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10.1016/j.bbrc.2014.03.017 http://scihub22266oqcxt.onion/10.1016/j.bbrc.2014.03.017 C4696041!4696041 !24657443     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=24657443 &cmd=llinks): Failed to open stream: HTTP request failed! 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Identification of prosaposin and transgelin as potential biomarkers for gallbladder cancer using quantitative proteomics |pdf=|usr=}}{{24657443 }} gab.com Text Identification of prosaposin and transgelin as potential biomarkers for gallbladder cancer using quantitative proteomics JO: Biochem Biophys Res Commun http://www.kidney.de/pget.php?&tw=1&pmid=24657443 #FOAvip Gallbladder cancer is an uncommon but lethal malignancy with particularly high incidence in Chile, India, Japan and China. There is a paucity of unbiased large-scale studies investigating molecular basis of gallbladder cancer. To systematically identify differentially regulated proteins in gallbladder cancer, iTRAQ-based quantitative proteomics of gallbladder cancer was carried out using Fourier transform high resolution mass spectrometry. Of the 2575 proteins identified, proteins upregulated in gallbladder cancer included several lysosomal proteins such as prosaposin, cathepsin Z and cathepsin H. Downregulated proteins included serine protease HTRA1 and transgelin, which have been reported to be downregulated in several other cancers. Novel biomarker candidates including prosaposin and transgelin were validated to be upregulated and downregulated, respectively, in gallbladder cancer using tissue microarrays. Our study provides the first large scale proteomic characterization of gallbladder cancer which will serve as a resource for future discovery of biomarkers for gallbladder cancer. Twit Text FOAVip Identification of prosaposin and transgelin as potential biomarkers for gallbladder cancer using quantitative proteomics ????Biochem Biophys Res Commun http://www.kidney.de/pget.php?&tw=1&pmid=24657443 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=24657443 #FOAvip English Wikipedia <ref>{{Cite pmid|24657443 }}</ref> Identification of prosaposin and transgelin as potential biomarkers for gallbladder cancer using quantitative proteomics #MMPMID24657443 Sahasrabuddhe NA ; Barbhuiya MA ; Bhunia S ; Subbannayya T ; Gowda H ; Advani J ; Shrivastav BR ; Navani S ; Leal P ; Roa JC ; Chaerkady R ; Gupta S ; Chatterjee A ; Pandey A ; Tiwari PK Biochem Biophys Res Commun 2014[Apr]; 446 (4 ): 863-9 PMID24657443 show ga Gallbladder cancer is an uncommon but lethal malignancy with particularly high incidence in Chile, India, Japan and China. There is a paucity of unbiased large-scale studies investigating molecular basis of gallbladder cancer. To systematically identify differentially regulated proteins in gallbladder cancer, iTRAQ-based quantitative proteomics of gallbladder cancer was carried out using Fourier transform high resolution mass spectrometry. Of the 2575 proteins identified, proteins upregulated in gallbladder cancer included several lysosomal proteins such as prosaposin, cathepsin Z and cathepsin H. Downregulated proteins included serine protease HTRA1 and transgelin, which have been reported to be downregulated in several other cancers. Novel biomarker candidates including prosaposin and transgelin were validated to be upregulated and downregulated, respectively, in gallbladder cancer using tissue microarrays. Our study provides the first large scale proteomic characterization of gallbladder cancer which will serve as a resource for future discovery of biomarkers for gallbladder cancer. |Biomarkers, Tumor/*analysis/genetics [MESH] |Chromatography, Liquid [MESH] |Gallbladder Neoplasms/genetics/*pathology [MESH] |Gallbladder/metabolism/*pathology [MESH] |Gene Expression Regulation, Neoplastic [MESH] |Humans [MESH] |Immunohistochemistry [MESH] |Microfilament Proteins/*analysis/genetics [MESH] |Muscle Proteins/*analysis/genetics [MESH] |Proteome/analysis/genetics [MESH] |Proteomics [MESH] |Saposins/*analysis/genetics [MESH] |Tandem Mass Spectrometry [MESH]Identification of prosaposin and transgelin as potential biomarkers fo(epmc).pdf DeepDyve Pubget Overpricing