数:7
相关论文
共 38 条
[11]  
LIJNEN HR, 1998, CELL, V37, P469
[12]   Regulation of the expression of stromelysin-2 by growth factors in keratinocytes: Implications for normal and impaired wound healing [J].
Madlener, M ;
Mauch, C ;
Conca, W ;
Brauchle, M ;
Parks, WC ;
Werner, S .
BIOCHEMICAL JOURNAL, 1996, 320 :659-664
[13]   EXPRESSION OF COLLAGENASE-RELATED METALLOPROTEINASE GENES IN HUMAN LUNG OR HEAD AND NECK TUMORS [J].
MULLER, D ;
BREATHNACH, R ;
ENGELMANN, A ;
MILLON, R ;
BRONNER, G ;
FLESCH, H ;
DUMONT, P ;
EBER, M ;
ABECASSIS, J .
INTERNATIONAL JOURNAL OF CANCER, 1991, 48 (04) :550-556
[14]   MATRIX METALLOPROTEINASE DEGRADATION OF ELASTIN, TYPE-IV COLLAGEN AND PROTEOGLYCAN - A QUANTITATIVE COMPARISON OF THE ACTIVITIES OF 95 KDA AND 72 KDA GELATINASES, STROMELYSIN-1 AND STROMELYSIN-2 AND PUNCTUATED METALLOPROTEINASE (PUMP) [J].
MURPHY, G ;
COCKETT, MI ;
WARD, RV ;
DOCHERTY, AJP .
BIOCHEMICAL JOURNAL, 1991, 277 :277-279
[15]  
Murray GI, 1998, J PATHOL, V185, P256
[16]  
Ohashi K, 2000, CANCER-AM CANCER SOC, V88, P2201, DOI 10.1002/(SICI)1097-0142(20000515)88:10<2201::AID-CNCR2>3.3.CO
[17]  
2-E
[18]   Angiostatin-converting enzyme activities of human matrilysin (MMP-7) and gelatinase B type IV collagenase (MMP-9) [J].
Patterson, BC ;
Sang, QXA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (46) :28823-28825
[19]  
POLETTE M, 1991, INVAS METAST, V11, P76
[20]   Assay of matrix metalloproteinases types 1, 2, 3 and 9 in breast cancer [J].
Remacle, AG ;
Noël, A ;
Duggan, C ;
McDermott, E ;
O'Higgins, N ;
Foidart, JM ;
Duffy, MJ .
BRITISH JOURNAL OF CANCER, 1998, 77 (06) :926-931