Investigating the synergy of Shikonin and Valproic acid in inducing apoptosis of osteosarcoma cells via ROS-mediated EGR1 expression

• Published in: Phytomedicine (Stuttgart) 2024-04, Vol.126, p.155459-155459, Article 155459
• Main Authors: Chen, Zhuo, Wu, Feng-feng, Li, Jing, Dong, Jia-bao, He, Hong-yi, Li, Xiong-feng, Lu, Qian, Zhang, Wen-xuan, Shao, Chang-ming, Yao, Zhao-nong, Lin, Nong, Ye, Zhao-ming, Xu, Jun-tao, Li, Heng-yuan
• Format: Article
• Language: English
• Subjects: Apoptosis; bcl-2-Associated X Protein; Bone Neoplasms - metabolism; Cell Line, Tumor; Cell Proliferation; Early Growth Response Protein 1 - pharmacology; EGR1; Humans; Naphthoquinones; Osteosarcoma; Osteosarcoma - pathology; Reactive Oxygen Species - metabolism; ROS; Shikonin; Synergism; Valproic acid; Valproic Acid - pharmacology; Valproic Acid - therapeutic use
• ISSN: 0944-7113; 1618-095X
• DOI: 10.1016/j.phymed.2024.155459

Osteosarcoma is the most prevalent malignant bone tumour with a poor prognosis. Shikonin (SHK) is derived from the traditional Chinese medicine Lithospermum that has been extensively studied for its notable anti-tumour effects, including for osteosarcoma. However, its application has certain limitations. Valproic acid (VPA) is a histone deacetylase inhibitor (HDACI) that has recently been employed as an adjunctive therapeutic agent that allows chromatin to assume a more relaxed state, thereby enhancing anti-tumour efficacy. This study was aimed to investigate the synergistic anti-tumour efficacy of SHK in combination with VPA and elucidate its underlying mechanism. CCK-8 assays were utilized to calculate the combination index. Additional assays, including colony formation, acridine orange/ethidium bromide double fluorescent staining, and flow cytometry, were employed to evaluate the effects on osteosarcoma cells. Wound healing and transwell assays were utilized to assess cell mobility. RNA sequencing, PCR, and Western blot analyses were conducted to uncover the underlying mechanism. Rescue experiments were performed to validate the mechanism of apoptotic induction. The impact of SHK and VPA combination treatment on primary osteosarcoma cells was also assessed. Finally, in vivo experiments were conducted to validate its anti-tumour effects and mechanism. The combination of SHK and VPA synergistically inhibited the proliferation and migration of osteosarcoma cells in vitro and induced apoptosis in these cells. Through a comprehensive analysis involving RNA sequencing, PCR, Western blot, and rescue experiments, we have substantiated our hypothesis that the combination of SHK and VPA induced apoptosis via the ROS-EGR1-Bax axis. Importantly, our in vivo experiments corroborated these findings, demonstrating the potential of the SHK and VPA combination as a promising therapeutic approach for osteosarcoma. The combination of SHK and VPA exerted an anti-tumour effect by inducing apoptosis through the ROS-EGR1-Bax pathway. Repurposing the old drug VPA demonstrated its effectiveness as an adjunctive therapeutic agent for SHK, enhancing its anti-tumour efficacy and revealing its potential value. Furthermore, our study expanded the application of natural compounds in the anti-tumour field and overcame some of their limitations through combination therapy. Finally, we enhanced the understanding of the mechanistic pathways linking reactive oxygen species (ROS) accumulat