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侵袭性变异相关肿瘤抑制基因在前列腺癌各阶段新兴的预测和预后作用。

The Emerging Predictive and Prognostic Role of Aggressive-Variant-Associated Tumor Suppressor Genes Across Prostate Cancer Stages.

作者信息

Pedrani Martino, Barizzi Jessica, Salfi Giuseppe, Nepote Alessandro, Testi Irene, Merler Sara, Castelo-Branco Luis, Mestre Ricardo Pereira, Turco Fabio, Tortola Luigi, Theurillat Jean-Philippe, Gillessen Silke, Vogl Ursula

机构信息

Oncology Institute of Southern Switzerland (IOSI), Ente Ospedaliero Cantonale (EOC), 6500 Bellinzona, Switzerland.

Department of Oncology and Hemato-Oncology, Università degli Studi di Milano, 20122 Milan, Italy.

出版信息

Int J Mol Sci. 2025 Jan 1;26(1):318. doi: 10.3390/ijms26010318.

Abstract

Aggressive variant prostate cancer (AVPC) is characterized by a molecular signature involving combined defects in , , and/or (AVPC-TSGs), identifiable through immunohistochemistry or genomic analysis. The reported prevalence of AVPC-TSG alterations varies widely, reflecting differences in assay sensitivity, treatment pressure, and disease stage evolution. Although robust clinical evidence is still emerging, the study of AVPC-TSG alterations in prostate cancer (PCa) is promising. Alterations in , , and , as well as the combined loss of AVPC-TSGs, may have significant implications for prognosis and treatment. These biomarkers might help predict responses to various therapies, including hormonal treatments, cytotoxic agents, radiotherapy, and targeted therapies. Understanding the impact of these molecular alterations in patients with PCa is crucial for personalized management. In this review, we provide a comprehensive overview of the emerging prognostic and predictive roles of AVPC-TSG alterations across PCa stages. Moreover, we discuss the implications of different methods used for detecting AVPC-TSG alterations and summarize factors influencing their prevalence. As our comprehension of the genomic landscape of PCa disease deepens, incorporating genomic profiling into clinical decision making will become increasingly important for improving patient outcomes.

摘要

侵袭性前列腺癌变异型(AVPC)的特征是具有一种分子特征,涉及[具体基因1]、[具体基因2]和/或[具体基因3](AVPC-肿瘤抑制基因)的联合缺陷,可通过免疫组织化学或基因组分析来识别。报道的AVPC-肿瘤抑制基因改变的患病率差异很大,这反映了检测灵敏度、治疗压力和疾病阶段演变的差异。尽管强有力的临床证据仍在不断涌现,但对前列腺癌(PCa)中AVPC-肿瘤抑制基因改变的研究很有前景。[具体基因1]、[具体基因2]和[具体基因3]的改变,以及AVPC-肿瘤抑制基因的联合缺失,可能对预后和治疗具有重要意义。这些生物标志物可能有助于预测对各种疗法的反应,包括激素治疗、细胞毒性药物、放射治疗和靶向治疗。了解这些分子改变对PCa患者的影响对于个性化管理至关重要。在这篇综述中,我们全面概述了AVPC-肿瘤抑制基因改变在PCa各阶段新兴的预后和预测作用。此外,我们讨论了用于检测AVPC-肿瘤抑制基因改变的不同方法的影响,并总结了影响其患病率的因素。随着我们对PCa疾病基因组格局的理解不断深入,将基因组分析纳入临床决策对于改善患者预后将变得越来越重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77bc/11719667/43edcc60576c/ijms-26-00318-g001.jpg

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