Department of Neuroscience, Biomedicine and Movement Sciences, University of Verona, 37134, Verona, Italy.
Department of Biochemistry and Molecular Biology, Faculty of Biology, Complutense University, 28040, Madrid, Spain.
Cell Commun Signal. 2024 Jan 12;22(1):36. doi: 10.1186/s12964-023-01462-0.
Prostate cancer, as one of the most prevalent malignancies in males, exhibits an approximate 5-year survival rate of 95% in advanced stages. A myriad of molecular events and mutations, including the accumulation of oncometabolites, underpin the genesis and progression of this cancer type. Despite growing research demonstrating the pivotal role of oncometabolites in supporting various cancers, including prostate cancer, the root causes of their accumulation, especially in the absence of enzymatic mutations, remain elusive. Consequently, identifying a tangible therapeutic target poses a formidable challenge. In this review, we aim to delve deeper into the implications of oncometabolite accumulation in prostate cancer. We center our focus on the consequential epigenetic alterations and impacts on cancer stem cells, with the ultimate goal of outlining novel therapeutic strategies.
前列腺癌是男性最常见的恶性肿瘤之一,晚期的 5 年生存率约为 95%。许多分子事件和突变,包括致癌代谢物的积累,是这种癌症类型发生和发展的基础。尽管越来越多的研究表明,致癌代谢物在支持包括前列腺癌在内的各种癌症方面发挥着关键作用,但它们积累的根本原因,特别是在没有酶突变的情况下,仍然难以捉摸。因此,确定一个切实可行的治疗靶点是一个巨大的挑战。在这篇综述中,我们旨在更深入地探讨致癌代谢物在前列腺癌中的积累所带来的影响。我们的重点是致癌代谢物积累对表观遗传改变和癌症干细胞的影响,最终目的是概述新的治疗策略。