Astragaloside IV Inhibits the Proliferation of Human Uterine Leiomyomas by Targeting IDO1

• Published in: Cancers Vol. 14; no. 18; p. 4424
• Main Authors: Qiu, Tiantian, Li, Donghua, Liu, Yu, Ren, Hui, Yang, Xuan, Luo, Wenting
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01.09.2022; MDPI
• Subjects: 1-Phosphatidylinositol 3-kinase; AKT protein; Antibodies; Antitumor activity; Apoptosis; Astragalus membranaceus; Autophagy; Cancer therapies; Care and treatment; CD25 antigen; CD3 antigen; CD4 antigen; Cell culture; Cell proliferation; Cholecystokinin; Dioxygenase; Fibroids; Flow cytometry; Foxp3 protein; Glycosides; Health aspects; Hysterectomy; Immunofluorescence; Immunohistochemistry; Immunomodulation; Immunosuppression; Immunotherapy; Leiomyoma; Lymphocytes T; Oxidases; Phagocytosis; Prevention; Proteins; Sex hormones; Signal transduction; Surgery; Transmission electron microscopy; Tumors; Uterine cancer; Uterus; Western blotting; China; Beijing China; United States > US
• ISSN: 2072-6694; 2072-6694
• DOI: 10.3390/cancers14184424

Astragaloside IV (AS-IV) is a chemical found in traditional Chinese medicine called Astragalus membranaceus (Fisch.) Bunge that has antitumor properties. However, the roles and mechanisms of AS-IV in uterine leiomyomas (ULMs) are unclear. The immunosuppressive enzyme indoleamine-2,3-dioxygenase-1 (IDO1) is involved in tumor formation. IDO1 is a new and reliable prognostic indicator for several cancers. In this work, AS-IV was applied to ULM cells in various concentrations. CCK-8, immunofluorescence, and flow cytometry were used to examine the proliferation and apoptosis of ULM cells caused by AS-IV. After lentiviral vector transduction with IDO1 short hairpin RNA (shRNA), the knockdown and overexpression of IDO1 were stable in ULM cells. To verify the antitumor effect of AS-IV in vivo, we established a rat model of uterine leiomyoma. HE staining, Masson staining, and transmission electron microscopy were used to observe pathological changes in the uterus, and the levels of serum sex hormones were measured by radio immune assay (RIA). The levels of CD3+T, CD4+T, and CD25+ Foxp3+Treg in rat peripheral blood were detected by flow cytometry. Western blotting and immunohistochemistry were used to examine protein expression. We found that AS-IV dramatically increased the apoptotic rate of ULM cells and reduced viability in a time- and dosage-dependent manner. After sh-IDO1 lentiviral transfection, we discovered that knocking down IDO1 reversed the effects of AS-IV on ULM cell proliferation and autophagy. We also found that AS-IV can effectively inhibit the growth of ULMs in vivo. AS-IV may promote apoptosis and autophagy in ULMs by activating PTEN/PI3K/AKT signaling through inhibition of IDO1. These findings imply that AS-IV exerts antifibroid effects, and the underlying mechanism may be IDO1, which is involved in proliferation, apoptosis, and autophagy.