甲状腺乳头状癌的高侵袭性:从临床证据到细胞调控网络。

IF 6.1 2区 生物学 Q1 CELL BIOLOGY Cell Death Discovery Pub Date : 2024-08-26 DOI:10.1038/s41420-024-02157-2
Junsi Zhang, Sunwang Xu
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引用次数: 0

摘要

近几十年来,甲状腺癌的全球发病率不断上升。甲状腺乳头状癌(PTC)是最常见的甲状腺癌类型,占所有病例的近 90%。通常情况下,PTC 的预后良好。然而,一些PTC变种表现出更强的侵袭性,这大大增加了术后复发的风险。在过去十年中,PTC 的高转移潜力引起了许多研究人员的关注,这些研究为改进诊断、风险分层和临床方法提供了有用的分子标记。本综述旨在讨论与 PTC 侵袭性相关的流行病学、转移特征、风险因素和分子机制方面的进展。我们详细介绍了上皮细胞向间质转化、癌症代谢重编程、重要信号通路的改变、表观遗传畸变和肿瘤微环境是 PTC 转移的关键驱动因素。要更全面地阐明 PTC 侵袭性背后的发病机制和生物学行为,还需要进一步的研究。
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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High aggressiveness of papillary thyroid cancer: from clinical evidence to regulatory cellular networks.

The global incidence of thyroid cancer has increased over recent decades. Papillary thyroid cancer (PTC) is the most common type of thyroid cancer and accounts for nearly 90% of all cases. Typically, PTC has a good prognosis. However, some PTC variants exhibit more aggressive behaviour, which significantly increases the risk of postoperative recurrence. Over the past decade, the high metastatic potential of PTC has drawn the attention of many researchers and these studies have provided useful molecular markers for improved diagnosis, risk stratification and clinical approaches. The aim of this review is to discuss the progress in epidemiology, metastatic features, risk factors and molecular mechanisms associated with PTC aggressiveness. We present a detailed picture showing that epithelial-to-mesenchymal transition, cancer metabolic reprogramming, alterations in important signalling pathways, epigenetic aberrations and the tumour microenvironment are crucial drivers of PTC metastasis. Further research is needed to more fully elucidate the pathogenesis and biological behaviour underlying the aggressiveness of PTC.

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来源期刊
Cell Death Discovery
Cell Death Discovery Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
8.30
自引率
1.40%
发文量
468
审稿时长
9 weeks
期刊介绍: Cell Death Discovery is a multidisciplinary, international, online-only, open access journal, dedicated to publishing research at the intersection of medicine with biochemistry, pharmacology, immunology, cell biology and cell death, provided it is scientifically sound. The unrestricted access to research findings in Cell Death Discovery will foster a dynamic and highly productive dialogue between basic scientists and clinicians, as well as researchers in industry with a focus on cancer, neurobiology and inflammation research. As an official journal of the Cell Death Differentiation Association (ADMC), Cell Death Discovery will build upon the success of Cell Death & Differentiation and Cell Death & Disease in publishing important peer-reviewed original research, timely reviews and editorial commentary. Cell Death Discovery is committed to increasing the reproducibility of research. To this end, in conjunction with its sister journals Cell Death & Differentiation and Cell Death & Disease, Cell Death Discovery provides a unique forum for scientists as well as clinicians and members of the pharmaceutical and biotechnical industry. It is committed to the rapid publication of high quality original papers that relate to these subjects, together with topical, usually solicited, reviews, editorial correspondence and occasional commentaries on controversial and scientifically informative issues.
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