m6A methylation modification and immune infiltration analysis in osteonecrosis of the femoral head

被引:0
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作者
Weihua Fang
Peng Peng
Kun Lin
Fangjun Xiao
Wei He
Mincong He
Qiushi Wei
机构
[1] Guangzhou University of Chinese Medicine,Department of Orthopaedics, The Third Affiliated Hospital
[2] Guangdong Research Institute for Orthopedics and Traumatology of Chinese Medicine,undefined
[3] Guangzhou University of Chinese Medicine,undefined
关键词
RNA N6-methyladenosine; Osteonecrosis of the femoral head; Immune microenvironment; Subtype classification; Bioinformatic analysis;
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学科分类号
摘要
Osteonecrosis of the femoral head (ONFH) is a elaborate hip disease characterized by collapse of femoral head and osteoarthritis. RNA N6-methyladenosine (m6A) plays a crucial role in a lot of biological processes within eukaryotic cells. However, the role of m6A in the regulation of ONFH remains unclear. In this study, we identified the m6A regulators in ONFH and performed subtype classification. We identified 7 significantly differentially expressed m6A regulators through the analysis of differences between ONFH and normal samples in the Gene Expression Omnibus (GEO) database. A random forest algorithm was employed to monitor these regulators to assess the risk of developing ONFH. We constructed a nomogram based on these 7 regulators. The decision curve analysis suggested that patients can benefit from the nomogram model. We classified the ONFH samples into two m6A models according to these 7 regulators through consensus clustering algorithm. After that, we evaluated those two m6A patterns using principal component analysis. We assessed the scores of those two m6A patterns and their relationship with immune infiltration. We observed a higher m6A score of type A than that of type B. Finally, we performed a cross-validation of crucial m6A regulatory factors in ONFH using external datasets and femoral head bone samples. In conclusion, we believed that the m6A pattern could provide a novel diagnostic strategy and offer new insights for molecularly targeted therapy of ONFH.
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