Author(s): Wu YC, Wang PH, Tsai A, Yang SF, Chen SC
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Abstract BACKGROUND AND OBJECTIVE: Because matrix metalloproteinase-2 (MMP-2) is associated with tumor progression and tissue inhibitor of MMP-2 (TIMP-2) selectively inhibits MMP-2, we investigate the implication of TIMP-2 in carcinogenesis of uterine cervix. METHODS: Twenty-six cervical cancer tissues and their normal counterparts were collected to evaluate semi-quantitative mRNA expression of TIMP-2. Eighty-two cervical cancer, 26 high-grade and 26 low-grade dysplasia, and 26 normal tissues were collected to construct tissue microarrays for immunohistochemical study. We evaluated TIMP-2 immunoreactivity using H scores in cervical carcinogenesis. Semi-quantitative expression of MMP-2 was also detected for comparison. RESULTS: Cervical cancer tissues exhibited statistically lower semi-quantitative TIMP-2 (P = 0.028) or higher MMP-2 (P = 0.036) mRNA expression than their normal counterparts. None of cervical cancer tissues exerted elevated TIMP-2 and reduced MMP-2 mRNA expression simultaneously. Cancer tissues have significantly lower TIMP-2 or higher MMP-2 H scores than high-grade and low-grade dysplasia or normal tissues of uterine cervix. CONCLUSIONS: Low expression of TIMP-2 or high expression of MMP-2 is semi-quantitatively demonstrated in cancer of uterine cervix. TIMP-2 is implicated in cervical carcinogenesis. Copyright © 2011 Wiley-Liss, Inc.
This article was published in J Surg Oncol
and referenced in Journal of Cytology & Histology
- Ji-Zhong Bai
Astrocytic contribution to deficient Ca2+ signalling and oxidative stress mediated by TRPV4 channels in A40-induced hippocampal cell death
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