Aggressive variants of prostate cancer: underlying mechanisms of neuroendocrine transdifferentiation

转分化 雄激素受体 前列腺癌 背景(考古学) 生物 生物信息学 表观遗传学 神经内分泌分化 癌症研究 癌症 医学 遗传学 细胞 基因 古生物学
作者
Lina Merkens,Verena Sailer,Davor Lessel,Ella Janzen,Sarah Greimeier,Jutta Kirfel,Sven Perner,Klaus Pantel,Stefan Werner,Gunhild von Amsberg
出处
期刊:Journal of Experimental & Clinical Cancer Research [BioMed Central]
卷期号:41 (1): 46-46 被引量:106
标识
DOI:10.1186/s13046-022-02255-y
摘要

Abstract Prostate cancer is a hormone-driven disease and its tumor cell growth highly relies on increased androgen receptor (AR) signaling. Therefore, targeted therapy directed against androgen synthesis or AR activation is broadly used and continually improved. However, a subset of patients eventually progresses to castration-resistant disease. To date, various mechanisms of resistance have been identified including the development of AR-independent aggressive variant prostate cancer based on neuroendocrine transdifferentiation (NED). Here, we review the highly complex processes contributing to NED. Genetic, epigenetic, transcriptional aberrations and posttranscriptional modifications are highlighted and the potential interplay of the different factors is discussed. Background Aggressive variant prostate cancer (AVPC) with traits of neuroendocrine differentiation emerges in a rising number of patients in recent years. Among others, advanced therapies targeting the androgen receptor axis have been considered causative for this development. Cell growth of AVPC often occurs completely independent of the androgen receptor signal transduction pathway and cells have mostly lost the typical cellular features of prostate adenocarcinoma. This complicates both diagnosis and treatment of this very aggressive disease. We believe that a deeper understanding of the complex molecular pathological mechanisms contributing to transdifferentiation will help to improve diagnostic procedures and develop effective treatment strategies. Indeed, in recent years, many scientists have made important contributions to unravel possible causes and mechanisms in the context of neuroendocrine transdifferentiation. However, the complexity of the diverse molecular pathways has not been captured completely, yet. This narrative review comprehensively highlights the individual steps of neuroendocrine transdifferentiation and makes an important contribution in bringing together the results found so far.
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