4.7 Article

Exosomal circRNA as a novel potential therapeutic target for multiple myeloma-related myocardial damage

Journal

CANCER CELL INTERNATIONAL
Volume 21, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12935-021-02011-w

Keywords

Multiple myeloma; Myocardial damage; Exosome; Circular RNA

Categories

Funding

  1. National Natural Science Foundation of China [81774080]
  2. Taishan Scholar Project [tsqn201812145]
  3. Key Technology Research and Development Program of Shandong [2019GSF108162]

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This study investigated the role of exosomal circular RNAs (exo-circRNAs) in multiple myeloma (MM) related myocardial damage. Bioinformatics analysis revealed that upregulated circRNAs may promote MM-related myocardial damage. Cell experiments showed that the circ-G042080/hsa-miR-4268/TLR4 axis may exist in H9C2 cells and cause abnormal autophagy. Abnormal expression of serum exo-circRNAs was found to be associated with MM-related myocardial damage, suggesting their potential as diagnostic markers and therapeutic targets.
Introduction Myocardial damage is a mostly incurable complication of multiple myeloma (MM) that seriously affects the treatment outcome and quality of life of patients. Exosomal circular RNAs (exo-circRNAs) play an important role in tumor occurrence and development and are considered key factors in MM pathogenesis. However, the role and mechanism of action of exo-circRNAs in MM-related myocardial damage are still unclear. This study aimed to investigate correlations between exo-circRNAs and MM and to preliminarily explore the role of exo-circRNAs in MM-related myocardial damage. Methods Six MM patients and five healthy controls (HCs) were included in the study. High-throughput sequencing and qRT-PCR verification were used to obtain a profile of abnormally expressed exo-circRNAs. GO, KEGG, miRanda, TargetScan and Metascape were used for bioinformatics analyses. H9C2 cells treated with exosomes from U266 cells were used in cell experiments. CCK-8, PCR, immunofluorescence and western blotting assays were used to detect cell proliferation and expression of autophagy-related indicators. Electron microscopy was used to observe the number of autophagic vesicles. Results Bioinformatics analysis showed that circRNAs with upregulated expression had the potential to promote MM-related myocardial damage. In addition, PCR results confirmed that circ-G042080 was abundantly expressed in the serum exosomes of 20 MM patients. Correlation analysis showed that the expression level of circ-G042080 was positively correlated with the clinical level of MM and MM-related myocardial damage and that circ-G042080 might interfere with MM-related myocardial damage through a downstream miRNA/TLR4 axis. Cell experiments demonstrated that the circ-G042080/hsa-miR-4268/TLR4 axis might exist in H9C2 cells incubated with exosomes and cause abnormal autophagy. Conclusion Abnormal expression of serum exo-circRNAs was found to be associated with MM-related myocardial damage, suggesting that exo-circRNAs might become a new diagnostic marker of MM-related myocardial damage and a therapeutic target.

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