Abstract
Abstract Obesity is a worldwide public health issue which can lead to cardiovascular disease, type 2 diabetes, and cancers. Bariatric surgery can provide sustained weight loss and a significant reduction of cancer risk. MicroRNAs are approximately 22 nucleotide long post transcription regulators. MicroRNAs are suggested to play important roles in obesity and metabolic syndrome related biological processes, but also are involved in different types of cancer. Recently microRNAs have been shown to be present in blood, and it is proposed that circulating microRNAs may be biomarker of tissue biochemistry and pathology. The aim of this study is to investigate if the circulation microRNA profile is changed by bariatric surgery and whether the altered microRNA expression could contribute to the long term reduced predisposition cancer risk associated with such surgery. Total plasma RNA from 53 days post bariatric surgery and sham operated rats were isolated and then examined using Taqman Rodent MicroRNA A+B Cards which have the capacity to evaluate expression levels of 373 rat microRNAs. Four different normalization methods (Global, cel-miR-39 spiked in, U6 endogenous and five endogenous microRNAs normalization) were tested. Five endogenous microRNAs normalization was found to be optimal and selected for all downstream analysis. Our preliminary data showed that 113 microRNAs were expressed in the plasma of bariatric surgical rats and 92 in sham operated rats. Furthermore, an OPLS-DA model clearly showed that bariatric surgery changed the circulating microRNA expression profile. Among nineteen of the most significantly changed microRNAs, nine of them are relevant to cancer. In summary, our data suggest that bariatric surgery fundamentally changed circulating microRNA expression. Understanding the significance of these changes in circulating microRNA may give clues to the mechanisms whereby bariatric surgery affords health benefits to individual undergoing such surgery, including a reduced predisposition to disease such as cancer. Citation Format: {Authors}. {Abstract title} [abstract]. In: Proceedings of the 103rd Annual Meeting of the American Association for Cancer Research; 2012 Mar 31-Apr 4; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2012;72(8 Suppl):Abstract nr 4130. doi:1538-7445.AM2012-4130
Published Version
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