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Clinicopathological Features and Overexpression of Matrix Metalloproteinases in Intramucosal Gastric Carcinoma with Lymph Node Metastasis
Endoscopic mucosal resection, which has been widely accepted for the treatment of intramucosal gastric carcinoma (IMGC) because of the minimal invasiveness of the procedure and the sustained quality of life it provides, can only be used on the premise that the carcinoma has no lymph node metastasis....
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Published in: | Clinical cancer research 2000-09, Vol.6 (9), p.3581-3584 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | Endoscopic mucosal resection, which has been widely
accepted for the treatment of intramucosal gastric carcinoma (IMGC)
because of the minimal invasiveness of the procedure and the sustained
quality of life it provides, can only be used on the premise that the
carcinoma has no lymph node metastasis. We evaluated the
clinicopathological and biological features of IMGC with lymph node
metastases in relation to matrix metalloproteinase (MMP) expression.
Fifteen cases of lymph node metastasis-positive [n(+)] IMGC
and 59 cases of lymph node metastatic-negative [n(–)] IMGC were
obtained. The expression of MMP-2 and MMP-9 was investigated with
immunohistochemical methods. Clinicopathologically, n(+)-IMGCs were
more likely to be of a larger size, to be of poorly differentiated
adenocarcinoma, to have had lymphatic permeation [ly(+)], and
to have ulcerations within the lesion compared to n(–)-IMGCs. The
incidence of the positive expression of MMP-9 in n(+)-IMGCs (67%) or
ly(+)-IMGCs (86%) was significantly higher than that in n(–)-IMGCs
(32%) or ly(–)-IMGCs (34%). Even in IMGCs, carcinoma cells may
produce MMPs that can degrade the basement membrane, allowing them to
permeate the lymph capillary. Ulcerations within the lesion may also
facilitate the interchange of lymphatic flow between the mucosa and the
submucosa, promoting the development of lymph node metastases. |
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ISSN: | 1078-0432 1557-3265 |