4.7 Article

Circular RNA Sequencing Reveals Serum Exosome Circular RNA Panel for High-Grade Astrocytoma Diagnosis

期刊

CLINICAL CHEMISTRY
卷 68, 期 2, 页码 332-343

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/clinchem/hvab254

关键词

high-grade astrocytoma; circular RNA; exosome; liquid biopsy; diagnosis

资金

  1. National Science Foundation for Young Scientists of China [81802871]
  2. Hunan Provincial Natural Science Foundation for Young Scientists of China [2019JJ50935]
  3. National Key Technology Research and Development program of the Ministry of Science and Technology of China
  4. Hunan Province Key RD projects [2020SK2053]

向作者/读者索取更多资源

This study revealed a comprehensive landscape of circRNAs in exosomes and cells of high-grade astrocytoma (HGA). The serum exosome circRNA panel and tissue circRNAs have potential for liquid biopsy and prognosis monitoring in HGA. Exosome circRNAs as novel targets should facilitate further biomarker discovery and aid in HGA diagnosis and therapy monitoring.
Background Although major advances have been made in the histopathological diagnosis of high-grade astrocytoma (HGA), methods for effective and noninvasive diagnosis remain largely unknown. Exosomes can cross the blood-brain barrier and are readily accessible in human biofluids, making them promising biomarkers for HGA. Circular RNAs (circRNAs) have potential as tumor biomarkers owing to their stability, conservation, and tissue specificity. However, the landscape and characteristics of exosome circRNAs in HGA remain to be studied. Methods CircRNA deep sequencing and bioinformatics approaches were used to generate a circRNA profiling database and analyze the features of HGA cell circRNAs and HGA cell-derived exosome circRNAs. Exosome circRNA expression in the serum and tissues of healthy individuals and patients with HGA was detected using reverse transcription-quantitative PCR. Additionally, the receiver operating characteristic curve and overall survival curves were analyzed. Results By investigating the characteristics of HGA cell-derived exosome circRNAs and HGA cell circRNAs, we observed that exosomes were more likely to enrich short-exon and suppressor circRNAs than HGA cells. Moreover, a serum exosome circRNA panel including hsa_circ_0075828, hsa_circ_0003828, and hsa_circ_0002976 could be used to screen for HGA, whereas a good prognosis panel comprised high concentrations of hsa_circ_0005019, hsa_circ_0000880, hsa_circ_0051680, and hsa_circ_0006365. Conclusions This study revealed a comprehensive circRNA landscape in HGA exosomes and cells. The serum exosome circexosome circRNA panel and tissue circRNAs are potentially useful for HGA liquid biopsy and prognosis monitoring. Exosome circRNAs as novel targets should facilitate further biomarker discovery and aid in HGA diagnosis and therapy monitoring.

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