CircNRIP1 Modulates the miR-515-5p/IL-25 Axis to Control 5-Fu and Cisplatin Resistance in Nasopharyngeal Carcinoma
Authors Lin J, Qin H, Han Y, Li X, Zhao Y, Zhai G
Received 14 November 2020
Accepted for publication 24 December 2020
Published 27 January 2021 Volume 2021:15 Pages 323—330
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 4
Editor who approved publication: Dr Anastasios Lymperopoulos
Junwu Lin,1,* Hong Qin,2,* Yue Han,3 Xinghua Li,4 YuJuan Zhao,5 Guangsheng Zhai6
1Department of Otolaryngology, Central Hospital, Qingdao, Shandong, People’s Republic of China; 2Department of Otolaryngology, Women and Children’s Hospital, Qingdao, Shandong, People’s Republic of China; 3Department of Urology, Zhangqiu District People’s Hospital, Jinan, Shandong, People’s Republic of China; 4Department of Critical Care Medicine, Zhangqiu District People’s Hospital, Jinan, Shandong, People’s Republic of China; 5Department of Otolaryngology, Rizhao Second People’s Hospital, Rizhao, Shandong, People’s Republic of China; 6Department of Radiotherapy, Zibo Central Hospital, Zibo, Shandong, People’s Republic of China
*These authors contributed equally to this work
Correspondence: Guangsheng Zhai
Department of Radiotherapy, Zibo Central Hospital, No. 54, Communist Youth League West Road, Zhangdian District, Zibo 255036, Shandong, People’s Republic of China
Background: The development of drug resistance leads many NPC patients to experience disease relapse following the completion of chemotherapy. It is thus essential that the mechanistic basis for such chemoresistance be clarified in an effort to identify approaches to sensitizing NPC tumors to treatment with cisplatin and related agents.
Methods: A qRT-PCR approach was used to measure the expression of circNRIP1 in NPC, while luciferase assays were used to identify interactions with downstream targets of circNRIP1 activity including miR-515-5p and IL-25. CCK8 assays were also utilized to detect IC50 values for cisplatin and 5-Fu.
Results: The expression of circNRIP1 was significantly increased in the serum of chemoresistant NPC patients. At a functional level, we determined that circNRIP1 is able to sequester miR-515-5p, thereby inhibiting its ability to post-transcriptionally suppress IL-25 expression. We observed a significant negative correlation between the expression of miR-515-5p and circNRIP1 in serum samples from chemoresistant NPC patients, consistent with a functional interaction between these two factors. We further found that 5-Fu and CDDP IC50 values in NPC cells in which circNRIP1 had been knocked down were restored following miR-515-5p inhibitor transfection. Similarly, changes in these IC50 values were reversed in NPC cells transfected with miR-515-5p mimics following the overexpression of IL-25 in these same cells.
Conclusion: These data highlight the circNRIP1/miR-515-5p/IL-25 as a novel regulator of 5-Fu and cisplatin resistance in NPC, suggesting that this pathway may be amenable to therapeutic targeting as an approach to treating this cancer type.
Keywords: circNRIP1, 5-Fu resistance, cisplatin resistance, NPC, miR-515-5p, IL-25
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