Fengxia Li1, Zhenwei Liu1, Bing Zhang1, Shan Jiang1, Qiongdan Wang1,2, Lifeng Du1, Huangqi Xue1, Yu Zhang1, Mengmeng Jin3, Xiaochun Zhu3, Matthew A Brown4,5, Jinyu Wu1, Xiaobing Wang3. 1. Institute of Genomic Medicine, Wenzhou Medical University. 2. Department of Clinical Laboratory, The First Affiliated Hospital of Wenzhou Medical University. 3. Department of Rheumatology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China. 4. Guy's & St Thomas NHS Foundation Trust and King's College London NIHR Biomedical Research Centre, London, UK. 5. Centre for Precision Medicine, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Abstract
OBJECTIVES: This study aims to characterize the expression profiles of circRNAs in primary Sjogren's Syndrome (pSS) and examine the potential of noninvasive circular RNAs (circRNAs) as biomarkers of pSS. METHODS: We performed RNA sequencing of minor salivary gland (MSG) biopsies from four pSS and four non-pSS individuals (subjects undergoing MSG biopsies but not meeting 2012 or 2016 ACR classification criteria for SS). Differentially expressed circRNAs were identified by DESeq2, and confirmed by quantitative real-time PCR in the MSGs as well as in plasma exosomes in 37 pSS and 14 non-pSS subjects. Discriminatory capacity testing using receiver operating characteristic analysis was used to evaluate the performance of circRNAs as diagnostic biomarkers for pSS. RESULTS: Circ-IQGAP2 and circ-ZC3H6 had significantly upregulated expression in the MSGs of pSS patients, and this elevated expression was confirmed by quantitative real-time PCR of plasma exosome RNA. The expression of these circRNAs also showed significant correlation with both clinical features, serum IgG level and MSG focus scores. Receiver operating characteristic analysis showed that the indices comprised of both the two circRNAs and clinical features were better able to distinguish pSS from non-pSS subjects with high mean areas under the curve of 0.93 in the MSGs and 0.92 in the plasma exosomes. CONCLUSION: This study indicated the potential roles of circ-IQGAP2 and circ-ZC3H6 as noninvasive biomarkers for the diagnosis of pSS.
OBJECTIVES: This study aims to characterize the expression profiles of circRNAs in primary Sjogren's Syndrome (pSS) and examine the potential of noninvasive circular RNAs (circRNAs) as biomarkers of pSS. METHODS: We performed RNA sequencing of minor salivary gland (MSG) biopsies from four pSS and four non-pSS individuals (subjects undergoing MSG biopsies but not meeting 2012 or 2016 ACR classification criteria for SS). Differentially expressed circRNAs were identified by DESeq2, and confirmed by quantitative real-time PCR in the MSGs as well as in plasma exosomes in 37 pSS and 14 non-pSS subjects. Discriminatory capacity testing using receiver operating characteristic analysis was used to evaluate the performance of circRNAs as diagnostic biomarkers for pSS. RESULTS: Circ-IQGAP2 and circ-ZC3H6 had significantly upregulated expression in the MSGs of pSSpatients, and this elevated expression was confirmed by quantitative real-time PCR of plasma exosome RNA. The expression of these circRNAs also showed significant correlation with both clinical features, serum IgG level and MSG focus scores. Receiver operating characteristic analysis showed that the indices comprised of both the two circRNAs and clinical features were better able to distinguish pSS from non-pSS subjects with high mean areas under the curve of 0.93 in the MSGs and 0.92 in the plasma exosomes. CONCLUSION: This study indicated the potential roles of circ-IQGAP2 and circ-ZC3H6 as noninvasive biomarkers for the diagnosis of pSS.
Authors: Akinsola Oyelakin; Erich Horeth; Eun-Ah Christine Song; Sangwon Min; Monika Che; Brandon Marzullo; Christopher J Lessard; Astrid Rasmussen; Lida Radfar; R Hal Scofield; David M Lewis; Donald U Stone; Kiely Grundahl; Scott S De Rossi; Zoya Kurago; A Darise Farris; Kathy L Sivils; Satrajit Sinha; Jill M Kramer; Rose-Anne Romano Journal: Front Immunol Date: 2021-01-08 Impact factor: 7.561