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浅析甲胎蛋白(AFP)在肝细胞癌发生发展中的作用。

An Insight Into the Role of Alpha-Fetoprotein (AFP) in the Development and Progression of Hepatocellular Carcinoma.

机构信息

Department of Pharmacognosy, Amrita School of Pharmacy, AIMS Health Science Campus, Amrita Vishwa Vidyapeetham, Ponekkara P.O., Kochi, Kerala, India.

Department of Anatomy and Cell Biology, University of Florida, Gainesville, FL, 32610, USA.

出版信息

Mol Biotechnol. 2024 Oct;66(10):2697-2709. doi: 10.1007/s12033-023-00890-0. Epub 2023 Oct 2.

Abstract

Hepatocellular carcinoma (HCC) is the primary malignancy of hepatocytes and the second most common cause of cancer-related mortality across the globe. Despite significant advancements in screening, diagnosis, and treatment modalities for HCC, the mortality-to-incidence ratio remain unacceptably high. A recent study indicates that a minor population of HCCs are AFP negative or express the normal range of AFP levels. Although it is a gold standard and a more reliable biomarker in the advanced stage of HCC and poorly differentiated tumors, it does not serve as a suitable means for screening HCC. AFP plays a significant role in the development and progression of HCC and understanding its role is crucial. By examining the molecular mechanisms involved in AFP-mediated tumorigenesis, we can better understand HCC pathogenesis and identify potential therapeutic targets. This article details the role of alpha-fetoprotein (AFP) in the carcinogenic transformation of hepatocytes. The article also focuses on information about the structure, biosynthesis, and regulation of AFP at the gene level. Additionally, it discusses the immune evasion, metastasis, and control of gene expression that AFP mediates during HCC.

摘要

肝细胞癌 (HCC) 是肝细胞的原发性恶性肿瘤,也是全球癌症相关死亡的第二大主要原因。尽管 HCC 的筛查、诊断和治疗方法有了显著进展,但死亡率与发病率的比例仍然高得不可接受。最近的一项研究表明,一小部分 HCC 患者的 AFP 呈阴性或表达正常范围的 AFP 水平。尽管 AFP 是 HCC 晚期和分化不良肿瘤的金标准和更可靠的生物标志物,但它不适合用于 HCC 的筛查。AFP 在 HCC 的发生和发展中起着重要作用,了解其作用至关重要。通过研究 AFP 介导的肿瘤发生的分子机制,我们可以更好地了解 HCC 的发病机制并确定潜在的治疗靶点。本文详细介绍了甲胎蛋白 (AFP) 在肝细胞癌发生中的作用。本文还重点介绍了 AFP 在基因水平上的结构、生物合成和调控信息。此外,还讨论了 AFP 在 HCC 中介导的免疫逃逸、转移和基因表达控制。

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