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. 2021 Jan 19;13:7. doi: 10.1186/s13098-021-00625-8

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© The Author(s) 2021

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 1 — Circ-FANCA was overexpressed in septic AKI patients and LPS-treated HK2 cells. a The level of circ-FANCA was examined by qRT-PCR in serum samples of septic AKI patients (n = 19) and healthy controls (n = 19). b The expression of circ-FANCA in HK2 cells treated with different concentrations of LPS for 24 h was detected by qRT-PCR. c QRT-PCR assay was conducted for circ-FANCA expression in nuclear and cytoplasmic fractions. d After RNase R treatment, the levels of circ-FANCA and linear FANCA mRNA were determined using qRT-PCR. *P < 0.05, ****P < 0.0001