RT‐qPCR and WB were performed according to a previous study [28 (link)]. RT‐qPCR was performed on an iQ5 real‐time detection system using the SYBR Kit (TaKaRa, Tokyo, Japan). Relative expression levels of genes among different samples were calculated using the ΔΔCt method, with GAPDH being used as the normalization control. The primer sequences are listed in supplementary material, Table S3. As for the WB assay, all blots were incubated with primary and secondary antibodies (TransGen Biotech, Beijing, PR China; 1:10,000) for 1 h. After incubating with ECL reagents (Proteintech, Wuhan, PR China), the blots were visualized using E‐blot. The primary antibodies recognized CARD11 (Proteintech; No. 28483‐1‐AP; 1:1,000), GATA2 (Proteintech; No. 11103‐1‐AP; 1:1,000), and β‐tubulin (Abiocode, Agoura Hills, CA, USA; No. R0742‐3; 1:1,000).