Publication Type:

Journal Article


Biochemical and Biophysical Research Communications, Academic Press Inc., Volume 446, Number 4, p.863-869 (2014)



Biological, Biomarkers, Chromatography, Gallbladder, gallbladder cancer, Gallbladder Neoplasms, Gene Expression Regulation, Humans, immunohistochemistry, iTRAQ, liquid, Microfilament Proteins, Muscle Proteins, Neoplastic, prosaposin, proteome, proteomics, Quantitative proteomics, Saposins, tandem mass spectrometry, Tissue Array Analysis, Transgelin, Tumor Markers


<p>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. © 2014 Elsevier Inc. All rights reserved.</p>


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Cite this Research Publication

N. Aa Sahasrabuddhe, Barbhuiya, M. Abc, Bhunia, Sb, Subbannayya, Tae, Gowda, Ha, Advani, Ja, Shrivastav, B. Rf, Navani, Sg, Leal, Pdh, Roa, J. Ci, Chaerkady, Rd, Gupta, Sf, Chatterjee, Aa, Pandey, Aad j k l, and Tiwari, P. Kbc, “Identification of prosaposin and transgelin as potential biomarkers for gallbladder cancer using quantitative proteomics”, Biochemical and Biophysical Research Communications, vol. 446, pp. 863-869, 2014.