Cigarette smoke and chewing tobacco alter expression of different sets of miRNAs in oral keratinocytes

被引:37
作者
Bhat, Mohd Younis [1 ,2 ]
Advani, Jayshree [1 ,3 ]
Rajagopalan, Pavithra [1 ,4 ]
Patel, Krishna [1 ,2 ]
Nanjappa, Vishalakshi [1 ]
Solanki, Hitendra S. [1 ,4 ]
Patil, Arun H. [1 ,4 ,5 ]
Bhat, Firdous A. [1 ,2 ]
Mathur, Premendu P. [4 ]
Nair, Bipin [2 ]
Prasad, T. S. Keshava [1 ,5 ]
Califano, Joseph A. [6 ]
Sidransky, David [7 ]
Gowda, Harsha [1 ]
Chatterjee, Aditi [1 ]
机构
[1] Int Technol Pk, Inst Bioinformat, Bangalore 560066, Karnataka, India
[2] Amrita Vishwa Vidyapeetham, Sch Biotechnol, Kollam 690525, India
[3] Manipal Acad Higher Educ, Manipal 576104, Karnataka, India
[4] Kalinga Inst Ind Technol, Sch Biotechnol, Bhubaneswar 751024, Odisha, India
[5] Yenepoya Deemed Be Univ, Yenepoya Res Ctr, Ctr Syst Biol & Mol Med, Mangalore 575018, India
[6] Univ Calif San Diego, Dept Surg, Moores Canc Ctr, La Jolla, CA 92093 USA
[7] Johns Hopkins Univ, Sch Med, Dept Otolaryngol Head & Neck Surg, Baltimore, MD 21231 USA
来源
SCIENTIFIC REPORTS | 2018年 / 8卷
关键词
SQUAMOUS-CELL CARCINOMA; EPITHELIAL-MESENCHYMAL TRANSITION; LUNG-CANCER CELLS; TARGET INTERACTIONS; TUMOR-METASTASIS; UP-REGULATION; OVEREXPRESSION; MICRORNAS; PROMOTES; PROGRESSION;
D O I
10.1038/s41598-018-25498-2
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
Carcinogenic effect of tobacco in oral cancer is through chewing and/or smoking. Significant differences exist in development of oral cancer between tobacco users and non-users. However, molecular alterations induced by different forms of tobacco are yet to be fully elucidated. We developed cellular models of chronic exposure to chewing tobacco and cigarette smoke using immortalized oral keratinocytes. Chronic exposure to tobacco resulted in increased cell scattering and invasiveness in immortalized oral keratinocytes. miRNA sequencing using Illumina HiSeq 2500 resulted in the identification of 10 significantly dysregulated miRNAs (4 fold; p <= 0.05) in chewing tobacco treated cells and 6 in cigarette smoke exposed cells. We integrated this data with global proteomic data and identified 36 protein targets that showed inverse expression pattern in chewing tobacco treated cells and 16 protein targets that showed inverse expression in smoke exposed cells. In addition, we identified 6 novel miRNAs in chewing tobacco treated cells and 18 novel miRNAs in smoke exposed cells. Integrative analysis of dysregulated miRNAs and their targets indicates that signaling mechanisms leading to oncogenic transformation are distinct between both forms of tobacco. Our study demonstrates alterations in miRNA expression in oral cells in response to two frequently used forms of tobacco.
引用
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页数:13
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