Literature DB >> 21983884

Overexpression of a disintegrin and metalloprotease 8 in human gliomas is implicated in tumor progression and prognosis.

Shiming He1, Lianshu Ding, Yizhan Cao, Gang Li, Jianping Deng, Yanyang Tu, Boliang Wang.   

Abstract

A disintegrin and metalloprotease 8 (ADAM8) has been shown to be expressed in various cancer types, and its expression was associated with advanced progression of several tumors. However, little is known about ADAM8 in human gliomas. Therefore, we here evaluated the correlation of ADAM8 expression with the clinicopathological features and prognosis in the patients with gliomas. Immunohistochemistry and western blot were used to investigate the expression of ADAM8 protein, respectively, in 128 patients with gliomas. The expression levels of ADAM8 in glioma tissues were significantly higher (P = 0.002) than those in non-neoplastic brain tissues according to the immunohistochemistry analysis. In addition, a high level of ADAM8 expression was significantly more common in glioma tissues with advanced grade than those with low grade (P = 0.01), which were in line with the results of western blot analysis (P = 0.01). Moreover, the increased expression of ADAM8 was significantly correlated with low Karnofsky performance score (KPS) (P = 0.008), frequent intra-tumor necrosis (P = 0.01), and poor overall survival (P = 0.008). Furthermore, multivariate analysis identified the expression levels of ADAM8 (P = 0.01) and intra-tumor necrosis (P = 0.03) to be independent prognostic factors. These findings suggest for the first time that ADAM8 is frequently overexpressed in human gliomas and is closely associated with poor clinical outcome.

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Year:  2011        PMID: 21983884     DOI: 10.1007/s12032-011-0084-9

Source DB:  PubMed          Journal:  Med Oncol        ISSN: 1357-0560            Impact factor:   3.064


  16 in total

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Authors:  I Hernández; J L Moreno; C Zandueta; L Montuenga; F Lecanda
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2.  Metalloproteinase disintegrins ADAM8 and ADAM19 are highly regulated in human primary brain tumors and their expression levels and activities are associated with invasiveness.

Authors:  Dirk Wildeboer; Silvia Naus; Qing-Xiang Amy Sang; Jörg W Bartsch; Axel Pagenstecher
Journal:  J Neuropathol Exp Neurol       Date:  2006-05       Impact factor: 3.685

3.  Tumor necrosis factor alpha induces a metalloprotease-disintegrin, ADAM8 (CD 156): implications for neuron-glia interactions during neurodegeneration.

Authors:  U Schlomann; S Rathke-Hartlieb; S Yamamoto; H Jockusch; J W Bartsch
Journal:  J Neurosci       Date:  2000-11-01       Impact factor: 6.167

4.  Distinct expression patterns and levels of enzymatic activity of matrix metalloproteinases and their inhibitors in primary brain tumors.

Authors:  A Pagenstecher; E M Wussler; G Opdenakker; B Volk; I L Campbell
Journal:  J Neuropathol Exp Neurol       Date:  2001-06       Impact factor: 3.685

5.  ADAM8 expression in prostate cancer is associated with parameters of unfavorable prognosis.

Authors:  Florian R Fritzsche; Monika Jung; Chuanliang Xu; Anja Rabien; Hanka Schicktanz; Carsten Stephan; Manfred Dietel; Klaus Jung; Glen Kristiansen
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6.  ADAM8 as a novel serological and histochemical marker for lung cancer.

Authors:  Nobuhisa Ishikawa; Yataro Daigo; Wataru Yasui; Kouki Inai; Hitoshi Nishimura; Eiju Tsuchiya; Nobuoki Kohno; Yusuke Nakamura
Journal:  Clin Cancer Res       Date:  2004-12-15       Impact factor: 12.531

7.  Hypoxia-dependent expression of ADAM8 in human pancreatic cancer cell lines.

Authors:  N V Valkovskaya
Journal:  Exp Oncol       Date:  2008-06

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Authors:  Troii Hall; Lyle E Pegg; Adele M Pauley; H David Fischer; Alfredo G Tomasselli; Marc D Zack
Journal:  Arch Biochem Biophys       Date:  2009-09-18       Impact factor: 4.013

9.  The enzymatic activity of ADAM8 and ADAM9 is not regulated by TIMPs.

Authors:  Augustin Amour; C Graham Knight; William R English; Ailsa Webster; Patrick M Slocombe; Vera Knäuper; Andrew J P Docherty; J David Becherer; Carl P Blobel; Gillian Murphy
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Review 10.  The 2007 WHO classification of tumours of the central nervous system.

Authors:  David N Louis; Hiroko Ohgaki; Otmar D Wiestler; Webster K Cavenee; Peter C Burger; Anne Jouvet; Bernd W Scheithauer; Paul Kleihues
Journal:  Acta Neuropathol       Date:  2007-07-06       Impact factor: 17.088

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Journal:  Neuro Oncol       Date:  2015-02-01       Impact factor: 12.300

2.  The metalloprotease-disintegrin ADAM8 contributes to temozolomide chemoresistance and enhanced invasiveness of human glioblastoma cells.

Authors:  Fangyong Dong; Michael Eibach; Jörg W Bartsch; Amalia M Dolga; Uwe Schlomann; Catharina Conrad; Susanne Schieber; Oliver Schilling; Martin L Biniossek; Carsten Culmsee; Herwig Strik; Garrit Koller; Barbara Carl; Christopher Nimsky
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3.  Oncogenic reg IV is a novel prognostic marker for glioma patient survival.

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Journal:  Diagn Pathol       Date:  2012-06-19       Impact factor: 2.644

4.  The Metalloprotease-Disintegrin ADAM8 Alters the Tumor Suppressor miR-181a-5p Expression Profile in Glioblastoma Thereby Contributing to Its Aggressiveness.

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Journal:  Front Oncol       Date:  2022-03-15       Impact factor: 6.244

5.  The GBM Tumor Microenvironment as a Modulator of Therapy Response: ADAM8 Causes Tumor Infiltration of Tams through HB-EGF/EGFR-Mediated CCL2 Expression and Overcomes TMZ Chemosensitization in Glioblastoma.

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6.  Expression of A disintegrin and metalloprotease 8 is associated with cell growth and poor survival in colorectal cancer.

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  6 in total

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