Secretome analysis of oral keratinocytes chronically exposed to shisha.

IF 1.9
Shankargouda Patil, Niraj Babu, Tejaswini Subbannayya, Sonali V Mohan, Gajanan Sathe, Hitendra S Solanki, Pavithra Rajagopalan, Krishna Patel, Jayshree Advani, Shilpa Bhandi, David Sidransky, Aditi Chatterjee, Harsha Gowda, Marco Ferrari
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引用次数: 4

Abstract

Background: Shisha smoking has been associated with multiple diseases including oral cancer. However, a mechanistic study to investigate alteration of secreted proteins in oral cells due to shisha smoking is lacking.

Objectives: Elucidation of differentially secreted proteins by immortalized human normal oral keratinocytes (OKF6/TERT1) upon chronic exposure to shisha.

Methods: OKF6/TERT1 was chronically treated with 0.5% shisha extract for 8 months. Conditioned media from shisha treated (OKF6/TERT1-Shisha) and untreated (OKF6/TERT1-Parental) cells were subjected to TMT-based quantitative proteomic analysis. Bioinformatics analysis of differentially secreted proteins was carried out using SignalP, SecretomeP and TMHMM. Immunoblot validation of selected proteins was carried out to confirm the proteomics results.

Results: Proteomic analysis of OKF6/TERT1-Parental and OKF6/TERT1-Shisha secretome resulted in the identification of 1,598 proteins, of which 218 proteins were found to be differentially secreted (⩾ 1.5-fold; p-value ⩽ 0.05) in shisha treated cells. Bioinformatics analysis using prediction tools showed secretory potential of differentially secreted proteins identified in OKF6/TERT1-Shisha. Western blotting validated the expression of AKR1C2, HSPH1 and MMP9 in OKF6/TERT1-Shisha secretome in agreement with proteomic data.

Conclusion: This study serves as a useful resource to understand the effect of chronic shisha smoking on the milieu of secreted proteins of oral cells. In vivo studies are warranted to supplement our in vitro data to elucidate the role of these proteins as early diagnostic biomarkers for oral carcinogenesis among shisha smokers.

长期暴露于水烟的口腔角化细胞分泌组学分析。
背景:水烟与口腔癌等多种疾病有关。然而,关于水烟对口腔细胞分泌蛋白改变的机制研究尚缺乏。目的:阐明永生化人正常口腔角质形成细胞(OKF6/TERT1)在长期暴露于水烟后差异分泌蛋白的作用。方法:以0.5%水烟提取物长期治疗OKF6/TERT1 8个月。对水烟处理细胞(OKF6/ tert1 -水烟)和未处理细胞(OKF6/ tert1 -亲本)的条件培养基进行基于tmt的定量蛋白质组学分析。采用SignalP、SecretomeP和TMHMM对差异分泌蛋白进行生物信息学分析。对所选蛋白进行免疫印迹验证,以确认蛋白质组学结果。结果:OKF6/ tert1 -亲本和OKF6/ tert1 -水烟分泌组的蛋白质组学分析导致鉴定出1,598个蛋白质,其中发现218个蛋白质差异分泌(大于或等于1.5倍;水烟处理细胞p值< 0.05)。利用预测工具进行生物信息学分析,发现OKF6/ tert1 -水烟中差异分泌蛋白的分泌潜力。Western blotting验证了OKF6/ tert1 -水烟分泌组中AKR1C2、HSPH1和MMP9的表达与蛋白质组学数据一致。结论:本研究为了解慢性水烟对口腔细胞分泌蛋白环境的影响提供了有益的资源。体内研究有必要补充我们的体外数据,以阐明这些蛋白作为水烟吸烟者口腔癌发生的早期诊断生物标志物的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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