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前列腺癌生物标志物与探针的进展

Advances in Prostate Cancer Biomarkers and Probes.

作者信息

Li Keyi, Wang Qiao, Tang Xiaoying, Akakuru Ozioma Udochukwu, Li Ruobing, Wang Yan, Zhang Renran, Jiang Zhenqi, Yang Zhuo

机构信息

Department of Endoscope, General Hospital of Northern Theater Command, Shenyang, Liaoning, P. R. China.

School of Medical Technology, Beijing Institute of Technology, Beijing, P. R. China.

出版信息

Cyborg Bionic Syst. 2024 Jun 27;5:0129. doi: 10.34133/cbsystems.0129. eCollection 2024.

Abstract

Prostate cancer is one of the most prevalent malignant tumors in men worldwide, and early diagnosis is essential to improve patient survival. This review provides a comprehensive discussion of recent advances in prostate cancer biomarkers, including molecular, cellular, and exosomal biomarkers. The potential of various biomarkers such as gene fusions (TMPRSS2-ERG), noncoding RNAs (SNHG12), proteins (PSA, PSMA, AR), and circulating tumor cells (CTCs) in the diagnosis, prognosis, and targeted therapies of prostate cancer is emphasized. In addition, this review systematically explores how multi-omics data and artificial intelligence technologies can be used for biomarker discovery and personalized medicine applications. In addition, this review provides insights into the development of specific probes, including fluorescent, electrochemical, and radionuclide probes, for sensitive and accurate detection of prostate cancer biomarkers. In conclusion, this review provides a comprehensive overview of the status and future directions of prostate cancer biomarker research, emphasizing the potential for precision diagnosis and targeted therapy.

摘要

前列腺癌是全球男性中最常见的恶性肿瘤之一,早期诊断对于提高患者生存率至关重要。本综述全面讨论了前列腺癌生物标志物的最新进展,包括分子、细胞和外泌体生物标志物。强调了各种生物标志物如基因融合(TMPRSS2-ERG)、非编码RNA(SNHG12)、蛋白质(PSA、PSMA、AR)和循环肿瘤细胞(CTC)在前列腺癌诊断、预后和靶向治疗中的潜力。此外,本综述系统地探讨了多组学数据和人工智能技术如何用于生物标志物发现和个性化医学应用。此外,本综述还介绍了用于灵敏准确检测前列腺癌生物标志物的特定探针的开发情况,包括荧光、电化学和放射性核素探针。总之,本综述全面概述了前列腺癌生物标志物研究的现状和未来方向,强调了精准诊断和靶向治疗的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ade4/12063729/27e572e062be/cbsystems.0129.fig.002.jpg

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