N6‐methyladenosine modification in trophoblasts promotes circSETD2 expression, inhibits miR‐181a‐5p, and elevates MCL1 transcription to reduce apoptosis of trophoblasts

Abstract Preeclampsia (PE) is an obstetric disorder. N6‐methyladenosine (m6A) modification is related to PE trophoblast biological behaviors. This study explored the mechanism of m6A‐modified circSETD2 in trophoblast biological behaviors. Chorionic trophoblast apoptosis and circSETD2 expression in PE rat models were detected. HTR8/SVneo cells were induced by CoCl 2 to establish PE trophoblast models. circSETD2 was silenced or overexpressed to evaluate its effect on cell proliferation, invasion, and apoptosis. m6A level of circSETD2 in trophoblasts was changed by pcDNA3.1‐METTL3 and pcDNA3.1‐FTO. The targeting relations among miR‐181a‐5p, circSETD2, and MCL1 were verified by dual‐luciferase assay. miR‐181a‐5p and MCL1 expressions were interfered with to confirm the effect of m6A‐modified circSETD2. m6A methylation level was changed in PE rats for in vivo validation. PE rats showed diminished circSETD2 expression and increased apoptosis index. circSETD2 overexpression promoted trophoblast proliferation and invasion, and reduced apoptosis. METTL3 overexpression increased total m6A, circSETD2 m6A, and circSETD2 levels. m6A modification mediated circSETD2 upregulation. circSETD2 was a sponge of miR‐181a‐5p to elevate MCL1 transcription. miR‐181a‐5p overexpression or MCL1 silencing annulled the role of m6A‐modified circSETD2. circSETD2 inhibition negated suppression of METTL3 overexpression on chorionic trophoblast apoptosis in vivo. Collectively, m6A modification of circSETD2 suppressed miR‐181a‐5p and increased MCL1 transcription, thus regulating trophoblasts.