Baicalein facilitates gastric cancer cell apoptosis by triggering endoplasmic reticulum stress via repression of the PI3K/AKT pathway

• Published in: Applied biological chemistry Vol. 66; no. 1; p. 10
• Main Authors: Shen, Junjie, Yang, Zhiwen, Wu, Xinlin, Yao, Guodong, Hou, Mingxing
• Format: Journal Article
• Language: English
• Published: Singapore Springer Nature Singapore 01.12.2023; Springer Nature B.V; SpringerOpen; 한국응용생명화학회
• Subjects: 1-Phosphatidylinositol 3-kinase; AKT protein; Animal models; Anticancer properties; Apoptosis; Applied Microbiology; Baicalein; Biological Techniques; Bioorganic Chemistry; BTG3; calcium; Calcium (intracellular); Calcium ions; Cell apoptosis; Cell cycle; Cell proliferation; Chemistry; Chemistry and Materials Science; Endoplasmic reticulum; Endoplasmic reticulum stress; Flow cytometry; Fluo-3; fluorescence; Gastric cancer; Gentian violet; Immunohistochemistry; inhibitory concentration 50; mice; neoplasm cells; PI3K/AKT; Staining; stomach neoplasms; Tumors; viability; Western blotting; Xenotransplantation; 농학; BTG3; Cell apoptosis; Baicalein; Ki67; Gastric cancer; Ca; PI3K/AKT; Endoplasmic reticulum stress; Ca2
• ISSN: 2468-0842; 2468-0834; 2468-0842
• DOI: 10.1186/s13765-022-00759-x

Objective Gastric cancer (GC) remains a prevailing threat to life. Baicalein exhibits anti-cancer properties. This study estimated the mechanism of baicalein in GC cell apoptosis by mediating endoplasmic reticulum stress (ERS) through the PI3K/AKT pathway. Methods After treatment with different concentrations of baicalein, GC cell (HGC-27 and AGS) viability was detected by MTT assay. AGS cells more sensitive to baicalein treatment were selected as study subjects. The IC50 of baicalein on AGS cells was determined. Colony formation, cell cycle, and apoptosis were detected using crystal violet staining and flow cytometry. Levels of ERS-related and BTG3/PI3K/AKT pathway-related proteins were determined by Western blot. Intracellular Ca 2+ level was measured using Fluo-3 AM fluorescence working solution. GC mouse models were established by subcutaneously injecting AGS cells into the right rib and were intragastrically administrated with baicalein. Tumor volume and weight were recorded. Expression of Ki67 in tumor tissues and positive expression of apoptotic cells were detected by immunohistochemistry and TUNEL staining. Results Baicalein inhibited cell proliferation and induced G0/G1 arrest and apoptosis by regulating the cell cycle, and triggered ERS in GC cells. Baicalein impeded the PI3K/AKT pathway by activating BTG3, thereby triggering ERS and inducing apoptosis. BTG3 inhibition reversed baicalein-induced apoptosis and ERS. Baicalein regulated GC cells in a concentration-dependent manner. Moreover, in xenograft mice, baicalein prevented tumor growth, decreased Ki67-positive cells, activated BTG3, and inhibited the PI3K/AKT pathway, thus activating ERS and increasing apoptotic cells. Conclusion Baicalein facilitates GC cell apoptosis by triggering ERS via repression of the PI3K/AKT pathway.