Identification of potential biomarkers of head and neck squamous cell carcinoma using iTRAQ based quantitative proteomic approach

被引:6
|
作者
Babu, Niraj [1 ,2 ]
Mohan, Sonali [1 ]
Nanjappa, Vishalakshi [1 ]
Chavan, Sandip [1 ]
Advani, Jayshree [1 ,2 ]
Khan, Aafaque Ahmed [1 ,3 ]
Renuse, Santosh [1 ]
Radhakrishnan, Aneesha [1 ]
Prasad, T. S. Keshava [1 ]
Kumar, Rekha V. [4 ]
Ray, Jay Gopal [5 ]
Biswas, Manjusha [6 ]
Thiyagarajan, Saravanan [7 ]
Califano, Joseph A. [8 ,9 ]
Sidransky, David [8 ]
Gowda, Harsha [1 ,2 ]
Chatterjee, Aditi [1 ]
机构
[1] Inst Bioinformat, Int Tech Pk, Bangalore 560066, Karnataka, India
[2] Manipal Acad Higher Educ, Manipal 576104, Karnataka, India
[3] Kalinga Inst Ind Technol, Sch Biotechnol, Bhubaneswar 751024, Odisha, India
[4] Kidwai Mem Inst Oncol, Dept Pathol, Bangalore 560029, Karnataka, India
[5] Burdwan Dent Coll & Hosp, Dept Oral Pathol, Burdwan 713101, W Bengal, India
[6] Mitra Biotech, Div Mol Pathol, Bangalore 560099, Karnataka, India
[7] Mitra Biotech, Div Canc Biol, Bangalore 560099, Karnataka, India
[8] Johns Hopkins Univ, Sch Med, Dept Otolaryngol Head & Neck Surg, Baltimore, MD 21205 USA
[9] Univ Calif San Diego, Dept Surg, Moores Canc Ctr, La Jolla, CA 92093 USA
来源
DATA IN BRIEF | 2018年 / 19卷
关键词
HNSCC; iTRAQ; Parallel reaction monitoring; Mass spectrometry; OKF6/TERT1;
D O I
10.1016/j.dib.2018.05.100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Head and neck squamous cell carcinoma (HNSCC) is one of the most common cancers in India. Despite improvements in treatment strategy, the survival rates of HNSCC patients remain poor. Thus, it is necessary to identify biomarkers that can be used for early detection of disease. In this study, we employed iTRAQ-based quantitative mass spectrometry analysis to identify dysregulated proteins from a panel of head and neck squamous cell carcinoma (HNSCC) cell lines. We identified 2468 proteins, of which 496 proteins were found to be dysregulated in at least two out of three HNSCC cell lines compared to immortalized normal oral keratinocytes. We detected increased expression of replication protein Al (RPA1) and heat shock protein family H (Hsp110) member 1 (HSPH1), in HNSCC cell lines compared to control. The differentially expressed proteins were further validated using parallel reaction monitoring (PRM) and western blot analysis in HNSCC cell lines. Immunohistochemistry-based validation using HNSCC tissue microarrays revealed overexpression of RPA1 and HSPH1 in 15.7% and 322% of the tested cases, respectively. Our study illustrates quantitative proteomics as a robust approach for identification of potential HNSCC biomarkers. The proteomic data has been submitted to ProteomeXchange Consortium (hlip://www.proLeomecentraLpro teomexchange.org) via the PRIDE public data repository accessible using the data identifier - PXD009241. (C) 2018 The Authors. Published by Elsevier Inc.
引用
收藏
页码:1124 / 1130
页数:7
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