Gajbhiye , A. and Dabhi , R. and Taunk , K. and Vannuruswamy, G. and RoyChoudhury , S. and Adhav , R. and Seal , S. and Mane , A. and Santhakumari , B. and Santra , M.K. and Chaudhury , K. and Rapole, S. (2016) Urinary proteome alterations in HER2 enriched breast cancer revealed by multipronged quantitative proteomics. Proteomics.

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Abstract

Globally, breast cancer is the second most common cancer amongst women. Although biomarker discoveries through various proteomic approaches of tissue and serum samples have been studied in breast cancer, urinary proteome alterations in breast cancer is least studied. Urine, being a non-invasive biofluid and a significant source of proteins has potential in early diagnosis of breast cancer. The present study used complementary quantitative gel based and gel free proteomic approaches to find a panel of urinary protein markers that could discriminate HER2 enriched (HE) subtype breast cancer from the healthy controls. A total of 183 differentially expressed proteins were identified using three complementary approaches viz. 2D-DIGE, iTRAQ and SWATH. The differentially expressed proteins were subjected to various bioinformatic analyses for deciphering the biological context of these proteins using PANTHER, DAVID and STRING. Multivariate statistical analysis was undertaken to identify the set of most significant proteins, which could discriminate HE breast cancer from healthy controls. Immunoblotting and MRM based validation in a separate cohort testified a panel of 21 proteins such as ZA2G, A2GL, RET4, ANXA1, SAP3, SRC8, GELS, KNG1, CO9, CLUS, CERU and A1AT could be a panel of candidate markers that could discriminate HE breast cancer from healthy controls. This article is protected by copyright. All rights reserved.

Item Type:	Article
Subjects:	Bioinformatics and Proteomics
Depositing User:	Mr. Rameshwar Nema
Date Deposited:	15 Jul 2016 07:38
Last Modified:	15 Jul 2016 07:39
URI:	http://nccs.sciencecentral.in/id/eprint/292

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