State-of-the-art in transposable element modulation affected by drugs in malignant prostatic cancer cells

IF 3 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Anna Terrazzan, Riccardo Vanini, Pietro Ancona, Nicoletta Bianchi, Cristian Taccioli, Gianluca Aguiari
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引用次数: 0

Abstract

Over recent years, the investigation of transposable elements (TEs) has granted researchers a deeper comprehension of their characteristics and functions, particularly regarding their significance in the mechanisms contributing to cancer development. This manuscript focuses on prostate carcinoma cell lines and offers a comprehensive review intended to scrutinize the associations and interactions between TEs and genes, as well as their response to treatment using various chemical drugs, emphasizing their involvement in cancer progression. We assembled a compendium of articles retrieved from the PubMed database to construct networks demonstrating correlations with genes and pharmaceuticals. In doing so, we linked the transposition of certain TE types to the expression of specific transcripts directly implicated in carcinogenesis. Additionally, we underline that treatment employing different drugs revealed unique patterns of TE reactivation. Our hypothesis gathers the current understanding and guides research toward evidence-based investigations, emphasizing the association between antiviral drugs, chemotherapy, and the reduced expression of TEs in patients affected by prostate cancer.

恶性前列腺癌细胞中受药物影响的转座元件调控的最新进展。
近年来,通过对转座元件(TE)的研究,研究人员对其特性和功能有了更深入的了解,尤其是它们在癌症发展机制中的重要作用。本手稿以前列腺癌细胞系为研究对象,全面回顾了转座元件与基因之间的关联和相互作用,以及它们对各种化学药物治疗的反应,强调了它们在癌症进展中的作用。我们汇集了从 PubMed 数据库中检索到的大量文章,构建了显示基因与药物相关性的网络。在此过程中,我们将某些 TE 类型的转座与直接参与致癌的特定转录本的表达联系起来。此外,我们还强调,使用不同药物进行治疗会发现 TE 重新激活的独特模式。我们的假设收集了当前的认识,并引导研究走向循证调查,强调了抗病毒药物、化疗和前列腺癌患者体内 TEs 表达减少之间的关联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of cellular biochemistry
Journal of cellular biochemistry 生物-生化与分子生物学
CiteScore
9.90
自引率
0.00%
发文量
164
审稿时长
1 months
期刊介绍: The Journal of Cellular Biochemistry publishes descriptions of original research in which complex cellular, pathogenic, clinical, or animal model systems are studied by biochemical, molecular, genetic, epigenetic or quantitative ultrastructural approaches. Submission of papers reporting genomic, proteomic, bioinformatics and systems biology approaches to identify and characterize parameters of biological control in a cellular context are encouraged. The areas covered include, but are not restricted to, conditions, agents, regulatory networks, or differentiation states that influence structure, cell cycle & growth control, structure-function relationships.
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