AI Article Synopsis

  • Extracellular vesicles (EVs), particularly exosomes, play a crucial role in cell communication and are emerging as valuable indicators for cancer diagnosis due to their molecular similarities to parent cells and stability of their bioactive cargo.
  • Uterine aspirate (UA) samples from epithelial ovarian cancer (EOC) patients and healthy donors can be analyzed for EVs, which are more abundant in this localized fluid than in other body fluids.
  • Profiling of small RNAs from these UA-derived EVs revealed significant differences in miRNA expression between EOC patients and healthy individuals, suggesting their potential as diagnostic markers for gynecological cancers.

Article Abstract

Extracellular vesicles (EVs), including exosomes, are key factors of intercellular communication, performing both local and distant transfers of bioactive molecules. The increasingly obvious role of EVs in carcinogenesis, similarity of molecular signatures with parental cells, precise selection and high stability of cargo molecules make exosomes a promising source of liquid biopsy markers for cancer diagnosis. The uterine cavity fluid, unlike blood, urine and other body fluids commonly used to study EVs, is of local origin and therefore enriched in EVs secreted by cells of the female reproductive tract. Here, we show that EVs, including those corresponding to exosomes, could be isolated from individual samples of uterine aspirates (UA) obtained from epithelial ovarian cancer (EOC) patients and healthy donors using the ultracentrifugation technique. First, the conducted profiling of small RNAs (small RNA-seq) from UA-derived EVs demonstrated the presence of non-coding RNA molecules belonging to various classes. The analysis of the miRNA content in EVs from UA performed on a pilot sample revealed significant differences in the expression levels of a number of miRNAs in EVs obtained from EOC patients compared to healthy individuals. The results open up prospects for using UA-derived EVs as a source of markers for the diagnostics of gynecological cancers, including EOC.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8997481PMC
http://dx.doi.org/10.3390/cells11071064DOI Listing

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