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   <subfield code="a">10.1245/s10434-011-1574-x</subfield>
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   <subfield code="a">(NATIONALLICENCE)springer-10.1245/s10434-011-1574-x</subfield>
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   <subfield code="a">Role of MMP14 Gene Polymorphisms in Susceptibility and Pathological Development to Hepatocellular Carcinoma</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Tzy-Yen Chen, Yi-Ching Li, Yu-Fan Liu, Chiung-Man Tsai, Yi-Hsien Hsieh, Chiao-Wen Lin, Shun-Fa Yang, Chia-Jui Weng]</subfield>
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   <subfield code="a">Background: Early detection of hepatocellular carcinoma (HCC) is seldom available because of the lack of reliable markers. Matrix metalloproteinase (MMP) 14 is a cell surface proteinase that displays a broad spectrum of activity against extracellular matrix components and promotes the invasion/metastasis of cells. MMP14 is overexpressed in HCC, and the level is correlated with poor overall survival. The purpose of this study was to examine whether the MMP14 gene polymorphisms are associated with the susceptibility and clinicopathological development of HCC. Methods: A total of 135 patients with HCC and 496 healthy control subjects were recruited. Six single nucleotide polymorphisms (SNPs) of MMP14 genes were analyzed by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) genotyping and haplotype-base analysis. Results: A significant (p&lt;0.05) lower risk for HCC was shown in the individuals with MMP14 +6767 G/A and +7096 C/C genotypes compared with those with corresponding wild-type homozygotes; high frequency for anti-hepatitis C virus and cirrhosis positive were shown in the HCC patients with MMP14 +7096 TC/CC genotype after adjusting for other confounding factors. The distribution frequency of −165 T: +221 T: +6727 C: +6767 G: +7096 T: +8153 G haplotype and diplotype was significantly higher in the HCC patients than healthy control subjects. Conclusions: The +6767 and +7096 polymorphic genotypes and haplotype −165 T: +221 T: +6727 C: +6767 G: +7096 T: +8153 G of MMP14 gene might contribute to the prediction of susceptibility and pathological development to HCC.</subfield>
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   <subfield code="a">Society of Surgical Oncology, 2011</subfield>
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   <subfield code="u">School of Medicine, Chung Shan Medical University, Taichung, Taiwan</subfield>
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   <subfield code="u">Department of Pharmacology, School of Medicine, Chung Shan Medical University, Taichung, Taiwan</subfield>
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   <subfield code="u">Department of Biomedical Sciences, Chung Shan Medical University, Taichung, Taiwan</subfield>
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   <subfield code="u">Institute of Biochemistry and Biotechnology, Chung Shan Medical University, Taichung, Taiwan</subfield>
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   <subfield code="u">Department of Medical Research, Chung Shan Medical University Hospital, Taichung, Taiwan</subfield>
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   <subfield code="u">Graduate Institute of Applied Science of Living, Tainan University of Technology, Tainan City, Taiwan</subfield>
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   <subfield code="t">Annals of Surgical Oncology</subfield>
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