RNA adenosine modifications related to prognosis and immune infiltration in osteosarcoma

• Published in: Journal of translational medicine 2022-05, Vol.20 (1), p.228-228, Article 228
• Main Authors: Chen, Shijie, Zeng, Jin, Huang, Liping, Peng, Yi, Yan, Zuyun, Zhang, Aiqian, Zhao, Xingping, Li, Jun, Zhou, Ziting, Wang, Sidan, Jing, Shengyu, Hu, Minghua, Li, Yuezhan, Wang, Dong, Wang, Weiguo, Yu, Haiyang, Miao, Jinglei, Li, Jinsong, Deng, Youwen, Li, Yusheng, Liu, Tang, Xu, Dabao
• Format: Article
• Language: English
• Subjects: Adenosine; Adenylic acid; Analysis; Antitumor activity; Biomarkers; Bone cancer; Care and treatment; Cell cycle; Datasets; Diagnosis; Drugs; Editing; Epigenetic inheritance; Epigenetics; Experiments; G1 phase; Gene expression; Immune; Immunosuppressive agents; Infiltration; Macrophages; Medical prognosis; Metastases; Osteosarcoma; Prognosis; Regression analysis; Risk factors; Risk groups; RNA adenosine modifications; Sarcoma; Survival analysis; Tumorigenesis; Tumors
• ISSN: 1479-5876; 1479-5876
• DOI: 10.1186/s12967-022-03415-6

RNA adenosine modifications, which are primarily mediated by "writer" enzymes (RMWs), play a key role in epigenetic regulation in various biological processes, including tumorigenesis. However, the expression and prognostic role of these genes in osteosarcoma (OS) remain unclear. Univariate and multivariate Cox analyses were used to construct the RMW signature for OS using Target datasets. RMW expression in OS tissue was detected by qPCR analysis. Xcell and GSVA were used to determine the relationship between RMWs and immune infiltration. The DGIdb and CMap databases were used for drug prediction. In vivo and in vitro experiments showed that strophanthidin elicited antitumor activity against OS. A 3-RMW (CSTF2, ADAR and WTAP) prognostic signature in OS was constructed using the Target dataset and verified using GEO datasets and 63 independent OS tissues via qPCR analysis. High-risk OS patients had poor overall survival, and the prognostic signature was an independent prognostic factor for OS. Functional studies showed that tumour-, metabolism-, cell cycle- and immune-related pathways were related to high risk. Next, we found that RMW-derived high-risk patients exhibited increased infiltration of M2 macrophages and cDCs. Furthermore, we predicted the potential drugs for OS using the DGIdb and CMap databases. In vivo and in vitro experiments showed that strophanthidin elicited antitumor activity against OS by repressing cell growth and inducing cell cycle arrest at the G1 phase. The 3-RWM-based prognostic signature established in this study is a novel gene signature associated with immune infiltration, and strophanthidin was identified as a candidate therapy for OS by repressing OS cell growth and the cell cycle.