Identification of lactylation gene CALML5 and its correlated lncRNAs in cutaneous melanoma by machine learning

医学 免疫系统 疾病 免疫抑制 基因 肿瘤微环境 黑色素瘤 机制(生物学) 计算生物学 癌症研究 生物信息学 免疫学 生物 遗传学 内科学 哲学 认识论
作者
Hailiang Feng,Wei Chen,Chen Zhang
出处
期刊:Medicine [Wolters Kluwer]
卷期号:102 (47): e35999-e35999 被引量:5
标识
DOI:10.1097/md.0000000000035999
摘要

As a product of glycolysis, lactate contributes to cancer proliferation, immunosuppression, and metastasis via histone lactylation. However, the relationship between cutaneous melanoma (CM) and lactylation-associated genes and lncRNAs has remained unclear. In this study, 4 mechanism learning algorithms and integrated bioinformatic analyses were employed to identify the core lactylation-associated genes and lncRNAs. Subsequently, 2 risk signatures based on the hub lactylation-associated genes and lncRNAs were constructed for CM patients. As a result, CALML5 was identified as a core lactylation-associated gene in CM, and its expression was found to be associated with patients survival and immune infiltration, suggesting its relevance as a potential therapeutic target. Additionally, this study provided clarification on hub CALML5-associated lncRNAs in CM, offering insights into their roles in the disease. Meanwhile, 2 identified risk signatures were both strongly linked to the prognosis and cancer growth of CM, underscoring their potential as valuable prognostic indicators. Furthermore, mechanistic analyses suggested a significant association between the risk signature and the immune microenvironment in CM, highlighting potential immune-related implications in disease progression. In conclusion, we propose that lactylation-associated genes and lncRNAs hold promise as potential targets in CM. Moreover, our findings revealed a significant correlation between lactylation and the immune microenvironment, providing crucial insights for guiding individualized treatment strategies in CM.
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