Sinomenine regulates circTRPM7‐related pathway to inhibit gastric cancer cell growth and metastasis

Abstract

AbstractSinomenine has been found to have antitumor effects in a variety of cancers, including gastric cancer. Circular RNA (circRNA) is an important regulator of gastric cancer progression. However, it is not known whether Sinomenine mediates gastric cancer processes by regulating circRNA‐related pathways. Quantitative real‐time PCR was used to measure the expression of circTRPM7, microRNA‐145‐5p (miR‐145‐5p), and pre‐B‐cell leukemia homeobox 3 (PBX3). MTT assay, colony formation assay, EdU assay, transwell assay, wound‐healing assay, and flow cytometry were used to detect cell proliferation, migration, invasion, and apoptosis. The expression of related proteins was detected by Western blot. Mechanically, the interaction of miR‐145‐5p with circTRPM7/PBX3 was validated by dual‐luciferase reporter assay and RIP assay. Our study showed that circTRPM7 expression was reduced in Sinomenine‐treated gastric cancer cells. Moreover, overexpression of circTRPM7 upregulated the growth and metastasis of Sinomenine‐treated gastric cancer cells. CircTRPM7 could sponge miR‐145‐5p, and miR‐145‐5p reversed the effect of circTRPM7 on the growth and metastasis of Sinomenine‐treated gastric cancer cells. PBX3 was the target of miR‐145‐5p, and knockdown of PBX3 could restore the in‐miR‐145‐5p promotion effect on the malignant behavior of Sinomenine‐treated gastric cancer cells. To sum up, our data indicated that Sinomenine played an antitumor role in gastric cancer cells via circTRPM7/miR‐145‐5p/PBX3 axis.