Literature DB >> 15375490

Expression spectra of matrix metalloproteinases in metastatic non-small cell lung cancer.

Torng-Sen Lin1, Shiow-Her Chiou, Liang-Shun Wang, Hsuan-Hua Huang, Shu-Fen Chiang, Alex Y H Shih, Ya-Lin Chen, Chih-Yi Chen, Chung-Ping Hsu, Nan-Yung Hsu, Ming-Chih Chou, Shou-Jen Kuo, Kuan-Chih Chow.   

Abstract

By combining suppression subtractive hybridization and microarray to examine gene expressions between metastatic and non-metastatic non-small cell lung cancer (NSCLC), we have identified differential expression spectra of matrix metalloproteinases (MMP). Among MMPs, expressions of MMP-13, -14, -15 and -24 decreased, those of MMP-9, -11, -12, -16, -17, -19 and -23B did not change, and those of MMP-1, -2, -7, -8 and -10 increased dramatically. Overexpressions of MMP-1, -2, -7 and -10 were confirmed by reverse transcription-polymerase chain reaction. In this study we further assessed the clinical significance of MMP-1, -2, -7 and -10. Specimens from 472 patients with completely resected NSCLC were examined by immunohistochemistry. The median follow-up period was 38 months (range, 2-113 months). Overexpression of MMP-1 was observed in 72.9% (n=344) of 472 patients, that of MMP-2 was 77.9% (n=352), MMP-7 63.3% (n=299) and that of MMP-10 was 27.1% (n=128). For patients with lymph node metastasis, MMP-1 and -2 overexpressions were not only independent prognostic factors for unfavorable outcome, but also associated with decreased survival (p=0.0015, and p=0.011 respectively). The present study showed that MMP expression spectrum in NSCLC was heterogeneous: expression of some MMP increased, some unchanged, while some decreased. Therefore, it should be worth determining MMP expression pattern as a regimen reference for NSCLC patients who were scheduled to receive MMP inhibitor, which was class-specific, as adjuvant therapeutic agent.

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Year:  2004        PMID: 15375490

Source DB:  PubMed          Journal:  Oncol Rep        ISSN: 1021-335X            Impact factor:   3.906


  19 in total

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7.  Signaling through urokinase and urokinase receptor in lung cancer cells requires interactions with beta1 integrins.

Authors:  Chi-Hui Tang; Marla L Hill; Alexis N Brumwell; Harold A Chapman; Ying Wei
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Authors:  Hen Prizant; Manisha Taya; Irina Lerman; Allison Light; Aritro Sen; Soumya Mitra; Thomas H Foster; Stephen R Hammes
Journal:  Endocr Relat Cancer       Date:  2016-02-15       Impact factor: 5.678

9.  Fibulin-5 suppresses lung cancer invasion by inhibiting matrix metalloproteinase-7 expression.

Authors:  Wen Yue; Quanhong Sun; Rodney Landreneau; Chuanyue Wu; Jill M Siegfried; Jian Yu; Lin Zhang
Journal:  Cancer Res       Date:  2009-07-07       Impact factor: 12.701

10.  Genetic polymorphisms in MMP 2, 3, 7, and 9 genes and the susceptibility and clinical outcome of cervical cancer in a Chinese Han population.

Authors:  Beibei Xie; Zhen Zhang; Hui Wang; Zhaojie Chen; Yongsheng Wang; Huazheng Liang; Gaoyuan Yang; Xingsheng Yang; Haiyan Zhang
Journal:  Tumour Biol       Date:  2015-11-02
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