Hsa-mir-135a Shows Potential As A Putative Diagnostic Biomarker in Saliva and Plasma for Endometriosis
Overview
Molecular Biology
Authors
Affiliations
Endometriosis is a chronic disease characterized by the implantation and proliferation of endometrial tissue outside of the uterine cavity. The nonspecific nature of the symptoms and the lack of sensitive, noninvasive diagnostic methods often lead to a significant delay in diagnosis, highlighting the need for diagnostic biomarkers. The correlation of circulating miRNAs with altered inflammatory signals seen in patients with endometriosis has raised the possibility that miRNAs can serve as biomarkers for the disease. In our study, we analyzed miRNA expression in saliva of women with and without endometriosis using a FireFly custom multiplex circulating miRNA assay. This focused panel included 28 human miRNAs, 25 of which have been previously found to be differentially expressed either in plasma, serum, and/or blood of women with endometriosis, compared to controls. We found that hsa-mir-135a was expressed significantly higher in the saliva of women with endometriosis, independent of disease stage and menstrual cycle phase. We confirmed that hsa-mir-135a also showed significantly elevated expression in the plasma of endometriosis patients. This indicates that hsa-mir-135a is a putative noninvasive biomarker of endometriosis in both saliva and plasma, but further validation studies are required to assess its clinical value as a biomarker.
Brady P, Yousif A, Sasamoto N, Vitonis A, Fendler W, Stawiski K Front Reprod Health. 2024; 6:1360417.
PMID: 38665804 PMC: 11043576. DOI: 10.3389/frph.2024.1360417.
An integrated multi-tissue approach for endometriosis candidate biomarkers: a systematic review.
Brulport A, Bourdon M, Vaiman D, Drouet C, Pocate-Cheriet K, Bouzid K Reprod Biol Endocrinol. 2024; 22(1):21.
PMID: 38341605 PMC: 10858544. DOI: 10.1186/s12958-023-01181-8.
Diet in Prevention and Treatment of Endometriosis: Current State of Knowledge.
Oszajca K, Adamus A Curr Nutr Rep. 2024; 13(1):49-58.
PMID: 38324218 DOI: 10.1007/s13668-024-00518-y.