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Omata, Yuji; Haraguchi, Mai; Yoshinaga, Sae; Ogino, Takashi; Okawa, Maseri; Tsuruta, Akito; Koyanagi, Satoru; Ohdo, Shigehiro
Biochemical and biophysical research communications, 09/2024, Letnik: 726Journal Article
Among the various RNA modifications, adenosine-to-inosine RNA editing, catalyzed by adenosine deaminase acting on RNA (ADAR) family, ADAR1 and ADAR2, is the most common nucleotide conversion in mammalian cells. The pathological relevance of ADAR expression has been highlighted in recent human genetic studies. Low expression of the ADAR2 gene is correlated with a poor prognosis in breast cancer patients, but the underlying mechanism remains enigmatic. In this study, we constructed Adar2-knockdown (Adar2-KD) murine breast cancer 4T1 cells and observed their reduced susceptibility to chemotherapeutic drug doxorubicin. Downregulation of ADAR2 induced the expression of P-glycoprotein (P-gp), leading to a reduction in the intracellular accumulation of doxorubicin. The upregulation of P-gp occurred at the post-transcriptional level due to the decreased miR-195a-3p function. The search for the underlying cause of the induction of P-gp expression in Adar2-KD 4T1 cells led to the identification of circular RNA (circRNA) circHif1a as a sponge for miR-195a-3p. The enhanced expression of circHif1a inhibited miR-195a-3p function, resulting in the upregulation of P-gp expression. These results suggest that ADAR2 acts as a suppressor of circHif1a biogenesis and then allows miR-195a-3p to interfere with P-gp translation. Our findings may help to improve drug efficacy by clarifying the mechanism of chemoresistance in breast cancer. Display omitted •RNA editing enzyme ADAR2 is involved in chemoresistance in breast cancer cells.•Downregulation of ADAR2 increases P-glycoprotein, promoting doxorubicin efflux.•Downregulation of ADAR2 induces circHif1a expression.•CircHif1a inhibits miR-195a-3p, resulting in the increased P-glycoprotein expression.
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